Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 441024 |
|---|---|
| ensemblid | ENSG00000163738.19 |
| hgncid | 31865 |
| symbol | MTHFD2L |
| name | methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like |
| refseq_nuc | NM_001144978.3 |
| refseq_prot | NP_001138450.1 |
| ensembl_nuc | ENST00000325278.7 |
| ensembl_prot | ENSP00000321984.7 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 74158118 |
| end | 74303099 |
| strand | + |
| ver | v1.2 |
| region | chr4:74158118-74303099 |
| region5000 | chr4:74153118-74308099 |
| regionname0 | MTHFD2L_chr4_74158118_74303099 |
| regionname5000 | MTHFD2L_chr4_74153118_74308099 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 347 | 199 | 74 | 32 | 71 | 2 | 18 | 49 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0002 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1044 | 196 | 72 | 32 | 70 | 2 | 18 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| c0002 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| c0003 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| c0004 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| c0005 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1312 | 105 | 27 | 23 | 43 | 1 | 9 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| t0002 | 0/0 | 1312 | 45 | 28 | 4 | 9 | 0 | 4 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| t0003 | 0/0 | 1312 | 43 | 13 | 5 | 20 | 1 | 4 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| t0004 | 0/0 | 1312 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| t0005 | 0/0 | 1312 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| t0006 | 0/0 | 1312 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| t0007 | 0/0 | 1312 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1044 | 196 | 72 | 32 | 70 | 2 | 18 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0003 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0004 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0005 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0002c0002 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2355 | 102 | 26 | 23 | 41 | 1 | 9 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0001t0002 | 0/0 | 2355 | 45 | 28 | 4 | 9 | 0 | 4 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0001t0003 | 0/0 | 2355 | 43 | 13 | 5 | 20 | 1 | 4 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0001t0004 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0001t0005 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0001t0006 | 0/0 | 2355 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0001t0007 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0003t0004 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0004t0001 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0001c0005t0001 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| a0002c0002t0001 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | copy fasta | chr4 | 74153118 | 74308099 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0111 | EUR | FIN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CDX | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ESN | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | BEB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0103 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18522 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18975 | hp1 | a0001 | c0005 | t0001 | g0099 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | USA | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | USA | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | LWK | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0069 | REF | REF | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0191 | REF | REF | MTHFD2L_chr4_74153118_74308099 | MTHFD2L | chr4 | 74153118 | 74308099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:74201285
|
T | A | 1 | a0002 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.627T>A | p.Asn209Lys | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/8 | 648/2355 | 627/1044 | 209/347 | chr4 | 74201285 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:74158171
|
C | G | 1 | a0001c0005 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.33C>G | p.Leu11Leu | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/8 | 54/2355 | 33/1044 | 11/347 | chr4 | 74158171 | ||
| chr4:74174533
|
C | T | 1 | a0001c0004 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.171C>T | p.Thr57Thr | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/8 | 192/2355 | 171/1044 | 57/347 | chr4 | 74174533 | ||
| chr4:74281501
|
C | T | 1 | a0001c0003 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.882C>T | p.His294His | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/8 | 903/2355 | 882/1044 | 294/347 | chr4 | 74281501 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:74301815
|
A | G | 2 | a0001c0001t0004a0001c0003t0004 | 3 | HG02615.hp2 HG03516.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 6 | chr4 | 74301815 | |||||
| chr4:74302006
|
C | T | 1 | a0001c0001t0007 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 197 | chr4 | 74302006 | |||||
| chr4:74302056
|
A | G | 1 | a0001c0001t0006 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 247 | chr4 | 74302056 | |||||
| chr4:74302458
|
C | T | 2 | a0001c0001t0003a0001c0001t0006 | 44 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*649C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 649 | chr4 | 74302458 | |||||
| chr4:74302854
|
T | C | 2 | a0001c0001t0002a0001c0001t0007 | 46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1045T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 1045 | chr4 | 74302854 | |||||
| chr4:74303068
|
A | G | 5 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(2): Show | 92 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1259A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 8/8 | 1259 | chr4 | 74303068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:74158577
|
A | G | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.143+296A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158577 | ||||||
| chr4:74158626
|
T | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+345T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158626 | ||||||
| chr4:74158748
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.143+467T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158748 | ||||||
| chr4:74158755
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.143+474A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158755 | ||||||
| chr4:74158805
|
C | T | 5 | a0001c0001t0001g0193a0001c0001t0002g0194a0001c0001t0002g0195others(2): Show | 5 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.143+524C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158805 | ||||||
| chr4:74158906
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.143+625G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74158906 | ||||||
| chr4:74159244
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.143+963A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159244 | ||||||
| chr4:74159269
|
A | G | 7 | a0001c0001t0002g0177a0001c0001t0003g0171a0001c0001t0003g0172others(4): Show | 7 | HG01109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.143+988A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159269 | ||||||
| chr4:74159411
|
A | G | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA18968.hp2 NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.143+1130A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159411 | ||||||
| chr4:74159497
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143+1216G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159497 | ||||||
| chr4:74159642
|
G | T | 5 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+1361G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159642 | ||||||
| chr4:74159652
|
C | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.143+1371C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159652 | ||||||
| chr4:74159676
|
C | G | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.143+1395C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159676 | ||||||
| chr4:74159767
|
C | G | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.143+1486C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159767 | ||||||
| chr4:74159880
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.143+1599G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159880 | ||||||
| chr4:74159917
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.143+1636G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74159917 | ||||||
| chr4:74160170
|
C | G | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.143+1889C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160170 | ||||||
| chr4:74160192
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.143+1911G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160192 | ||||||
| chr4:74160351
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+2070G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160351 | ||||||
| chr4:74160814
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010 | 3 | HG01070.hp2 HG01071.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.143+2533G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74160814 | ||||||
| chr4:74161170
|
T | A | 2 | a0001c0001t0003g0011a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.143+2889T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161170 | ||||||
| chr4:74161241
|
C | T | 14 | a0001c0001t0001g0193a0001c0001t0002g0008a0001c0001t0002g0009others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.143+2960C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161241 | ||||||
| chr4:74161297
|
A | C | 3 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143+3016A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161297 | ||||||
| chr4:74161506
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.143+3225T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161506 | ||||||
| chr4:74161532
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.143+3251G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74161532 | ||||||
| chr4:74162216
|
CTG | C | 2 | a0001c0001t0003g0011a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.143+3939_143+3940d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74162216 | |||||
| chr4:74162370
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.143+4089A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74162370 | ||||||
| chr4:74162475
|
G | A | 1 | a0001c0001t0003g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.143+4194G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74162475 | ||||||
| chr4:74162505
|
CT | C | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(67): Show | 70 | HG00408.hp1 HG00438.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.143+4244delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74162505 | |||||
| chr4:74162678
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.143+4397C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74162678 | ||||||
| chr4:74163075
|
AT | A | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+4805delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74163075 | |||||
| chr4:74163075
|
ATT | A | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(77): Show | 80 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(77): Show |
intron_variant | MODIFIER | c.143+4804_143+4805d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74163075 | |||||
| chr4:74163075
|
ATTT | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0061others(102): Show | 106 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.143+4803_143+4805d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74163075 | |||||
| chr4:74163098
|
G | A | 3 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143+4817G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163098 | ||||||
| chr4:74163154
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.143+4873G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163154 | ||||||
| chr4:74163254
|
T | A | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.143+4973T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163254 | ||||||
| chr4:74163317
|
A | G | 1 | a0001c0001t0003g0059 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143+5036A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163317 | ||||||
| chr4:74163378
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.143+5097G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163378 | ||||||
| chr4:74163411
|
C | A | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.143+5130C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163411 | ||||||
| chr4:74163744
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.143+5463T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163744 | ||||||
| chr4:74163842
|
A | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.143+5561A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163842 | ||||||
| chr4:74163897
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0061others(102): Show | 106 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.143+5616G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74163897 | ||||||
| chr4:74164065
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 7 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.143+5784C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164065 | ||||||
| chr4:74164092
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.143+5811C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164092 | ||||||
| chr4:74164122
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+5841C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164122 | ||||||
| chr4:74164166
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+5885A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164166 | ||||||
| chr4:74164167
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+5886T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164167 | ||||||
| chr4:74164171
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.143+5890T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164171 | ||||||
| chr4:74164331
|
T | A | 3 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0003g0167 | 3 | HG01243.hp2 HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.143+6050T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164331 | ||||||
| chr4:74164802
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.143+6521C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164802 | ||||||
| chr4:74164914
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.143+6633A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74164914 | ||||||
| chr4:74165077
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.143+6796G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165077 | ||||||
| chr4:74165360
|
CTTTG | C | 12 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG00408.hp1 HG00438.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.143+7083_143+7086d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74165360 | |||||
| chr4:74165364
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.143+7083G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165364 | ||||||
| chr4:74165443
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143+7162C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165443 | ||||||
| chr4:74165494
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.143+7213A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165494 | ||||||
| chr4:74165524
|
A | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 72 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.143+7243A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165524 | ||||||
| chr4:74165546
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.143+7265C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165546 | ||||||
| chr4:74165784
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.143+7503A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74165784 | ||||||
| chr4:74165951
|
ATAGTT | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 72 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.143+7673_143+7677d others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74165951 | |||||
| chr4:74166077
|
A | C | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+7796A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166077 | ||||||
| chr4:74166412
|
A | G | 1 | a0001c0001t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.144-8094A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166412 | ||||||
| chr4:74166443
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.144-8063A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166443 | ||||||
| chr4:74166679
|
A | G | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-7827A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166679 | ||||||
| chr4:74166852
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.144-7654C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166852 | ||||||
| chr4:74166969
|
G | C | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-7537G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74166969 | ||||||
| chr4:74167272
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.144-7234T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167272 | ||||||
| chr4:74167398
|
C | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.144-7108C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167398 | ||||||
| chr4:74167636
|
G | T | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-6870G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167636 | ||||||
| chr4:74167911
|
T | C | 108 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.144-6595T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74167911 | ||||||
| chr4:74168006
|
C | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-6500C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168006 | ||||||
| chr4:74168029
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.144-6477C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168029 | ||||||
| chr4:74168034
|
GT | G | 18 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-6469delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74168034 | |||||
| chr4:74168068
|
C | G | 108 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0029others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.144-6438C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168068 | ||||||
| chr4:74168101
|
C | T | 2 | a0001c0001t0002g0165a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.144-6405C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168101 | ||||||
| chr4:74168161
|
T | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-6345T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168161 | ||||||
| chr4:74168421
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.144-6085G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168421 | ||||||
| chr4:74168952
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0164 | 2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.144-5554A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74168952 | ||||||
| chr4:74169341
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.144-5165G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169341 | ||||||
| chr4:74169382
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0147 | 3 | NA18945.hp2 NA18964.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.144-5124C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169382 | ||||||
| chr4:74169435
|
T | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-5071T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169435 | ||||||
| chr4:74169464
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(112): Show | 116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.144-5042C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169464 | ||||||
| chr4:74169497
|
G | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-5009G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169497 | ||||||
| chr4:74169572
|
A | C | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.144-4934A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169572 | ||||||
| chr4:74169654
|
A | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0053others(1): Show | 4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-4852A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169654 | ||||||
| chr4:74169659
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.144-4847C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169659 | ||||||
| chr4:74169808
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.144-4698A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169808 | ||||||
| chr4:74169963
|
A | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-4543A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74169963 | ||||||
| chr4:74170009
|
C | T | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.144-4497C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170009 | ||||||
| chr4:74170072
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005 | 3 | HG01884.hp2 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.144-4434A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170072 | ||||||
| chr4:74170327
|
A | G | 100 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.144-4179A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170327 | ||||||
| chr4:74170329
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.144-4177T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170329 | ||||||
| chr4:74170341
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(112): Show | 116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.144-4165C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170341 | ||||||
| chr4:74170374
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.144-4132T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170374 | ||||||
| chr4:74170688
|
G | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-3818G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170688 | ||||||
| chr4:74170742
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.144-3764C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170742 | ||||||
| chr4:74170816
|
A | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-3690A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170816 | ||||||
| chr4:74170965
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.144-3541T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170965 | ||||||
| chr4:74170990
|
A | G | 1 | a0001c0001t0003g0153 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.144-3516A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74170990 | ||||||
| chr4:74171004
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.144-3502G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171004 | ||||||
| chr4:74171026
|
C | G | 1 | a0001c0001t0002g0002 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.144-3480C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171026 | ||||||
| chr4:74171243
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02145.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.144-3263G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171243 | ||||||
| chr4:74171263
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.144-3243G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171263 | ||||||
| chr4:74171449
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.144-3057G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171449 | ||||||
| chr4:74171667
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 7 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.144-2839G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171667 | ||||||
| chr4:74171798
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-2708C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171798 | ||||||
| chr4:74171798
|
C | G | 112 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.144-2708C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171798 | ||||||
| chr4:74171909
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.144-2597G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74171909 | ||||||
| chr4:74171937
|
TAAAC | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.144-2565_144-2562d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74171937 | |||||
| chr4:74172129
|
G | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.144-2377G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172129 | ||||||
| chr4:74172150
|
G | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.144-2356G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172150 | ||||||
| chr4:74172443
|
TAATG | T | 14 | a0001c0001t0001g0144a0001c0001t0001g0193a0001c0001t0002g0137others(11): Show | 14 | HG01496.hp2 HG02258.hp2 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-2060_144-2057d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 74172443 | |||||
| chr4:74172475
|
T | C | 2 | a0001c0001t0002g0163a0001c0001t0002g0164 | 2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.144-2031T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172475 | ||||||
| chr4:74172524
|
G | T | 1 | a0001c0001t0003g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.144-1982G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172524 | ||||||
| chr4:74172746
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.144-1760T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74172746 | ||||||
| chr4:74173010
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.144-1496G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173010 | ||||||
| chr4:74173092
|
T | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.144-1414T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173092 | ||||||
| chr4:74173186
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.144-1320A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173186 | ||||||
| chr4:74173227
|
G | A | 8 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.144-1279G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173227 | ||||||
| chr4:74173326
|
C | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-1180C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173326 | ||||||
| chr4:74173562
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.144-944A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173562 | ||||||
| chr4:74173722
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-784A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173722 | ||||||
| chr4:74173742
|
A | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.144-764A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173742 | ||||||
| chr4:74173918
|
G | A | 18 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.144-588G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173918 | ||||||
| chr4:74173933
|
T | C | 1 | a0001c0001t0003g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.144-573T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173933 | ||||||
| chr4:74173990
|
A | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.144-516A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74173990 | ||||||
| chr4:74174266
|
A | T | 6 | a0001c0001t0001g0193a0001c0001t0002g0137a0001c0001t0002g0194others(3): Show | 6 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-240A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 1/7 | chr4 | 74174266 | ||||||
| chr4:74174716
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.328+26A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74174716 | ||||||
| chr4:74174750
|
T | C | 1 | a0001c0001t0003g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.328+60T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74174750 | ||||||
| chr4:74174979
|
G | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.328+289G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74174979 | ||||||
| chr4:74175012
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-269T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175012 | ||||||
| chr4:74175061
|
T | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.329-220T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175061 | ||||||
| chr4:74175146
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.329-135A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175146 | ||||||
| chr4:74175227
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.329-54T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 2/7 | chr4 | 74175227 | ||||||
| chr4:74175646
|
T | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.451+243T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74175646 | ||||||
| chr4:74175743
|
C | T | 18 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.451+340C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74175743 | ||||||
| chr4:74176232
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.451+829A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176232 | ||||||
| chr4:74176336
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.451+933T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176336 | ||||||
| chr4:74176352
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.451+949C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176352 | ||||||
| chr4:74176484
|
T | C | 2 | a0001c0001t0001g0075a0002c0002t0001g0076 | 2 | NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.451+1081T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176484 | ||||||
| chr4:74176554
|
G | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+1151G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176554 | ||||||
| chr4:74176867
|
G | C | 61 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.451+1464G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74176867 | ||||||
| chr4:74177372
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.451+1969G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177372 | ||||||
| chr4:74177382
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+1979C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177382 | ||||||
| chr4:74177404
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0002g0131 | 2 | HG02015.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.451+2001A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177404 | ||||||
| chr4:74177427
|
A | G | 1 | a0001c0001t0003g0130 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.451+2024A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177427 | ||||||
| chr4:74177518
|
A | G | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+2115A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177518 | ||||||
| chr4:74177643
|
G | A | 34 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(31): Show | 34 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.451+2240G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177643 | ||||||
| chr4:74177661
|
T | C | 45 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(42): Show | 45 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.451+2258T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177661 | ||||||
| chr4:74177809
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0007g0055 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.451+2406C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177809 | ||||||
| chr4:74177910
|
A | G | 6 | a0001c0001t0001g0193a0001c0001t0002g0137a0001c0001t0002g0194others(3): Show | 6 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+2507A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74177910 | ||||||
| chr4:74178058
|
CAT | C | 102 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(99): Show | 102 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.451+2657_451+2658d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74178058 | |||||
| chr4:74178713
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.451+3310A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178713 | ||||||
| chr4:74178871
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.451+3468A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178871 | ||||||
| chr4:74178894
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.451+3491G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178894 | ||||||
| chr4:74178941
|
C | G | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.451+3538C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178941 | ||||||
| chr4:74178972
|
G | A | 43 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(40): Show | 43 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.451+3569G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74178972 | ||||||
| chr4:74179143
|
G | A | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.451+3740G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179143 | ||||||
| chr4:74179543
|
G | T | 2 | a0001c0001t0002g0019a0001c0001t0002g0050 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.451+4140G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179543 | ||||||
| chr4:74179588
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+4185C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179588 | ||||||
| chr4:74179645
|
CT | C | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+4246delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74179645 | |||||
| chr4:74179734
|
C | G | 1 | a0001c0001t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.451+4331C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179734 | ||||||
| chr4:74179950
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+4547C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74179950 | ||||||
| chr4:74180109
|
G | A | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+4706G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180109 | ||||||
| chr4:74180217
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+4814A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180217 | ||||||
| chr4:74180296
|
A | G | 6 | a0001c0001t0001g0193a0001c0001t0002g0137a0001c0001t0002g0194others(3): Show | 6 | HG03704.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+4893A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180296 | ||||||
| chr4:74180354
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.451+4951C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180354 | ||||||
| chr4:74180500
|
G | C | 2 | a0001c0001t0003g0041a0001c0001t0003g0058 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.451+5097G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180500 | ||||||
| chr4:74180593
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.451+5190A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180593 | ||||||
| chr4:74180620
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.451+5217T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180620 | ||||||
| chr4:74180655
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+5252A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180655 | ||||||
| chr4:74180748
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.451+5345C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180748 | ||||||
| chr4:74180904
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.451+5501T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180904 | ||||||
| chr4:74180925
|
A | T | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+5522A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180925 | ||||||
| chr4:74180930
|
A | T | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5527A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180930 | ||||||
| chr4:74180931
|
T | A | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5528T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74180931 | ||||||
| chr4:74181036
|
A | G | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+5633A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181036 | ||||||
| chr4:74181087
|
A | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+5684A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181087 | ||||||
| chr4:74181149
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0003g0148others(1): Show | 4 | HG00597.hp1 HG00621.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+5746T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181149 | ||||||
| chr4:74181403
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.451+6000C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181403 | ||||||
| chr4:74181414
|
A | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+6011A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181414 | ||||||
| chr4:74181434
|
G | A | 2 | a0001c0001t0003g0041a0001c0001t0003g0058 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.451+6031G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181434 | ||||||
| chr4:74181527
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+6124C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181527 | ||||||
| chr4:74181659
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.451+6256T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74181659 | ||||||
| chr4:74182132
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+6729C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182132 | ||||||
| chr4:74182138
|
G | A | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+6735G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182138 | ||||||
| chr4:74182311
|
C | G | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+6908C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182311 | ||||||
| chr4:74182471
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.451+7068T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182471 | ||||||
| chr4:74182561
|
C | A | 3 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA18968.hp2 NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.451+7158C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182561 | ||||||
| chr4:74182675
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0002g0164 | 2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451+7272C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182675 | ||||||
| chr4:74182719
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.451+7316G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182719 | ||||||
| chr4:74182738
|
G | A | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+7335G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182738 | ||||||
| chr4:74182774
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.451+7371A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74182774 | ||||||
| chr4:74183253
|
T | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+7850T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183253 | ||||||
| chr4:74183385
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.451+7982C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183385 | ||||||
| chr4:74183386
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+7983G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183386 | ||||||
| chr4:74183415
|
G | C | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+8012G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183415 | ||||||
| chr4:74183526
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.451+8123C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183526 | ||||||
| chr4:74183812
|
GTTCTTA | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.451+8418_451+8423d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74183812 | |||||
| chr4:74183962
|
C | T | 3 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.451+8559C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74183962 | ||||||
| chr4:74184046
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.451+8643C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184046 | ||||||
| chr4:74184296
|
A | C | 22 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(19): Show | 22 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.451+8893A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184296 | ||||||
| chr4:74184308
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.451+8905G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184308 | ||||||
| chr4:74184966
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.451+9563G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74184966 | ||||||
| chr4:74185151
|
C | CA | 32 | a0001c0001t0001g0029a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00438.hp1 HG00438.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.451+9776dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAA | 7 | a0001c0001t0001g0100a0001c0001t0001g0156a0001c0001t0002g0002others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+9775_451+9776d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAA | 16 | a0001c0001t0001g0048a0001c0001t0002g0050a0001c0001t0002g0154others(13): Show | 16 | HG02040.hp2 HG02165.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+9773_451+9776d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAA | 15 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0049others(12): Show | 15 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+9772_451+9776d others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAAA | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0043others(4): Show | 7 | HG01169.hp1 HG01891.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+9771_451+9776d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+9768_451+9776d others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0197others(1): Show | 4 | HG01243.hp2 HG03486.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+9767_451+9776d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0163a0001c0001t0003g0026a0001c0001t0005g0141 | 3 | HG03486.hp1 HG04184.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451+9766_451+9776d others(13): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+9765_451+9776d others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185151
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451+9763_451+9776d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185151 | |||||
| chr4:74185180
|
T | A | 57 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 57 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.451+9777T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185180 | ||||||
| chr4:74185543
|
A | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+10140A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185543 | ||||||
| chr4:74185585
|
T | C | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+10182T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185585 | ||||||
| chr4:74185673
|
TAAATG | T | 3 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.451+10276_451+1028 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74185673 | |||||
| chr4:74185898
|
C | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0106others(2): Show | 5 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+10495C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74185898 | ||||||
| chr4:74186104
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.451+10701A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186104 | ||||||
| chr4:74186142
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.451+10739A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186142 | ||||||
| chr4:74186438
|
G | GA | 19 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0098others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+11056dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | |||||
| chr4:74186438
|
G | GAA | 90 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0062others(87): Show | 90 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.451+11055_451+1105 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | |||||
| chr4:74186438
|
G | GAAA | 21 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.451+11054_451+1105 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | |||||
| chr4:74186438
|
GA | G | 41 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(38): Show | 41 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.451+11056delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | |||||
| chr4:74186438
|
GAAAA | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+11053_451+1105 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74186438 | |||||
| chr4:74186457
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+11054A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186457 | ||||||
| chr4:74186615
|
T | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.451+11212T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186615 | ||||||
| chr4:74186632
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.451+11229A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186632 | ||||||
| chr4:74186771
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+11368A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186771 | ||||||
| chr4:74186875
|
A | G | 100 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.451+11472A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186875 | ||||||
| chr4:74186920
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.451+11517C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186920 | ||||||
| chr4:74186961
|
T | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.451+11558T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74186961 | ||||||
| chr4:74187112
|
C | G | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.451+11709C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187112 | ||||||
| chr4:74187253
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0003g0138 | 2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.451+11850C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187253 | ||||||
| chr4:74187288
|
G | A | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.451+11885G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187288 | ||||||
| chr4:74187312
|
C | A | 1 | a0001c0001t0003g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.451+11909C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187312 | ||||||
| chr4:74187396
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.451+11993T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187396 | ||||||
| chr4:74187432
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.451+12029G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187432 | ||||||
| chr4:74187707
|
G | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.452-12087G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187707 | ||||||
| chr4:74187733
|
T | TAC | 24 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0068others(21): Show | 24 | HG00280.hp1 HG01123.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-12024_452-1202 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | |||||
| chr4:74187733
|
T | TACAC | 10 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(7): Show | 11 | HG01891.hp2 HG02083.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.452-12026_452-1202 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | |||||
| chr4:74187733
|
TAC | T | 15 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.452-12024_452-1202 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | |||||
| chr4:74187733
|
TACAC | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG01109.hp2 HG01123.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.452-12026_452-1202 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | |||||
| chr4:74187733
|
TACACAC | T | 43 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(40): Show | 43 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.452-12028_452-1202 others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | |||||
| chr4:74187733
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0065a0001c0001t0002g0066a0001c0001t0002g0155 | 3 | HG02965.hp1 HG03041.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.452-12030_452-1202 others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187733 | |||||
| chr4:74187786
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.452-12008T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187786 | ||||||
| chr4:74187800
|
T | TAC | 14 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0002g0008others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-11960_452-1195 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACAC | 2 | a0001c0001t0002g0155a0001c0001t0003g0060 | 2 | HG01496.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.452-11962_452-1195 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACAC | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-11964_452-1195 others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(1): Show |
8 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG01123.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-11966_452-1195 others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(3): Show |
5 | a0001c0001t0001g0042a0001c0001t0002g0177a0001c0001t0003g0174others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-11968_452-1195 others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(5): Show |
10 | a0001c0001t0001g0015a0001c0001t0001g0193a0001c0001t0002g0050others(7): Show | 10 | HG02647.hp2 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-11970_452-1195 others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0051a0001c0001t0002g0154a0001c0001t0003g0041others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-11972_452-1195 others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(9): Show |
6 | a0001c0001t0002g0137a0001c0001t0002g0194a0001c0001t0003g0059others(3): Show | 6 | HG02129.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-11974_452-1195 others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(11): Show |
3 | a0001c0001t0001g0048a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | NA18973.hp1 NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.452-11976_452-1195 others(22): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(13): Show |
5 | a0001c0001t0001g0049a0001c0001t0002g0045a0001c0001t0003g0038others(2): Show | 5 | HG02040.hp2 HG03239.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-11978_452-1195 others(24): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(15): Show |
3 | a0001c0001t0003g0036a0001c0001t0003g0046a0001c0003t0004g0047 | 3 | HG02165.hp1 NA18522.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.452-11980_452-1195 others(26): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(17): Show |
4 | a0001c0001t0001g0044a0001c0001t0003g0034a0001c0001t0003g0035others(1): Show | 4 | HG01106.hp2 HG02735.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-11982_452-1195 others(28): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(19): Show |
2 | a0001c0001t0001g0043a0001c0001t0003g0037 | 2 | NA18994.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.452-11984_452-1195 others(30): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(21): Show |
1 | a0001c0001t0003g0028 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.452-11986_452-1195 others(32): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
T | TACACACA others(23): Show |
1 | a0001c0001t0003g0027 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.452-11988_452-1195 others(34): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0002g0002others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-11968_452-1195 others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187800
|
TACACACA others(5): Show |
T | 110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(107): Show | 111 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.452-11970_452-1195 others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74187800 | |||||
| chr4:74187850
|
C | G | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.452-11944C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187850 | ||||||
| chr4:74187888
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.452-11906T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74187888 | ||||||
| chr4:74188122
|
CTG | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.452-11669_452-1166 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188122 | |||||
| chr4:74188172
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.452-11622C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188172 | ||||||
| chr4:74188419
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.452-11375T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188419 | ||||||
| chr4:74188488
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0002g0066 | 2 | HG03041.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.452-11306C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188488 | ||||||
| chr4:74188517
|
T | C | 61 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-11277T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188517 | ||||||
| chr4:74188678
|
GTA | G | 60 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(57): Show | 60 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.452-11104_452-1110 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188678 | |||||
| chr4:74188680
|
A | ATATATAT others(133): Show |
1 | a0001c0001t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.452-11105_452-1110 others(144): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188680 | |||||
| chr4:74188682
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.452-11103_452-1110 others(40): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188682 | |||||
| chr4:74188682
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.452-11105_452-1110 others(38): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188682 | |||||
| chr4:74188698
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0136a0001c0001t0002g0045 | 3 | HG01071.hp1 NA18954.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.452-11096G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188698 | ||||||
| chr4:74188698
|
G | GCATATGT others(27): Show |
106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(103): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.452-11069_452-1106 others(38): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188698 | |||||
| chr4:74188716
|
GTATATAT others(33): Show |
G | 7 | a0001c0001t0001g0156a0001c0001t0002g0002a0001c0001t0002g0003others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-11068_452-1102 others(44): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188716 | |||||
| chr4:74188728
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.452-11066G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188728 | ||||||
| chr4:74188735
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.452-11059C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188735 | ||||||
| chr4:74188740
|
GTA | G | 6 | a0001c0001t0001g0151a0001c0001t0002g0045a0001c0001t0002g0157others(3): Show | 6 | HG02486.hp1 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-11044_452-1104 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188740 | |||||
| chr4:74188742
|
A | ATATATAT others(135): Show |
4 | a0001c0001t0003g0034a0001c0001t0003g0036a0001c0001t0003g0037others(1): Show | 4 | NA18973.hp1 NA18991.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(146): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(27): Show |
18 | a0001c0001t0001g0180a0001c0001t0001g0188a0001c0001t0002g0008others(15): Show | 18 | HG01070.hp2 HG01071.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(38): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(135): Show |
1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.452-11045_452-1104 others(146): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(133): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(144): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(169): Show |
1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.452-11045_452-1104 others(180): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(61): Show |
2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-11045_452-1104 others(72): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(133): Show |
38 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(144): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(169): Show |
7 | a0001c0001t0001g0144a0001c0001t0002g0142a0001c0001t0002g0143others(4): Show | 7 | HG02258.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-11045_452-1104 others(180): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(131): Show |
2 | a0001c0001t0003g0171a0001c0001t0003g0172 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.452-11045_452-1104 others(142): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATATAT others(167): Show |
1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.452-11045_452-1104 others(178): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188742
|
A | ATATGGGT others(23): Show |
1 | a0001c0001t0001g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.452-11049_452-1104 others(34): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188742 | |||||
| chr4:74188750
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(100): Show | 104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.452-11044A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188750 | ||||||
| chr4:74188751
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(100): Show | 104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.452-11043T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188751 | ||||||
| chr4:74188753
|
G | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(100): Show | 104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.452-11041G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188753 | ||||||
| chr4:74188754
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(100): Show | 104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.452-11040G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188754 | ||||||
| chr4:74188778
|
GTA | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.452-11006_452-1100 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188778 | |||||
| chr4:74188792
|
GTA | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-10992_452-1099 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74188792 | |||||
| chr4:74188822
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.452-10972A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188822 | ||||||
| chr4:74188875
|
C | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.452-10919C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74188875 | ||||||
| chr4:74189030
|
C | T | 61 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-10764C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189030 | ||||||
| chr4:74189441
|
G | A | 2 | a0001c0001t0003g0101a0001c0005t0001g0099 | 2 | NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.452-10353G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189441 | ||||||
| chr4:74189485
|
C | CCTTTTT | 5 | a0001c0001t0001g0049a0001c0001t0003g0046a0001c0001t0003g0054others(2): Show | 5 | HG02165.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
