geneid | 54842 |
---|---|
ensemblid | ENSG00000151690.15 |
hgncid | 24711 |
symbol | MFSD6 |
name | major facilitator superfamily domain containing 6 |
refseq_nuc | NM_017694.4 |
refseq_prot | NP_060164.3 |
ensembl_nuc | ENST00000392328.6 |
ensembl_prot | ENSP00000376141.1 |
mane_status | MANE Select |
chr | chr2 |
start | 190408355 |
end | 190502314 |
strand | + |
ver | v1.2 |
region | chr2:190408355-190502314 |
region5000 | chr2:190403355-190507314 |
regionname0 | MFSD6_chr2_190408355_190502314 |
regionname5000 | MFSD6_chr2_190403355_190507314 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 791 | 177 | 44 | 26 | 79 | 9 | 18 | 61 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002 | 0/1 | 791 | 157 | 21 | 29 | 93 | 3 | 10 | 75 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0003 | 0/0 | 791 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0004 | 0/0 | 791 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0005 | 0/0 | 791 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0006 | 0/0 | 791 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0007 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0008 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2376 | 175 | 43 | 26 | 78 | 9 | 18 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0002 | 0/1 | 2376 | 156 | 20 | 29 | 93 | 3 | 10 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0003 | 0/0 | 2376 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0004 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0005 | 0/0 | 2376 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0006 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0007 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0008 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0009 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0010 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
c0011 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2421 | 172 | 36 | 27 | 93 | 5 | 10 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0002 | 0/0 | 2421 | 81 | 18 | 9 | 47 | 2 | 5 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0003 | 0/0 | 2421 | 49 | 0 | 14 | 21 | 4 | 10 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0004 | 0/0 | 2421 | 6 | 0 | 5 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0005 | 0/0 | 2421 | 5 | 5 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0006 | 0/0 | 2421 | 4 | 0 | 0 | 4 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0007 | 0/0 | 2420 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0008 | 0/0 | 2421 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0009 | 0/0 | 2421 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0010 | 0/0 | 2419 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0011 | 0/0 | 2421 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0012 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0013 | 0/0 | 2421 | 2 | 0 | 1 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0014 | 1/0 | 2421 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0015 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0016 | 0/0 | 2421 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0017 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0018 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0019 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0020 | 0/0 | 2421 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0021 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0022 | 0/0 | 2419 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
t0023 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2376 | 175 | 43 | 26 | 78 | 9 | 18 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0007 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0010 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002 | 0/1 | 2376 | 156 | 20 | 29 | 93 | 3 | 10 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0011 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0003c0003 | 0/0 | 2376 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0004c0005 | 0/0 | 2376 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0005c0004 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0006c0008 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0007c0009 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0008c0006 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4796 | 29 | 19 | 4 | 1 | 2 | 3 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0002 | 0/0 | 4796 | 80 | 17 | 9 | 47 | 2 | 5 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0003 | 0/0 | 4796 | 47 | 0 | 13 | 21 | 4 | 9 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0006 | 0/0 | 4796 | 4 | 0 | 0 | 4 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0007 | 0/0 | 4795 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0008 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0011 | 0/0 | 4796 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0012 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0014 | 1/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0016 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0017 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0018 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0020 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0021 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0001t0023 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0007t0001 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0001c0010t0002 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0001 | 0/1 | 4796 | 136 | 13 | 23 | 89 | 3 | 7 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0003 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0004 | 0/0 | 4796 | 6 | 0 | 5 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0005 | 0/0 | 4796 | 5 | 5 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0008 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0009 | 0/0 | 4796 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0013 | 0/0 | 4796 | 2 | 0 | 1 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0002t0019 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0002c0011t0001 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0003c0003t0010 | 0/0 | 4794 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0003c0003t0022 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0004c0005t0001 | 0/0 | 4796 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0005c0004t0001 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0006c0008t0003 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0007c0009t0015 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
a0008c0006t0001 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | copy fasta | chr2 | 190403355 | 190507314 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0011g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0011g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0014g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0016g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0017g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0020g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0021g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0001t0023g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0001c0010t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0009g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0009g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0013g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0013g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0002t0019g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0002c0011t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0003c0003t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0003c0003t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0003c0003t0022g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0004c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0004c0005t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0005c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0005c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0006c0008t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0007c0009t0015g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
a0008c0006t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0001 | g0159 | EUR | GBR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0058 | EUR | GBR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00323 | hp1 | a0001 | c0001 | t0016 | g0117 | EUR | FIN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | FIN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00408 | hp2 | a0001 | c0001 | t0011 | g0041 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00639 | hp2 | a0002 | c0002 | t0013 | g0305 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01070 | hp2 | a0002 | c0002 | t0004 | g0168 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01071 | hp1 | a0002 | c0002 | t0004 | g0160 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01074 | hp1 | a0006 | c0008 | t0003 | g0032 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01256 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01258 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01884 | hp2 | a0002 | c0011 | t0001 | g0320 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0289 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02015 | hp2 | a0001 | c0001 | t0018 | g0057 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02074 | hp2 | a0002 | c0002 | t0009 | g0304 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0247 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CDX | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | CDX | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02258 | hp2 | a0002 | c0002 | t0005 | g0200 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02280 | hp1 | a0002 | c0002 | t0005 | g0218 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02647 | hp1 | a0002 | c0002 | t0005 | g0204 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02818 | hp1 | a0001 | c0001 | t0021 | g0210 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0322 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02970 | hp2 | a0005 | c0004 | t0001 | g0321 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03098 | hp1 | a0002 | c0002 | t0005 | g0185 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03195 | hp2 | a0003 | c0003 | t0022 | g0207 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03225 | hp1 | a0002 | c0002 | t0005 | g0149 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03239 | hp2 | a0002 | c0002 | t0013 | g0314 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03453 | hp1 | a0003 | c0003 | t0010 | g0331 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03579 | hp1 | a0003 | c0003 | t0010 | g0330 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0214 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03669 | hp1 | a0002 | c0002 | t0003 | g0067 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0284 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG04228 | hp1 | a0001 | c0001 | t0020 | g0248 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18522 | hp1 | a0007 | c0009 | t0015 | g0208 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18522 | hp2 | a0002 | c0002 | t0008 | g0205 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0236 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18957 | hp2 | a0002 | c0002 | t0009 | g0296 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18963 | hp2 | a0001 | c0001 | t0017 | g0048 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18977 | hp1 | a0004 | c0005 | t0001 | g0270 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18986 | hp1 | a0001 | c0007 | t0001 | g0043 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18992 | hp1 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18993 | hp2 | a0001 | c0001 | t0023 | g0047 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19004 | hp2 | a0002 | c0002 | t0009 | g0317 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19007 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19007 | hp2 | a0004 | c0005 | t0001 | g0287 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19030 | hp2 | a0001 | c0010 | t0002 | g0098 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19078 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19089 | hp1 | a0002 | c0002 | t0019 | g0295 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01123 | hp1 | a0002 | c0002 | t0004 | g0213 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02559 | hp1 | a0008 | c0006 | t0001 | g0324 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03471 | hp1 | a0002 | c0002 | t0008 | g0211 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0332 | AFR | USA | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA21309 | hp1 | a0005 | c0004 | t0001 | g0323 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0306 | REF | REF | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0014 | g0209 | REF | REF | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190436190
|
T | C | 2 | a0005a0008 | 3 | HG02559.hp1 HG02970.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.161T>C | p.Ile54Thr | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 485/4796 | 161/2376 | 54/791 | chr2 | 190436190 | ||
chr2:190436567
|
C | T | 1 | a0007 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.538C>T | p.Pro180Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 862/4796 | 538/2376 | 180/791 | chr2 | 190436567 | ||
chr2:190436597
|
A | T | 1 | a0003 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.568A>T | p.Thr190Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 892/4796 | 568/2376 | 190/791 | chr2 | 190436597 | ||
chr2:190436642
|
A | G | 4 | a0002a0004a0005others(1): Show | 162 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(159): Show |
missense_variant | MODERATE | c.613A>G | p.Arg205Gly | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 937/4796 | 613/2376 | 205/791 | chr2 | 190436642 | ||
chr2:190436709
|
A | C | 1 | a0008 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.680A>C | p.Gln227Pro | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 1004/4796 | 680/2376 | 227/791 | chr2 | 190436709 | ||
chr2:190436768
|
G | A | 1 | a0004 | 2 | NA18977.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.739G>A | p.Ala247Thr | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 1063/4796 | 739/2376 | 247/791 | chr2 | 190436768 | ||
chr2:190500102
|
C | T | 1 | a0006 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2260C>T | p.Pro754Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2584/4796 | 2260/2376 | 754/791 | chr2 | 190500102 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190436119
|
C | T | 1 | a0002c0011 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.90C>T | p.Ser30Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 414/4796 | 90/2376 | 30/791 | chr2 | 190436119 | ||
chr2:190436227
|
C | T | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.198C>T | p.Asn66Asn | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 522/4796 | 198/2376 | 66/791 | chr2 | 190436227 | ||
chr2:190436566
|
G | T | 1 | a0007c0009 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.537G>T | p.Leu179Leu | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 861/4796 | 537/2376 | 179/791 | chr2 | 190436566 | ||
chr2:190500137
|
C | T | 1 | a0001c0007 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.2295C>T | p.Thr765Thr | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2619/4796 | 2295/2376 | 765/791 | chr2 | 190500137 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190408382
|
A | G | 1 | a0001c0001t0023 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-297A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/8 | 27648 | chr2 | 190408382 | |||||
chr2:190408424
|
C | G | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 340 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(337): Show |
5_prime_UTR_variant | MODIFIER | c.-255C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/8 | 27606 | chr2 | 190408424 | |||||
chr2:190415331
|
C | T | 1 | a0002c0002t0013 | 2 | HG00639.hp2 HG03239.hp2 |
5_prime_UTR_variant | MODIFIER | c.-136C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/8 | 20699 | chr2 | 190415331 | |||||
chr2:190415332
|
G | A | 1 | a0001c0001t0016 | 1 | HG00323.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-135G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/8 | chr2 | 190415332 | ||||||
chr2:190500317
|
A | G | 1 | a0002c0002t0004 | 6 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*99A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 99 | chr2 | 190500317 | |||||
chr2:190500397
|
G | A | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0017others(4): Show | 55 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*179G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 179 | chr2 | 190500397 | |||||
chr2:190500504
|
GC | G | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG03453.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*288delC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 288 | INFO_REALIGN_3_PRIME | chr2 | 190500504 | ||||
chr2:190500568
|
G | A | 1 | a0002c0002t0005 | 5 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 350 | chr2 | 190500568 | |||||
chr2:190500736
|
T | C | 1 | a0001c0001t0006 | 4 | NA18982.hp1 NA19002.hp1 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*518T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 518 | chr2 | 190500736 | |||||
chr2:190500964
|
ATTTCAAA others(17): Show |
A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748_*771delTTCAAA others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 748 | INFO_REALIGN_3_PRIME | chr2 | 190500964 | ||||
chr2:190501020
|
A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 802 | chr2 | 190501020 | |||||
chr2:190501021
|
A | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 803 | chr2 | 190501021 | |||||
chr2:190501026
|
A | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 808 | chr2 | 190501026 | |||||
chr2:190501029
|
G | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 811 | chr2 | 190501029 | |||||
chr2:190501030
|
A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*812A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 812 | chr2 | 190501030 | |||||
chr2:190501031
|
T | TTTTTGAA others(3): Show |
1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*813_*814insTTTTGA others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 814 | chr2 | 190501031 | |||||
chr2:190501033
|
C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 815 | chr2 | 190501033 | |||||
chr2:190501035
|
G | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 817 | chr2 | 190501035 | |||||
chr2:190501040
|
T | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 822 | chr2 | 190501040 | |||||
chr2:190501044
|
C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 826 | chr2 | 190501044 | |||||
chr2:190501048
|
C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 830 | chr2 | 190501048 | |||||
chr2:190501050
|
C | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 832 | chr2 | 190501050 | |||||
chr2:190501054
|
A | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*836A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 836 | chr2 | 190501054 | |||||
chr2:190501059
|
C | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 841 | chr2 | 190501059 | |||||
chr2:190501062
|
T | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 844 | chr2 | 190501062 | |||||
chr2:190501063
|
C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 845 | chr2 | 190501063 | |||||
chr2:190501065
|
T | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*847T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 847 | chr2 | 190501065 | |||||
chr2:190501072
|
A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*854A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 854 | chr2 | 190501072 | |||||
chr2:190501085
|
T | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 867 | chr2 | 190501085 | |||||
chr2:190501087
|
A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*869A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 869 | chr2 | 190501087 | |||||
chr2:190501088
|
G | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 870 | chr2 | 190501088 | |||||
chr2:190501107
|
C | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 889 | chr2 | 190501107 | |||||
chr2:190501127
|
A | C | 1 | a0003c0003t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 909 | chr2 | 190501127 | |||||
chr2:190501138
|
A | G | 1 | a0001c0001t0021 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*920A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 920 | chr2 | 190501138 | |||||
chr2:190501255
|
G | A | 2 | a0001c0001t0008a0002c0002t0008 | 3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1037 | chr2 | 190501255 | |||||
chr2:190501292
|
