geneid | 113115 |
---|---|
ensemblid | ENSG00000146410.12 |
hgncid | 21115 |
symbol | MTFR2 |
name | mitochondrial fission regulator 2 |
refseq_nuc | NM_001099286.3 |
refseq_prot | NP_001092756.1 |
ensembl_nuc | ENST00000420702.6 |
ensembl_prot | ENSP00000395232.1 |
mane_status | MANE Select |
chr | chr6 |
start | 136231034 |
end | 136250311 |
strand | - |
ver | v1.2 |
region | chr6:136231034-136250311 |
region5000 | chr6:136226034-136255311 |
regionname0 | MTFR2_chr6_136231034_136250311 |
regionname5000 | MTFR2_chr6_136226034_136255311 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 385 | 374 | 58 | 73 | 197 | 16 | 28 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0002 | 0/0 | 385 | 24 | 23 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0003 | 0/0 | 385 | 8 | 6 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0004 | 0/0 | 385 | 4 | 4 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0005 | 0/0 | 385 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0006 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0007 | 0/0 | 212 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0008 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0009 | 0/0 | 385 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0010 | 0/0 | 385 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1158 | 340 | 49 | 62 | 185 | 15 | 27 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0002 | 0/0 | 1158 | 24 | 23 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0003 | 0/0 | 1158 | 16 | 0 | 7 | 8 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0004 | 0/0 | 1158 | 9 | 8 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0005 | 0/0 | 1158 | 8 | 6 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0006 | 0/0 | 1158 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0007 | 0/0 | 1158 | 3 | 0 | 2 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0008 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0009 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0010 | 0/0 | 1283 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0011 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0012 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0013 | 0/0 | 1158 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0014 | 0/0 | 1158 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0015 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0016 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0017 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
c0018 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 632 | 392 | 95 | 75 | 177 | 16 | 27 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
t0002 | 0/0 | 632 | 10 | 0 | 0 | 10 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
t0003 | 0/0 | 632 | 8 | 0 | 0 | 8 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
t0004 | 0/0 | 632 | 5 | 0 | 0 | 5 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
t0005 | 0/0 | 610 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
t0006 | 0/0 | 632 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
t0007 | 0/0 | 632 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 17 | 1 | 3 | 13 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0002 | 0/0 | 14 | 0 | 3 | 7 | 1 | 3 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0003 | 0/0 | 13 | 0 | 2 | 8 | 1 | 2 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0004 | 0/0 | 11 | 0 | 3 | 6 | 1 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0005 | 0/0 | 6 | 1 | 1 | 0 | 3 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0009 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0024 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0040 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/1 | 340 | 49 | 62 | 185 | 15 | 27 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 16 | 0 | 7 | 8 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0004 | a0001 | c0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0007 | a0001 | c0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0011 | a0001 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0013 | a0001 | c0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0014 | a0001 | c0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0002c0002 | a0002 | c0002 | 0/0 | 24 | 23 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0003c0005 | a0003 | c0005 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0004c0009 | a0004 | c0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0004c0018 | a0004 | c0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0005c0008 | a0005 | c0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0006c0017 | a0006 | c0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0007c0010 | a0007 | c0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0008c0016 | a0008 | c0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0009c0015 | a0009 | c0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0010c0012 | a0010 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 314 | 48 | 61 | 162 | 15 | 26 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 16 | 0 | 7 | 8 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0007t0001 | a0001 | c0007 | t0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0011t0001 | a0001 | c0011 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0001c0014t0001 | a0001 | c0014 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 24 | 23 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0003c0005t0001 | a0003 | c0005 | t0001 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0004c0009t0001 | a0004 | c0009 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0004c0018t0001 | a0004 | c0018 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0005c0008t0001 | a0005 | c0008 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0006c0017t0001 | a0006 | c0017 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0007c0010t0001 | a0007 | c0010 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0008c0016t0001 | a0008 | c0016 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0009c0015t0001 | a0009 | c0015 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
a0010c0012t0001 | a0010 | c0012 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 17 | 1 | 3 | 13 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 14 | 0 | 3 | 7 | 1 | 3 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 13 | 0 | 2 | 8 | 1 | 2 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 11 | 0 | 3 | 6 | 1 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 6 | 1 | 1 | 0 | 3 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0261 | a0001 | c0001 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0262 | a0001 | c0001 | t0001 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0275 | a0001 | c0001 | t0002 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0276 | a0001 | c0001 | t0002 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0277 | a0001 | c0001 | t0002 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0278 | a0001 | c0001 | t0002 | g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0002g0279 | a0001 | c0001 | t0002 | g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0003g0280 | a0001 | c0001 | t0003 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0003g0281 | a0001 | c0001 | t0003 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0003g0282 | a0001 | c0001 | t0003 | g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0003g0283 | a0001 | c0001 | t0003 | g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0004g0053 | a0001 | c0001 | t0004 | g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0004g0272 | a0001 | c0001 | t0004 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0004g0273 | a0001 | c0001 | t0004 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0004g0274 | a0001 | c0001 | t0004 | g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0005g0055 | a0001 | c0001 | t0005 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0006g0133 | a0001 | c0001 | t0006 | g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0001t0007g0271 | a0001 | c0001 | t0007 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0021 | a0001 | c0003 | t0001 | g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0025 | a0001 | c0003 | t0001 | g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0042 | a0001 | c0003 | t0001 | g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0101 | a0001 | c0003 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0120 | a0001 | c0003 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0121 | a0001 | c0003 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0149 | a0001 | c0003 | t0001 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0187 | a0001 | c0003 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0200 | a0001 | c0003 | t0001 | g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0259 | a0001 | c0003 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0003t0001g0260 | a0001 | c0003 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0051 | a0001 | c0004 | t0001 | g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0109 | a0001 | c0004 | t0001 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0206 | a0001 | c0004 | t0001 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0209 | a0001 | c0004 | t0001 | g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0242 | a0001 | c0004 | t0001 | g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0243 | a0001 | c0004 | t0001 | g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0246 | a0001 | c0004 | t0001 | g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0004t0001g0269 | a0001 | c0004 | t0001 | g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0006t0001g0124 | a0001 | c0006 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0006t0001g0136 | a0001 | c0006 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0006t0001g0163 | a0001 | c0006 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0007t0001g0135 | a0001 | c0007 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0007t0001g0254 | a0001 | c0007 | t0001 | g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0007t0001g0255 | a0001 | c0007 | t0001 | g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0011t0001g0263 | a0001 | c0011 | t0001 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0013t0001g0166 | a0001 | c0013 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0001c0014t0001g0156 | a0001 | c0014 | t0001 | g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0015 | a0002 | c0002 | t0001 | g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0016 | a0002 | c0002 | t0001 | g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0032 | a0002 | c0002 | t0001 | g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0048 | a0002 | c0002 | t0001 | g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0059 | a0002 | c0002 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0060 | a0002 | c0002 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0097 | a0002 | c0002 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0224 | a0002 | c0002 | t0001 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0226 | a0002 | c0002 | t0001 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0227 | a0002 | c0002 | t0001 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0228 | a0002 | c0002 | t0001 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0232 | a0002 | c0002 | t0001 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0233 | a0002 | c0002 | t0001 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0234 | a0002 | c0002 | t0001 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0237 | a0002 | c0002 | t0001 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0239 | a0002 | c0002 | t0001 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0248 | a0002 | c0002 | t0001 | g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0002c0002t0001g0249 | a0002 | c0002 | t0001 | g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0003c0005t0001g0049 | a0003 | c0005 | t0001 | g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0003c0005t0001g0050 | a0003 | c0005 | t0001 | g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0003c0005t0001g0229 | a0003 | c0005 | t0001 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0003c0005t0001g0230 | a0003 | c0005 | t0001 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0003c0005t0001g0235 | a0003 | c0005 | t0001 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0003c0005t0001g0238 | a0003 | c0005 | t0001 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0004c0009t0001g0265 | a0004 | c0009 | t0001 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0004c0009t0001g0266 | a0004 | c0009 | t0001 | g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0004c0009t0001g0267 | a0004 | c0009 | t0001 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0004c0018t0001g0264 | a0004 | c0018 | t0001 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0005c0008t0001g0056 | a0005 | c0008 | t0001 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0005c0008t0001g0244 | a0005 | c0008 | t0001 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0005c0008t0001g0245 | a0005 | c0008 | t0001 | g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0006c0017t0001g0205 | a0006 | c0017 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0007c0010t0001g0218 | a0007 | c0010 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0008c0016t0001g0100 | a0008 | c0016 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0009c0015t0001g0058 | a0009 | c0015 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
a0010c0012t0001g0208 | a0010 | c0012 | t0001 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR2_chr6_136226034_136255311 | MTFR2 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0120 | EUR | FIN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0259 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00673 | hp1 | a0001 | c0006 | t0001 | g0124 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01167 | hp2 | a0003 | c0005 | t0001 | g0229 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01168 | hp1 | a0001 | c0007 | t0001 | g0254 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01169 | hp1 | a0003 | c0005 | t0001 | g0230 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01169 | hp2 | a0001 | c0007 | t0001 | g0255 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0200 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0206 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0042 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0042 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0246 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01975 | hp1 | a0001 | c0014 | t0001 | g0156 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0149 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02135 | hp2 | a0006 | c0017 | t0001 | g0205 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02145 | hp1 | a0001 | c0004 | t0001 | g0051 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02257 | hp2 | a0003 | c0005 | t0001 | g0238 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02280 | hp1 | a0004 | c0009 | t0001 | g0266 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02523 | hp1 | a0001 | c0006 | t0001 | g0136 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02615 | hp1 | a0003 | c0005 | t0001 | g0050 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0269 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0209 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02622 | hp2 | a0004 | c0009 | t0001 | g0267 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02630 | hp1 | a0005 | c0008 | t0001 | g0244 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02809 | hp1 | a0003 | c0005 | t0001 | g0049 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02818 | hp1 | a0003 | c0005 | t0001 | g0050 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02922 | hp2 | a0003 | c0005 | t0001 | g0235 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0243 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03041 | hp2 | a0004 | c0009 | t0001 | g0265 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03098 | hp1 | a0005 | c0008 | t0001 | g0245 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03139 | hp1 | a0010 | c0012 | t0001 | g0208 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03195 | hp1 | a0001 | c0011 | t0001 | g0263 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0242 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03225 | hp2 | a0003 | c0005 | t0001 | g0049 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0055 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03579 | hp2 | a0005 | c0008 | t0001 | g0056 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04204 | hp1 | a0001 | c0013 | t0001 | g0166 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18522 | hp1 | a0004 | c0018 | t0001 | g0264 | AFR | YRI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0051 | AFR | YRI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | YRI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18980 | hp2 | a0007 | c0010 | t0001 | g0218 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18986 | hp2 | a0001 | c0006 | t0001 | g0163 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19030 | hp2 | a0009 | c0015 | t0001 | g0058 | AFR | LWK | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | LWK | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19065 | hp1 | a0001 | c0007 | t0001 | g0135 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19067 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19086 | hp1 | a0008 | c0016 | t0001 | g0100 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ASW | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0109 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | MTFR2_chr6_136226034_136255311 | MTFR2 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | USA | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | USA | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | MTFR2_chr6_136226034_136255311 | MTFR2 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | MTFR2_chr6_136226034_136255311 | MTFR2 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0040 | REF | REF | MTFR2_chr6_136226034_136255311 | MTFR2 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0257 | REF | REF | MTFR2_chr6_136226034_136255311 | MTFR2 |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136231354
|
C | G | 1 | a0003 | 8 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(5): Show |
missense_variant | MODERATE | c.1079G>C | p.Arg360Pro | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 8/8 | 1469/1789 | 1079/1158 | 360/385 | chr6 | 136231354 | ||
chr6:136231354
|
C | T | 1 | a0002 | 24 | HG01099.hp1 HG02055.hp1 HG02109.hp2 others(21): Show |
missense_variant | MODERATE | c.1079G>A | p.Arg360Gln | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 8/8 | 1469/1789 | 1079/1158 | 360/385 | chr6 | 136231354 | ||
chr6:136233476
|
T | A | 1 | a0010 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.893A>T | p.His298Leu | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/8 | 1283/1789 | 893/1158 | 298/385 | chr6 | 136233476 | ||
chr6:136239479
|
G | A | 1 | a0005 | 3 | HG02630.hp1 HG03098.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.856C>T | p.Arg286Cys | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1246/1789 | 856/1158 | 286/385 | chr6 | 136239479 | ||
chr6:136239689
|
G | C | 1 | a0009 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.646C>G | p.Pro216Ala | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1036/1789 | 646/1158 | 216/385 | chr6 | 136239689 | ||
chr6:136239700
|
G | A | 1 | a0008 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.635C>T | p.Pro212Leu | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1025/1789 | 635/1158 | 212/385 | chr6 | 136239700 | ||
chr6:136239708
|
A | AGGAGGAG others(118): Show |
1 | a0007 | 1 | NA18980.hp2 | frameshift_variant&stop_gained | HIGH | c.515-13_626dupACTTT others(120): Show |
p.Pro210fs | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1016/1789 | 626/1158 | 209/385 | chr6 | 136239708 | ||
chr6:136244850
|
T | A | 1 | a0006 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.83A>T | p.Asn28Ile | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/8 | 473/1789 | 83/1158 | 28/385 | chr6 | 136244850 | ||
chr6:136249083
|
T | C | 1 | a0004 | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.17A>G | p.Asn6Ser | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/8 | 407/1789 | 17/1158 | 6/385 | chr6 | 136249083 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136233490
|
G | A | 2 | a0001c0003a0008c0016 | 17 | HG00323.hp2 HG00558.hp2 HG01106.hp1 others(14): Show |
synonymous_variant | LOW | c.879C>T | p.Gly293Gly | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/8 | 1269/1789 | 879/1158 | 293/385 | chr6 | 136233490 | ||
chr6:136239537
|
T | C | 1 | a0001c0007 | 3 | HG01168.hp1 HG01169.hp2 NA19065.hp1 |
synonymous_variant | LOW | c.798A>G | p.Arg266Arg | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1188/1789 | 798/1158 | 266/385 | chr6 | 136239537 | ||
chr6:136239582
|
C | G | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.753G>C | p.Pro251Pro | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1143/1789 | 753/1158 | 251/385 | chr6 | 136239582 | ||