C | CCTTTTTT | 25 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 25 | HG01099.hp2 HG01106.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
C | CCTTTTTT others(1): Show |
15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0042others(12): Show | 15 | HG01109.hp2 HG01891.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
C | CCTTTTTT others(3): Show |
2 | a0001c0001t0002g0164a0001c0001t0003g0026 | 2 | HG01243.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.452-10309_452-1030 others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
C | CCTTTTTT others(4): Show |
9 | a0001c0001t0001g0144a0001c0001t0002g0137a0001c0001t0002g0142others(6): Show | 9 | HG02258.hp2 HG03041.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-10309_452-1030 others(15): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
C | CCTTTTTT others(5): Show |
3 | a0001c0001t0001g0193a0001c0001t0002g0145a0001c0001t0002g0194 | 3 | HG03471.hp2 HG03704.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452-10309_452-1030 others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
C | CCTTTTTT others(6): Show |
1 | a0001c0001t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-10309_452-1030 others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189485 | ||||||
| chr4:74189485
|
CT | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-10284delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | |||||
| chr4:74189485
|
CTT | C | 12 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0124others(9): Show | 12 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-10285_452-1028 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | |||||
| chr4:74189485
|
CTTT | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(88): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.452-10286_452-1028 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | |||||
| chr4:74189485
|
CTTTT | C | 15 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0085others(12): Show | 15 | HG01070.hp1 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-10287_452-1028 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | |||||
| chr4:74189485
|
CTTTTT | C | 8 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0018others(5): Show | 8 | HG01071.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-10288_452-1028 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74189485 | |||||
| chr4:74189487
|
T | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-10307T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189487 | ||||||
| chr4:74189488
|
T | C | 12 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0124others(9): Show | 12 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-10306T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189488 | ||||||
| chr4:74189489
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(88): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.452-10305T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189489 | ||||||
| chr4:74189490
|
T | C | 15 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0085others(12): Show | 15 | HG01070.hp1 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-10304T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189490 | ||||||
| chr4:74189491
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0018others(5): Show | 8 | HG01071.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-10303T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189491 | ||||||
| chr4:74189492
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.452-10302T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189492 | ||||||
| chr4:74189691
|
A | G | 1 | a0001c0001t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.452-10103A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189691 | ||||||
| chr4:74189754
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.452-10040T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189754 | ||||||
| chr4:74189768
|
A | G | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.452-10026A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189768 | ||||||
| chr4:74189816
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.452-9978T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74189816 | ||||||
| chr4:74190112
|
A | G | 1 | a0001c0001t0002g0169 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.452-9682A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190112 | ||||||
| chr4:74190174
|
C | CT | 3 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG02486.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.452-9619dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74190174 | |||||
| chr4:74190275
|
T | C | 64 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.452-9519T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190275 | ||||||
| chr4:74190373
|
G | A | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-9421G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190373 | ||||||
| chr4:74190499
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0002g0197 | 2 | HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.452-9295C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190499 | ||||||
| chr4:74190614
|
C | T | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-9180C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190614 | ||||||
| chr4:74190932
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.452-8862G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74190932 | ||||||
| chr4:74191146
|
C | T | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-8648C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191146 | ||||||
| chr4:74191214
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.452-8580T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191214 | ||||||
| chr4:74191283
|
T | C | 9 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.452-8511T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191283 | ||||||
| chr4:74191363
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.452-8431C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191363 | ||||||
| chr4:74191364
|
G | GT | 39 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(36): Show | 39 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.452-8419dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74191364 | |||||
| chr4:74191379
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-8415G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191379 | ||||||
| chr4:74191388
|
G | T | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-8406G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191388 | ||||||
| chr4:74191540
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.452-8254T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191540 | ||||||
| chr4:74191581
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 197 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.452-8213T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191581 | ||||||
| chr4:74191660
|
C | T | 19 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-8134C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191660 | ||||||
| chr4:74191718
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0003g0192 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.452-8076T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74191718 | ||||||
| chr4:74192035
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.452-7759A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192035 | ||||||
| chr4:74192095
|
T | G | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.452-7699T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192095 | ||||||
| chr4:74192174
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.452-7620C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192174 | ||||||
| chr4:74192249
|
C | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-7545C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192249 | ||||||
| chr4:74192254
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-7540C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192254 | ||||||
| chr4:74192321
|
T | C | 20 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.452-7473T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192321 | ||||||
| chr4:74192362
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.452-7432A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192362 | ||||||
| chr4:74192521
|
T | G | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-7273T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192521 | ||||||
| chr4:74192633
|
C | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(125): Show | 129 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.452-7161C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192633 | ||||||
| chr4:74192719
|
A | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.452-7075A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192719 | ||||||
| chr4:74192790
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.452-7004A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74192790 | ||||||
| chr4:74193066
|
T | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.452-6728T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193066 | ||||||
| chr4:74193115
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-6679T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193115 | ||||||
| chr4:74193223
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0110a0001c0001t0003g0192 | 3 | HG01169.hp2 HG03579.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.452-6571C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193223 | ||||||
| chr4:74193240
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.452-6554G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193240 | ||||||
| chr4:74193314
|
TTGTC | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.452-6476_452-6473d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74193314 | |||||
| chr4:74193370
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.452-6424T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193370 | ||||||
| chr4:74193597
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0002g0159a0001c0001t0002g0163others(1): Show | 4 | HG01243.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-6197T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193597 | ||||||
| chr4:74193623
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.452-6171T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193623 | ||||||
| chr4:74193776
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.452-6018T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193776 | ||||||
| chr4:74193789
|
T | G | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-6005T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193789 | ||||||
| chr4:74193877
|
C | A | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.452-5917C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193877 | ||||||
| chr4:74193879
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.452-5915A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193879 | ||||||
| chr4:74193935
|
G | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 191 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.452-5859G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193935 | ||||||
| chr4:74193976
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.452-5818T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74193976 | ||||||
| chr4:74194385
|
A | AT | 10 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0189others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-5400dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74194385 | |||||
| chr4:74194418
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0065others(20): Show | 24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-5376A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194418 | ||||||
| chr4:74194708
|
G | C | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.452-5086G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194708 | ||||||
| chr4:74194850
|
C | CT | 40 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.452-4937dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74194850 | |||||
| chr4:74194850
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(44): Show | 48 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.452-4944C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194850 | ||||||
| chr4:74194866
|
ATCT | A | 6 | a0001c0001t0001g0078a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG00597.hp2 NA18945.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-4921_452-4919d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74194866 | |||||
| chr4:74194881
|
G | A | 88 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(85): Show | 88 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.452-4913G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74194881 | ||||||
| chr4:74195382
|
C | A | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(21): Show | 24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-4412C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195382 | ||||||
| chr4:74195423
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.452-4371G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195423 | ||||||
| chr4:74195471
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0065others(20): Show | 24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-4323T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195471 | ||||||
| chr4:74195779
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.452-4015T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195779 | ||||||
| chr4:74195843
|
G | T | 1 | a0001c0001t0001g0033 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.452-3951G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195843 | ||||||
| chr4:74195927
|
G | A | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-3867G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74195927 | ||||||
| chr4:74196348
|
T | G | 3 | a0001c0001t0002g0159a0001c0001t0002g0163a0001c0001t0002g0164 | 3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.452-3446T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196348 | ||||||
| chr4:74196501
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.452-3293T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196501 | ||||||
| chr4:74196553
|
A | T | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-3241A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196553 | ||||||
| chr4:74196622
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(48): Show | 52 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.452-3172A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196622 | ||||||
| chr4:74196727
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.452-3067C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196727 | ||||||
| chr4:74196771
|
C | T | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(21): Show | 24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-3023C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196771 | ||||||
| chr4:74196895
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.452-2899G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74196895 | ||||||
| chr4:74196945
|
C | CA | 19 | a0001c0001t0001g0033a0001c0001t0001g0061a0001c0001t0001g0078others(16): Show | 19 | HG00597.hp2 HG01070.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.452-2831dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74196945 | |||||
| chr4:74197384
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-2410C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197384 | ||||||
| chr4:74197608
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.452-2186G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197608 | ||||||
| chr4:74197659
|
T | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0002g0008others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-2135T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197659 | ||||||
| chr4:74197689
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.452-2105C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74197689 | ||||||
| chr4:74198013
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(44): Show | 48 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.452-1781T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198013 | ||||||
| chr4:74198024
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.452-1770G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198024 | ||||||
| chr4:74198290
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.452-1504C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198290 | ||||||
| chr4:74198506
|
CT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(44): Show | 48 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.452-1284delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74198506 | |||||
| chr4:74198552
|
T | C | 1 | a0001c0001t0002g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.452-1242T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198552 | ||||||
| chr4:74198606
|
T | A | 2 | a0001c0001t0001g0081a0001c0003t0004g0047 | 2 | HG01261.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-1188T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198606 | ||||||
| chr4:74198607
|
A | T | 14 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-1187A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198607 | ||||||
| chr4:74198880
|
T | TTAAAG | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.452-911_452-910ins others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74198880 | |||||
| chr4:74198884
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.452-910G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74198884 | ||||||
| chr4:74199351
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-443C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199351 | ||||||
| chr4:74199387
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-407A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199387 | ||||||
| chr4:74199487
|
C | G | 1 | a0001c0001t0003g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-307C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199487 | ||||||
| chr4:74199645
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-149G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199645 | ||||||
| chr4:74199647
|
A | AAAT | 22 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(19): Show | 22 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.452-125_452-123dup others(3): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74199647 | |||||
| chr4:74199647
|
A | AAATAAT | 3 | a0001c0001t0002g0159a0001c0001t0002g0163a0001c0001t0002g0164 | 3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.452-128_452-123dup others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 74199647 | |||||
| chr4:74199761
|
T | A | 1 | a0001c0003t0004g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.452-33T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 3/7 | chr4 | 74199761 | ||||||
| chr4:74200341
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.604+395A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200341 | ||||||
| chr4:74200369
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.604+423C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200369 | ||||||
| chr4:74200698
|
G | A | 2 | a0001c0001t0002g0056a0001c0001t0007g0055 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.605-565G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200698 | ||||||
| chr4:74200847
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.605-416A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200847 | ||||||
| chr4:74200869
|
CTT | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0065others(20): Show | 24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.605-391_605-390del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 74200869 | |||||
| chr4:74200894
|
G | A | 14 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0074others(11): Show | 14 | HG01109.hp2 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.605-369G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74200894 | ||||||
| chr4:74201129
|
CATATT | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.605-130_605-126del others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 74201129 | |||||
| chr4:74201148
|
A | G | 16 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(13): Show | 16 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.605-115A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74201148 | ||||||
| chr4:74201257
|
T | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0002g0008others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.605-6T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 4/7 | chr4 | 74201257 | ||||||
| chr4:74201399
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+29C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201399 | ||||||
| chr4:74201421
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.712+51T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201421 | ||||||
| chr4:74201452
|
A | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.712+82A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201452 | ||||||
| chr4:74201502
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712+132A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201502 | ||||||
| chr4:74201568
|
AT | A | 143 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.712+212delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74201568 | |||||
| chr4:74201568
|
ATT | A | 43 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(40): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.712+211_712+212del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74201568 | |||||
| chr4:74201568
|
ATTT | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+210_712+212del others(3): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74201568 | |||||
| chr4:74201616
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0005g0141others(1): Show | 4 | HG02895.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+246T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201616 | ||||||
| chr4:74201710
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(136): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.712+340G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74201710 | ||||||
| chr4:74202021
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.712+651C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202021 | ||||||
| chr4:74202036
|
G | A | 1 | a0001c0001t0003g0059 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.712+666G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202036 | ||||||
| chr4:74202082
|
C | T | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(21): Show | 24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+712C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202082 | ||||||
| chr4:74202094
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.712+724C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202094 | ||||||
| chr4:74202125
|
C | T | 88 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(85): Show | 88 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.712+755C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202125 | ||||||
| chr4:74202157
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0005g0141others(1): Show | 4 | HG02895.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+787T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202157 | ||||||
| chr4:74202224
|
G | T | 1 | a0001c0001t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.712+854G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202224 | ||||||
| chr4:74202225
|
G | T | 1 | a0001c0001t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.712+855G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202225 | ||||||
| chr4:74202537
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0065others(20): Show | 24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+1167T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202537 | ||||||
| chr4:74202715
|
C | T | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(21): Show | 24 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+1345C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202715 | ||||||
| chr4:74202870
|
G | A | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+1500G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202870 | ||||||
| chr4:74202942
|
C | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.712+1572C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74202942 | ||||||
| chr4:74203200
|
T | TAAAAAGC others(327): Show |
4 | a0001c0001t0001g0193a0001c0001t0002g0045a0001c0001t0002g0194others(1): Show | 4 | HG03704.hp2 NA18954.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.712+1847_712+1848i others(336): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203200 | |||||
| chr4:74203200
|
T | TAAAAAGC others(328): Show |
3 | a0001c0001t0002g0137a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG03831.hp1 HG03927.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.712+1847_712+1848i others(337): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203200 | |||||
| chr4:74203331
|
T | TTC | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+1973_712+1974d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203331 | |||||
| chr4:74203372
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+2002C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74203372 | ||||||
| chr4:74203411
|
G | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0002g0008others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+2041G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74203411 | ||||||
| chr4:74203474
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.712+2104G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74203474 | ||||||
| chr4:74203897
|
GT | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 191 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.712+2540delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74203897 | |||||
| chr4:74204039
|
C | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+2669C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204039 | ||||||
| chr4:74204194
|
C | T | 11 | a0001c0001t0001g0065a0001c0001t0001g0193a0001c0001t0002g0045others(8): Show | 11 | HG02486.hp1 HG02970.hp2 HG03579.hp1 others(8): Show |
intron_variant | MODIFIER | c.712+2824C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204194 | ||||||
| chr4:74204247
|
CAAT | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0065others(20): Show | 24 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+2882_712+2884d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74204247 | |||||
| chr4:74204822
|
T | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0156a0001c0001t0002g0008others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+3452T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204822 | ||||||
| chr4:74204960
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0109a0001c0001t0001g0123 | 3 | HG03927.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.712+3590C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74204960 | ||||||
| chr4:74205040
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.712+3670C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205040 | ||||||
| chr4:74205258
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0080 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.712+3888C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205258 | ||||||
| chr4:74205314
|
G | A | 19 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 19 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.712+3944G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205314 | ||||||
| chr4:74205448
|
G | A | 10 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0002g0019others(7): Show | 10 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.712+4078G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205448 | ||||||
| chr4:74205473
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0152 | 2 | HG02040.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.712+4103T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205473 | ||||||
| chr4:74205588
|
T | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+4218T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205588 | ||||||
| chr4:74205696
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+4326G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205696 | ||||||
| chr4:74205852
|
A | AT | 24 | a0001c0001t0001g0048a0001c0001t0001g0077a0001c0001t0001g0079others(21): Show | 24 | HG00438.hp2 HG00621.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.712+4483dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74205852 | |||||
| chr4:74205884
|
A | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.712+4514A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74205884 | ||||||
| chr4:74206010
|
A | G | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(21): Show | 24 | HG00438.hp1 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.712+4640A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206010 | ||||||
| chr4:74206134
|
T | TA | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.712+4778dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206134 | |||||
| chr4:74206187
|
AT | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0088 | 2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.712+4820delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206187 | |||||