G | A | 1 | a0001c0001t0018 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1074G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1074 | chr2 | 190501292 | |||||
chr2:190501485
|
G | A | 1 | a0002c0002t0009 | 3 | HG02074.hp2 NA18957.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1267 | chr2 | 190501485 | |||||
chr2:190501819
|
G | A | 1 | a0002c0002t0019 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1601G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1601 | chr2 | 190501819 | |||||
chr2:190501853
|
T | G | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(5): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1635T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1635 | chr2 | 190501853 | |||||
chr2:190501981
|
A | G | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(3): Show | 88 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1763A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1763 | chr2 | 190501981 | |||||
chr2:190502110
|
A | G | 2 | a0003c0003t0010a0003c0003t0022 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1892A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1892 | chr2 | 190502110 | |||||
chr2:190502213
|
G | A | 1 | a0001c0001t0020 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1995G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1995 | chr2 | 190502213 | |||||
chr2:190502244
|
G | A | 1 | a0001c0001t0012 | 2 | HG02145.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2026G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2026 | chr2 | 190502244 | |||||
chr2:190502248
|
CTT | C | 2 | a0003c0003t0010a0003c0003t0022 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034_*2035delTT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2034 | INFO_REALIGN_3_PRIME | chr2 | 190502248 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190408511
|
G | A | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.-176+8G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408511 | ||||||
chr2:190408536
|
C | T | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-176+33C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408536 | ||||||
chr2:190408632
|
C | T | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-176+129C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408632 | ||||||
chr2:190408694
|
G | GCTCC | 4 | a0002c0002t0001g0322a0005c0004t0001g0321a0005c0004t0001g0323others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176+209_-176+212d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190408694 | |||||
chr2:190408694
|
G | GCTCCCTC others(1): Show |
7 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0327others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176+205_-176+212d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190408694 | |||||
chr2:190408694
|
GCTCCCTC others(1): Show |
G | 56 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-176+205_-176+212d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190408694 | |||||
chr2:190408754
|
G | A | 85 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(82): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176+251G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408754 | ||||||
chr2:190408755
|
G | C | 56 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-176+252G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408755 | ||||||
chr2:190408769
|
T | A | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-176+266T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408769 | ||||||
chr2:190409090
|
G | C | 2 | a0002c0002t0001g0145a0002c0002t0001g0146 | 2 | HG01255.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-176+587G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409090 | ||||||
chr2:190409267
|
A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-176+764A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409267 | ||||||
chr2:190409407
|
A | G | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-176+904A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409407 | ||||||
chr2:190409483
|
G | T | 1 | a0002c0002t0001g0318 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-176+980G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409483 | ||||||
chr2:190409543
|
G | T | 1 | a0001c0001t0003g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-176+1040G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409543 | ||||||
chr2:190410078
|
C | T | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-176+1575C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410078 | ||||||
chr2:190410368
|
T | C | 1 | a0002c0002t0001g0147 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-176+1865T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410368 | ||||||
chr2:190410525
|
C | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-176+2022C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410525 | ||||||
chr2:190410537
|
A | T | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-176+2034A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410537 | ||||||
chr2:190410557
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-176+2054T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410557 | ||||||
chr2:190410790
|
G | A | 1 | a0002c0002t0005g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-176+2287G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410790 | ||||||
chr2:190410801
|
T | C | 4 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071others(1): Show | 4 | HG00741.hp2 HG01074.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-176+2298T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410801 | ||||||
chr2:190410852
|
T | TC | 69 | a0001c0001t0002g0313a0001c0001t0003g0282a0002c0002t0001g0010others(66): Show | 70 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.-176+2350dupC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190410852 | |||||
chr2:190410954
|
G | T | 1 | a0001c0001t0002g0144 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-176+2451G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410954 | ||||||
chr2:190411009
|
C | T | 69 | a0001c0001t0002g0313a0001c0001t0003g0282a0002c0002t0001g0010others(66): Show | 70 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.-176+2506C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411009 | ||||||
chr2:190411010
|
G | A | 84 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0001others(81): Show | 89 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-176+2507G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411010 | ||||||
chr2:190411011
|
C | T | 34 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(31): Show | 35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-176+2508C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411011 | ||||||
chr2:190411074
|
A | G | 1 | a0001c0001t0007g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-176+2571A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411074 | ||||||
chr2:190411156
|
CAGT | C | 9 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0136others(6): Show | 9 | HG01433.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176+2657_-176+265 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190411156 | |||||
chr2:190411158
|
GTAGT | G | 75 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0001others(72): Show | 80 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-176+2657_-176+266 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190411158 | |||||
chr2:190411161
|
G | GT | 30 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(27): Show | 30 | HG01169.hp2 HG01192.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-176+2675dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190411161 | |||||
chr2:190411189
|
C | G | 1 | a0002c0002t0001g0215 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-176+2686C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411189 | ||||||
chr2:190411194
|
T | C | 85 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(82): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176+2691T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411194 | ||||||
chr2:190411795
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0002g0129a0001c0001t0002g0131others(2): Show | 5 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+3292C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411795 | ||||||
chr2:190411885
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-176+3382C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411885 | ||||||
chr2:190411944
|
A | G | 2 | a0002c0002t0004g0213a0002c0002t0004g0214 | 2 | HG01123.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-175-3348A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411944 | ||||||
chr2:190412495
|
T | G | 1 | a0002c0002t0001g0150 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-175-2797T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412495 | ||||||
chr2:190412496
|
A | T | 1 | a0002c0002t0001g0150 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-175-2796A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412496 | ||||||
chr2:190412565
|
G | A | 1 | a0002c0002t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-175-2727G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412565 | ||||||
chr2:190412626
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-175-2666C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412626 | ||||||
chr2:190413184
|
C | G | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-175-2108C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413184 | ||||||
chr2:190413615
|
G | A | 235 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(232): Show | 246 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-175-1677G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413615 | ||||||
chr2:190413671
|
G | A | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-175-1621G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413671 | ||||||
chr2:190413692
|
C | T | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-175-1600C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413692 | ||||||
chr2:190413912
|
C | A | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-175-1380C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413912 | ||||||
chr2:190414005
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-175-1287G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414005 | ||||||
chr2:190414260
|
A | G | 36 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(33): Show | 37 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.-175-1032A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414260 | ||||||
chr2:190414439
|
G | A | 1 | a0002c0002t0001g0243 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-175-853G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414439 | ||||||
chr2:190414446
|
T | TAAAAGAC others(30): Show |
1 | a0002c0002t0001g0243 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-175-836_-175-835i others(39): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190414446 | |||||
chr2:190414640
|
A | G | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-175-652A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414640 | ||||||
chr2:190415479
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-54+66A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190415479 | ||||||
chr2:190415709
|
G | T | 330 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(327): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-54+296G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190415709 | ||||||
chr2:190415943
|
A | G | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+530A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190415943 | ||||||
chr2:190416032
|
A | C | 2 | a0002c0002t0001g0308a0002c0002t0001g0309 | 2 | HG02040.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-54+619A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416032 | ||||||
chr2:190416155
|
A | G | 2 | a0002c0002t0001g0306a0002c0002t0001g0307 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-54+742A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416155 | ||||||
chr2:190416306
|
A | C | 32 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(29): Show | 33 | HG01192.hp1 HG01261.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.-54+893A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416306 | ||||||
chr2:190416320
|
C | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-54+907C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416320 | ||||||
chr2:190416442
|
A | C | 35 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0221others(32): Show | 36 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.-54+1029A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416442 | ||||||
chr2:190416594
|
C | T | 56 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-54+1181C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416594 | ||||||
chr2:190417182
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-54+1769A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417182 | ||||||
chr2:190417268
|
G | A | 330 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(327): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-54+1855G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417268 | ||||||
chr2:190417465
|
T | G | 2 | a0001c0001t0003g0016a0001c0001t0003g0017 | 2 | HG01517.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-54+2052T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417465 | ||||||
chr2:190417525
|
A | G | 34 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(31): Show | 35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-54+2112A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417525 | ||||||
chr2:190417684
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+2271C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417684 | ||||||
chr2:190417698
|
T | C | 272 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(269): Show | 284 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.-54+2285T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417698 | ||||||
chr2:190417703
|
C | A | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-54+2290C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417703 | ||||||
chr2:190417965
|
G | GGT | 15 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0003g0016others(12): Show | 16 | HG00140.hp2 HG01517.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-54+2587_-54+2588d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
G | GGTGT | 21 | a0001c0001t0001g0143a0001c0001t0003g0059a0001c0001t0021g0210others(18): Show | 21 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-54+2585_-54+2588d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
G | GGTGTGT | 57 | a0001c0001t0001g0148a0001c0001t0001g0232a0001c0001t0001g0233others(54): Show | 60 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-54+2583_-54+2588d others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
G | GGTGTGTG others(1): Show |
41 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(38): Show | 42 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-54+2581_-54+2588d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
G | GGTGTGTG others(3): Show |
12 | a0001c0001t0001g0242a0001c0001t0001g0251a0002c0002t0001g0206others(9): Show | 12 | HG01891.hp1 HG02486.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54+2579_-54+2588d others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
G | GGTGTGTG others(5): Show |
5 | a0002c0002t0001g0302a0002c0002t0001g0303a0002c0002t0009g0304others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+2577_-54+2588d others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
GGTGTGT | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0244a0003c0003t0010g0330others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+2583_-54+2588d others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
GGTGTGTG others(3): Show |
G | 75 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(72): Show | 80 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-54+2579_-54+2588d others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417965
|
GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-54+2567_-54+2588d others(24): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | |||||
chr2:190417998
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0012g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+2588_-54+2589i others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417998 | |||||
chr2:190418000
|
GTA | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG00735.hp2 HG01070.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+2589_-54+2590d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190418000 | |||||
chr2:190418002
|
A | G | 53 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-54+2589A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418002 | ||||||
chr2:190418005
|
T | A | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(2): Show | 5 | HG02135.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+2592T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418005 | ||||||
chr2:190418088
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+2675C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418088 | ||||||
chr2:190418308
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0003g0062 | 2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-54+2895T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418308 | ||||||
chr2:190418523
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-54+3110A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418523 | ||||||
chr2:190418752
|
A | G | 330 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(327): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-54+3339A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418752 | ||||||
chr2:190418774
|
A | C | 1 | a0002c0002t0003g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-54+3361A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418774 | ||||||
chr2:190418775
|
A | G | 1 | a0002c0002t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-54+3362A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418775 | ||||||
chr2:190418982
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-54+3569C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418982 | ||||||
chr2:190419092
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-54+3679A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419092 | ||||||
chr2:190419181
|
T | C | 1 | a0002c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-54+3768T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419181 | ||||||
chr2:190419244
|
G | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-54+3831G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419244 | ||||||
chr2:190419271
|
C | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0251 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-54+3858C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419271 | ||||||
chr2:190419392
|
C | T | 1 | a0002c0002t0001g0005 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-54+3979C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419392 | ||||||
chr2:190419625
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-54+4212C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419625 | ||||||
chr2:190419840
|
G | T | 1 | a0002c0002t0005g0200 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-54+4427G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419840 | ||||||
chr2:190419929
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-54+4516A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419929 | ||||||
chr2:190420057
|
CAA | C | 153 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(150): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-54+4645_-54+4646d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420057 | ||||||
chr2:190420139
|
C | G | 44 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(41): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-54+4726C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420139 | ||||||
chr2:190420172
|
TATATAGC others(27): Show |
T | 330 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(327): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-54+4761_-54+4794d others(36): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190420172 | |||||
chr2:190420390
|
T | G | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-54+4977T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420390 | ||||||
chr2:190420391
|
C | A | 1 | a0002c0002t0013g0314 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-54+4978C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420391 | ||||||
chr2:190420531
|
A | G | 1 | a0002c0002t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-54+5118A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420531 | ||||||
chr2:190420888
|
T | C | 154 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(151): Show | 161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-54+5475T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420888 | ||||||
chr2:190421006
|