chr6:136239648
|
T | C | 1 | a0001c0013 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.687A>G | p.Val229Val | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1077/1789 | 687/1158 | 229/385 | chr6 | 136239648 | ||
chr6:136239651
|
G | A | 1 | a0001c0014 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.684C>T | p.Pro228Pro | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1074/1789 | 684/1158 | 228/385 | chr6 | 136239651 | ||
chr6:136239720
|
C | T | 1 | a0001c0006 | 3 | HG00673.hp1 HG02523.hp1 NA18986.hp2 |
synonymous_variant | LOW | c.615G>A | p.Val205Val | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 1005/1789 | 615/1158 | 205/385 | chr6 | 136239720 | ||
chr6:136239810
|
G | A | 3 | a0001c0004a0004c0018a0005c0008 | 13 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(10): Show |
synonymous_variant | LOW | c.525C>T | p.Gly175Gly | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/8 | 915/1789 | 525/1158 | 175/385 | chr6 | 136239810 |
chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136231173
|
A | G | 1 | a0001c0001t0006 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*102T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 8/8 | 102 | chr6 | 136231173 | |||||
chr6:136250024
|
G | A | 1 | a0001c0001t0007 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-103C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/8 | 925 | chr6 | 136250024 | |||||
chr6:136250100
|
G | C | 2 | a0001c0001t0003a0001c0001t0004 | 13 | NA18939.hp2 NA18970.hp2 NA18980.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-179C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/8 | 1001 | chr6 | 136250100 | |||||
chr6:136250192
|
T | C | 1 | a0001c0001t0002 | 10 | HG00408.hp1 HG02027.hp2 NA18948.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-271A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/8 | 1093 | chr6 | 136250192 | |||||
chr6:136250256
|
C | A | 1 | a0001c0001t0003 | 8 | NA18970.hp2 NA18980.hp1 NA19002.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-335G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/8 | chr6 | 136250256 | ||||||
chr6:136250281
|
CGGACTGC others(15): Show |
C | 1 | a0001c0001t0005 | 1 | HG03490.hp2 | 5_prime_UTR_variant | MODIFIER | c.-382_-361delTGTCAT others(16): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/8 | 1183 | chr6 | 136250281 |
chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:136231415
|
G | T | 1 | a0004c0018t0001g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1045-27C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231415 | ||||||
chr6:136231431
|
C | CA | 19 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0130others(16): Show | 20 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1045-44dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231431 | ||||||
chr6:136231431
|
CA | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0082others(5): Show | 10 | HG00438.hp1 HG00544.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1045-44delT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231431 | ||||||
chr6:136231503
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0169 | 3 | HG00597.hp2 NA18997.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1045-115C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231503 | ||||||
chr6:136231565
|
G | T | 24 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0032others(21): Show | 32 | HG01099.hp1 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1045-177C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231565 | ||||||
chr6:136231669
|
T | TA | 15 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0061others(12): Show | 19 | HG00423.hp1 HG00423.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1045-282dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAA | 6 | a0001c0001t0001g0014a0001c0001t0001g0072a0001c0001t0001g0074others(3): Show | 8 | NA18942.hp2 NA18945.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1045-283_1045-282d others(4): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAA | 27 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0068others(24): Show | 31 | HG00558.hp1 HG00609.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.1045-284_1045-282d others(5): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(3): Show |
11 | a0002c0002t0001g0015a0002c0002t0001g0032a0002c0002t0001g0048others(8): Show | 15 | HG01099.hp1 HG02109.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1045-291_1045-282d others(12): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(4): Show |
5 | a0002c0002t0001g0016a0002c0002t0001g0060a0002c0002t0001g0097others(2): Show | 7 | HG02055.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1045-292_1045-282d others(13): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(5): Show |
2 | a0002c0002t0001g0059a0003c0005t0001g0229 | 2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1045-293_1045-282d others(14): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(6): Show |
6 | a0001c0001t0001g0090a0002c0002t0001g0239a0003c0005t0001g0049others(3): Show | 7 | HG01169.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1045-294_1045-282d others(15): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(7): Show |
1 | a0003c0005t0001g0050 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1045-295_1045-282d others(16): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0045 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1045-297_1045-282d others(18): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0046 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1045-298_1045-282d others(19): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
TA | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0017others(37): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.1045-282delT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
TAAA | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0084a0001c0001t0001g0086others(12): Show | 16 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1045-284_1045-282d others(5): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231669
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1045-291_1045-282d others(12): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231669 | ||||||
chr6:136231693
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1045-305C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231693 | ||||||
chr6:136231785
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1045-397G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231785 | ||||||
chr6:136231829
|
A | G | 2 | a0003c0005t0001g0229a0003c0005t0001g0230 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1045-441T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231829 | ||||||
chr6:136231845
|
GCATCCTC others(11): Show |
G | 13 | a0001c0001t0007g0271a0001c0004t0001g0051a0001c0004t0001g0109others(10): Show | 14 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1045-475_1045-458d others(20): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136231845 | ||||||
chr6:136232001
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1045-613A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232001 | ||||||
chr6:136232100
|
G | A | 1 | a0004c0018t0001g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1045-712C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232100 | ||||||
chr6:136232161
|
T | C | 4 | a0001c0001t0001g0092a0001c0001t0001g0207a0001c0001t0001g0212others(1): Show | 4 | HG02109.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-773A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232161 | ||||||
chr6:136232195
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 7 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1045-807C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232195 | ||||||
chr6:136232196
|
C | T | 1 | a0001c0004t0001g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1045-808G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232196 | ||||||
chr6:136232264
|
T | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0112 | 3 | HG00735.hp1 HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1045-876A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232264 | ||||||
chr6:136232336
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1045-948G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232336 | ||||||
chr6:136232375
|
C | T | 1 | a0009c0015t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1044+950G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232375 | ||||||
chr6:136232400
|
A | C | 19 | a0002c0002t0001g0015a0002c0002t0001g0016a0002c0002t0001g0032others(16): Show | 25 | HG01099.hp1 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1044+925T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232400 | ||||||
chr6:136232407
|
T | C | 61 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(58): Show | 78 | HG00639.hp1 HG00733.hp1 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.1044+918A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232407 | ||||||
chr6:136232430
|
C | T | 6 | a0001c0001t0001g0093a0001c0001t0001g0106a0001c0001t0001g0126others(3): Show | 6 | HG01099.hp2 HG02602.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+895G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232430 | ||||||
chr6:136232451
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1044+874C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232451 | ||||||
chr6:136232459
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1044+866C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232459 | ||||||
chr6:136232559
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1044+766A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232559 | ||||||
chr6:136232606
|
C | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 5 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+719G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232606 | ||||||
chr6:136232640
|
T | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0185 | 3 | HG00099.hp1 HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1044+685A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232640 | ||||||
chr6:136232687
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1044+638A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232687 | ||||||
chr6:136232703
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0223 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1044+622G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232703 | ||||||
chr6:136232837
|
C | A | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044+488G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232837 | ||||||