| chr4:74206322
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(12): Show | 16 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.712+4952G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206322 | ||||||
| chr4:74206383
|
C | CTGGAATT others(1): Show |
25 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0002g0050others(22): Show | 25 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.712+5016_712+5023d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206383 | |||||
| chr4:74206389
|
T | G | 1 | a0002c0002t0001g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.712+5019T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206389 | ||||||
| chr4:74206399
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+5029G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74206399 | ||||||
| chr4:74206843
|
TACTA | T | 2 | a0001c0001t0003g0185a0001c0003t0004g0047 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.712+5477_712+5480d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74206843 | |||||
| chr4:74207092
|
G | T | 63 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.712+5722G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207092 | ||||||
| chr4:74207159
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.712+5789C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207159 | ||||||
| chr4:74207165
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0156 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.712+5795G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207165 | ||||||
| chr4:74207198
|
C | T | 155 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.712+5828C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207198 | ||||||
| chr4:74207313
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.712+5943T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207313 | ||||||
| chr4:74207585
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.712+6215C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207585 | ||||||
| chr4:74207589
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.712+6219G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207589 | ||||||
| chr4:74207683
|
C | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+6313C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207683 | ||||||
| chr4:74207759
|
A | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+6389A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207759 | ||||||
| chr4:74207760
|
A | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+6390A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207760 | ||||||
| chr4:74207766
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0052a0001c0001t0003g0171a0001c0001t0003g0172others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+6403_712+6412d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207766
|
C | CTTTTTTT others(4): Show |
59 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.712+6402_712+6412d others(13): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207766
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0189others(5): Show | 8 | HG01123.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+6401_712+6412d others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207766
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.712+6400_712+6412d others(15): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207766
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0002g0155a0001c0001t0003g0167 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.712+6399_712+6412d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207766
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01884.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+6398_712+6412d others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207766
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0020others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.712+6397_712+6412d others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207766 | |||||
| chr4:74207776
|
T | TTTTTTTT others(8): Show |
1 | a0001c0001t0002g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.712+6412_712+6413i others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74207776 | |||||
| chr4:74207915
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.712+6545T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207915 | ||||||
| chr4:74207983
|
A | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+6613A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74207983 | ||||||
| chr4:74208082
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.712+6712A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208082 | ||||||
| chr4:74208303
|
A | ATTCAGTG others(10): Show |
169 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.712+6935_712+6951d others(19): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74208303 | |||||
| chr4:74208303
|
A | ATTTCAGT others(11): Show |
1 | a0001c0001t0001g0112 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.712+6935_712+6936i others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74208303 | |||||
| chr4:74208414
|
C | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.712+7044C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208414 | ||||||
| chr4:74208470
|
C | T | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.712+7100C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208470 | ||||||
| chr4:74208671
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.712+7301G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208671 | ||||||
| chr4:74208707
|
C | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.712+7337C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208707 | ||||||
| chr4:74208832
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.712+7462A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208832 | ||||||
| chr4:74208854
|
A | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0108others(3): Show | 6 | HG02004.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.712+7484A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74208854 | ||||||
| chr4:74209136
|
C | T | 87 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0042others(84): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.712+7766C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209136 | ||||||
| chr4:74209285
|
T | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.712+7915T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209285 | ||||||
| chr4:74209586
|
G | T | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+8216G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209586 | ||||||
| chr4:74209768
|
A | G | 8 | a0001c0001t0002g0045a0001c0001t0002g0131a0001c0001t0002g0137others(5): Show | 8 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.712+8398A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209768 | ||||||
| chr4:74209952
|
A | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+8582A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74209952 | ||||||
| chr4:74210176
|
C | CA | 170 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.712+8806_712+8807i others(3): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210176 | ||||||
| chr4:74210288
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.712+8918G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210288 | ||||||
| chr4:74210561
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712+9191C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210561 | ||||||
| chr4:74210655
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+9285G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210655 | ||||||
| chr4:74210672
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+9302C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210672 | ||||||
| chr4:74210992
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(12): Show | 16 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.712+9622T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74210992 | ||||||
| chr4:74211082
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.712+9712G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211082 | ||||||
| chr4:74211135
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.712+9765C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211135 | ||||||
| chr4:74211299
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.712+9929A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211299 | ||||||
| chr4:74211308
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.712+9938T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211308 | ||||||
| chr4:74211340
|
T | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+9970T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211340 | ||||||
| chr4:74211349
|
A | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+9979A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74211349 | ||||||
| chr4:74212294
|
G | A | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0004g0016others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.712+10924G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212294 | ||||||
| chr4:74212402
|
C | G | 4 | a0001c0001t0002g0131a0001c0001t0002g0137a0001c0001t0002g0195others(1): Show | 4 | HG03927.hp1 NA19004.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.712+11032C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212402 | ||||||
| chr4:74212443
|
C | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.712+11073C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212443 | ||||||
| chr4:74212546
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(22): Show | 26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.712+11176G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212546 | ||||||
| chr4:74212712
|
G | A | 60 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.712+11342G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212712 | ||||||
| chr4:74212801
|
T | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+11431T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212801 | ||||||
| chr4:74212900
|
A | T | 25 | a0001c0001t0001g0048a0001c0001t0003g0027a0001c0001t0003g0028others(22): Show | 25 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.712+11530A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74212900 | ||||||
| chr4:74213106
|
G | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(22): Show | 26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.712+11736G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213106 | ||||||
| chr4:74213119
|
C | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(22): Show | 26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.712+11749C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213119 | ||||||
| chr4:74213349
|
C | T | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-11953C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213349 | ||||||
| chr4:74213781
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0084a0002c0002t0001g0076 | 3 | HG00408.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.713-11521G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74213781 | ||||||
| chr4:74214059
|
A | C | 3 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0004t0001g0012 | 3 | HG02572.hp2 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-11243A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214059 | ||||||
| chr4:74214165
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 109 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.713-11137T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214165 | ||||||
| chr4:74214186
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.713-11116C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214186 | ||||||
| chr4:74214311
|
G | C | 8 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(5): Show | 8 | HG01106.hp2 HG02015.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-10991G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214311 | ||||||
| chr4:74214341
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(22): Show | 26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.713-10961G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214341 | ||||||
| chr4:74214403
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.713-10899G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214403 | ||||||
| chr4:74214730
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(22): Show | 26 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.713-10572G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214730 | ||||||
| chr4:74214874
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713-10428G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214874 | ||||||
| chr4:74214923
|
T | C | 4 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0053others(1): Show | 4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.713-10379T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214923 | ||||||
| chr4:74214924
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.713-10378G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74214924 | ||||||
| chr4:74215076
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 109 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.713-10226C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215076 | ||||||
| chr4:74215325
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-9977G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215325 | ||||||
| chr4:74215362
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-9940G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215362 | ||||||
| chr4:74215399
|
G | A | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-9903G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215399 | ||||||
| chr4:74215404
|
G | A | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-9898G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215404 | ||||||
| chr4:74215467
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.713-9835G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74215467 | ||||||
| chr4:74215968
|
GA | G | 18 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.713-9323delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74215968 | |||||
| chr4:74216067
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713-9235G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216067 | ||||||
| chr4:74216395
|
T | C | 170 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.713-8907T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216395 | ||||||
| chr4:74216488
|
C | T | 87 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0042others(84): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.713-8814C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216488 | ||||||
| chr4:74216785
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.713-8517A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216785 | ||||||
| chr4:74216834
|
C | A | 87 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0042others(84): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.713-8468C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74216834 | ||||||
| chr4:74217010
|
C | T | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-8292C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217010 | ||||||
| chr4:74217112
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.713-8190C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217112 | ||||||
| chr4:74217285
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.713-8017A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217285 | ||||||
| chr4:74217344
|
A | G | 155 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.713-7958A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217344 | ||||||
| chr4:74217384
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.713-7918A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217384 | ||||||
| chr4:74217619
|
C | T | 87 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0042others(84): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.713-7683C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217619 | ||||||
| chr4:74217872
|
A | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-7430A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217872 | ||||||
| chr4:74217899
|
T | C | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-7403T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74217899 | ||||||
| chr4:74218027
|
G | A | 3 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0004t0001g0012 | 3 | HG02572.hp2 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.713-7275G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218027 | ||||||
| chr4:74218050
|
T | G | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-7252T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218050 | ||||||
| chr4:74218250
|
A | T | 89 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0042others(86): Show | 89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.713-7052A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218250 | ||||||
| chr4:74218296
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | NA18939.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.713-7006A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218296 | ||||||
| chr4:74218519
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0002g0183 | 3 | HG02630.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.713-6783T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218519 | ||||||
| chr4:74218614
|
G | GC | 31 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0122others(28): Show | 32 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.713-6678dupC | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74218614 | |||||
| chr4:74218614
|
GC | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0082others(28): Show | 31 | HG01099.hp1 HG01109.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.713-6678delC | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74218614 | |||||
| chr4:74218661
|
T | C | 45 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(42): Show | 45 | HG00408.hp1 HG01099.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.713-6641T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218661 | ||||||
| chr4:74218839
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.713-6463C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218839 | ||||||
| chr4:74218992
|
T | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0134 | 2 | HG02132.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.713-6310T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74218992 | ||||||
| chr4:74219087
|
G | A | 162 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.713-6215G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219087 | ||||||
| chr4:74219185
|
G | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(14): Show | 18 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.713-6117G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219185 | ||||||
| chr4:74219464
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.713-5838C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219464 | ||||||
| chr4:74219525
|
G | T | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.713-5777G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219525 | ||||||
| chr4:74219820
|
A | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-5482A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219820 | ||||||
| chr4:74219841
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-5461C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219841 | ||||||
| chr4:74219927
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.713-5375C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219927 | ||||||
| chr4:74219929
|
C | T | 162 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.713-5373C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74219929 | ||||||
| chr4:74220092
|
A | AT | 164 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 165 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.713-5199dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74220092 | |||||
| chr4:74220467
|
T | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.713-4835T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220467 | ||||||
| chr4:74220509
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.713-4793T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220509 | ||||||
| chr4:74220516
|
A | G | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.713-4786A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220516 | ||||||
| chr4:74220704
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.713-4598G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220704 | ||||||
| chr4:74220754
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-4548C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220754 | ||||||
| chr4:74220875
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.713-4427A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74220875 | ||||||
| chr4:74221132
|
G | A | 2 | a0001c0001t0002g0019a0001c0001t0002g0182 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.713-4170G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221132 | ||||||
| chr4:74221208
|
TATTA | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-4088_713-4085d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74221208 | |||||
| chr4:74221382
|
A | G | 1 | a0001c0001t0003g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.713-3920A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221382 | ||||||
| chr4:74221455
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-3847T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221455 | ||||||
| chr4:74221874
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-3428T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221874 | ||||||
| chr4:74221921
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-3381T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221921 | ||||||
| chr4:74221942
|
T | C | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.713-3360T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74221942 | ||||||
| chr4:74222119
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.713-3183A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222119 | ||||||
| chr4:74222128
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.713-3174A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222128 | ||||||
| chr4:74222180
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.713-3122C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222180 | ||||||
| chr4:74222338
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.713-2964C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222338 | ||||||
| chr4:74222665
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-2637G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222665 | ||||||
| chr4:74222911
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.713-2391A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74222911 | ||||||
| chr4:74223125
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG02965.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.713-2177T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223125 | ||||||
| chr4:74223262
|
T | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.713-2040T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223262 | ||||||
| chr4:74223404
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.713-1898G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223404 | ||||||
| chr4:74223457
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.713-1845A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74223457 | ||||||
| chr4:74223638
|
A | AAAAT | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.713-1654_713-1651d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74223638 | |||||
| chr4:74224025
|
T | A | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.713-1277T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224025 | ||||||
| chr4:74224057
|
G | T | 18 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(15): Show | 18 | HG00408.hp1 HG00597.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.713-1245G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224057 | ||||||
| chr4:74224159
|
C | A | 2 | a0001c0001t0003g0036a0001c0001t0003g0039 | 2 | NA18973.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.713-1143C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224159 | ||||||
| chr4:74224187
|
C | T | 10 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0002g0181others(7): Show | 10 | HG02572.hp1 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.713-1115C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224187 | ||||||
| chr4:74224315
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0002g0018 | 2 | HG02622.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.713-987C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224315 | ||||||
| chr4:74224511
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.713-791G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224511 | ||||||
| chr4:74224531
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.713-771G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224531 | ||||||
| chr4:74224800
|
A | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.713-502A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74224800 | ||||||
| chr4:74224906
|
CA | C | 6 | a0001c0001t0002g0181a0001c0001t0002g0183a0001c0001t0002g0184others(3): Show | 6 | HG02572.hp1 HG02630.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.713-394delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 74224906 | |||||
| chr4:74225055
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-247T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74225055 | ||||||
| chr4:74225120
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.713-182G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 5/7 | chr4 | 74225120 | ||||||
| chr4:74225521
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+127A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74225521 | ||||||
| chr4:74225870
|
A | G | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+476A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74225870 | ||||||
| chr4:74225881
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805+487T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74225881 | ||||||
| chr4:74226190
|
CA | C | 47 | a0001c0001t0001g0048a0001c0001t0001g0061a0001c0001t0001g0063others(44): Show | 47 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.805+806delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74226190 | |||||
| chr4:74226213
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+819A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74226213 | ||||||
| chr4:74227743
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+2349A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227743 | ||||||
| chr4:74227825
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+2431A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227825 | ||||||
| chr4:74227922
|
A | T | 10 | a0001c0001t0003g0011a0001c0001t0003g0025a0001c0001t0003g0026others(7): Show | 10 | HG00280.hp1 HG00621.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.805+2528A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227922 | ||||||
| chr4:74227923
|
A | T | 10 | a0001c0001t0003g0011a0001c0001t0003g0025a0001c0001t0003g0026others(7): Show | 10 | HG00280.hp1 HG00621.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.805+2529A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227923 | ||||||
| chr4:74227991
|
C | T | 72 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(69): Show | 72 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.805+2597C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227991 | ||||||
| chr4:74227992
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0156 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.805+2598A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227992 | ||||||
| chr4:74227995
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+2601T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74227995 | ||||||
| chr4:74228474
|
T | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+3080T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228474 | ||||||
| chr4:74228737
|
G | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+3343G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228737 | ||||||
| chr4:74228874
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+3480G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228874 | ||||||
| chr4:74228938
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.805+3544G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74228938 | ||||||
| chr4:74229119
|
C | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+3725C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229119 | ||||||
| chr4:74229245
|
A | G | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+3851A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229245 | ||||||
| chr4:74229344
|
C | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+3950C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229344 | ||||||
| chr4:74229463
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.805+4069A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229463 | ||||||
| chr4:74229504