A | G | 75 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(72): Show | 79 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-54+5593A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421006 | ||||||
chr2:190421484
|
A | G | 1 | a0001c0001t0003g0055 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-54+6071A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421484 | ||||||
chr2:190421494
|
G | GGTTT | 330 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(327): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-54+6084_-54+6085i others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190421494 | |||||
chr2:190421611
|
C | A | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-54+6198C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421611 | ||||||
chr2:190421658
|
T | C | 330 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(327): Show | 342 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-54+6245T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421658 | ||||||
chr2:190421676
|
A | C | 154 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(151): Show | 161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-54+6263A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421676 | ||||||
chr2:190421725
|
T | TAA | 115 | a0001c0001t0001g0097a0001c0001t0001g0143a0001c0001t0001g0148others(112): Show | 120 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-54+6321_-54+6322d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190421725 | |||||
chr2:190421736
|
T | A | 6 | a0001c0001t0001g0130a0001c0001t0002g0129a0001c0001t0002g0131others(3): Show | 6 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+6323T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421736 | ||||||
chr2:190421758
|
A | G | 271 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(268): Show | 283 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.-54+6345A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421758 | ||||||
chr2:190421790
|
A | C | 108 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(105): Show | 111 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.-54+6377A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421790 | ||||||
chr2:190421932
|
A | G | 272 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(269): Show | 284 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.-54+6519A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421932 | ||||||
chr2:190422065
|
A | G | 56 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-54+6652A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422065 | ||||||
chr2:190422114
|
C | T | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-54+6701C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422114 | ||||||
chr2:190422396
|
T | A | 154 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(151): Show | 161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-54+6983T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422396 | ||||||
chr2:190422415
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-54+7002T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422415 | ||||||
chr2:190422651
|
G | A | 1 | a0001c0001t0002g0325 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-54+7238G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422651 | ||||||
chr2:190422656
|
G | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(115): Show | 123 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-54+7243G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422656 | ||||||
chr2:190422788
|
T | C | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-54+7375T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422788 | ||||||
chr2:190422861
|
G | T | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-54+7448G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422861 | ||||||
chr2:190422888
|
C | CT | 8 | a0001c0001t0002g0124a0001c0001t0002g0126a0001c0001t0002g0128others(5): Show | 10 | NA18949.hp1 NA18960.hp2 NA18980.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+7484dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190422888 | |||||
chr2:190422957
|
A | G | 81 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0001others(78): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-54+7544A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422957 | ||||||
chr2:190422959
|
A | C | 81 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0001others(78): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-54+7546A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422959 | ||||||
chr2:190423345
|
G | T | 83 | a0001c0001t0003g0212a0002c0002t0001g0002a0002c0002t0001g0007others(80): Show | 88 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-54+7932G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190423345 | ||||||
chr2:190423688
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-54+8275G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190423688 | ||||||
chr2:190423968
|
T | C | 154 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(151): Show | 161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-54+8555T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190423968 | ||||||
chr2:190424107
|
A | G | 202 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(199): Show | 212 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-54+8694A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424107 | ||||||
chr2:190424181
|
C | T | 83 | a0001c0001t0003g0212a0002c0002t0001g0002a0002c0002t0001g0007others(80): Show | 88 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-54+8768C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424181 | ||||||
chr2:190424235
|
CT | C | 160 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(157): Show | 169 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-54+8835delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190424235 | |||||
chr2:190424578
|
G | A | 2 | a0001c0001t0001g0222a0002c0002t0001g0206 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-54+9165G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424578 | ||||||
chr2:190424706
|
T | C | 4 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(1): Show | 4 | NA18986.hp2 NA18993.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+9293T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424706 | ||||||
chr2:190424785
|
A | G | 70 | a0001c0001t0002g0313a0001c0001t0003g0282a0002c0002t0001g0005others(67): Show | 72 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.-54+9372A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424785 | ||||||
chr2:190425290
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-54+9877C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425290 | ||||||
chr2:190425408
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+9995C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425408 | ||||||
chr2:190425473
|
T | C | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+10060T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425473 | ||||||
chr2:190425568
|
T | G | 10 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(7): Show | 10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+10155T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425568 | ||||||
chr2:190425828
|
T | C | 56 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-53-10149T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425828 | ||||||
chr2:190425886
|
G | A | 1 | a0002c0002t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-53-10091G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425886 | ||||||
chr2:190426019
|
A | T | 154 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(151): Show | 161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-53-9958A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426019 | ||||||
chr2:190426023
|
T | C | 34 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(31): Show | 35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-53-9954T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426023 | ||||||
chr2:190426555
|
G | C | 1 | a0002c0002t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-53-9422G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426555 | ||||||
chr2:190426749
|
G | A | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-9228G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426749 | ||||||
chr2:190426828
|
CTG | C | 34 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(31): Show | 35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-53-9146_-53-9145d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190426828 | |||||
chr2:190426914
|
G | A | 1 | a0005c0004t0001g0321 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-53-9063G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426914 | ||||||
chr2:190427069
|
G | A | 1 | a0001c0001t0002g0128 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-53-8908G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427069 | ||||||
chr2:190427288
|
G | A | 1 | a0001c0001t0003g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-53-8689G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427288 | ||||||
chr2:190427360
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-53-8617C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427360 | ||||||
chr2:190427412
|
C | T | 82 | a0001c0001t0003g0212a0002c0002t0001g0002a0002c0002t0001g0007others(79): Show | 87 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-53-8565C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427412 | ||||||
chr2:190427657
|
T | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-8320T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427657 | ||||||
chr2:190427727
|
CT | C | 116 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(113): Show | 122 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-53-8239delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190427727 | |||||
chr2:190427846
|
C | A | 44 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(41): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-53-8131C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427846 | ||||||
chr2:190427963
|
C | T | 1 | a0002c0002t0001g0170 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-53-8014C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427963 | ||||||
chr2:190427981
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-53-7996C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427981 | ||||||
chr2:190427983
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-53-7994C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427983 | ||||||
chr2:190428027
|
C | G | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-7950C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428027 | ||||||
chr2:190428071
|
T | C | 82 | a0001c0001t0003g0212a0002c0002t0001g0002a0002c0002t0001g0007others(79): Show | 87 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-53-7906T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428071 | ||||||
chr2:190428083
|
C | G | 82 | a0001c0001t0003g0212a0002c0002t0001g0002a0002c0002t0001g0007others(79): Show | 87 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-53-7894C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428083 | ||||||
chr2:190428085
|
A | G | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-7892A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428085 | ||||||
chr2:190428228
|
C | T | 1 | a0001c0001t0007g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-53-7749C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428228 | ||||||
chr2:190428240
|
T | G | 5 | a0001c0001t0001g0130a0001c0001t0002g0129a0001c0001t0002g0131others(2): Show | 5 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53-7737T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428240 | ||||||
chr2:190428329
|
A | G | 83 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(80): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-53-7648A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428329 | ||||||
chr2:190428558
|
T | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-53-7419T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428558 | ||||||
chr2:190428572
|
T | G | 2 | a0001c0001t0002g0124a0002c0002t0001g0125 | 2 | NA18960.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-53-7405T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428572 | ||||||
chr2:190428647
|
ATGCT | A | 33 | a0001c0001t0001g0246a0001c0001t0002g0001a0001c0001t0002g0014others(30): Show | 35 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-53-7324_-53-7321d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428647 | |||||
chr2:190428650
|
C | CTTAT | 26 | a0001c0001t0002g0019a0001c0001t0002g0069a0001c0001t0002g0070others(23): Show | 26 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-53-7325_-53-7324i others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428650 | |||||
chr2:190428650
|
CTTGCTTA others(1): Show |
C | 140 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0221others(137): Show | 144 | HG00621.hp1 HG00741.hp1 HG01069.hp2 others(141): Show |
intron_variant | MODIFIER | c.-53-7324_-53-7317d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428650 | |||||
chr2:190428650
|
CTTGCTTA others(5): Show |
C | 1 | a0002c0002t0001g0182 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-53-7324_-53-7313d others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428650 | |||||
chr2:190428653
|
G | A | 153 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0015others(150): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-53-7324G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428653 | ||||||
chr2:190428654
|
C | T | 153 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0015others(150): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-53-7323C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428654 | ||||||
chr2:190428874
|
C | T | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-53-7103C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428874 | ||||||
chr2:190428875
|
A | G | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-7102A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428875 | ||||||
chr2:190428969
|
A | G | 329 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(326): Show | 341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-53-7008A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428969 | ||||||
chr2:190429046
|
G | A | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-6931G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429046 | ||||||
chr2:190429086
|
A | G | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-6891A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429086 | ||||||
chr2:190429127
|
T | C | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-53-6850T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429127 | ||||||
chr2:190429227
|
C | CGT | 182 | a0001c0001t0001g0148a0001c0001t0001g0221a0001c0001t0001g0222others(179): Show | 189 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(186): Show |
intron_variant | MODIFIER | c.-53-6729_-53-6728d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190429227 | |||||
chr2:190429364
|
C | T | 5 | a0002c0002t0001g0002a0002c0002t0001g0179a0002c0002t0001g0197others(2): Show | 7 | NA18941.hp2 NA18956.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-6613C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429364 | ||||||
chr2:190429388
|
C | T | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-6589C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429388 | ||||||
chr2:190429443
|
A | T | 1 | a0002c0002t0001g0005 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-53-6534A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429443 | ||||||
chr2:190429448
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-53-6529C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429448 | ||||||
chr2:190429454
|
C | A | 44 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(41): Show | 48 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-53-6523C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429454 | ||||||
chr2:190429534
|
G | A | 1 | a0002c0002t0001g0158 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-53-6443G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429534 | ||||||
chr2:190429583
|
A | G | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-6394A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429583 | ||||||
chr2:190429803
|
A | C | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-6174A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429803 | ||||||
chr2:190429999
|
T | C | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-5978T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429999 | ||||||
chr2:190430009
|
C | G | 2 | a0001c0001t0001g0251a0002c0002t0001g0275 | 2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-53-5968C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430009 | ||||||
chr2:190430026
|
G | C | 20 | a0001c0001t0002g0001a0001c0001t0002g0076a0001c0001t0002g0077others(17): Show | 22 | HG00408.hp1 HG00423.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.-53-5951G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430026 | ||||||
chr2:190430207
|
C | CT | 143 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(140): Show | 150 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.-53-5754dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430207 | |||||
chr2:190430207
|
CT | C | 7 | a0001c0001t0001g0237a0001c0001t0002g0111a0001c0001t0003g0031others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-5754delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430207 | |||||
chr2:190430278
|
T | C | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-5699T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430278 | ||||||
chr2:190430320
|
A | G | 1 | a0002c0002t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-53-5657A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430320 | ||||||
chr2:190430350
|
C | T | 56 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-53-5627C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430350 | ||||||
chr2:190430359
|
G | A | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-5618G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430359 | ||||||
chr2:190430389
|
T | G | 1 | a0001c0001t0003g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-53-5588T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430389 | ||||||
chr2:190430621
|
A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-5356A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430621 | ||||||
chr2:190430631
|
C | T | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-5346C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430631 | ||||||
chr2:190430698
|
C | A | 1 | a0002c0002t0001g0280 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-53-5279C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430698 | ||||||
chr2:190430718
|
GGGTACAC others(5): Show |
G | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-5258_-53-5247d others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430718 | ||||||
chr2:190430738
|
G | A | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-5239G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430738 | ||||||
chr2:190430769
|
C | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-53-5208C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430769 | ||||||
chr2:190430799
|
C | CCCCCCCC others(88): Show |
1 | a0002c0002t0001g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-53-5160_-53-5159i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | |||||
chr2:190430799
|
C | CCCCCCCC others(88): Show |
51 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-5160_-53-5159i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | |||||
chr2:190430799
|
C | CCCCCCCC others(88): Show |
1 | a0002c0002t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-53-5160_-53-5159i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | |||||
chr2:190430799
|
C | CCCCCCCC others(89): Show |
2 | a0002c0002t0001g0276a0002c0002t0001g0316 | 2 | HG02056.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-53-5171_-53-5170i others(98): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | |||||
chr2:190430800
|
CCCCCCCA others(40): Show |
C | 6 | a0001c0001t0001g0130a0001c0001t0002g0129a0001c0001t0002g0131others(3): Show | 6 | HG01106.hp1 HG02083.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53-5147_-53-5101d others(49): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430800 | |||||
chr2:190430818
|
G | C | 98 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0007others(95): Show | 103 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-53-5159G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430818 | ||||||
chr2:190430820
|
A | G | 55 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(52): Show | 56 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-53-5157A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430820 | ||||||