chr6:136232923
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+402C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232923 | ||||||
chr6:136232954
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1044+371C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136232954 | ||||||
chr6:136233138
|
A | T | 12 | a0001c0004t0001g0051a0001c0004t0001g0109a0001c0004t0001g0206others(9): Show | 13 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1044+187T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 7/7 | chr6 | 136233138 | ||||||
chr6:136233509
|
A | T | 78 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(75): Show | 97 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(94): Show |
intron_variant | MODIFIER | c.870-10T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136233509 | ||||||
chr6:136233510
|
A | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096others(7): Show | 13 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.870-11T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136233510 | ||||||
chr6:136233523
|
A | C | 3 | a0004c0009t0001g0265a0004c0009t0001g0266a0004c0009t0001g0267 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-24T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136233523 | ||||||
chr6:136233632
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0007g0271 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.870-133G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136233632 | ||||||
chr6:136233678
|
G | C | 1 | a0001c0004t0001g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.870-179C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136233678 | ||||||
chr6:136233995
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.870-496A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136233995 | ||||||
chr6:136234016
|
C | A | 28 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0095others(25): Show | 32 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.870-517G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234016 | ||||||
chr6:136234239
|
T | C | 3 | a0005c0008t0001g0056a0005c0008t0001g0244a0005c0008t0001g0245 | 3 | HG02630.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.870-740A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234239 | ||||||
chr6:136234304
|
C | CA | 36 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(33): Show | 46 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.870-806dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234304 | ||||||
chr6:136234418
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.870-919G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234418 | ||||||
chr6:136234758
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.870-1259G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234758 | ||||||
chr6:136234759
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0207others(3): Show | 6 | HG02109.hp1 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1260C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234759 | ||||||
chr6:136234774
|
A | G | 6 | a0003c0005t0001g0049a0003c0005t0001g0050a0003c0005t0001g0229others(3): Show | 8 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.870-1275T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234774 | ||||||
chr6:136234837
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.870-1338A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136234837 | ||||||
chr6:136235148
|
T | C | 1 | a0010c0012t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.870-1649A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235148 | ||||||
chr6:136235212
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1713G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235212 | ||||||
chr6:136235254
|
G | GAAAGAAC others(19): Show |
72 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(69): Show | 90 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(87): Show |
intron_variant | MODIFIER | c.870-1781_870-1756d others(28): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235254 | ||||||
chr6:136235254
|
G | GAAAGAAC others(19): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 5 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-1756_870-1755i others(28): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235254 | ||||||
chr6:136235301
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.870-1802T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235301 | ||||||
chr6:136235348
|
A | T | 1 | a0002c0002t0001g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.870-1849T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235348 | ||||||
chr6:136235717
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.870-2218G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235717 | ||||||
chr6:136235774
|
A | T | 6 | a0003c0005t0001g0049a0003c0005t0001g0050a0003c0005t0001g0229others(3): Show | 8 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.870-2275T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235774 | ||||||
chr6:136235784
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.870-2285A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235784 | ||||||
chr6:136235825
|
G | A | 3 | a0004c0009t0001g0265a0004c0009t0001g0266a0004c0009t0001g0267 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-2326C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235825 | ||||||
chr6:136235918
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.870-2419C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136235918 | ||||||
chr6:136236142
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.870-2643T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236142 | ||||||
chr6:136236184
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.870-2685C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236184 | ||||||
chr6:136236311
|
C | G | 2 | a0004c0009t0001g0265a0004c0009t0001g0266 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.870-2812G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236311 | ||||||
chr6:136236344
|
T | C | 7 | a0001c0001t0001g0236a0003c0005t0001g0049a0003c0005t0001g0050others(4): Show | 9 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.870-2845A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236344 | ||||||
chr6:136236382
|
C | T | 12 | a0001c0001t0001g0057a0001c0001t0001g0236a0001c0001t0007g0271others(9): Show | 14 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.870-2883G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236382 | ||||||
chr6:136236385
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.870-2886C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236385 | ||||||
chr6:136236477
|
T | C | 19 | a0001c0001t0001g0047a0002c0002t0001g0015a0002c0002t0001g0016others(16): Show | 26 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.870-2978A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236477 | ||||||
chr6:136236479
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.870-2980C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236479 | ||||||
chr6:136236530
|
G | A | 9 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(6): Show | 9 | HG00639.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.869+2936C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236530 | ||||||
chr6:136236606
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.869+2860G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236606 | ||||||
chr6:136236768
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0125 | 3 | HG01361.hp1 HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.869+2698G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236768 | ||||||
chr6:136236773
|
C | A | 1 | a0001c0001t0001g0041 | 2 | NA18997.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.869+2693G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236773 | ||||||
chr6:136236864
|
C | T | 19 | a0001c0001t0001g0047a0002c0002t0001g0015a0002c0002t0001g0016others(16): Show | 26 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.869+2602G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236864 | ||||||
chr6:136236901
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.869+2565A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236901 | ||||||
chr6:136236963
|
C | T | 76 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(73): Show | 95 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(92): Show |
intron_variant | MODIFIER | c.869+2503G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236963 | ||||||
chr6:136236999
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.869+2467C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136236999 | ||||||
chr6:136237089
|
C | G | 1 | a0002c0002t0001g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.869+2377G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237089 | ||||||
chr6:136237097
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.869+2369G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237097 | ||||||
chr6:136237320
|
T | A | 1 | a0010c0012t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.869+2146A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237320 | ||||||
chr6:136237435
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.869+2031A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237435 | ||||||
chr6:136237449
|
G | A | 3 | a0004c0009t0001g0265a0004c0009t0001g0266a0004c0009t0001g0267 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.869+2017C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237449 | ||||||
chr6:136237526
|
T | A | 3 | a0001c0003t0001g0042a0001c0003t0001g0120a0001c0003t0001g0121 | 4 | HG00323.hp2 HG01928.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.869+1940A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237526 | ||||||
chr6:136237637
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0113 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.869+1829G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237637 | ||||||
chr6:136237639
|
G | GTC | 12 | a0001c0004t0001g0051a0001c0004t0001g0109a0001c0004t0001g0206others(9): Show | 13 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+1825_869+1826d others(4): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237639 | ||||||
chr6:136237746
|
G | A | 2 | a0001c0007t0001g0254a0001c0007t0001g0255 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.869+1720C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237746 | ||||||
chr6:136237814
|
T | TA | 42 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(39): Show | 57 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.869+1651dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136237814 | ||||||
chr6:136238128