|
G | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+4110G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229504 | ||||||
| chr4:74229528
|
A | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+4134A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229528 | ||||||
| chr4:74229688
|
G | A | 76 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+4294G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74229688 | ||||||
| chr4:74230029
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.805+4635G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230029 | ||||||
| chr4:74230244
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+4850C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230244 | ||||||
| chr4:74230318
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 83 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.805+4924A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230318 | ||||||
| chr4:74230591
|
GA | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 165 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.805+5211delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74230591 | |||||
| chr4:74230602
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+5208A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230602 | ||||||
| chr4:74230684
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.805+5290C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230684 | ||||||
| chr4:74230735
|
G | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.805+5341G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230735 | ||||||
| chr4:74230767
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.805+5373C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230767 | ||||||
| chr4:74230823
|
A | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+5429A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74230823 | ||||||
| chr4:74231002
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.805+5608C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231002 | ||||||
| chr4:74231058
|
T | A | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+5664T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231058 | ||||||
| chr4:74231297
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+5903G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231297 | ||||||
| chr4:74231483
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+6089A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231483 | ||||||
| chr4:74231771
|
A | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+6377A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74231771 | ||||||
| chr4:74232404
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.805+7010C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232404 | ||||||
| chr4:74232774
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.805+7380T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232774 | ||||||
| chr4:74232869
|
G | GAT | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0108others(3): Show | 6 | HG02004.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+7479_805+7480d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74232869 | |||||
| chr4:74232951
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.805+7557G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232951 | ||||||
| chr4:74232952
|
C | A | 1 | a0001c0001t0002g0131 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.805+7558C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232952 | ||||||
| chr4:74232992
|
C | T | 77 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+7598C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74232992 | ||||||
| chr4:74233005
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+7611G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233005 | ||||||
| chr4:74233037
|
ATTAC | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.805+7647_805+7650d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74233037 | |||||
| chr4:74233083
|
A | G | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.805+7689A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233083 | ||||||
| chr4:74233398
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.805+8004T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233398 | ||||||
| chr4:74233951
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.805+8557T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74233951 | ||||||
| chr4:74234203
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0088 | 2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.805+8809T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234203 | ||||||
| chr4:74234497
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+9103T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234497 | ||||||
| chr4:74234796
|
A | AATGT | 5 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+9402_805+9403i others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234796 | ||||||
| chr4:74234796
|
A | AGT | 8 | a0001c0001t0001g0098a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG01123.hp2 HG01496.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.805+9425_805+9426d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
A | AGTGT | 11 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(8): Show | 12 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.805+9423_805+9426d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
A | AGTGTGT | 19 | a0001c0001t0001g0065a0001c0001t0001g0193a0001c0001t0002g0002others(16): Show | 19 | HG01106.hp2 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.805+9421_805+9426d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
A | AGTGTGTG others(1): Show |
54 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(51): Show | 54 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.805+9419_805+9426d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0002g0056a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.805+9417_805+9426d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+9415_805+9426d others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
AGT | A | 26 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0002g0018others(23): Show | 26 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.805+9425_805+9426d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234796
|
AGTGT | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0159 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.805+9423_805+9426d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74234796 | |||||
| chr4:74234810
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.805+9416T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234810 | ||||||
| chr4:74234824
|
C | T | 78 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(75): Show | 78 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.805+9430C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234824 | ||||||
| chr4:74234978
|
A | G | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.805+9584A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74234978 | ||||||
| chr4:74235000
|
A | G | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+9606A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235000 | ||||||
| chr4:74235420
|
T | C | 11 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0002g0158others(8): Show | 11 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.805+10026T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235420 | ||||||
| chr4:74235582
|
T | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+10188T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235582 | ||||||
| chr4:74235586
|
G | A | 2 | a0001c0001t0003g0083a0001c0001t0003g0092 | 2 | NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.805+10192G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235586 | ||||||
| chr4:74235678
|
G | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+10284G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235678 | ||||||
| chr4:74235784
|
G | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+10390G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235784 | ||||||
| chr4:74235851
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+10457C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74235851 | ||||||
| chr4:74236142
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+10748T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236142 | ||||||
| chr4:74236154
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.805+10760C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236154 | ||||||
| chr4:74236282
|
T | A | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+10888T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236282 | ||||||
| chr4:74236372
|
T | G | 1 | a0001c0001t0003g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.805+10978T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236372 | ||||||
| chr4:74236538
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+11144T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236538 | ||||||
| chr4:74236705
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.805+11311G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236705 | ||||||
| chr4:74236905
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+11511T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236905 | ||||||
| chr4:74236931
|
A | G | 76 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+11537A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236931 | ||||||
| chr4:74236972
|
G | C | 77 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+11578G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74236972 | ||||||
| chr4:74237028
|
A | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(74): Show | 78 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.805+11634A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237028 | ||||||
| chr4:74237065
|
C | T | 13 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0002g0018others(10): Show | 13 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.805+11671C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237065 | ||||||
| chr4:74237170
|
G | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+11776G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237170 | ||||||
| chr4:74237186
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805+11792A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237186 | ||||||
| chr4:74237276
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.805+11882T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237276 | ||||||
| chr4:74237569
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+12175G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237569 | ||||||
| chr4:74237571
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.805+12177A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237571 | ||||||
| chr4:74237585
|
G | T | 18 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(15): Show | 18 | HG00408.hp1 HG00597.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.805+12191G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237585 | ||||||
| chr4:74237693
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.805+12299G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237693 | ||||||
| chr4:74237952
|
C | T | 76 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+12558C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237952 | ||||||
| chr4:74237959
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.805+12565C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237959 | ||||||
| chr4:74237981
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(74): Show | 78 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.805+12587G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74237981 | ||||||
| chr4:74238049
|
T | C | 4 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0053others(1): Show | 4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+12655T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238049 | ||||||
| chr4:74238272
|
G | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+12878G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238272 | ||||||
| chr4:74238276
|
G | A | 1 | a0001c0001t0006g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.805+12882G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238276 | ||||||
| chr4:74238289
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+12895T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238289 | ||||||
| chr4:74238300
|
G | C | 3 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0165 | 3 | HG03041.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.805+12906G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238300 | ||||||
| chr4:74238604
|
C | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.805+13210C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238604 | ||||||
| chr4:74238679
|
A | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+13285A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238679 | ||||||
| chr4:74238800
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0024others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.805+13406G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238800 | ||||||
| chr4:74238971
|
G | C | 3 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0165 | 3 | HG03041.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.805+13577G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74238971 | ||||||
| chr4:74239110
|
A | C | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805+13716A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239110 | ||||||
| chr4:74239222
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 80 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.805+13828A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239222 | ||||||
| chr4:74239294
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+13900T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239294 | ||||||
| chr4:74239429
|
T | C | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.805+14035T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239429 | ||||||
| chr4:74239489
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.805+14095T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239489 | ||||||
| chr4:74239489
|
T | TA | 85 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 85 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.805+14095_805+1409 others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239489 | ||||||
| chr4:74239490
|
T | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+14096T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239490 | ||||||
| chr4:74239491
|
A | T | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.805+14097A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239491 | ||||||
| chr4:74239706
|
C | A | 3 | a0001c0001t0002g0159a0001c0001t0002g0163a0001c0001t0002g0164 | 3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.805+14312C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239706 | ||||||
| chr4:74239731
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0129others(1): Show | 4 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+14337T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239731 | ||||||
| chr4:74239885
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+14491C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74239885 | ||||||
| chr4:74240203
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+14809G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240203 | ||||||
| chr4:74240397
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.805+15003G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240397 | ||||||
| chr4:74240474
|
G | C | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+15080G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240474 | ||||||
| chr4:74240648
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.805+15254C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240648 | ||||||
| chr4:74240712
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.805+15318T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240712 | ||||||
| chr4:74240768
|
A | G | 22 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 22 | HG00438.hp1 HG00621.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.805+15374A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240768 | ||||||
| chr4:74240774
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.805+15380A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74240774 | ||||||
| chr4:74241006
|
TG | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+15614delG | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74241006 | |||||
| chr4:74241110
|
G | A | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.805+15716G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241110 | ||||||
| chr4:74241151
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805+15757A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241151 | ||||||
| chr4:74241153
|
A | G | 66 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.805+15759A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241153 | ||||||
| chr4:74241161
|
A | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+15767A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241161 | ||||||
| chr4:74241418
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+16024G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241418 | ||||||
| chr4:74241538
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 83 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.805+16144T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241538 | ||||||
| chr4:74241540
|
C | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+16146C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241540 | ||||||
| chr4:74241608
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+16214A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241608 | ||||||
| chr4:74241673
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.805+16279C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241673 | ||||||
| chr4:74241680
|
A | G | 66 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.805+16286A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241680 | ||||||
| chr4:74241708
|
C | T | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+16314C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241708 | ||||||
| chr4:74241807
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+16413T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241807 | ||||||
| chr4:74241843
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+16449C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241843 | ||||||
| chr4:74241948
|
C | T | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+16554C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74241948 | ||||||
| chr4:74242080
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.805+16686G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242080 | ||||||
| chr4:74242200
|
A | AAAAAT | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+16811_805+1681 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74242200 | |||||
| chr4:74242234
|
A | C | 1 | a0001c0001t0001g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.805+16840A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242234 | ||||||
| chr4:74242235
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0109 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.805+16841G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242235 | ||||||
| chr4:74242603
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+17209C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242603 | ||||||
| chr4:74242670
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.805+17276G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242670 | ||||||
| chr4:74242769
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+17375A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242769 | ||||||
| chr4:74242797
|
T | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+17403T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242797 | ||||||
| chr4:74242854
|
A | G | 45 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(42): Show | 45 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.805+17460A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242854 | ||||||
| chr4:74242873
|
C | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.805+17479C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74242873 | ||||||
| chr4:74243291
|
C | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.805+17897C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243291 | ||||||
| chr4:74243343
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0002g0142 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.805+17949C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243343 | ||||||
| chr4:74243423
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+18029C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243423 | ||||||
| chr4:74243770
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.805+18376C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243770 | ||||||
| chr4:74243862
|
A | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.805+18468A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243862 | ||||||
| chr4:74243994
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.805+18600A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74243994 | ||||||
| chr4:74244040
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+18646G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244040 | ||||||
| chr4:74244050
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+18656C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244050 | ||||||
| chr4:74244078
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+18684A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244078 | ||||||
| chr4:74244215
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805+18821A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244215 | ||||||
| chr4:74244291
|
T | C | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+18897T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244291 | ||||||
| chr4:74244389
|
T | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0053others(1): Show | 4 | HG01099.hp2 HG01169.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+18995T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244389 | ||||||
| chr4:74244412
|
G | C | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.805+19018G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244412 | ||||||
| chr4:74244470
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805+19076A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244470 | ||||||
| chr4:74244512
|
TTA | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 83 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.805+19122_805+1912 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74244512 | |||||
| chr4:74244796
|
A | G | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+19402A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244796 | ||||||
| chr4:74244803
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.805+19409A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244803 | ||||||
| chr4:74244823
|
T | G | 81 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.805+19429T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244823 | ||||||
| chr4:74244916
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805+19522C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74244916 | ||||||
| chr4:74245051
|
G | A | 14 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(11): Show | 14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.805+19657G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245051 | ||||||
| chr4:74245068
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+19674G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245068 | ||||||
| chr4:74245097
|
A | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+19703A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245097 | ||||||
| chr4:74245119
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.805+19725C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245119 | ||||||
| chr4:74245120
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0064a0001c0001t0001g0120 | 3 | HG00438.hp1 HG00621.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.805+19726G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245120 | ||||||
| chr4:74245159
|
C | A | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.805+19765C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245159 | ||||||
| chr4:74245194
|
C | CA | 6 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0122others(3): Show | 6 | HG00408.hp1 HG01243.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.805+19825dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74245194 | |||||
| chr4:74245194
|
CA | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(128): Show | 132 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.805+19825delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74245194 | |||||
| chr4:74245298
|
T | A | 5 | a0001c0001t0003g0034a0001c0001t0003g0036a0001c0001t0003g0037others(2): Show | 5 | HG02015.hp2 NA18973.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+19904T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245298 | ||||||
| chr4:74245385
|
T | C | 1 | a0001c0001t0006g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.805+19991T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245385 | ||||||
| chr4:74245481
|
AT | A | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20095delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74245481 | |||||
| chr4:74245601
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+20207A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245601 | ||||||
| chr4:74245662
|
G | A | 45 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(42): Show | 45 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.805+20268G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245662 | ||||||
| chr4:74245723
|
T | C | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20329T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245723 | ||||||
| chr4:74245738
|
T | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0129others(1): Show | 4 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+20344T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245738 | ||||||
| chr4:74245839
|
G | C | 2 | a0001c0001t0002g0019a0001c0001t0002g0182 | 2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.805+20445G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245839 | ||||||
| chr4:74245950
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.805+20556A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74245950 | ||||||
| chr4:74246027
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.805+20633G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246027 | ||||||
| chr4:74246054
|
G | C | 76 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+20660G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246054 | ||||||
| chr4:74246063
|
A | G | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20669A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246063 | ||||||
| chr4:74246101
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.805+20707A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246101 | ||||||
| chr4:74246210
|
G | A | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+20816G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246210 | ||||||
| chr4:74246229
|
T | A | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.805+20835T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246229 | ||||||
| chr4:74246249
|
T | C | 13 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(10): Show | 13 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.805+20855T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246249 | ||||||
| chr4:74246286
|
G | T | 2 | a0001c0001t0002g0155a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+20892G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246286 | ||||||
| chr4:74246354
|
G | A | 66 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.805+20960G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246354 | ||||||
| chr4:74246622
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.805+21228T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246622 | ||||||
| chr4:74246727
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+21333A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246727 | ||||||
| chr4:74246770
|
T | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.805+21376T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246770 | ||||||
| chr4:74246785
|
G | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805+21391G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246785 | ||||||
| chr4:74246786
|
A | T | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805+21392A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246786 | ||||||
| chr4:74246796
|
C | T | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+21402C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246796 | ||||||
| chr4:74246797
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.805+21403G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246797 | ||||||
| chr4:74246807