chr2:190430834
|
C | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-5143C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430834 | ||||||
chr2:190430855
|
C | T | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-5122C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430855 | ||||||
chr2:190430864
|
C | CGGACGGG others(88): Show |
2 | a0002c0002t0001g0306a0002c0002t0001g0307 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-53-5101_-53-5100i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | |||||
chr2:190430864
|
C | CGGACGGG others(88): Show |
88 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0007others(85): Show | 93 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-53-5101_-53-5100i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | |||||
chr2:190430864
|
C | CGGACGGG others(89): Show |
1 | a0002c0002t0001g0274 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(98): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | |||||
chr2:190430864
|
C | CGGACGGG others(71): Show |
1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(80): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | |||||
chr2:190430864
|
C | CGGACGGG others(89): Show |
1 | a0002c0002t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(98): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | |||||
chr2:190430864
|
C | CGGGCGGG others(40): Show |
3 | a0002c0002t0005g0149a0002c0002t0005g0218a0002c0002t0008g0211 | 3 | HG02280.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-53-5111_-53-5110i others(49): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | |||||
chr2:190430864
|
C | T | 58 | a0001c0001t0002g0313a0001c0001t0003g0033a0001c0001t0003g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-53-5113C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430864 | ||||||
chr2:190430867
|
A | ACGGGGCG others(41): Show |
1 | a0002c0002t0001g0176 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(50): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430867 | |||||
chr2:190430873
|
C | CGGCCGGC others(88): Show |
1 | a0002c0002t0001g0275 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430873 | |||||
chr2:190430948
|
C | T | 1 | a0002c0002t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-53-5029C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430948 | ||||||
chr2:190431006
|
ACGCTCCT others(33): Show |
A | 46 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(43): Show | 50 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-53-4943_-53-4904d others(42): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190431006 | |||||
chr2:190431026
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-53-4951G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431026 | ||||||
chr2:190431048
|
G | A | 1 | a0002c0002t0001g0281 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-53-4929G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431048 | ||||||
chr2:190431087
|
C | T | 59 | a0001c0001t0002g0001a0001c0001t0002g0069a0001c0001t0002g0070others(56): Show | 63 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-53-4890C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431087 | ||||||
chr2:190431114
|
G | A | 2 | a0002c0002t0001g0181a0002c0002t0001g0183 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-53-4863G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431114 | ||||||
chr2:190431143
|
G | A | 3 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0327 | 3 | HG02622.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-4834G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431143 | ||||||
chr2:190431194
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-53-4783G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431194 | ||||||
chr2:190431244
|
C | T | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-4733C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431244 | ||||||
chr2:190431297
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0246 | 2 | HG01261.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-53-4680C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431297 | ||||||
chr2:190431382
|
G | A | 2 | a0001c0001t0012g0236a0001c0001t0012g0247 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-4595G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431382 | ||||||
chr2:190431453
|
G | A | 2 | a0001c0001t0002g0124a0002c0002t0001g0125 | 2 | NA18960.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-53-4524G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431453 | ||||||
chr2:190431490
|
A | G | 152 | a0001c0001t0002g0313a0001c0001t0003g0212a0001c0001t0003g0282others(149): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-53-4487A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431490 | ||||||
chr2:190431506
|
T | C | 297 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(294): Show | 308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-53-4471T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431506 | ||||||
chr2:190431524
|
G | C | 1 | a0002c0002t0001g0197 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-53-4453G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431524 | ||||||
chr2:190431547
|
A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-4430A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431547 | ||||||
chr2:190431570
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-53-4407C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431570 | ||||||
chr2:190431690
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-53-4287G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431690 | ||||||
chr2:190431695
|
AAG | A | 58 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-53-4277_-53-4276d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190431695 | |||||
chr2:190431703
|
G | A | 81 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0001others(78): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-53-4274G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431703 | ||||||
chr2:190431892
|
T | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-53-4085T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431892 | ||||||
chr2:190431997
|
TCTGATTT others(7): Show |
T | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-3974_-53-3961d others(16): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190431997 | |||||
chr2:190432245
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-3732G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432245 | ||||||
chr2:190432320
|
C | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0244 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-53-3657C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432320 | ||||||
chr2:190432394
|
C | A | 1 | a0002c0002t0001g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-53-3583C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432394 | ||||||
chr2:190432425
|
T | G | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-3552T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432425 | ||||||
chr2:190432426
|
G | T | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-3551G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432426 | ||||||
chr2:190432427
|
T | G | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-3550T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432427 | ||||||
chr2:190432721
|
T | C | 295 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(292): Show | 306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-53-3256T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432721 | ||||||
chr2:190432821
|
C | T | 1 | a0002c0002t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-53-3156C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432821 | ||||||
chr2:190432840
|
A | T | 1 | a0006c0008t0003g0032 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-53-3137A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432840 | ||||||
chr2:190432842
|
T | A | 136 | a0001c0001t0003g0212a0001c0001t0003g0282a0002c0002t0001g0002others(133): Show | 142 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.-53-3135T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432842 | ||||||
chr2:190432869
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-53-3108T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432869 | ||||||
chr2:190433047
|
C | T | 151 | a0001c0001t0003g0212a0002c0002t0001g0002a0002c0002t0001g0005others(148): Show | 158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-2930C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433047 | ||||||
chr2:190433183
|
A | C | 1 | a0002c0002t0013g0314 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-53-2794A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433183 | ||||||
chr2:190433260
|
AT | A | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0035others(1): Show | 4 | HG01069.hp1 HG01243.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-2713delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190433260 | |||||
chr2:190433812
|
C | G | 1 | a0001c0001t0002g0095 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-53-2165C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433812 | ||||||
chr2:190433886
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095 | 3 | NA18959.hp2 NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-53-2091C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433886 | ||||||
chr2:190434017
|
C | A | 1 | a0001c0001t0003g0055 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-53-1960C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434017 | ||||||
chr2:190434098
|
G | C | 150 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0007others(147): Show | 157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-53-1879G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434098 | ||||||
chr2:190434182
|
C | CA | 216 | a0001c0001t0001g0222a0001c0001t0002g0014a0001c0001t0002g0015others(213): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-53-1782dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190434182 | |||||
chr2:190434196
|
G | A | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-1781G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434196 | ||||||
chr2:190434240
|
G | A | 1 | a0002c0002t0001g0283 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-53-1737G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434240 | ||||||
chr2:190434326
|
A | G | 2 | a0003c0003t0022g0207a0007c0009t0015g0208 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-53-1651A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434326 | ||||||
chr2:190434576
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-53-1401C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434576 | ||||||
chr2:190434580
|
C | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-1397C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434580 | ||||||
chr2:190434795
|
G | A | 16 | a0002c0002t0001g0252a0002c0002t0001g0253a0002c0002t0001g0254others(13): Show | 16 | HG01981.hp1 HG02015.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53-1182G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434795 | ||||||
chr2:190434983
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-53-994G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434983 | ||||||
chr2:190435171
|
G | A | 297 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(294): Show | 308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-53-806G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435171 | ||||||
chr2:190435270
|
G | T | 297 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(294): Show | 308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-53-707G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435270 | ||||||
chr2:190435392
|
G | A | 215 | a0001c0001t0001g0143a0001c0001t0002g0014a0001c0001t0002g0015others(212): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-53-585G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435392 | ||||||
chr2:190435452
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-53-525C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435452 | ||||||
chr2:190435637
|
AAC | A | 150 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0007others(147): Show | 157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-53-338_-53-337del others(2): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190435637 | |||||
chr2:190435676
|
A | G | 151 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0005others(148): Show | 158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-301A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435676 | ||||||
chr2:190435713
|
A | G | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-264A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435713 | ||||||
chr2:190435796
|
G | A | 2 | a0002c0002t0001g0196a0002c0002t0001g0319 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-53-181G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435796 | ||||||
chr2:190437577
|
C | T | 1 | a0002c0002t0001g0158 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1532+16C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190437577 | ||||||
chr2:190438013
|
C | T | 103 | a0001c0001t0001g0130a0002c0002t0001g0005a0002c0002t0001g0008others(100): Show | 107 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1532+452C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438013 | ||||||
chr2:190438025
|
T | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+464T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438025 | ||||||
chr2:190438061
|
G | A | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1532+500G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438061 | ||||||
chr2:190438176
|
T | C | 1 | a0002c0002t0001g0158 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1532+615T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438176 | ||||||
chr2:190438181
|
C | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1532+620C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438181 | ||||||
chr2:190438215
|
T | TA | 302 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0222others(299): Show | 314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.1532+665dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190438215 | |||||
chr2:190438215
|
T | TAA | 8 | a0002c0002t0001g0125a0002c0002t0001g0145a0002c0002t0001g0146others(5): Show | 8 | HG01255.hp2 HG03195.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1532+664_1532+665d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190438215 | |||||
chr2:190438305
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1532+744C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438305 | ||||||
chr2:190438313
|
C | T | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+752C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438313 | ||||||
chr2:190438393
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1532+832G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438393 | ||||||
chr2:190438520
|
A | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+959A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438520 | ||||||
chr2:190438531
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1532+970C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438531 | ||||||
chr2:190438673
|
G | A | 1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1532+1112G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438673 | ||||||
chr2:190438794
|
T | G | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1532+1233T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438794 | ||||||
chr2:190438799
|
A | G | 61 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+1238A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438799 | ||||||
chr2:190438986
|
G | T | 2 | a0002c0002t0001g0173a0002c0002t0013g0305 | 2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1532+1425G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438986 | ||||||
chr2:190438987
|
G | A | 2 | a0002c0002t0001g0173a0002c0002t0013g0305 | 2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1532+1426G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438987 | ||||||
chr2:190439260
|
C | T | 103 | a0001c0001t0001g0130a0002c0002t0001g0005a0002c0002t0001g0008others(100): Show | 107 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1532+1699C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439260 | ||||||
chr2:190439423
|
A | G | 219 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(216): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1532+1862A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439423 | ||||||
chr2:190439533
|
T | C | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+1972T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439533 | ||||||
chr2:190439643
|
T | G | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1532+2082T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439643 | ||||||
chr2:190439786
|
T | C | 1 | a0004c0005t0001g0287 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1532+2225T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439786 | ||||||
chr2:190439887
|
T | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+2326T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439887 | ||||||
chr2:190440034
|
T | C | 1 | a0002c0002t0001g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1532+2473T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440034 | ||||||
chr2:190440286
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1532+2725C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440286 | ||||||
chr2:190440309
|
A | G | 2 | a0002c0002t0008g0211a0002c0011t0001g0320 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1532+2748A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440309 | ||||||
chr2:190440760
|
C | T | 2 | a0001c0001t0001g0230a0002c0002t0001g0219 | 2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1532+3199C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440760 | ||||||
chr2:190440808
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1532+3247T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440808 | ||||||
chr2:190440821
|
A | G | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1532+3260A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440821 | ||||||
chr2:190440921
|
C | T | 153 | a0001c0001t0001g0130a0001c0001t0001g0143a0002c0002t0001g0002others(150): Show | 161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.1532+3360C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440921 | ||||||
chr2:190440936
|
G | A | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+3375G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440936 | ||||||
chr2:190441094
|
C | G | 1 | a0001c0001t0002g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1532+3533C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441094 | ||||||
chr2:190441098
|
T | C | 215 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(212): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1532+3537T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441098 | ||||||
chr2:190441180
|
T | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1532+3619T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441180 | ||||||
chr2:190441257
|
T | C | 218 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(215): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1532+3696T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441257 | ||||||
chr2:190441307
|
G | A | 1 | a0002c0002t0001g0263 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1532+3746G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441307 | ||||||
chr2:190441422
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1532+3861G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441422 | ||||||
chr2:190441428
|
C | A | 1 | a0001c0001t0002g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1532+3867C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441428 | ||||||
chr2:190441488
|
G | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1532+3927G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441488 | ||||||
chr2:190441813
|
C | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1532+4252C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441813 | ||||||
chr2:190441816
|
C | T | 165 | a0001c0001t0001g0130a0001c0001t0002g0014a0001c0001t0002g0015others(162): Show | 169 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1532+4255C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441816 | ||||||
chr2:190442000
|
A | G | 219 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(216): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1532+4439A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442000 | ||||||
chr2:190442164
|
C | G | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+4603C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442164 | ||||||
chr2:190442374
|
T | G | 2 | a0001c0001t0012g0236a0001c0001t0012g0247 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1532+4813T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442374 | ||||||