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.869+1338A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238128 | ||||||
chr6:136238235
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 6 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.869+1231G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238235 | ||||||
chr6:136238332
|
G | C | 1 | a0001c0001t0001g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.869+1134C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238332 | ||||||
chr6:136238374
|
C | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 6 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.869+1092G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238374 | ||||||
chr6:136238375
|
G | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(43): Show | 62 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.869+1091C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238375 | ||||||
chr6:136238603
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.869+863G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238603 | ||||||
chr6:136238669
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0113 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.869+797C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238669 | ||||||
chr6:136238678
|
C | CCA | 62 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(59): Show | 91 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.869+786_869+787dup others(2): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238678 | ||||||
chr6:136238678
|
C | CCACA | 8 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 12 | HG01255.hp2 NA18522.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.869+784_869+787dup others(4): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238678 | ||||||
chr6:136238678
|
C | CCACACAC others(1): Show |
3 | a0004c0009t0001g0265a0004c0009t0001g0266a0004c0009t0001g0267 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.869+780_869+787dup others(8): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238678 | ||||||
chr6:136238707
|
CAT | C | 5 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0122others(2): Show | 5 | HG01993.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+757_869+758del others(2): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238707 | ||||||
chr6:136238709
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0018others(47): Show | 65 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.869+757A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238709 | ||||||
chr6:136238791
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.869+675C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238791 | ||||||
chr6:136238792
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.869+674G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136238792 | ||||||
chr6:136239040
|
C | T | 2 | a0001c0001t0001g0037a0006c0017t0001g0205 | 3 | HG02135.hp2 NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.869+426G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136239040 | ||||||
chr6:136239064
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(9): Show | 20 | HG02040.hp2 HG02723.hp1 HG02895.hp1 others(17): Show |
intron_variant | MODIFIER | c.869+402G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136239064 | ||||||
chr6:136239152
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG00639.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.869+314G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136239152 | ||||||
chr6:136239306
|
T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(9): Show | 20 | HG02040.hp2 HG02723.hp1 HG02895.hp1 others(17): Show |
intron_variant | MODIFIER | c.869+160A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 6/7 | chr6 | 136239306 | ||||||
chr6:136239899
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.515-79G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136239899 | ||||||
chr6:136239919
|
T | G | 1 | a0001c0001t0007g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.515-99A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136239919 | ||||||
chr6:136239932
|
G | A | 1 | a0009c0015t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.515-112C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136239932 | ||||||
chr6:136239936
|
T | G | 12 | a0001c0004t0001g0051a0001c0004t0001g0109a0001c0004t0001g0206others(9): Show | 13 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.515-116A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136239936 | ||||||
chr6:136239982
|
A | G | 12 | a0001c0004t0001g0051a0001c0004t0001g0109a0001c0004t0001g0206others(9): Show | 13 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.515-162T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136239982 | ||||||
chr6:136240009
|
T | TAATCCAG others(5): Show |
1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.515-201_515-190dup others(12): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240009 | ||||||
chr6:136240031
|
T | C | 12 | a0001c0004t0001g0051a0001c0004t0001g0109a0001c0004t0001g0206others(9): Show | 13 | HG01891.hp1 HG01952.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.515-211A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240031 | ||||||
chr6:136240050
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.515-230G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240050 | ||||||
chr6:136240069
|
T | TAAAC | 70 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(67): Show | 87 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(84): Show |
intron_variant | MODIFIER | c.515-253_515-250dup others(4): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240069 | ||||||
chr6:136240071
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.515-251T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240071 | ||||||
chr6:136240077
|
C | CAAACA | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.515-258_515-257ins others(5): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240077 | ||||||
chr6:136240103
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-283G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240103 | ||||||
chr6:136240264
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.515-444G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240264 | ||||||
chr6:136240311
|
T | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(10): Show | 19 | HG02040.hp2 HG02280.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.515-491A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240311 | ||||||
chr6:136240338
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG00639.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.515-518T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240338 | ||||||
chr6:136240469
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.515-649T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240469 | ||||||
chr6:136240503
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.515-683G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240503 | ||||||
chr6:136240814
|
G | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(32): Show | 49 | HG01099.hp1 HG02040.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.514+630C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240814 | ||||||
chr6:136240814
|
G | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+630C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240814 | ||||||
chr6:136240819
|
C | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(32): Show | 50 | HG01099.hp1 HG02040.hp2 HG02109.hp2 others(47): Show |
intron_variant | MODIFIER | c.514+625G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240819 | ||||||
chr6:136240822
|
T | C | 19 | a0001c0001t0001g0225a0002c0002t0001g0015a0002c0002t0001g0016others(16): Show | 25 | HG01099.hp1 HG02109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.514+622A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240822 | ||||||
chr6:136240826
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.514+618A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240826 | ||||||
chr6:136240827
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.514+617G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240827 | ||||||
chr6:136240828
|
A | ACGCCTGT others(127): Show |
1 | a0001c0001t0001g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.514+615_514+616ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240828 | ||||||
chr6:136240828
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.514+616T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240828 | ||||||
chr6:136240830
|
G | A | 1 | a0001c0006t0001g0136 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.514+614C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240830 | ||||||
chr6:136240835
|
T | C | 1 | a0001c0006t0001g0136 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.514+609A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240835 | ||||||
chr6:136240835
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.514+609A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240835 | ||||||
chr6:136240841
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.514+603G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240841 | ||||||
chr6:136240848
|
T | A | 1 | a0001c0001t0001g0034 | 2 | HG01361.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.514+596A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240848 | ||||||
chr6:136240857
|
C | T | 1 | a0001c0001t0001g0019 | 3 | HG01192.hp2 HG02004.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.514+587G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240857 | ||||||
chr6:136240858
|
A | G | 15 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 19 | HG01175.hp1 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.514+586T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240858 | ||||||
chr6:136240862
|
C | T | 17 | a0001c0001t0001g0225a0002c0002t0001g0015a0002c0002t0001g0016others(14): Show | 23 | HG01099.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.514+582G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240862 | ||||||
chr6:136240863
|
G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(34): Show | 47 | HG02040.hp2 HG02280.hp1 HG02451.hp2 others(44): Show |
intron_variant | MODIFIER | c.514+581C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240863 | ||||||
chr6:136240867
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.514+577T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240867 | ||||||
chr6:136240874
|
G | A | 1 | a0007c0010t0001g0218 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.514+570C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240874 | ||||||
chr6:136240882