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.805+21413C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246807 | ||||||
| chr4:74246829
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.805+21435T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246829 | ||||||
| chr4:74246951
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.805+21557T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246951 | ||||||
| chr4:74246954
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.805+21560C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246954 | ||||||
| chr4:74246959
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.805+21565C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246959 | ||||||
| chr4:74246989
|
C | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 171 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.805+21595C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74246989 | ||||||
| chr4:74247087
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.805+21693A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247087 | ||||||
| chr4:74247149
|
T | C | 3 | a0001c0001t0003g0011a0001c0001t0003g0052a0001c0001t0003g0167 | 3 | HG02145.hp1 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.805+21755T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247149 | ||||||
| chr4:74247254
|
G | A | 1 | a0001c0003t0004g0047 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.805+21860G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247254 | ||||||
| chr4:74247351
|
T | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.805+21957T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247351 | ||||||
| chr4:74247365
|
G | T | 41 | a0001c0001t0001g0051a0001c0001t0003g0011a0001c0001t0003g0025others(38): Show | 41 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.805+21971G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247365 | ||||||
| chr4:74247388
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+21994A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247388 | ||||||
| chr4:74247490
|
G | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.805+22096G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247490 | ||||||
| chr4:74247556
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.805+22162C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247556 | ||||||
| chr4:74247582
|
G | T | 14 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(11): Show | 14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.805+22188G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247582 | ||||||
| chr4:74247630
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.805+22236G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247630 | ||||||
| chr4:74247640
|
T | A | 2 | a0001c0001t0002g0155a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+22246T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247640 | ||||||
| chr4:74247695
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 93 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.805+22301G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247695 | ||||||
| chr4:74247742
|
T | A | 9 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0143others(6): Show | 9 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.805+22348T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247742 | ||||||
| chr4:74247798
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.805+22404A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247798 | ||||||
| chr4:74247810
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.805+22416T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247810 | ||||||
| chr4:74247876
|
G | T | 2 | a0001c0001t0002g0155a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+22482G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247876 | ||||||
| chr4:74247948
|
G | T | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+22554G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247948 | ||||||
| chr4:74247994
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+22600T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74247994 | ||||||
| chr4:74248099
|
C | A | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.805+22705C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248099 | ||||||
| chr4:74248166
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.805+22772C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248166 | ||||||
| chr4:74248256
|
G | C | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.805+22862G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248256 | ||||||
| chr4:74248349
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805+22955C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248349 | ||||||
| chr4:74248350
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.805+22956G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248350 | ||||||
| chr4:74248365
|
C | T | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+22971C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248365 | ||||||
| chr4:74248473
|
T | C | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+23079T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248473 | ||||||
| chr4:74248559
|
T | G | 1 | a0001c0001t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.805+23165T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248559 | ||||||
| chr4:74248846
|
C | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.805+23452C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248846 | ||||||
| chr4:74248967
|
G | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.805+23573G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74248967 | ||||||
| chr4:74249157
|
G | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.805+23763G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249157 | ||||||
| chr4:74249294
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.805+23900G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249294 | ||||||
| chr4:74249347
|
C | T | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.805+23953C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249347 | ||||||
| chr4:74249431
|
A | T | 1 | a0001c0001t0003g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805+24037A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249431 | ||||||
| chr4:74249436
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.805+24042A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249436 | ||||||
| chr4:74249576
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.805+24182T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249576 | ||||||
| chr4:74249606
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.805+24212C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249606 | ||||||
| chr4:74249674
|
T | C | 8 | a0001c0001t0002g0019a0001c0001t0002g0143a0001c0001t0002g0145others(5): Show | 8 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+24280T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249674 | ||||||
| chr4:74249732
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.805+24338A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249732 | ||||||
| chr4:74249815
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.805+24421C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249815 | ||||||
| chr4:74249838
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.805+24444G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249838 | ||||||
| chr4:74249839
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.805+24445C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249839 | ||||||
| chr4:74249896
|
T | C | 77 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+24502T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249896 | ||||||
| chr4:74249942
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.805+24548A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249942 | ||||||
| chr4:74249963
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.805+24569G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74249963 | ||||||
| chr4:74250021
|
T | TG | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 171 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.805+24628dupG | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74250021 | |||||
| chr4:74250042
|
A | G | 77 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(74): Show | 77 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.805+24648A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250042 | ||||||
| chr4:74250141
|
C | G | 1 | a0001c0001t0003g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.805+24747C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250141 | ||||||
| chr4:74250198
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.805+24804A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250198 | ||||||
| chr4:74250242
|
T | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.805+24848T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250242 | ||||||
| chr4:74250280
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.805+24886A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250280 | ||||||
| chr4:74250296
|
T | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+24902T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250296 | ||||||
| chr4:74250633
|
C | T | 11 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0066others(8): Show | 11 | HG01243.hp2 HG02622.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.805+25239C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250633 | ||||||
| chr4:74250750
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.805+25356T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74250750 | ||||||
| chr4:74251020
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0143others(6): Show | 9 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.805+25626A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251020 | ||||||
| chr4:74251146
|
A | G | 41 | a0001c0001t0001g0051a0001c0001t0003g0011a0001c0001t0003g0025others(38): Show | 41 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.805+25752A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251146 | ||||||
| chr4:74251377
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+25983A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251377 | ||||||
| chr4:74251392
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.805+25998A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251392 | ||||||
| chr4:74251643
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.805+26249C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251643 | ||||||
| chr4:74251716
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.805+26322A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251716 | ||||||
| chr4:74251737
|
A | G | 2 | a0001c0001t0002g0155a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+26343A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74251737 | ||||||
| chr4:74252023
|
T | C | 2 | a0001c0001t0002g0155a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.805+26629T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252023 | ||||||
| chr4:74252086
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.805+26692C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252086 | ||||||
| chr4:74252362
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.805+26968A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252362 | ||||||
| chr4:74252493
|
A | T | 1 | a0001c0001t0003g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.805+27099A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252493 | ||||||
| chr4:74252537
|
C | T | 5 | a0001c0001t0001g0098a0001c0001t0001g0106a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.805+27143C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252537 | ||||||
| chr4:74252537
|
CAAG | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0094 | 2 | HG00438.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.805+27146_805+2714 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74252537 | |||||
| chr4:74252646
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.805+27252C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252646 | ||||||
| chr4:74252694
|
T | A | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+27300T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74252694 | ||||||
| chr4:74253022
|
G | T | 76 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(73): Show | 76 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.805+27628G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253022 | ||||||
| chr4:74253251
|
A | G | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.805+27857A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253251 | ||||||
| chr4:74253284
|
C | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.805+27890C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253284 | ||||||
| chr4:74253351
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.805+27957T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253351 | ||||||
| chr4:74253356
|
G | A | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.805+27962G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74253356 | ||||||
| chr4:74254114
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.806-27311G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254114 | ||||||
| chr4:74254239
|
T | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0184 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.806-27186T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254239 | ||||||
| chr4:74254330
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.806-27095C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254330 | ||||||
| chr4:74254510
|
T | C | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.806-26915T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254510 | ||||||
| chr4:74254570
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26855A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254570 | ||||||
| chr4:74254571
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26854A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254571 | ||||||
| chr4:74254587
|
C | CA | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.806-26825dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74254587 | |||||
| chr4:74254587
|
C | CAA | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.806-26826_806-2682 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74254587 | |||||
| chr4:74254636
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26789A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254636 | ||||||
| chr4:74254645
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.806-26780C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254645 | ||||||
| chr4:74254714
|
G | A | 74 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.806-26711G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254714 | ||||||
| chr4:74254757
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26668A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254757 | ||||||
| chr4:74254762
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26663G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254762 | ||||||
| chr4:74254767
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-26658G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254767 | ||||||
| chr4:74254781
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806-26644A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254781 | ||||||
| chr4:74254807
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.806-26618C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254807 | ||||||
| chr4:74254830
|
T | TTA | 169 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 170 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.806-26594_806-2659 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74254830 | |||||
| chr4:74254836
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.806-26589G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254836 | ||||||
| chr4:74254909
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.806-26516C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254909 | ||||||
| chr4:74254990
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-26435C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74254990 | ||||||
| chr4:74255028
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.806-26397G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255028 | ||||||
| chr4:74255136
|
C | CA | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(23): Show | 26 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.806-26264dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | |||||
| chr4:74255136
|
C | CAA | 48 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0043others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.806-26265_806-2626 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | |||||
| chr4:74255136
|
C | CAAA | 12 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0051others(9): Show | 12 | HG00621.hp1 HG01109.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-26266_806-2626 others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | |||||
| chr4:74255136
|
CA | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 82 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.806-26264delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255136 | |||||
| chr4:74255140
|
A | C | 8 | a0001c0001t0002g0158a0001c0001t0002g0177a0001c0001t0002g0181others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-26285A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255140 | ||||||
| chr4:74255351
|
A | G | 6 | a0001c0001t0003g0083a0001c0001t0003g0086a0001c0001t0003g0087others(3): Show | 6 | HG02083.hp2 NA18939.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.806-26074A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255351 | ||||||
| chr4:74255436
|
AGAAAG | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0167 | 2 | HG02145.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.806-25985_806-2598 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74255436 | |||||
| chr4:74255491
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.806-25934T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255491 | ||||||
| chr4:74255540
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.806-25885C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255540 | ||||||
| chr4:74255631
|
C | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0128 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.806-25794C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255631 | ||||||
| chr4:74255641
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.806-25784C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255641 | ||||||
| chr4:74255688
|
T | A | 2 | a0001c0001t0002g0155a0001c0004t0001g0012 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.806-25737T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74255688 | ||||||
| chr4:74256003
|
A | T | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.806-25422A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256003 | ||||||
| chr4:74256255
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806-25170G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256255 | ||||||
| chr4:74256656
|
C | G | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.806-24769C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256656 | ||||||
| chr4:74256780
|
G | A | 1 | a0001c0001t0003g0130 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.806-24645G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256780 | ||||||
| chr4:74256825
|
T | C | 9 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0143others(6): Show | 9 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-24600T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256825 | ||||||
| chr4:74256915
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.806-24510T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74256915 | ||||||
| chr4:74257184
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.806-24241T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257184 | ||||||
| chr4:74257335
|
C | T | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-24090C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257335 | ||||||
| chr4:74257337
|
G | A | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-24088G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257337 | ||||||
| chr4:74257381
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.806-24044G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257381 | ||||||
| chr4:74257418
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-24007A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257418 | ||||||
| chr4:74257942
|
T | C | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-23483T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257942 | ||||||
| chr4:74257987
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.806-23438C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74257987 | ||||||
| chr4:74258318
|
G | C | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.806-23107G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74258318 | ||||||
| chr4:74258389
|
A | AAC | 11 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-23016_806-2301 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74258389 | |||||
| chr4:74258643
|
T | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-22782T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74258643 | ||||||
| chr4:74258787
|
C | T | 29 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(26): Show | 29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-22638C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74258787 | ||||||
| chr4:74259093
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.806-22332A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259093 | ||||||
| chr4:74259123
|
A | C | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-22302A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259123 | ||||||
| chr4:74259148
|
C | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-22277C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259148 | ||||||
| chr4:74259293
|
G | C | 49 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(46): Show | 49 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.806-22132G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259293 | ||||||
| chr4:74259558
|
T | C | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-21867T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259558 | ||||||
| chr4:74259932
|
A | G | 1 | a0001c0001t0003g0111 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.806-21493A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74259932 | ||||||
| chr4:74260302
|
C | T | 3 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0165 | 3 | HG03041.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.806-21123C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260302 | ||||||
| chr4:74260373
|
A | G | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-21052A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260373 | ||||||
| chr4:74260709
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-20716C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260709 | ||||||
| chr4:74260756
|
C | G | 1 | a0001c0001t0007g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.806-20669C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260756 | ||||||
| chr4:74260856
|
C | T | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-20569C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74260856 | ||||||
| chr4:74260923
|
CAAAG | C | 99 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(96): Show | 99 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.806-20498_806-2049 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74260923 | |||||
| chr4:74261011
|
G | GAA | 15 | a0001c0001t0001g0070a0001c0001t0002g0008a0001c0001t0002g0009others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.806-20408_806-2040 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261011 | |||||
| chr4:74261011
|
GA | G | 11 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-20407delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261011 | |||||
| chr4:74261017
|
A | AAT | 3 | a0001c0001t0001g0118a0001c0001t0002g0137a0001c0001t0007g0055 | 3 | HG02109.hp2 HG02647.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.806-20394_806-2039 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261017 | |||||
| chr4:74261018
|
AT | A | 69 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(66): Show | 69 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.806-20406delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261018 | ||||||
| chr4:74261019
|
T | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0109a0001c0001t0002g0010others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-20406T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261019 | ||||||
| chr4:74261375
|
TCA | T | 29 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(26): Show | 29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-20047_806-2004 others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74261375 | |||||
| chr4:74261727
|
A | G | 2 | a0001c0001t0002g0181a0001c0001t0002g0184 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.806-19698A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261727 | ||||||
| chr4:74261745
|
A | G | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-19680A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74261745 | ||||||
| chr4:74262055
|
A | ATATAT | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-19368_806-1936 others(9): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74262055 | |||||
| chr4:74262077
|
C | G | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-19348C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262077 | ||||||
| chr4:74262188
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-19237G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262188 | ||||||
| chr4:74262200
|
A | C | 29 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(26): Show | 29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-19225A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262200 | ||||||
| chr4:74262248
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.806-19177T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262248 | ||||||
| chr4:74262310
|
C | G | 1 | a0001c0001t0002g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.806-19115C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262310 | ||||||
| chr4:74262319
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.806-19106A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262319 | ||||||
| chr4:74262362
|
A | C | 3 | a0001c0001t0002g0159a0001c0001t0002g0163a0001c0001t0002g0164 | 3 | HG01243.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.806-19063A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262362 | ||||||
| chr4:74262514
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0033 | 2 | NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.806-18911G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262514 | ||||||
| chr4:74262759
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.806-18666A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262759 | ||||||
| chr4:74262771
|
T | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0146 | 2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.806-18654T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262771 | ||||||
| chr4:74262789
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG02280.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.806-18636T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262789 | ||||||
| chr4:74262959
|
A | G | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-18466A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74262959 | ||||||
| chr4:74263200
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.806-18225G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74263200 | ||||||
| chr4:74263784
|
T | G | 29 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(26): Show | 29 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.806-17641T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74263784 | ||||||
| chr4:74263823
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.806-17602C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74263823 | ||||||
| chr4:74264017
|
A | T | 11 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0002g0155others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-17408A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264017 | ||||||
| chr4:74264523
|
T | G | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-16902T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264523 | ||||||
| chr4:74264744
|
G | A | 14 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(11): Show | 14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-16681G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264744 | ||||||
| chr4:74264768
|
T | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-16657T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264768 | ||||||
| chr4:74264779
|
C | A | 2 | a0001c0001t0003g0036a0001c0001t0003g0039 | 2 | NA18973.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.806-16646C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74264779 | ||||||
| chr4:74265112
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.806-16313A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74265112 | ||||||