chr2:190442493
|
C | G | 215 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(212): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1532+4932C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442493 | ||||||
chr2:190442541
|
T | C | 2 | a0002c0002t0001g0201a0002c0002t0001g0322 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1532+4980T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442541 | ||||||
chr2:190442614
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+5053G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442614 | ||||||
chr2:190442682
|
G | T | 103 | a0001c0001t0001g0130a0002c0002t0001g0005a0002c0002t0001g0008others(100): Show | 107 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1532+5121G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442682 | ||||||
chr2:190442818
|
T | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+5257T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442818 | ||||||
chr2:190442821
|
T | C | 2 | a0002c0002t0001g0181a0002c0002t0001g0183 | 2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1532+5260T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442821 | ||||||
chr2:190442836
|
C | T | 166 | a0001c0001t0001g0130a0001c0001t0001g0222a0001c0001t0002g0014others(163): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1532+5275C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442836 | ||||||
chr2:190442900
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1532+5339G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442900 | ||||||
chr2:190443751
|
G | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532+6190G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190443751 | ||||||
chr2:190443847
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1532+6286G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190443847 | ||||||
chr2:190443906
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1532+6345G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190443906 | ||||||
chr2:190444066
|
G | T | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+6505G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444066 | ||||||
chr2:190444124
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1532+6563T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444124 | ||||||
chr2:190444145
|
T | C | 1 | a0002c0002t0009g0304 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1532+6584T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444145 | ||||||
chr2:190444338
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1532+6777C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444338 | ||||||
chr2:190444563
|
T | C | 7 | a0001c0001t0002g0112a0001c0001t0002g0122a0001c0001t0002g0223others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1532+7002T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444563 | ||||||
chr2:190444572
|
C | T | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+7011C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444572 | ||||||
chr2:190444663
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0137 | 3 | HG02145.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1532+7102C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444663 | ||||||
chr2:190444880
|
A | G | 1 | a0002c0002t0001g0157 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1532+7319A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444880 | ||||||
chr2:190444958
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1532+7397A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444958 | ||||||
chr2:190444997
|
C | T | 2 | a0002c0002t0001g0220a0002c0002t0001g0243 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1532+7436C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444997 | ||||||
chr2:190445129
|
G | C | 1 | a0002c0002t0005g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1532+7568G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445129 | ||||||
chr2:190445281
|
T | G | 2 | a0002c0002t0001g0264a0002c0002t0001g0283 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1532+7720T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445281 | ||||||
chr2:190445343
|
C | T | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+7782C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445343 | ||||||
chr2:190445392
|
A | G | 61 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+7831A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445392 | ||||||
chr2:190445457
|
C | CA | 80 | a0001c0001t0001g0097a0001c0001t0001g0245a0001c0001t0002g0001others(77): Show | 84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1532+7907dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | |||||
chr2:190445457
|
C | CAA | 63 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1532+7906_1532+790 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | |||||
chr2:190445457
|
C | CAAAA | 32 | a0001c0001t0001g0130a0002c0002t0001g0008a0002c0002t0001g0009others(29): Show | 34 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1532+7904_1532+790 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | |||||
chr2:190445457
|
C | CAAAAA | 60 | a0002c0002t0001g0005a0002c0002t0001g0010a0002c0002t0001g0125others(57): Show | 62 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+7903_1532+790 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | |||||
chr2:190445469
|
C | A | 4 | a0001c0001t0002g0103a0001c0001t0002g0114a0001c0001t0002g0123others(1): Show | 4 | HG00544.hp2 NA18747.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532+7908C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445469 | ||||||
chr2:190445473
|
G | A | 164 | a0001c0001t0001g0130a0001c0001t0002g0014a0001c0001t0002g0015others(161): Show | 168 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1532+7912G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445473 | ||||||
chr2:190445497
|
G | A | 1 | a0001c0001t0018g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1532+7936G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445497 | ||||||
chr2:190445499
|
A | AT | 164 | a0001c0001t0001g0130a0001c0001t0002g0014a0001c0001t0002g0015others(161): Show | 168 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1532+7948dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445499 | |||||
chr2:190445510
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0092 | 2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1532+7949C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445510 | ||||||
chr2:190445704
|
G | A | 61 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+8143G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445704 | ||||||
chr2:190445743
|
T | C | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095 | 3 | NA18959.hp2 NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1532+8182T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445743 | ||||||
chr2:190445802
|
CGTG | C | 99 | a0001c0001t0001g0130a0002c0002t0001g0005a0002c0002t0001g0008others(96): Show | 103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1532+8244_1532+824 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445802 | |||||
chr2:190445858
|
G | A | 9 | a0001c0001t0002g0096a0001c0001t0002g0112a0001c0001t0002g0113others(6): Show | 9 | HG01891.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1532+8297G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445858 | ||||||
chr2:190445861
|
A | AT | 14 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071others(11): Show | 14 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1532+8308dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445861 | |||||
chr2:190446270
|
A | C | 1 | a0002c0002t0001g0215 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1532+8709A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446270 | ||||||
chr2:190446286
|
A | G | 218 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(215): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1532+8725A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446286 | ||||||
chr2:190446332
|
C | T | 2 | a0001c0001t0002g0119a0001c0001t0002g0120 | 2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1532+8771C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446332 | ||||||
chr2:190446333
|
A | T | 1 | a0001c0001t0003g0018 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1532+8772A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446333 | ||||||
chr2:190446594
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1532+9033G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446594 | ||||||
chr2:190446684
|
T | C | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1532+9123T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446684 | ||||||
chr2:190446770
|
A | T | 2 | a0001c0001t0003g0064a0001c0001t0017g0048 | 2 | NA18963.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1532+9209A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446770 | ||||||
chr2:190446857
|
C | T | 1 | a0001c0001t0018g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1532+9296C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446857 | ||||||
chr2:190447098
|
A | AT | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+9537_1532+953 others(5): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447098 | ||||||
chr2:190447142
|
C | T | 2 | a0002c0002t0001g0258a0002c0002t0019g0295 | 2 | NA18940.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1532+9581C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447142 | ||||||
chr2:190447158
|
G | A | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9597G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447158 | ||||||
chr2:190447160
|
C | G | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9599C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447160 | ||||||
chr2:190447161
|
A | G | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9600A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447161 | ||||||
chr2:190447377
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1532+9816T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447377 | ||||||
chr2:190447413
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1532+9852G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447413 | ||||||
chr2:190447498
|
GTCATAGC others(5): Show |
G | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9939_1532+995 others(16): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190447498 | |||||
chr2:190447761
|
G | C | 19 | a0001c0001t0001g0130a0002c0002t0001g0008a0002c0002t0001g0009others(16): Show | 21 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1532+10200G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447761 | ||||||
chr2:190447779
|
G | T | 1 | a0001c0001t0003g0025 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1532+10218G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447779 | ||||||
chr2:190447937
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1532+10376A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447937 | ||||||
chr2:190448145
|
C | A | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1532+10584C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448145 | ||||||
chr2:190448180
|
T | C | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+10619T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448180 | ||||||
chr2:190448423
|
T | C | 3 | a0002c0002t0004g0006a0002c0002t0004g0160a0002c0002t0004g0168 | 4 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1532+10862T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448423 | ||||||
chr2:190448603
|
G | A | 99 | a0001c0001t0001g0130a0002c0002t0001g0005a0002c0002t0001g0008others(96): Show | 103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1532+11042G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448603 | ||||||
chr2:190448669
|
G | C | 4 | a0002c0002t0001g0002a0002c0002t0001g0197a0002c0002t0001g0198others(1): Show | 6 | NA18941.hp2 NA18956.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.1532+11108G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448669 | ||||||
chr2:190448918
|
C | T | 2 | a0002c0002t0004g0160a0002c0002t0004g0168 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1532+11357C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448918 | ||||||
chr2:190448986
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1532+11425A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448986 | ||||||
chr2:190449172
|
A | G | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+11611A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449172 | ||||||
chr2:190449176
|
T | G | 59 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1532+11615T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449176 | ||||||
chr2:190449178
|
T | C | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+11617T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449178 | ||||||
chr2:190449662
|
A | AC | 68 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(65): Show | 68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1532+12101_1532+12 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449662 | ||||||
chr2:190449842
|
C | T | 2 | a0002c0002t0001g0220a0002c0002t0001g0243 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1532+12281C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449842 | ||||||
chr2:190449878
|
G | C | 61 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+12317G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449878 | ||||||
chr2:190449878
|
G | T | 1 | a0001c0001t0003g0029 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1532+12317G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449878 | ||||||
chr2:190449900
|
A | G | 1 | a0002c0002t0001g0293 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1532+12339A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449900 | ||||||
chr2:190449930
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+12369G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449930 | ||||||
chr2:190449976
|
G | A | 2 | a0002c0002t0001g0186a0002c0002t0001g0203 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1532+12415G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449976 | ||||||
chr2:190450032
|
A | T | 2 | a0001c0001t0003g0023a0001c0001t0003g0062 | 2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1532+12471A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450032 | ||||||
chr2:190450153
|
T | C | 3 | a0002c0002t0008g0205a0002c0002t0008g0211a0002c0011t0001g0320 | 3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+12592T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450153 | ||||||
chr2:190450291
|
G | A | 1 | a0002c0002t0001g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1532+12730G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450291 | ||||||
chr2:190450312
|
C | T | 1 | a0002c0002t0001g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1532+12751C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450312 | ||||||
chr2:190450419
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1532+12858T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450419 | ||||||
chr2:190450488
|
C | CT | 68 | a0001c0001t0001g0143a0001c0001t0001g0222a0001c0001t0001g0224others(65): Show | 72 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1532+12948dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | |||||
chr2:190450488
|
C | CTT | 161 | a0001c0001t0001g0130a0001c0001t0002g0001a0001c0001t0002g0069others(158): Show | 169 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1532+12947_1532+12 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | |||||
chr2:190450488
|
C | CTTT | 17 | a0001c0001t0002g0072a0001c0001t0002g0077a0001c0001t0002g0090others(14): Show | 17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1532+12946_1532+12 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | |||||
chr2:190450488
|
C | CTTTT | 50 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0313others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1532+12945_1532+12 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | |||||
chr2:190450488
|
C | CTTTTT | 9 | a0001c0001t0002g0019a0001c0001t0003g0018a0001c0001t0003g0022others(6): Show | 9 | HG01243.hp2 HG02602.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1532+12944_1532+12 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | |||||
chr2:190450519
|
G | T | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+12958G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450519 | ||||||
chr2:190450589
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1532+13028C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450589 | ||||||
chr2:190450631
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+13070T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450631 | ||||||
chr2:190450752
|
G | A | 1 | a0002c0002t0003g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1532+13191G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450752 | ||||||
chr2:190450803
|
TTC | T | 6 | a0002c0002t0001g0008a0002c0002t0001g0182a0002c0002t0001g0192others(3): Show | 7 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1532+13244_1532+13 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450803 | |||||
chr2:190450922
|
T | C | 15 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0174others(12): Show | 17 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1532+13361T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450922 | ||||||
chr2:190451069
|
C | G | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1532+13508C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451069 | ||||||
chr2:190451072
|
T | C | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1532+13511T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451072 | ||||||
chr2:190451073
|
G | T | 1 | a0002c0002t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1532+13512G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451073 | ||||||
chr2:190451149
|
G | T | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+13588G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451149 | ||||||
chr2:190451307
|
G | C | 1 | a0001c0001t0003g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1532+13746G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451307 | ||||||
chr2:190451322
|
T | C | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+13761T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451322 | ||||||
chr2:190452269
|
T | C | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1532+14708T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452269 | ||||||
chr2:190452639
|
C | G | 1 | a0002c0002t0009g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1532+15078C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452639 | ||||||
chr2:190452784
|
T | C | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1532+15223T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452784 | ||||||
chr2:190452950
|
C | T | 218 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(215): Show | 226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1532+15389C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452950 | ||||||
chr2:190453069
|
G | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0039 | 3 | HG00735.hp2 HG01070.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1532+15508G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453069 | ||||||
chr2:190453222
|
C | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1532+15661C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453222 | ||||||
chr2:190453270
|
C | A | 1 | a0002c0002t0001g0005 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1532+15709C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453270 | ||||||
chr2:190453294
|
G | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+15733G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453294 | ||||||
chr2:190453332
|
A | G | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+15771A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453332 | ||||||
chr2:190453368
|
T | C | 1 | a0008c0006t0001g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1532+15807T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453368 | ||||||
chr2:190453427
|
T | C | 26 | a0001c0001t0001g0130a0002c0002t0001g0008a0002c0002t0001g0009others(23): Show | 28 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+15866T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453427 | ||||||
chr2:190453454
|
C | G | 1 | a0001c0001t0003g0029 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1532+15893C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453454 | ||||||
chr2:190453530
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1532+15969C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453530 | ||||||
chr2:190453756
|
C | G | 3 | a0002c0002t0008g0205a0002c0002t0008g0211a0002c0011t0001g0320 | 3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-16002C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453756 | ||||||
chr2:190454050
|