|
G | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 332 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.514+562C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240882 | ||||||
chr6:136240887
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+557G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240887 | ||||||
chr6:136240888
|
G | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(48): Show | 63 | HG01167.hp2 HG01169.hp1 HG02040.hp2 others(60): Show |
intron_variant | MODIFIER | c.514+556C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240888 | ||||||
chr6:136240888
|
G | GAGACCAT others(127): Show |
1 | a0001c0001t0001g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.514+555_514+556ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240888 | ||||||
chr6:136240888
|
G | GAGACCAT others(127): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+555_514+556ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240888 | ||||||
chr6:136240888
|
G | GAGACCAT others(127): Show |
1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.514+555_514+556ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240888 | ||||||
chr6:136240892
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.514+552G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240892 | ||||||
chr6:136240894
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+550T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240894 | ||||||
chr6:136240898
|
T | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0191a0001c0001t0001g0261others(2): Show | 5 | HG00558.hp1 HG04115.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.514+546A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240898 | ||||||
chr6:136240901
|
C | A | 1 | a0001c0001t0001g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.514+543G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240901 | ||||||
chr6:136240902
|
T | C | 5 | a0001c0001t0001g0159a0001c0001t0007g0271a0004c0009t0001g0265others(2): Show | 5 | HG02165.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.514+542A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240902 | ||||||
chr6:136240908
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(69): Show | 89 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.514+536C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240908 | ||||||
chr6:136240908
|
G | GGTGAAAC others(127): Show |
2 | a0003c0005t0001g0229a0003c0005t0001g0230 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.514+535_514+536ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240908 | ||||||
chr6:136240918
|
C | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0241others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.514+526G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240918 | ||||||
chr6:136240918
|
C | CATCTCTA others(127): Show |
2 | a0001c0001t0001g0207a0005c0008t0001g0245 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.514+525_514+526ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240918 | ||||||
chr6:136240919
|
G | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(30): Show | 42 | HG01346.hp1 HG02040.hp2 HG02280.hp1 others(39): Show |
intron_variant | MODIFIER | c.514+525C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240919 | ||||||
chr6:136240919
|
G | GTCTCTAC others(127): Show |
3 | a0001c0004t0001g0051a0001c0004t0001g0206a0005c0008t0001g0056 | 4 | HG01891.hp1 HG02145.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+524_514+525ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240919 | ||||||
chr6:136240919
|
G | GTCTCTAC others(127): Show |
1 | a0001c0004t0001g0246 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.514+524_514+525ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240919 | ||||||
chr6:136240919
|
G | GTCTCTAC others(127): Show |
18 | a0001c0001t0001g0047a0001c0001t0001g0225a0002c0002t0001g0015others(15): Show | 25 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.514+524_514+525ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240919 | ||||||
chr6:136240931
|
A | T | 1 | a0001c0013t0001g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.514+513T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240931 | ||||||
chr6:136240948
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.514+496C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240948 | ||||||
chr6:136240964
|
G | A | 2 | a0001c0001t0001g0241a0001c0004t0001g0109 | 2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.514+480C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240964 | ||||||
chr6:136240964
|
G | GCCTGTAG others(127): Show |
2 | a0001c0004t0001g0242a0001c0004t0001g0243 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.514+479_514+480ins others(134): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240964 | ||||||
chr6:136240972
|
T | C | 1 | a0001c0006t0001g0163 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.514+472A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240972 | ||||||
chr6:136240985
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.514+459T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240985 | ||||||
chr6:136240989
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.514+455C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136240989 | ||||||
chr6:136241008
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.514+436C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241008 | ||||||
chr6:136241022
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.514+422A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241022 | ||||||
chr6:136241040
|
A | G | 4 | a0001c0001t0001g0241a0001c0004t0001g0109a0001c0004t0001g0242others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+404T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241040 | ||||||
chr6:136241047
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0092others(1): Show | 6 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.514+397A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241047 | ||||||
chr6:136241048
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(35): Show | 48 | HG01891.hp1 HG01952.hp2 HG02040.hp2 others(45): Show |
intron_variant | MODIFIER | c.514+396C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241048 | ||||||
chr6:136241070
|
G | A | 3 | a0001c0004t0001g0051a0001c0004t0001g0206a0002c0002t0001g0234 | 4 | HG01891.hp1 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+374C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241070 | ||||||
chr6:136241078
|
A | G | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0216others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.514+366T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241078 | ||||||
chr6:136241084
|
G | C | 2 | a0003c0005t0001g0229a0003c0005t0001g0230 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.514+360C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241084 | ||||||
chr6:136241090
|
C | CA | 17 | a0001c0001t0001g0071a0001c0001t0001g0081a0001c0001t0001g0194others(14): Show | 21 | HG01433.hp2 NA18939.hp2 NA18970.hp2 others(18): Show |
intron_variant | MODIFIER | c.514+353dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241090 | ||||||
chr6:136241090
|
CA | C | 13 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0001t0001g0085others(10): Show | 13 | HG00639.hp1 HG02559.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.514+353delT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241090 | ||||||
chr6:136241110
|
T | A | 7 | a0001c0001t0001g0236a0003c0005t0001g0049a0003c0005t0001g0050others(4): Show | 9 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.514+334A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241110 | ||||||
chr6:136241187
|
A | C | 1 | a0001c0001t0001g0221 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.514+257T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241187 | ||||||
chr6:136241273
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.514+171C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241273 | ||||||
chr6:136241354
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.514+90A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 5/7 | chr6 | 136241354 | ||||||
chr6:136241830
|
AC | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 5 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-155delG | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136241830 | ||||||
chr6:136242019
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.282-343C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242019 | ||||||
chr6:136242079
|
C | CA | 83 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(80): Show | 105 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.282-404dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242079 | ||||||
chr6:136242079
|
C | CAA | 22 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0034others(19): Show | 27 | HG01346.hp2 HG01358.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.282-405_282-404dup others(2): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242079 | ||||||
chr6:136242079
|
CA | C | 22 | a0001c0001t0001g0027a0001c0001t0001g0077a0001c0001t0001g0089others(19): Show | 24 | HG00733.hp1 HG01168.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.282-404delT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242079 | ||||||
chr6:136242079
|
CAA | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0001t0001g0085others(8): Show | 11 | HG00639.hp1 HG01074.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-405_282-404del others(2): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242079 | ||||||
chr6:136242079
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.282-418_282-404del others(15): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242079 | ||||||
chr6:136242093
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-417T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242093 | ||||||
chr6:136242098
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-422T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242098 | ||||||
chr6:136242106
|
A | C | 12 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0001t0001g0085others(9): Show | 12 | HG00639.hp1 HG01074.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-430T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242106 | ||||||
chr6:136242131
|
T | C | 3 | a0004c0009t0001g0265a0004c0009t0001g0266a0004c0009t0001g0267 | 3 | HG02280.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.282-455A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242131 | ||||||
chr6:136242229
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.282-553C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242229 | ||||||