| chr4:74265243
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-16182T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74265243 | ||||||
| chr4:74265726
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 150 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.806-15699C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74265726 | ||||||
| chr4:74266182
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.806-15243G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266182 | ||||||
| chr4:74266228
|
TA | T | 17 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0045others(14): Show | 17 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.806-15196delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266228 | ||||||
| chr4:74266569
|
G | A | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-14856G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266569 | ||||||
| chr4:74266614
|
A | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-14811A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266614 | ||||||
| chr4:74266636
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0146 | 3 | HG01978.hp2 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.806-14789C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266636 | ||||||
| chr4:74266931
|
T | C | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-14494T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266931 | ||||||
| chr4:74266979
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.806-14446T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74266979 | ||||||
| chr4:74267081
|
C | T | 118 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(115): Show | 118 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.806-14344C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267081 | ||||||
| chr4:74267243
|
A | G | 1 | a0001c0005t0001g0099 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.806-14182A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267243 | ||||||
| chr4:74267304
|
CT | C | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-14117delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267304 | |||||
| chr4:74267319
|
CT | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0143 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.806-14103delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267319 | |||||
| chr4:74267327
|
CT | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0143 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.806-14095delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267327 | |||||
| chr4:74267371
|
T | TTTTC | 10 | a0001c0001t0001g0093a0001c0001t0002g0155a0001c0001t0002g0158others(7): Show | 10 | HG02135.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-14034_806-1403 others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267371 | |||||
| chr4:74267371
|
T | TTTTCTTT others(9): Show |
1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-14046_806-1403 others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267371 | |||||
| chr4:74267372
|
T | TTTCTTTC others(28): Show |
1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-14031_806-1403 others(39): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74267372 | |||||
| chr4:74267434
|
A | G | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-13991A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267434 | ||||||
| chr4:74267615
|
T | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-13810T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267615 | ||||||
| chr4:74267700
|
T | G | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-13725T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267700 | ||||||
| chr4:74267882
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-13543C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267882 | ||||||
| chr4:74267969
|
C | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-13456C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267969 | ||||||
| chr4:74267996
|
G | A | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-13429G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74267996 | ||||||
| chr4:74268021
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.806-13404G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268021 | ||||||
| chr4:74268189
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806-13236T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268189 | ||||||
| chr4:74268470
|
A | G | 2 | a0001c0001t0003g0185a0001c0003t0004g0047 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.806-12955A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268470 | ||||||
| chr4:74268665
|
A | T | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.806-12760A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268665 | ||||||
| chr4:74268906
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.806-12519A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74268906 | ||||||
| chr4:74269171
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.806-12254T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269171 | ||||||
| chr4:74269288
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-12137A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269288 | ||||||
| chr4:74269379
|
A | G | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-12046A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269379 | ||||||
| chr4:74269425
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0139others(1): Show | 5 | HG02280.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-12000A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269425 | ||||||
| chr4:74269460
|
T | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-11965T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74269460 | ||||||
| chr4:74270101
|
T | A | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806-11324T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270101 | ||||||
| chr4:74270177
|
A | G | 5 | a0001c0001t0001g0098a0001c0001t0001g0106a0001c0001t0001g0112others(2): Show | 5 | HG01123.hp2 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.806-11248A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270177 | ||||||
| chr4:74270355
|
G | C | 1 | a0001c0001t0002g0195 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.806-11070G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270355 | ||||||
| chr4:74270521
|
T | C | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-10904T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270521 | ||||||
| chr4:74270583
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.806-10842G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270583 | ||||||
| chr4:74270612
|
G | A | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-10813G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270612 | ||||||
| chr4:74270650
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.806-10775T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270650 | ||||||
| chr4:74270655
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.806-10770G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270655 | ||||||
| chr4:74270711
|
G | A | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-10714G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270711 | ||||||
| chr4:74270794
|
C | A | 110 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.806-10631C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270794 | ||||||
| chr4:74270919
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.806-10506C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270919 | ||||||
| chr4:74270925
|
G | T | 110 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.806-10500G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270925 | ||||||
| chr4:74270986
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0064a0001c0001t0001g0120 | 3 | HG00438.hp1 HG00621.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.806-10439T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74270986 | ||||||
| chr4:74271043
|
C | T | 108 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.806-10382C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271043 | ||||||
| chr4:74271297
|
G | A | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.806-10128G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271297 | ||||||
| chr4:74271304
|
G | T | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.806-10121G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271304 | ||||||
| chr4:74271371
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.806-10054T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271371 | ||||||
| chr4:74271407
|
G | A | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.806-10018G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271407 | ||||||
| chr4:74271442
|
T | G | 11 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0002g0155others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-9983T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271442 | ||||||
| chr4:74271454
|
C | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-9971C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271454 | ||||||
| chr4:74271523
|
G | C | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-9902G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271523 | ||||||
| chr4:74271537
|
T | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-9888T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271537 | ||||||
| chr4:74271587
|
T | A | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-9838T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271587 | ||||||
| chr4:74271610
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.806-9815C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271610 | ||||||
| chr4:74271643
|
G | C | 14 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(11): Show | 14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-9782G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271643 | ||||||
| chr4:74271651
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.806-9774G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271651 | ||||||
| chr4:74271680
|
A | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.806-9745A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271680 | ||||||
| chr4:74271874
|
GA | G | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.806-9550delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271874 | ||||||
| chr4:74271898
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.806-9527T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74271898 | ||||||
| chr4:74272010
|
T | C | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0177others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-9415T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272010 | ||||||
| chr4:74272023
|
A | C | 11 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0002g0155others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-9402A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272023 | ||||||
| chr4:74272050
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.806-9375G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272050 | ||||||
| chr4:74272307
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0013 | 2 | HG01123.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.806-9118C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272307 | ||||||
| chr4:74272581
|
G | A | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.806-8844G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272581 | ||||||
| chr4:74272662
|
A | T | 11 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0002g0155others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-8763A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272662 | ||||||
| chr4:74272805
|
C | T | 45 | a0001c0001t0001g0051a0001c0001t0003g0011a0001c0001t0003g0025others(42): Show | 45 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.806-8620C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272805 | ||||||
| chr4:74272949
|
A | T | 11 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0002g0155others(8): Show | 11 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.806-8476A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74272949 | ||||||
| chr4:74273143
|
A | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-8282A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273143 | ||||||
| chr4:74273524
|
C | T | 114 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 114 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.806-7901C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273524 | ||||||
| chr4:74273613
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0003g0057 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.806-7812A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273613 | ||||||
| chr4:74273938
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806-7487C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74273938 | ||||||
| chr4:74274012
|
A | AT | 86 | a0001c0001t0001g0118a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 86 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.806-7403dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74274012 | |||||
| chr4:74274290
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-7135G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274290 | ||||||
| chr4:74274596
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-6829A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274596 | ||||||
| chr4:74274602
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.806-6823C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274602 | ||||||
| chr4:74274734
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-6691C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274734 | ||||||
| chr4:74274814
|
A | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0100 | 3 | NA18965.hp2 NA18968.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.806-6611A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74274814 | ||||||
| chr4:74275039
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.806-6386C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275039 | ||||||
| chr4:74275406
|
T | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-6019T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275406 | ||||||
| chr4:74275445
|
C | T | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.806-5980C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275445 | ||||||
| chr4:74275570
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.806-5855A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275570 | ||||||
| chr4:74275640
|
C | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(190): Show | 194 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.806-5785C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275640 | ||||||
| chr4:74275934
|
A | C | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-5491A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275934 | ||||||
| chr4:74275969
|
T | A | 115 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.806-5456T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74275969 | ||||||
| chr4:74276008
|
G | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(42): Show | 45 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.806-5417G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276008 | ||||||
| chr4:74276361
|
A | G | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-5064A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276361 | ||||||
| chr4:74276571
|
C | A | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.806-4854C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276571 | ||||||
| chr4:74276596
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-4829G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276596 | ||||||
| chr4:74276631
|
A | T | 10 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0142others(7): Show | 10 | HG01243.hp2 HG02976.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-4794A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276631 | ||||||
| chr4:74276729
|
C | T | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.806-4696C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276729 | ||||||
| chr4:74276892
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.806-4533A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74276892 | ||||||
| chr4:74277135
|
C | T | 13 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(10): Show | 13 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.806-4290C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277135 | ||||||
| chr4:74277154
|
A | AT | 40 | a0001c0001t0001g0077a0001c0001t0002g0002a0001c0001t0002g0003others(37): Show | 40 | HG00280.hp1 HG00621.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.806-4256dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277154 | |||||
| chr4:74277154
|
A | ATT | 23 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0034others(20): Show | 23 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.806-4257_806-4256d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277154 | |||||
| chr4:74277154
|
AT | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(50): Show | 54 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.806-4256delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277154 | |||||
| chr4:74277305
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.806-4120A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277305 | ||||||
| chr4:74277355
|
C | T | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-4070C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277355 | ||||||
| chr4:74277356
|
G | A | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-4069G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277356 | ||||||
| chr4:74277365
|
G | A | 3 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176 | 3 | HG01109.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.806-4060G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277365 | ||||||
| chr4:74277418
|
G | C | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806-4007G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277418 | ||||||
| chr4:74277485
|
A | C | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-3940A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277485 | ||||||
| chr4:74277726
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.806-3699C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74277726 | ||||||
| chr4:74277805
|
A | ATTTG | 30 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(27): Show | 30 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.806-3592_806-3589d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277805 | |||||
| chr4:74277805
|
A | ATTTGTTT others(1): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0105a0001c0001t0007g0055 | 3 | HG01891.hp1 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.806-3596_806-3589d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74277805 | |||||
| chr4:74278023
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806-3402C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278023 | ||||||
| chr4:74278026
|
G | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.806-3399G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278026 | ||||||
| chr4:74278157
|
G | A | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.806-3268G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278157 | ||||||
| chr4:74278171
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.806-3254A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278171 | ||||||
| chr4:74278291
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.806-3134A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278291 | ||||||
| chr4:74278377
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.806-3048T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278377 | ||||||
| chr4:74278449
|
A | G | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.806-2976A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278449 | ||||||
| chr4:74278856
|
T | C | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-2569T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278856 | ||||||
| chr4:74278896
|
A | C | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-2529A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74278896 | ||||||
| chr4:74279005
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.806-2420C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279005 | ||||||
| chr4:74279079
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.806-2346C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279079 | ||||||
| chr4:74279199
|
A | G | 3 | a0001c0001t0003g0011a0001c0001t0003g0052a0001c0001t0003g0167 | 3 | HG02145.hp1 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.806-2226A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279199 | ||||||
| chr4:74279480
|
T | G | 2 | a0001c0001t0003g0148a0001c0001t0003g0153 | 2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.806-1945T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279480 | ||||||
| chr4:74279697
|
A | T | 57 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.806-1728A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279697 | ||||||
| chr4:74279749
|
A | G | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-1676A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279749 | ||||||
| chr4:74279818
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806-1607A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279818 | ||||||
| chr4:74279864
|
T | C | 115 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(112): Show | 115 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.806-1561T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279864 | ||||||
| chr4:74279922
|
A | G | 1 | a0001c0005t0001g0099 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.806-1503A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74279922 | ||||||
| chr4:74280047
|
A | G | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(87): Show | 90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.806-1378A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280047 | ||||||
| chr4:74280078
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806-1347G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280078 | ||||||
| chr4:74280215
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806-1210G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280215 | ||||||
| chr4:74280426
|
A | G | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.806-999A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280426 | ||||||
| chr4:74280607
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.806-818A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280607 | ||||||
| chr4:74280630
|
GT | G | 101 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(98): Show | 101 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.806-783delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280630 | |||||
| chr4:74280630
|
GTT | G | 8 | a0001c0001t0002g0050a0001c0001t0002g0158a0001c0001t0002g0177others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-784_806-783del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280630 | |||||
| chr4:74280642
|
T | A | 39 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0108others(36): Show | 39 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.806-783T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280642 | ||||||
| chr4:74280642
|
T | TA | 4 | a0001c0001t0001g0098a0001c0001t0001g0112a0001c0001t0001g0129others(1): Show | 4 | HG01978.hp2 HG01981.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-777dupA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280642 | |||||
| chr4:74280642
|
TA | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.806-777delA | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280642 | |||||
| chr4:74280643
|
A | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.806-782A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74280643 | ||||||
| chr4:74280840
|
TAAAA | T | 15 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.806-583_806-580del others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74280840 | |||||
| chr4:74281078
|
A | T | 1 | a0001c0001t0002g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.806-347A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281078 | ||||||
| chr4:74281108
|
G | A | 43 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(40): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.806-317G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281108 | ||||||
| chr4:74281196
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806-229G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281196 | ||||||
| chr4:74281271
|
C | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0084a0002c0002t0001g0076 | 3 | HG00408.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.806-154C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281271 | ||||||
| chr4:74281324
|
C | CGT | 2 | a0001c0001t0001g0098a0001c0001t0001g0109 | 2 | HG02083.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.806-76_806-75dupGT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281324
|
C | CGTGTGTG others(3): Show |
8 | a0001c0001t0001g0022a0001c0001t0002g0019a0001c0001t0002g0050others(5): Show | 8 | HG02970.hp2 HG03195.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.806-84_806-75dupGT others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281324
|
C | CGTGTGTG others(5): Show |
9 | a0001c0001t0002g0010a0001c0001t0002g0142a0001c0001t0002g0145others(6): Show | 9 | HG01243.hp2 HG02976.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.806-86_806-75dupGT others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281324
|
C | CGTGTGTG others(7): Show |
70 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0030others(67): Show | 70 | HG00280.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.806-88_806-75dupGT others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281324
|
C | CGTGTGTG others(9): Show |
15 | a0001c0001t0001g0033a0001c0001t0001g0065a0001c0001t0001g0189others(12): Show | 15 | HG00621.hp1 HG01109.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.806-90_806-75dupGT others(14): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281324
|
C | CGTGTGTG others(11): Show |
12 | a0001c0001t0001g0032a0001c0001t0002g0002a0001c0001t0002g0003others(9): Show | 12 | HG00408.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.806-92_806-75dupGT others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281324
|
C | CGTGTGTG others(13): Show |
4 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0009others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-94_806-75dupGT others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 74281324 | |||||
| chr4:74281341
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.806-84G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 6/7 | chr4 | 74281341 | ||||||
| chr4:74282108
|
A | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+558A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282108 | ||||||
| chr4:74282171
|
C | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.931+621C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282171 | ||||||
| chr4:74282278
|
C | G | 23 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0034others(20): Show | 23 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.931+728C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282278 | ||||||
| chr4:74282286
|
G | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+736G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282286 | ||||||
| chr4:74282404
|
G | GTTCTTCT others(12): Show |
12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+855_931+856ins others(19): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74282404 | |||||
| chr4:74282408
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+858C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282408 | ||||||
| chr4:74282653
|
T | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(87): Show | 90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+1103T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282653 | ||||||
| chr4:74282792
|
T | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(53): Show | 56 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.931+1242T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282792 | ||||||
| chr4:74282933
|
A | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.931+1383A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282933 | ||||||
| chr4:74282960
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+1410T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74282960 | ||||||
| chr4:74283004
|
G | GC | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(87): Show | 90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+1455dupC | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74283004 | |||||
| chr4:74283205
|
A | G | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(87): Show | 90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+1655A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283205 | ||||||
| chr4:74283237
|
T | A | 30 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(27): Show | 30 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.931+1687T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283237 | ||||||