T | C | 160 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0124others(157): Show | 170 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.1533-15708T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454050 | ||||||
chr2:190454084
|
G | A | 2 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1533-15674G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454084 | ||||||
chr2:190454268
|
C | G | 9 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | NA18940.hp2 NA18956.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-15490C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454268 | ||||||
chr2:190454335
|
T | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-15423T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454335 | ||||||
chr2:190454358
|
C | T | 1 | a0002c0002t0001g0169 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1533-15400C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454358 | ||||||
chr2:190454383
|
C | A | 2 | a0002c0002t0001g0306a0002c0002t0001g0307 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1533-15375C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454383 | ||||||
chr2:190454513
|
G | A | 2 | a0002c0002t0001g0073a0002c0002t0001g0074 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1533-15245G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454513 | ||||||
chr2:190454520
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1533-15238T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454520 | ||||||
chr2:190454534
|
CCCTTCCC others(15): Show |
C | 1 | a0002c0002t0001g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1533-15221_1533-15 others(28): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454534 | |||||
chr2:190454687
|
A | G | 1 | a0001c0001t0007g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1533-15071A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454687 | ||||||
chr2:190454932
|
G | GTATGTA | 45 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0229others(42): Show | 46 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.1533-14763_1533-14 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
G | GTATGTAT others(5): Show |
29 | a0001c0001t0001g0239a0001c0001t0007g0011a0002c0002t0001g0005others(26): Show | 30 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1533-14769_1533-14 others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
G | GTATGTAT others(11): Show |
13 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0234others(10): Show | 13 | HG01255.hp2 HG01261.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1533-14775_1533-14 others(24): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
G | GTATGTAT others(17): Show |
3 | a0001c0001t0001g0225a0001c0001t0001g0233a0001c0001t0001g0241 | 3 | HG01496.hp1 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1533-14781_1533-14 others(30): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
G | GTATGTAT others(23): Show |
7 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0242others(4): Show | 7 | HG01884.hp1 HG01981.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-14787_1533-14 others(36): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
GTATGTA | G | 24 | a0001c0001t0001g0130a0001c0001t0001g0231a0001c0001t0001g0238others(21): Show | 25 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1533-14763_1533-14 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
GTATGTAT others(5): Show |
G | 33 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0074others(30): Show | 36 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1533-14769_1533-14 others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
GTATGTAT others(11): Show |
G | 14 | a0002c0002t0001g0008a0002c0002t0001g0152a0002c0002t0001g0155others(11): Show | 15 | HG00609.hp2 HG00621.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533-14775_1533-14 others(24): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454932
|
GTATGTAT others(17): Show |
G | 3 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0195 | 3 | HG00423.hp2 NA18965.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1533-14781_1533-14 others(30): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | |||||
chr2:190454963
|
TATGTATA others(30): Show |
T | 3 | a0001c0001t0003g0022a0001c0001t0003g0055a0001c0001t0003g0212 | 3 | HG01081.hp2 HG02602.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1533-14772_1533-14 others(43): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454963 | |||||
chr2:190454967
|
T | C | 1 | a0002c0002t0003g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533-14791T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454967 | ||||||
chr2:190454969
|
TATGTATA others(24): Show |
T | 25 | a0001c0001t0002g0079a0001c0001t0003g0013a0001c0001t0003g0016others(22): Show | 25 | HG00735.hp2 HG01070.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1533-14766_1533-14 others(37): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454969 | |||||
chr2:190454975
|
TATGTATA others(18): Show |
T | 20 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0078others(17): Show | 20 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1533-14760_1533-14 others(31): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454975 | |||||
chr2:190454981
|
TATGTATA others(12): Show |
T | 15 | a0001c0001t0002g0019a0001c0001t0002g0131a0001c0001t0002g0313others(12): Show | 15 | HG00140.hp2 HG00323.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533-14757_1533-14 others(25): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454981 | |||||
chr2:190454987
|
TATGTATA others(6): Show |
T | 14 | a0001c0001t0002g0015a0001c0001t0002g0070a0001c0001t0002g0091others(11): Show | 14 | HG00544.hp1 HG01515.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1533-14757_1533-14 others(19): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454987 | |||||
chr2:190454993
|
TATGTATA | T | 31 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0014others(28): Show | 35 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1533-14757_1533-14 others(13): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454993 | |||||
chr2:190454999
|
TA | T | 11 | a0001c0001t0002g0081a0001c0001t0002g0083a0001c0001t0002g0084others(8): Show | 11 | HG02027.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533-14757delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454999 | |||||
chr2:190455000
|
A | ATGTAT | 14 | a0001c0001t0002g0090a0001c0001t0002g0093a0001c0001t0002g0104others(11): Show | 14 | HG00558.hp1 HG01123.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1533-14758_1533-14 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455000 | ||||||
chr2:190455000
|
A | ATGTATAT others(4): Show |
6 | a0001c0001t0002g0082a0001c0001t0002g0092a0001c0001t0002g0096others(3): Show | 6 | HG01433.hp1 HG02622.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1533-14758_1533-14 others(17): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455000 | ||||||
chr2:190455000
|
A | ATGTATAT others(10): Show |
2 | a0001c0001t0002g0123a0002c0002t0001g0277 | 2 | HG00544.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1533-14758_1533-14 others(23): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455000 | ||||||
chr2:190455044
|
A | G | 1 | a0002c0002t0001g0263 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1533-14714A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455044 | ||||||
chr2:190455198
|
A | G | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-14560A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455198 | ||||||
chr2:190455252
|
A | G | 5 | a0002c0002t0001g0008a0002c0002t0001g0182a0002c0002t0001g0193others(2): Show | 6 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1533-14506A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455252 | ||||||
chr2:190455253
|
TTATTAC | T | 3 | a0002c0002t0008g0205a0002c0002t0008g0211a0002c0011t0001g0320 | 3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-14499_1533-14 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455253 | |||||
chr2:190455280
|
TATTA | T | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-14472_1533-14 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455280 | |||||
chr2:190455377
|
T | A | 4 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533-14381T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455377 | ||||||
chr2:190455452
|
G | A | 14 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071others(11): Show | 14 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1533-14306G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455452 | ||||||
chr2:190455519
|
A | T | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1533-14239A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455519 | ||||||
chr2:190455934
|
C | CT | 97 | a0001c0001t0001g0130a0001c0001t0001g0224a0001c0001t0001g0226others(94): Show | 101 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1533-13800dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | |||||
chr2:190455934
|
C | CTT | 96 | a0001c0001t0001g0143a0001c0001t0001g0225a0001c0001t0001g0246others(93): Show | 98 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1533-13801_1533-13 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | |||||
chr2:190455934
|
C | CTTT | 28 | a0001c0001t0002g0015a0001c0001t0002g0111a0001c0001t0003g0017others(25): Show | 30 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1533-13802_1533-13 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | |||||
chr2:190455934
|
C | CTTTT | 68 | a0001c0001t0002g0001a0001c0001t0002g0069a0001c0001t0002g0070others(65): Show | 72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1533-13803_1533-13 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | |||||
chr2:190455934
|
C | CTTTTT | 14 | a0001c0001t0001g0097a0001c0001t0002g0084a0001c0001t0002g0086others(11): Show | 14 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1533-13804_1533-13 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | |||||
chr2:190456035
|
G | C | 49 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(46): Show | 53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1533-13723G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456035 | ||||||
chr2:190456417
|
G | A | 8 | a0002c0002t0001g0147a0002c0002t0001g0150a0002c0002t0001g0152others(5): Show | 8 | NA18960.hp1 NA18961.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1533-13341G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456417 | ||||||
chr2:190456499
|
T | TA | 3 | a0002c0002t0008g0205a0002c0002t0008g0211a0002c0011t0001g0320 | 3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-13258dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190456499 | |||||
chr2:190456527
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533-13231C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456527 | ||||||
chr2:190456632
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1533-13126C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456632 | ||||||
chr2:190456901
|
G | T | 3 | a0002c0002t0008g0205a0002c0002t0008g0211a0002c0011t0001g0320 | 3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-12857G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456901 | ||||||
chr2:190457000
|
G | A | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-12758G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457000 | ||||||
chr2:190457071
|
G | A | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-12687G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457071 | ||||||
chr2:190457178
|
C | T | 160 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0003g0020others(157): Show | 168 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.1533-12580C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457178 | ||||||
chr2:190457251
|
G | T | 1 | a0002c0002t0005g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1533-12507G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457251 | ||||||
chr2:190457411
|
C | A | 1 | a0001c0001t0002g0114 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1533-12347C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457411 | ||||||
chr2:190457546
|
G | C | 62 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-12212G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457546 | ||||||
chr2:190457888
|
C | A | 1 | a0002c0002t0001g0278 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1533-11870C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457888 | ||||||
chr2:190458167
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1533-11591G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458167 | ||||||
chr2:190458194
|
CCCTGAAG others(21): Show |
C | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1533-11561_1533-11 others(34): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190458194 | |||||
chr2:190458412
|
C | T | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-11346C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458412 | ||||||
chr2:190458457
|
T | G | 1 | a0001c0001t0001g0232 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1533-11301T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458457 | ||||||
chr2:190458464
|
CTT | C | 150 | a0001c0001t0001g0130a0001c0001t0001g0143a0002c0002t0001g0002others(147): Show | 158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1533-11291_1533-11 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190458464 | |||||
chr2:190458569
|
C | T | 81 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(78): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1533-11189C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458569 | ||||||
chr2:190458603
|
C | T | 59 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1533-11155C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458603 | ||||||
chr2:190458975
|
A | G | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1533-10783A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458975 | ||||||
chr2:190459477
|
G | T | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1533-10281G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459477 | ||||||
chr2:190459489
|
A | T | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533-10269A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459489 | ||||||
chr2:190459490
|
A | C | 4 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533-10268A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459490 | ||||||
chr2:190459490
|
A | G | 1 | a0002c0002t0001g0289 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1533-10268A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459490 | ||||||
chr2:190459932
|
T | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-9826T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459932 | ||||||
chr2:190460163
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1533-9595G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460163 | ||||||
chr2:190460235
|
A | C | 6 | a0002c0002t0001g0153a0002c0002t0001g0297a0002c0002t0001g0298others(3): Show | 6 | NA18944.hp1 NA18997.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-9523A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460235 | ||||||
chr2:190460267
|
G | A | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1533-9491G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460267 | ||||||
chr2:190460326
|
T | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-9432T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460326 | ||||||
chr2:190460446
|
C | T | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-9312C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460446 | ||||||
chr2:190460477
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1533-9281G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460477 | ||||||
chr2:190460498
|
A | G | 6 | a0002c0002t0001g0153a0002c0002t0001g0297a0002c0002t0001g0298others(3): Show | 6 | NA18944.hp1 NA18997.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-9260A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460498 | ||||||
chr2:190460529
|
C | G | 219 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0002g0014others(216): Show | 227 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1533-9229C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460529 | ||||||
chr2:190460676
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1533-9082C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460676 | ||||||
chr2:190460688
|
A | G | 83 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(80): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1533-9070A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460688 | ||||||
chr2:190460875
|
A | C | 80 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(77): Show | 84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1533-8883A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460875 | ||||||
chr2:190460899
|
A | C | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1533-8859A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460899 | ||||||
chr2:190461601
|
G | A | 151 | a0001c0001t0001g0130a0001c0001t0001g0143a0002c0002t0001g0002others(148): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1533-8157G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190461601 | ||||||
chr2:190461622
|
A | G | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1533-8136A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190461622 | ||||||
chr2:190461975
|
C | T | 307 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(304): Show | 319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.1533-7783C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190461975 | ||||||
chr2:190462215
|
G | T | 1 | a0001c0010t0002g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1533-7543G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462215 | ||||||
chr2:190462421
|
T | C | 83 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(80): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1533-7337T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462421 | ||||||
chr2:190462505
|
C | T | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1533-7253C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462505 | ||||||
chr2:190462545
|
A | T | 2 | a0002c0002t0001g0306a0002c0002t0001g0307 | 2 | HG01099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1533-7213A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462545 | ||||||
chr2:190462785
|
T | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1533-6973T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462785 | ||||||
chr2:190462989
|
G | C | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-6769G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462989 | ||||||
chr2:190463126
|
A | G | 80 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0069others(77): Show | 84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1533-6632A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463126 | ||||||
chr2:190463183
|
G | C | 2 | a0001c0001t0002g0087a0001c0001t0002g0134 | 2 | NA19004.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1533-6575G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463183 | ||||||
chr2:190463314
|
A | G | 1 | a0001c0001t0003g0034 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1533-6444A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463314 | ||||||
chr2:190463354
|
T | C | 1 | a0002c0002t0001g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1533-6404T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463354 | ||||||
chr2:190463493
|
T | A | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533-6265T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463493 | ||||||
chr2:190463576
|
T | C | 1 | a0002c0002t0008g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1533-6182T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463576 | ||||||
chr2:190463714
|
G | T | 79 | a0001c0001t0002g0001a0001c0001t0002g0069a0001c0001t0002g0070others(76): Show | 83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1533-6044G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463714 | ||||||
chr2:190464454
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-5304G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464454 | ||||||
chr2:190464642
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1533-5116T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464642 | ||||||
chr2:190464680
|
G | A | 99 | a0001c0001t0001g0097a0001c0001t0001g0130a0002c0002t0001g0005others(96): Show | 103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1533-5078G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464680 | ||||||
chr2:190464711
|
T | C | 1 | a0001c0001t0003g0049 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1533-5047T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464711 | ||||||
chr2:190464903
|
T | G | 9 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0024others(6): Show | 9 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-4855T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464903 | ||||||
chr2:190465063
|