chr6:136242296
|
T | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0202others(2): Show | 7 | HG01433.hp2 HG02293.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+565A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242296 | ||||||
chr6:136242559
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+302A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242559 | ||||||
chr6:136242659
|
T | G | 1 | a0001c0004t0001g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.281+202A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242659 | ||||||
chr6:136242715
|
C | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+146G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242715 | ||||||
chr6:136242841
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+20T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 4/7 | chr6 | 136242841 | ||||||
chr6:136243118
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-145C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243118 | ||||||
chr6:136243257
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(63): Show | 83 | HG00609.hp1 HG01070.hp1 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.169-284A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243257 | ||||||
chr6:136243418
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.169-445T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243418 | ||||||
chr6:136243435
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.169-462C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243435 | ||||||
chr6:136243436
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.169-463C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243436 | ||||||
chr6:136243443
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.169-470T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243443 | ||||||
chr6:136243461
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.169-488G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243461 | ||||||
chr6:136243553
|
A | C | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-580T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243553 | ||||||
chr6:136243575
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-602C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243575 | ||||||
chr6:136243683
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.169-710C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243683 | ||||||
chr6:136243690
|
C | A | 7 | a0001c0001t0001g0236a0002c0002t0001g0237a0002c0002t0001g0239others(4): Show | 9 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-717G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243690 | ||||||
chr6:136243712
|
C | G | 1 | a0001c0001t0001g0034 | 2 | HG01361.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.169-739G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243712 | ||||||
chr6:136243714
|
T | TA | 83 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(80): Show | 101 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(98): Show |
intron_variant | MODIFIER | c.169-742dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243714 | ||||||
chr6:136243714
|
TA | T | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0062others(5): Show | 10 | HG01099.hp2 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-742delT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136243714 | ||||||
chr6:136244067
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.168+698G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136244067 | ||||||
chr6:136244169
|
A | C | 2 | a0001c0004t0001g0206a0001c0011t0001g0263 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.168+596T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136244169 | ||||||
chr6:136244219
|
C | G | 1 | a0001c0003t0001g0101 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.168+546G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136244219 | ||||||
chr6:136244562
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.168+203G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136244562 | ||||||
chr6:136244576
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+189G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136244576 | ||||||
chr6:136244589
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+176A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 3/7 | chr6 | 136244589 | ||||||
chr6:136244945
|
TAAAAAAG others(2): Show |
T | 82 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(79): Show | 99 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-85_64-77delGTCT others(5): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136244945 | ||||||
chr6:136244945
|
TAAAAAAG others(3): Show |
T | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-86_64-77delTGTC others(6): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136244945 | ||||||
chr6:136245015
|
T | G | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-146A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245015 | ||||||
chr6:136245090
|
T | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG00639.hp1 HG02559.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-221A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245090 | ||||||
chr6:136245166
|
C | CA | 82 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(79): Show | 99 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-298dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245166 | ||||||
chr6:136245168
|
A | T | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-299T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245168 | ||||||
chr6:136245274
|
C | T | 2 | a0001c0001t0007g0271a0008c0016t0001g0100 | 2 | HG02280.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.64-405G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245274 | ||||||
chr6:136245318
|
A | T | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-449T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245318 | ||||||
chr6:136245329
|
G | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(65): Show | 84 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-460C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245329 | ||||||
chr6:136245494
|
G | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0029others(65): Show | 84 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-625C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245494 | ||||||
chr6:136245533
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-664T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245533 | ||||||
chr6:136245534
|
T | C | 88 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0027others(85): Show | 108 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(105): Show |
intron_variant | MODIFIER | c.64-665A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136245534 | ||||||
chr6:136246148
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.64-1279C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246148 | ||||||
chr6:136246174
|
A | C | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1305T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246174 | ||||||
chr6:136246175
|
C | A | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1306G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246175 | ||||||
chr6:136246273
|
T | G | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1404A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246273 | ||||||
chr6:136246644
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64-1775G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246644 | ||||||
chr6:136246654
|
T | G | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1785A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246654 | ||||||
chr6:136246671
|
A | G | 1 | a0009c0015t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-1802T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246671 | ||||||
chr6:136246706
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.64-1837C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246706 | ||||||
chr6:136246724
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.64-1855T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246724 | ||||||
chr6:136246734
|
T | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 11 | HG00609.hp1 NA18945.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-1865A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246734 | ||||||
chr6:136246753
|
G | A | 3 | a0002c0002t0001g0059a0002c0002t0001g0060a0009c0015t0001g0058 | 3 | HG02572.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64-1884C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246753 | ||||||
chr6:136246790
|
A | G | 1 | a0001c0001t0001g0033 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.64-1921T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246790 | ||||||
chr6:136246791
|
A | C | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1922T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246791 | ||||||
chr6:136246794
|
A | C | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1925T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246794 | ||||||
chr6:136246822
|
A | C | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1953T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246822 | ||||||
chr6:136246938
|
T | A | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-2069A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136246938 | ||||||
chr6:136247001
|
G | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 11 | HG00609.hp1 NA18945.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+2036C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247001 | ||||||
chr6:136247042
|
T | A | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+1995A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247042 | ||||||
chr6:136247049
|
C | T | 29 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0223others(26): Show | 38 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+1988G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247049 | ||||||
chr6:136247278
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0096 | 4 | HG02922.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1759C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247278 | ||||||
chr6:136247291
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 8 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+1746T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247291 | ||||||
chr6:136247388
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.63+1649G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247388 | ||||||
chr6:136247447
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.63+1590G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247447 | ||||||