| chr4:74283374
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.931+1824C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283374 | ||||||
| chr4:74283438
|
C | A | 5 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(2): Show | 5 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+1888C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283438 | ||||||
| chr4:74283649
|
G | C | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+2099G>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283649 | ||||||
| chr4:74283719
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.931+2169G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74283719 | ||||||
| chr4:74284035
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.931+2485A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284035 | ||||||
| chr4:74284094
|
G | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+2544G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284094 | ||||||
| chr4:74284363
|
T | C | 21 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 21 | HG00408.hp1 HG00597.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.931+2813T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284363 | ||||||
| chr4:74284419
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.931+2869T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284419 | ||||||
| chr4:74284443
|
T | C | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.931+2893T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284443 | ||||||
| chr4:74284493
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.931+2943C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284493 | ||||||
| chr4:74284584
|
G | T | 1 | a0001c0001t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.931+3034G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284584 | ||||||
| chr4:74284783
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.931+3233G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284783 | ||||||
| chr4:74284930
|
G | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+3380G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74284930 | ||||||
| chr4:74285024
|
C | G | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.931+3474C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285024 | ||||||
| chr4:74285106
|
T | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(43): Show | 46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.931+3556T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285106 | ||||||
| chr4:74285465
|
A | G | 44 | a0001c0001t0003g0011a0001c0001t0003g0025a0001c0001t0003g0026others(41): Show | 44 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.931+3915A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285465 | ||||||
| chr4:74285708
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.931+4158C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285708 | ||||||
| chr4:74285829
|
G | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0193 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.931+4279G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285829 | ||||||
| chr4:74285867
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+4317C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285867 | ||||||
| chr4:74285961
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.931+4411A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74285961 | ||||||
| chr4:74286103
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.931+4553A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286103 | ||||||
| chr4:74286192
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.931+4642C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286192 | ||||||
| chr4:74286262
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.931+4712T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286262 | ||||||
| chr4:74286719
|
G | A | 21 | a0001c0001t0003g0011a0001c0001t0003g0025a0001c0001t0003g0026others(18): Show | 21 | HG00280.hp1 HG00621.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.931+5169G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286719 | ||||||
| chr4:74286853
|
T | C | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+5303T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74286853 | ||||||
| chr4:74287013
|
A | C | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+5463A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287013 | ||||||
| chr4:74287020
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA18945.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.931+5470T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287020 | ||||||
| chr4:74287140
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.931+5590A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287140 | ||||||
| chr4:74287194
|
G | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+5644G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287194 | ||||||
| chr4:74287293
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.931+5743A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287293 | ||||||
| chr4:74287616
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.931+6066G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287616 | ||||||
| chr4:74287701
|
C | T | 23 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0034others(20): Show | 23 | HG01099.hp2 HG01106.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.931+6151C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287701 | ||||||
| chr4:74287964
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0105 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.931+6414G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287964 | ||||||
| chr4:74287993
|
A | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(53): Show | 56 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.931+6443A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74287993 | ||||||
| chr4:74288049
|
T | A | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+6499T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288049 | ||||||
| chr4:74288181
|
G | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0094 | 3 | HG00438.hp2 NA19081.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.931+6631G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288181 | ||||||
| chr4:74288206
|
G | A | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+6656G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288206 | ||||||
| chr4:74288240
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.931+6690G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288240 | ||||||
| chr4:74288304
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931+6754A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288304 | ||||||
| chr4:74288364
|
G | T | 1 | a0001c0001t0002g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.931+6814G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288364 | ||||||
| chr4:74288479
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.931+6929T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288479 | ||||||
| chr4:74288721
|
G | A | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.931+7171G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288721 | ||||||
| chr4:74288802
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.931+7252C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74288802 | ||||||
| chr4:74289179
|
C | A | 14 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(11): Show | 14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.931+7629C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289179 | ||||||
| chr4:74289509
|
C | G | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(87): Show | 90 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.931+7959C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289509 | ||||||
| chr4:74289717
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0013 | 2 | HG01123.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.931+8167G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289717 | ||||||
| chr4:74289946
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931+8396T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74289946 | ||||||
| chr4:74290019
|
C | A | 32 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(29): Show | 32 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.931+8469C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74290019 | ||||||
| chr4:74290303
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.931+8753G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74290303 | ||||||
| chr4:74290322
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0105 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.931+8772A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74290322 | ||||||
| chr4:74290640
|
C | CTGTG | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.931+9108_931+9111d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74290640 | |||||
| chr4:74291003
|
C | CTTT | 11 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0090others(8): Show | 11 | HG00597.hp2 HG00621.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+9483_931+9485d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTT | 7 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0001g0114others(4): Show | 7 | HG02004.hp1 HG02040.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+9482_931+9485d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0001g0133a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG01981.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9478_931+9485d others(10): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(2): Show |
11 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(8): Show | 11 | HG02004.hp2 HG02015.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+9477_931+9485d others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00408.hp1 HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.931+9476_931+9485d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.931+9475_931+9485d others(13): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.931+9473_931+9485d others(15): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0043 | 2 | HG02965.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.931+9472_931+9485d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.931+9471_931+9485d others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0015 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.931+9470_931+9485d others(18): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0180 | 3 | HG01123.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.931+9469_931+9485d others(19): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0014a0001c0001t0001g0072a0001c0001t0001g0144others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+9468_931+9485d others(20): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.931+9467_931+9485d others(21): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(13): Show |
9 | a0001c0001t0001g0048a0001c0001t0001g0068a0001c0001t0001g0073others(6): Show | 9 | HG01123.hp2 HG01981.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.931+9466_931+9485d others(22): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(14): Show |
9 | a0001c0001t0001g0063a0001c0001t0001g0080a0001c0001t0001g0094others(6): Show | 9 | HG01106.hp1 HG01978.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.931+9465_931+9485d others(23): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0091others(2): Show | 5 | HG00408.hp2 HG01261.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+9464_931+9485d others(24): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0123 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.931+9463_931+9485d others(25): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.931+9462_931+9485d others(26): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.931+9461_931+9485d others(27): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0079 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.931+9459_931+9485d others(29): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.931+9458_931+9485d others(30): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.931+9453C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291003 | ||||||
| chr4:74291003
|
CTTT | C | 8 | a0001c0001t0001g0150a0001c0001t0001g0178a0001c0001t0003g0036others(5): Show | 8 | HG00597.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.931+9483_931+9485d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
CTTTT | C | 37 | a0001c0001t0001g0071a0001c0001t0001g0149a0001c0001t0002g0005others(34): Show | 37 | HG00280.hp2 HG00621.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.931+9482_931+9485d others(6): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
CTTTTT | C | 14 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(11): Show | 14 | HG00280.hp1 HG01243.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.931+9481_931+9485d others(7): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
CTTTTTTT others(2): Show |
C | 29 | a0001c0001t0001g0067a0001c0001t0002g0008a0001c0001t0002g0009others(26): Show | 29 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.931+9477_931+9485d others(11): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0045a0001c0001t0002g0160 | 2 | NA18954.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.931+9476_931+9485d others(12): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.931+9472_931+9485d others(16): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291003
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.931+9471_931+9485d others(17): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74291003 | |||||
| chr4:74291034
|
TTGAGATG others(64): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.931+9485_931+9555d others(73): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291034 | ||||||
| chr4:74291163
|
G | A | 3 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176 | 3 | HG01109.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.931+9613G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291163 | ||||||
| chr4:74291315
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.931+9765C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291315 | ||||||
| chr4:74291372
|
T | G | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(86): Show | 89 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.931+9822T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291372 | ||||||
| chr4:74291587
|
T | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+10037T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291587 | ||||||
| chr4:74291785
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0002g0018 | 2 | HG02622.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.932-9912A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74291785 | ||||||
| chr4:74292281
|
T | C | 1 | a0001c0001t0003g0025 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.932-9416T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292281 | ||||||
| chr4:74292304
|
A | T | 5 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0004g0016others(2): Show | 5 | HG02615.hp2 HG03130.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-9393A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292304 | ||||||
| chr4:74292313
|
AT | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0084a0002c0002t0001g0076 | 3 | HG00408.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.932-9382delT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74292313 | |||||
| chr4:74292515
|
A | G | 88 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(85): Show | 88 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.932-9182A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292515 | ||||||
| chr4:74292623
|
A | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.932-9074A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292623 | ||||||
| chr4:74292803
|
G | A | 118 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(115): Show | 118 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.932-8894G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74292803 | ||||||
| chr4:74293137
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.932-8560C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293137 | ||||||
| chr4:74293188
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.932-8509C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293188 | ||||||
| chr4:74293336
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.932-8361T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293336 | ||||||
| chr4:74293348
|
A | G | 1 | a0001c0001t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.932-8349A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293348 | ||||||
| chr4:74293425
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.932-8272G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293425 | ||||||
| chr4:74293502
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-8195T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293502 | ||||||
| chr4:74293591
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.932-8106G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293591 | ||||||
| chr4:74293755
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.932-7942A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74293755 | ||||||
| chr4:74294078
|
C | G | 2 | a0001c0001t0003g0148a0001c0001t0003g0153 | 2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.932-7619C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294078 | ||||||
| chr4:74294338
|
A | AT | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-7357dupT | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74294338 | |||||
| chr4:74294486
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-7211G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294486 | ||||||
| chr4:74294494
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-7203A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294494 | ||||||
| chr4:74294500
|
A | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-7197A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294500 | ||||||
| chr4:74294506
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.932-7191A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294506 | ||||||
| chr4:74294859
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.932-6838A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294859 | ||||||
| chr4:74294936
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.932-6761G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74294936 | ||||||
| chr4:74295107
|
C | T | 46 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(43): Show | 46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.932-6590C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295107 | ||||||
| chr4:74295177
|
A | G | 46 | a0001c0001t0003g0011a0001c0001t0003g0025a0001c0001t0003g0026others(43): Show | 46 | HG00280.hp1 HG00621.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.932-6520A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295177 | ||||||
| chr4:74295599
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.932-6098A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295599 | ||||||
| chr4:74295670
|
T | C | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-6027T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295670 | ||||||
| chr4:74295712
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.932-5985T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295712 | ||||||
| chr4:74295935
|
C | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(41): Show | 44 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.932-5762C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74295935 | ||||||
| chr4:74296083
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.932-5614C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296083 | ||||||
| chr4:74296189
|
C | T | 1 | a0001c0001t0006g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.932-5508C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296189 | ||||||
| chr4:74296207
|
T | C | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-5490T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296207 | ||||||
| chr4:74296241
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.932-5456A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296241 | ||||||
| chr4:74296480
|
C | T | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-5217C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296480 | ||||||
| chr4:74296481
|
T | C | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-5216T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296481 | ||||||
| chr4:74296581
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.932-5116C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296581 | ||||||
| chr4:74296591
|
A | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.932-5106A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296591 | ||||||
| chr4:74296605
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.932-5092C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296605 | ||||||
| chr4:74296753
|
C | G | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-4944C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296753 | ||||||
| chr4:74296754
|
A | C | 1 | a0001c0001t0003g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.932-4943A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296754 | ||||||
| chr4:74296961
|
G | A | 118 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(115): Show | 118 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.932-4736G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74296961 | ||||||
| chr4:74297030
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.932-4667T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297030 | ||||||
| chr4:74297398
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-4299G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297398 | ||||||
| chr4:74297425
|
A | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(43): Show | 46 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.932-4272A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297425 | ||||||
| chr4:74297642
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.932-4055G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297642 | ||||||
| chr4:74297703
|
C | A | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.932-3994C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297703 | ||||||
| chr4:74297771
|
CTT | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0153 | 2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.932-3924_932-3923d others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74297771 | |||||
| chr4:74297780
|
A | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.932-3917A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297780 | ||||||
| chr4:74297787
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.932-3910A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74297787 | ||||||
| chr4:74298312
|
G | A | 14 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(11): Show | 14 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.932-3385G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298312 | ||||||
| chr4:74298450
|
T | G | 1 | a0001c0001t0005g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.932-3247T>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298450 | ||||||
| chr4:74298487
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.932-3210C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298487 | ||||||
| chr4:74298559
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.932-3138A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298559 | ||||||
| chr4:74298566
|
G | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0091 | 2 | HG02109.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.932-3131G>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298566 | ||||||
| chr4:74298851
|
T | C | 1 | a0001c0001t0003g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.932-2846T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298851 | ||||||
| chr4:74298862
|
T | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-2835T>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74298862 | ||||||
| chr4:74299026
|
A | G | 1 | a0001c0001t0002g0002 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.932-2671A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299026 | ||||||
| chr4:74299088
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.932-2609A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299088 | ||||||
| chr4:74299401
|
CAGCAGT | C | 4 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0003g0026others(1): Show | 4 | HG02723.hp2 HG03453.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-2267_932-2262d others(8): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74299401 | |||||
| chr4:74299404
|
CAGT | C | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-2290_932-2288d others(5): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74299404 | |||||
| chr4:74299413
|
T | C | 31 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(28): Show | 31 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.932-2284T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299413 | ||||||
| chr4:74299706
|
C | G | 13 | a0001c0001t0002g0045a0001c0001t0002g0115a0001c0001t0002g0131others(10): Show | 13 | HG03688.hp2 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.932-1991C>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299706 | ||||||
| chr4:74299755
|
A | G | 1 | a0001c0001t0003g0153 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.932-1942A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299755 | ||||||
| chr4:74299780
|
C | A | 2 | a0001c0001t0005g0141a0001c0001t0005g0166 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.932-1917C>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299780 | ||||||
| chr4:74299817
|
C | T | 3 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0003t0004g0047 | 3 | HG02615.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-1880C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74299817 | ||||||
| chr4:74300033
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.932-1664G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300033 | ||||||
| chr4:74300211
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.932-1486T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300211 | ||||||
| chr4:74300363
|
A | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.932-1334A>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300363 | ||||||
| chr4:74300463
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.932-1234T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300463 | ||||||
| chr4:74300853
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.932-844A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300853 | ||||||
| chr4:74300870
|
A | G | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-827A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74300870 | ||||||
| chr4:74301182
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0105 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.932-515G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301182 | ||||||
| chr4:74301262
|
A | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.932-435A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301262 | ||||||
| chr4:74301354
|
C | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-343C>T | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301354 | ||||||
| chr4:74301355
|
A | C | 1 | a0001c0001t0002g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.932-342A>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301355 | ||||||
| chr4:74301447
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | NA18961.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.932-250G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301447 | ||||||
| chr4:74301464
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.932-233G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301464 | ||||||
| chr4:74301530
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.932-167A>G | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301530 | ||||||
| chr4:74301532
|
C | CGT | 23 | a0001c0001t0002g0010a0001c0001t0002g0056a0001c0001t0003g0027others(20): Show | 23 | HG01099.hp2 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.932-140_932-139dup others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74301532 | |||||
| chr4:74301532
|
CGT | C | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 25 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.932-140_932-139del others(2): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74301532 | |||||
| chr4:74301532
|
CGTGT | C | 9 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0142others(6): Show | 9 | HG01243.hp2 HG02976.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.932-142_932-139del others(4): Show |
MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 74301532 | |||||
| chr4:74301549
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.932-148G>A | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301549 | ||||||
| chr4:74301563
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.932-134T>C | MTHFD2L | ENSG00000163738.19 | transcript | ENST00000325278.7 | protein_coding | 7/7 | chr4 | 74301563 |