A | G | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1533-4695A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465063 | ||||||
chr2:190465298
|
T | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-4460T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465298 | ||||||
chr2:190465425
|
CT | C | 49 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(46): Show | 53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1533-4324delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190465425 | |||||
chr2:190465436
|
A | G | 197 | a0001c0001t0001g0143a0001c0001t0002g0001a0001c0001t0002g0014others(194): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1533-4322A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465436 | ||||||
chr2:190465571
|
G | T | 59 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1533-4187G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465571 | ||||||
chr2:190465630
|
C | G | 6 | a0001c0001t0001g0097a0002c0002t0001g0196a0002c0002t0001g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-4128C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465630 | ||||||
chr2:190465632
|
G | T | 151 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(148): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1533-4126G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465632 | ||||||
chr2:190465728
|
C | CA | 14 | a0002c0002t0001g0002a0002c0002t0001g0153a0002c0002t0001g0176others(11): Show | 16 | NA18941.hp2 NA18944.hp1 NA18955.hp1 others(13): Show |
intron_variant | MODIFIER | c.1533-4029dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190465728 | |||||
chr2:190465756
|
G | T | 1 | a0001c0001t0018g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1533-4002G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465756 | ||||||
chr2:190465850
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1533-3908G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465850 | ||||||
chr2:190466004
|
G | A | 2 | a0002c0002t0005g0185a0002c0002t0005g0204 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1533-3754G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466004 | ||||||
chr2:190466060
|
C | G | 163 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0003g0013others(160): Show | 167 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1533-3698C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466060 | ||||||
chr2:190466111
|
C | T | 247 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0001others(244): Show | 255 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.1533-3647C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466111 | ||||||
chr2:190466130
|
G | T | 216 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(213): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1533-3628G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466130 | ||||||
chr2:190466135
|
A | T | 154 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(151): Show | 162 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.1533-3623A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466135 | ||||||
chr2:190466301
|
A | G | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1533-3457A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466301 | ||||||
chr2:190466338
|
A | G | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1533-3420A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466338 | ||||||
chr2:190466407
|
C | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-3351C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466407 | ||||||
chr2:190466488
|
C | T | 149 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(146): Show | 157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.1533-3270C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466488 | ||||||
chr2:190466578
|
G | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(76): Show | 83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1533-3180G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466578 | ||||||
chr2:190466658
|
A | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-3100A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466658 | ||||||
chr2:190466892
|
G | A | 1 | a0001c0001t0023g0047 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1533-2866G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466892 | ||||||
chr2:190466905
|
C | G | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1533-2853C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466905 | ||||||
chr2:190466925
|
G | C | 1 | a0001c0001t0002g0102 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1533-2833G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466925 | ||||||
chr2:190467321
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1533-2437C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467321 | ||||||
chr2:190467376
|
GC | G | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-2380delC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190467376 | |||||
chr2:190467443
|
T | A | 88 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(85): Show | 92 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1533-2315T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467443 | ||||||
chr2:190467620
|
G | T | 4 | a0002c0002t0001g0151a0002c0002t0001g0175a0002c0002t0001g0177others(1): Show | 4 | HG00609.hp1 HG00621.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-2138G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467620 | ||||||
chr2:190467914
|
A | G | 2 | a0002c0002t0001g0201a0002c0002t0001g0322 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1533-1844A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467914 | ||||||
chr2:190468011
|
C | T | 8 | a0002c0002t0001g0153a0002c0002t0001g0176a0002c0002t0001g0180others(5): Show | 8 | NA18944.hp1 NA18955.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.1533-1747C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468011 | ||||||
chr2:190468453
|
A | AT | 60 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(57): Show | 60 | HG00408.hp2 HG00544.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1533-1288dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468453 | |||||
chr2:190468453
|
AT | A | 6 | a0001c0001t0001g0233a0001c0001t0002g0100a0001c0001t0002g0112others(3): Show | 6 | HG01496.hp1 HG02451.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-1288delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468453 | |||||
chr2:190468619
|
A | AT | 9 | a0001c0001t0001g0148a0001c0001t0001g0232a0001c0001t0001g0233others(6): Show | 9 | HG01361.hp1 HG01496.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-1120dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468619 | |||||
chr2:190468619
|
AT | A | 222 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(219): Show | 234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1533-1120delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468619 | |||||
chr2:190468619
|
ATT | A | 9 | a0001c0001t0002g0120a0002c0002t0001g0186a0002c0002t0001g0203others(6): Show | 9 | HG01515.hp1 HG02486.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-1121_1533-112 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468619 | |||||
chr2:190468626
|
T | A | 1 | a0002c0002t0001g0268 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1533-1132T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468626 | ||||||
chr2:190468647
|
C | T | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-1111C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468647 | ||||||
chr2:190468807
|
A | G | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1533-951A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468807 | ||||||
chr2:190469002
|
C | T | 211 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(208): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1533-756C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469002 | ||||||
chr2:190469143
|
T | C | 1 | a0002c0002t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-615T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469143 | ||||||
chr2:190469305
|
G | C | 100 | a0001c0001t0001g0097a0001c0001t0001g0130a0002c0002t0001g0005others(97): Show | 104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1533-453G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469305 | ||||||
chr2:190469310
|
T | C | 1 | a0002c0002t0001g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1533-448T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469310 | ||||||
chr2:190469326
|
T | A | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-432T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469326 | ||||||
chr2:190469698
|
G | A | 150 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(147): Show | 158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1533-60G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469698 | ||||||
chr2:190469727
|
T | A | 1 | a0002c0002t0004g0006 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1533-31T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469727 | ||||||
chr2:190469733
|
A | ATTTTTAT | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
splice_region_variant&intron_variant | LOW | c.1533-12_1533-6dupA others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190469733 | |||||
chr2:190469733
|
A | T | 1 | a0002c0002t0001g0288 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1533-25A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469733 | ||||||
chr2:190469867
|
G | T | 1 | a0004c0005t0001g0287 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1630+12G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190469867 | ||||||
chr2:190470011
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1630+156G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470011 | ||||||
chr2:190470232
|
A | G | 1 | a0002c0002t0009g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1630+377A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470232 | ||||||
chr2:190470331
|
T | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+476T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470331 | ||||||
chr2:190470357
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1630+502T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470357 | ||||||
chr2:190470381
|
T | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1630+526T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470381 | ||||||
chr2:190470586
|
C | T | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1630+731C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470586 | ||||||
chr2:190470703
|
G | A | 2 | a0002c0002t0005g0185a0002c0002t0005g0204 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1630+848G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470703 | ||||||
chr2:190470757
|
T | A | 60 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1630+902T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470757 | ||||||
chr2:190470903
|
G | GTA | 50 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0019others(47): Show | 50 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1630+1061_1630+106 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190470903 | |||||
chr2:190470903
|
G | GTATA | 29 | a0001c0001t0002g0001a0001c0001t0002g0076a0001c0001t0002g0077others(26): Show | 33 | HG00408.hp1 HG00423.hp1 HG02165.hp1 others(30): Show |
intron_variant | MODIFIER | c.1630+1059_1630+106 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190470903 | |||||
chr2:190470970
|
A | G | 2 | a0001c0001t0021g0210a0002c0011t0001g0320 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1630+1115A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470970 | ||||||
chr2:190471208
|
G | A | 60 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1630+1353G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471208 | ||||||
chr2:190471226
|
A | C | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1630+1371A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471226 | ||||||
chr2:190471247
|
G | C | 2 | a0002c0002t0001g0201a0002c0002t0001g0322 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1630+1392G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471247 | ||||||
chr2:190471288
|
G | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1630+1433G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471288 | ||||||
chr2:190471525
|
C | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1630+1670C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471525 | ||||||
chr2:190471596
|
A | G | 1 | a0004c0005t0001g0287 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1630+1741A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471596 | ||||||
chr2:190471717
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1630+1862T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471717 | ||||||
chr2:190471812
|
G | A | 6 | a0001c0001t0001g0097a0002c0002t0001g0196a0002c0002t0001g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1630+1957G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471812 | ||||||
chr2:190471904
|
C | T | 2 | a0002c0002t0001g0264a0002c0002t0001g0283 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1630+2049C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471904 | ||||||
chr2:190471973
|
C | G | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+2118C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471973 | ||||||
chr2:190472066
|
T | C | 331 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(328): Show | 343 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.1630+2211T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472066 | ||||||
chr2:190472203
|
G | A | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1630+2348G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472203 | ||||||
chr2:190472421
|
C | T | 1 | a0001c0001t0012g0247 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1630+2566C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472421 | ||||||
chr2:190472555
|
C | T | 1 | a0002c0002t0003g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1630+2700C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472555 | ||||||
chr2:190472622
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1630+2767G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472622 | ||||||
chr2:190472692
|
A | G | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0039 | 3 | HG00735.hp2 HG01070.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1630+2837A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472692 | ||||||
chr2:190473272
|
A | G | 1 | a0002c0002t0001g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1630+3417A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473272 | ||||||
chr2:190473490
|
G | T | 62 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1630+3635G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473490 | ||||||
chr2:190473497
|
G | A | 1 | a0001c0010t0002g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1630+3642G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473497 | ||||||
chr2:190473785
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1630+3930C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473785 | ||||||
chr2:190474131
|
C | T | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1630+4276C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474131 | ||||||
chr2:190474159
|
G | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+4304G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474159 | ||||||
chr2:190474173
|
AAC | A | 59 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1630+4322_1630+432 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190474173 | |||||
chr2:190474210
|
A | T | 55 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1630+4355A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474210 | ||||||
chr2:190474314
|
G | A | 3 | a0001c0001t0002g0126a0001c0001t0006g0003a0001c0001t0006g0004 | 5 | NA18982.hp1 NA19002.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630+4459G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474314 | ||||||
chr2:190474407
|
A | G | 79 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(76): Show | 83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1630+4552A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474407 | ||||||
chr2:190474411
|
A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1630+4556A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474411 | ||||||
chr2:190474682
|
G | T | 1 | a0002c0002t0001g0191 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1630+4827G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474682 | ||||||
chr2:190474791
|
G | T | 1 | a0002c0002t0001g0272 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1630+4936G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474791 | ||||||
chr2:190474797
|
G | C | 150 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(147): Show | 154 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1630+4942G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474797 | ||||||
chr2:190474876
|
G | C | 1 | a0001c0001t0003g0034 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1630+5021G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474876 | ||||||
chr2:190474915
|
T | C | 1 | a0002c0002t0005g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1630+5060T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474915 | ||||||
chr2:190475169
|
C | G | 75 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(72): Show | 79 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1630+5314C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475169 | ||||||
chr2:190475537
|
A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1630+5682A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475537 | ||||||
chr2:190475670
|
G | C | 4 | a0001c0001t0001g0097a0002c0002t0001g0196a0002c0002t0001g0206others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630+5815G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475670 | ||||||
chr2:190475725
|
C | T | 1 | a0002c0002t0001g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1630+5870C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475725 | ||||||
chr2:190475821
|
C | G | 1 | a0002c0002t0005g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1630+5966C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475821 | ||||||
chr2:190475937
|
A | G | 1 | a0002c0002t0008g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1630+6082A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475937 | ||||||
chr2:190476114
|
A | G | 100 | a0001c0001t0001g0097a0001c0001t0001g0130a0002c0002t0001g0005others(97): Show | 104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1630+6259A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476114 | ||||||
chr2:190476160
|
T | G | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1630+6305T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476160 | ||||||
chr2:190476298
|
A | G | 49 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0073others(46): Show | 53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1630+6443A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476298 | ||||||
chr2:190476346
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1630+6491C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476346 | ||||||
chr2:190476469
|
G | C | 55 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1630+6614G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476469 | ||||||
chr2:190476528
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1630+6673G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476528 | ||||||
chr2:190476529
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1630+6674G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476529 | ||||||
chr2:190476640
|
G | C | 100 | a0001c0001t0001g0097a0001c0001t0001g0130a0002c0002t0001g0005others(97): Show | 104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1630+6785G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476640 | ||||||
chr2:190476646
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630+6791C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476646 | ||||||
chr2:190476774
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1630+6919A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476774 | ||||||
chr2:190476777
|
C | A | 2 | a0001c0001t0002g0082a0001c0001t0002g0092 | 2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1630+6922C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476777 | ||||||
chr2:190476852
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1630+6997C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476852 | ||||||
chr2:190476876
|
A | C | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1630+7021A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476876 | ||||||
chr2:190477035
|
C | T | 4 | a0001c0001t0001g0097a0002c0002t0001g0196a0002c0002t0001g0206others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630+7180C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477035 | ||||||
chr2:190477101
|