chr6:136247537
|
C | T | 1 | a0001c0001t0001g0031 | 2 | NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.63+1500G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247537 | ||||||
chr6:136247634
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.63+1403C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247634 | ||||||
chr6:136247778
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(9): Show | 13 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+1259G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136247778 | ||||||
chr6:136248012
|
C | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0220a0001c0001t0001g0253 | 4 | HG02293.hp1 NA18949.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1025G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248012 | ||||||
chr6:136248016
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG00423.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.63+1021A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248016 | ||||||
chr6:136248072
|
T | TA | 28 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(25): Show | 34 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.63+964dupT | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248072 | ||||||
chr6:136248137
|
C | G | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG00639.hp1 HG02559.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+900G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248137 | ||||||
chr6:136248409
|
T | A | 1 | a0001c0001t0007g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+628A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248409 | ||||||
chr6:136248419
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.63+618T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248419 | ||||||
chr6:136248424
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.63+613T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248424 | ||||||
chr6:136248439
|
T | C | 11 | a0001c0001t0001g0241a0001c0001t0001g0247a0001c0004t0001g0051others(8): Show | 12 | HG01952.hp2 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+598A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248439 | ||||||
chr6:136248453
|
A | C | 1 | a0001c0001t0002g0275 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.63+584T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248453 | ||||||
chr6:136248477
|
T | C | 4 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG00423.hp2 HG01081.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+560A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248477 | ||||||
chr6:136248494
|
T | C | 2 | a0001c0007t0001g0254a0001c0007t0001g0255 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+543A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248494 | ||||||
chr6:136248499
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.63+538T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248499 | ||||||
chr6:136248507
|
T | G | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+530A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248507 | ||||||
chr6:136248542
|
G | A | 4 | a0004c0009t0001g0265a0004c0009t0001g0266a0004c0009t0001g0267others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+495C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248542 | ||||||
chr6:136248607
|
C | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0076others(7): Show | 15 | NA18951.hp1 NA18964.hp1 NA18968.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+430G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248607 | ||||||
chr6:136248608
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.63+429C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248608 | ||||||
chr6:136248736
|
A | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0028others(13): Show | 23 | HG00438.hp2 HG00544.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+301T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248736 | ||||||
chr6:136248885
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0262 | 3 | HG01891.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.63+152G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248885 | ||||||
chr6:136248901
|
T | G | 1 | a0001c0011t0001g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+136A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 2/7 | chr6 | 136248901 | ||||||
chr6:136249277
|
T | G | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-54-124A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249277 | ||||||
chr6:136249703
|
C | T | 10 | a0001c0001t0001g0063a0001c0001t0003g0013a0001c0001t0003g0280others(7): Show | 14 | NA18939.hp2 NA18970.hp2 NA18973.hp2 others(11): Show |
intron_variant | MODIFIER | c.-55+273G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249703 | ||||||
chr6:136249708
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+268C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249708 | ||||||
chr6:136249709
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+267A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249709 | ||||||
chr6:136249712
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+264G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249712 | ||||||
chr6:136249713
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+263G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249713 | ||||||
chr6:136249714
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+262G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249714 | ||||||
chr6:136249715
|
T | G | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+261A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249715 | ||||||
chr6:136249724
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-55+252G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249724 | ||||||
chr6:136249725
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+251G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249725 | ||||||
chr6:136249726
|
T | G | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+250A>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249726 | ||||||
chr6:136249727
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+249G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249727 | ||||||
chr6:136249729
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+247A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249729 | ||||||
chr6:136249730
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+246C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249730 | ||||||
chr6:136249731
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+245G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249731 | ||||||
chr6:136249735
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+241G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249735 | ||||||
chr6:136249742
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+234C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249742 | ||||||
chr6:136249744
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+232T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249744 | ||||||
chr6:136249746
|
A | G | 7 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0061others(4): Show | 8 | HG02572.hp1 HG02965.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-55+230T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249746 | ||||||
chr6:136249747
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+229T>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249747 | ||||||
chr6:136249760
|
A | ATAACAGC others(4): Show |
1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+215_-55+216ins others(11): Show |
MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249760 | ||||||
chr6:136249761
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+215G>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249761 | ||||||
chr6:136249762
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+214A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249762 | ||||||
chr6:136249763
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+213G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249763 | ||||||
chr6:136249768
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+208C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249768 | ||||||
chr6:136249769
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+207G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249769 | ||||||
chr6:136249770
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+206G>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249770 | ||||||
chr6:136249773
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+203G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249773 | ||||||
chr6:136249774
|
A | G | 1 | a0005c0008t0001g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-55+202T>C | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249774 | ||||||
chr6:136249775
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+201C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249775 | ||||||
chr6:136249775
|
G | C | 1 | a0001c0004t0001g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-55+201C>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249775 | ||||||
chr6:136249776
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+200G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249776 | ||||||
chr6:136249779
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+197A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249779 | ||||||
chr6:136249781
|
A | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+195T>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249781 | ||||||
chr6:136249784
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+192C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249784 | ||||||
chr6:136249785
|
T | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+191A>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249785 | ||||||
chr6:136249786
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+190C>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249786 | ||||||
chr6:136249799
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+177G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249799 | ||||||
chr6:136249802
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+174A>G | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249802 | ||||||
chr6:136249803
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+173C>A | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249803 | ||||||
chr6:136249820
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-55+156G>T | MTFR2 | ENSG00000146410.12 | transcript | ENST00000420702.6 | protein_coding | 1/7 | chr6 | 136249820 |