GT | G | 4 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630+7248delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190477101 | |||||
chr2:190477145
|
G | A | 1 | a0002c0002t0001g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1630+7290G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477145 | ||||||
chr2:190477151
|
A | G | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1630+7296A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477151 | ||||||
chr2:190477199
|
TATA | T | 8 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0115others(5): Show | 8 | HG01099.hp1 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630+7358_1630+736 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190477199 | |||||
chr2:190477218
|
A | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1630+7363A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477218 | ||||||
chr2:190477487
|
G | T | 1 | a0006c0008t0003g0032 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1630+7632G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477487 | ||||||
chr2:190477491
|
C | G | 2 | a0002c0002t0001g0257a0002c0002t0001g0268 | 2 | HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1630+7636C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477491 | ||||||
chr2:190477606
|
A | G | 1 | a0001c0001t0003g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1630+7751A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477606 | ||||||
chr2:190477671
|
C | G | 2 | a0001c0001t0003g0023a0001c0001t0003g0062 | 2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1630+7816C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477671 | ||||||
chr2:190477684
|
A | C | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1630+7829A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477684 | ||||||
chr2:190477703
|
A | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+7848A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477703 | ||||||
chr2:190477739
|
C | T | 2 | a0002c0011t0001g0320a0007c0009t0015g0208 | 2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1630+7884C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477739 | ||||||
chr2:190477946
|
TG | T | 56 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1630+8096delG | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190477946 | |||||
chr2:190477989
|
G | A | 100 | a0001c0001t0001g0097a0001c0001t0001g0130a0002c0002t0001g0005others(97): Show | 104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1630+8134G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477989 | ||||||
chr2:190478001
|
A | G | 1 | a0002c0002t0001g0188 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1630+8146A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478001 | ||||||
chr2:190478112
|
T | A | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1630+8257T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478112 | ||||||
chr2:190478172
|
G | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+8317G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478172 | ||||||
chr2:190478214
|
T | G | 1 | a0003c0003t0010g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1630+8359T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478214 | ||||||
chr2:190478384
|
A | C | 1 | a0001c0001t0016g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1630+8529A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478384 | ||||||
chr2:190478442
|
T | G | 1 | a0001c0001t0003g0034 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1630+8587T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478442 | ||||||
chr2:190478599
|
G | A | 1 | a0001c0001t0003g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1630+8744G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478599 | ||||||
chr2:190478728
|
A | AGGCTGGG others(9): Show |
1 | a0002c0002t0001g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1630+8875_1630+889 others(20): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190478728 | |||||
chr2:190478835
|
T | TA | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1630+8990dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190478835 | |||||
chr2:190478980
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1630+9125C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478980 | ||||||
chr2:190479011
|
T | C | 1 | a0002c0002t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1630+9156T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479011 | ||||||
chr2:190479037
|
T | C | 151 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(148): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.1630+9182T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479037 | ||||||
chr2:190479087
|
A | T | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1630+9232A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479087 | ||||||
chr2:190479406
|
C | T | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1631-9251C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479406 | ||||||
chr2:190479511
|
C | G | 1 | a0002c0002t0001g0289 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1631-9146C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479511 | ||||||
chr2:190479522
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1631-9135T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479522 | ||||||
chr2:190479602
|
G | A | 1 | a0004c0005t0001g0287 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1631-9055G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479602 | ||||||
chr2:190479807
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1631-8850C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479807 | ||||||
chr2:190479823
|
A | G | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-8834A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479823 | ||||||
chr2:190479910
|
G | A | 4 | a0002c0002t0001g0278a0002c0002t0001g0294a0002c0002t0001g0310others(1): Show | 4 | NA18965.hp2 NA19058.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631-8747G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479910 | ||||||
chr2:190479916
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1631-8741C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479916 | ||||||
chr2:190480025
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1631-8632T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480025 | ||||||
chr2:190480052
|
A | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1631-8605A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480052 | ||||||
chr2:190480161
|
T | C | 57 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1631-8496T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480161 | ||||||
chr2:190480380
|
ATAGT | A | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1631-8272_1631-826 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190480380 | |||||
chr2:190480443
|
T | A | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1631-8214T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480443 | ||||||
chr2:190480518
|
C | T | 54 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(51): Show | 54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1631-8139C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480518 | ||||||
chr2:190480548
|
T | A | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1631-8109T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480548 | ||||||
chr2:190480771
|
A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1631-7886A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480771 | ||||||
chr2:190480820
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1631-7837A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480820 | ||||||
chr2:190481277
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1631-7380T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481277 | ||||||
chr2:190481356
|
C | T | 9 | a0001c0001t0003g0036a0001c0001t0003g0042a0001c0001t0003g0044others(6): Show | 9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631-7301C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481356 | ||||||
chr2:190481440
|
C | T | 57 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1631-7217C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481440 | ||||||
chr2:190481567
|
G | A | 51 | a0001c0001t0001g0143a0001c0001t0021g0210a0002c0002t0001g0002others(48): Show | 55 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1631-7090G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481567 | ||||||
chr2:190481673
|
T | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-6984T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481673 | ||||||
chr2:190481713
|
A | G | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1631-6944A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481713 | ||||||
chr2:190481811
|
T | C | 2 | a0002c0002t0001g0125a0002c0002t0001g0145 | 2 | NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1631-6846T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481811 | ||||||
chr2:190482058
|
TAGG | T | 104 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(101): Show | 108 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.1631-6594_1631-659 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482058 | |||||
chr2:190482076
|
C | T | 5 | a0001c0001t0001g0097a0002c0002t0001g0192a0002c0002t0001g0196others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1631-6581C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482076 | ||||||
chr2:190482109
|
T | G | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1631-6548T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482109 | ||||||
chr2:190482157
|
G | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0227 | 2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1631-6500G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482157 | ||||||
chr2:190482399
|
CT | C | 6 | a0001c0001t0001g0230a0001c0001t0002g0093a0001c0001t0002g0112others(3): Show | 6 | HG01255.hp1 HG01256.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1631-6243delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482399 | |||||
chr2:190482458
|
G | A | 142 | a0001c0001t0001g0143a0001c0001t0002g0001a0001c0001t0002g0014others(139): Show | 150 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1631-6199G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482458 | ||||||
chr2:190482554
|
A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1631-6103A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482554 | ||||||
chr2:190482584
|
G | T | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1631-6073G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482584 | ||||||
chr2:190482672
|
CT | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(82): Show | 89 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1631-5978delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482672 | |||||
chr2:190482719
|
G | A | 1 | a0003c0003t0010g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1631-5938G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482719 | ||||||
chr2:190482770
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-5887G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482770 | ||||||
chr2:190482868
|
C | CT | 6 | a0001c0001t0001g0234a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01192.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631-5754dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | |||||
chr2:190482868
|
CT | C | 11 | a0001c0001t0001g0221a0001c0001t0001g0232a0001c0001t0001g0235others(8): Show | 11 | HG01361.hp1 HG02145.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1631-5754delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | |||||
chr2:190482868
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0116a0001c0001t0021g0210 | 2 | HG01099.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1631-5764_1631-575 others(15): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | |||||
chr2:190482868
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1631-5768_1631-575 others(19): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | |||||
chr2:190482868
|
CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0100 | 3 | HG02451.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1631-5770_1631-575 others(21): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | |||||
chr2:190482868
|
CTTTTTTT others(15): Show |
C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-5775_1631-575 others(26): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | |||||
chr2:190482903
|
T | G | 71 | a0001c0001t0001g0143a0001c0001t0002g0070a0001c0001t0002g0100others(68): Show | 75 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1631-5754T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTG | 38 | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(35): Show | 40 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTG | 35 | a0001c0001t0002g0096a0001c0001t0002g0111a0001c0001t0002g0112others(32): Show | 36 | HG00609.hp2 HG00741.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTG | 42 | a0001c0001t0002g0099a0001c0001t0002g0137a0001c0001t0002g0223others(39): Show | 43 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTG | 30 | a0001c0001t0002g0081a0001c0001t0002g0327a0001c0001t0003g0017others(27): Show | 30 | HG01069.hp1 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(1): Show |
10 | a0001c0001t0002g0071a0001c0001t0002g0313a0001c0001t0003g0027others(7): Show | 10 | HG00544.hp1 HG01074.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(2): Show |
18 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0072others(15): Show | 20 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(13): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(3): Show |
22 | a0001c0001t0001g0130a0001c0001t0002g0014a0001c0001t0002g0069others(19): Show | 23 | HG00735.hp2 HG01243.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(4): Show |
12 | a0001c0001t0002g0015a0001c0001t0002g0078a0001c0001t0002g0079others(9): Show | 13 | HG02027.hp1 HG02071.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(15): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(5): Show |
3 | a0001c0001t0003g0033a0001c0001t0003g0052a0002c0002t0001g0196 | 3 | HG00323.hp2 HG02615.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(16): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(6): Show |
3 | a0001c0001t0002g0127a0001c0001t0003g0058a0002c0002t0001g0329 | 3 | HG00140.hp2 HG02055.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(17): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(7): Show |
3 | a0001c0001t0002g0080a0001c0001t0002g0082a0001c0001t0002g0092 | 3 | NA18969.hp2 NA18988.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(8): Show |
1 | a0001c0001t0002g0086 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(19): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(9): Show |
2 | a0001c0001t0002g0019a0002c0002t0001g0206 | 2 | HG01891.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(20): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(10): Show |
1 | a0001c0001t0002g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(21): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(14): Show |
1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(25): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(17): Show |
3 | a0001c0001t0002g0101a0001c0001t0002g0106a0001c0001t0002g0107 | 3 | NA18941.hp1 NA18942.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(28): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482903
|
T | TTTTTTTT others(18): Show |
1 | a0001c0001t0002g0108 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(29): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | ||||||
chr2:190482932
|
C | T | 1 | a0002c0002t0001g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1631-5725C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482932 | ||||||
chr2:190482939
|
C | A | 1 | a0001c0001t0002g0127 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1631-5718C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482939 | ||||||
chr2:190482940
|
G | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-5717G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482940 | ||||||
chr2:190483037
|
G | A | 4 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631-5620G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483037 | ||||||
chr2:190483047
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1631-5610G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483047 | ||||||
chr2:190483083
|
G | A | 52 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(49): Show | 56 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1631-5574G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483083 | ||||||
chr2:190483171
|
C | T | 1 | a0006c0008t0003g0032 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1631-5486C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483171 | ||||||
chr2:190483283
|
A | G | 2 | a0001c0001t0021g0210a0002c0011t0001g0320 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1631-5374A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483283 | ||||||
chr2:190483350
|
C | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-5307C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483350 | ||||||
chr2:190483619
|
G | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(76): Show | 83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1631-5038G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483619 | ||||||
chr2:190483696
|
G | A | 3 | a0002c0002t0001g0146a0002c0002t0008g0205a0002c0002t0008g0211 | 3 | HG01255.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1631-4961G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483696 | ||||||
chr2:190483775
|
C | T | 1 | a0002c0002t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1631-4882C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483775 | ||||||
chr2:190483835
|
C | CA | 68 | a0001c0001t0002g0116a0002c0002t0001g0005a0002c0002t0001g0010others(65): Show | 70 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1631-4801dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190483835 | |||||
chr2:190483835
|
CA | C | 11 | a0001c0001t0002g0107a0001c0001t0002g0120a0001c0001t0002g0144others(8): Show | 11 | HG01168.hp2 HG01515.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1631-4801delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190483835 | |||||
chr2:190483835
|
CAAA | C | 32 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(29): Show | 34 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1631-4803_1631-480 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190483835 | |||||
chr2:190484027
|
T | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0148a0001c0001t0001g0221others(115): Show | 122 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1631-4630T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484027 | ||||||
chr2:190484345
|
T | A | 27 | a0001c0001t0001g0130a0001c0007t0001g0043a0002c0002t0001g0008others(24): Show | 29 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1631-4312T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484345 | ||||||
chr2:190484351
|
A | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1631-4306A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484351 | ||||||
chr2:190484436
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1631-4221A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484436 | ||||||
chr2:190484646
|
T | A | 1 | a0001c0001t0002g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1631-4011T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484646 | ||||||
chr2:190484746
|
T | G | 3 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0137 | 3 | HG02145.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1631-3911T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484746 | ||||||
chr2:190484802
|
G | C | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1631-3855G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484802 | ||||||
chr2:190484956
|
T | G | 299 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1631-3701T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484956 | ||||||
chr2:190484957
|
C | G | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-3700C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484957 | ||||||
chr2:190485274
|
T | A | 3 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211 | 3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1631-3383T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485274 | ||||||
chr2:190485661
|
T | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1631-2996T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485661 | ||||||
chr2:190485703
|
G | A | 57 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1631-2954G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485703 | ||||||
chr2:190485803
|
TA | T | 103 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0002g0081others(100): Show | 108 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.1631-2840delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190485803 | |||||
chr2:190485819
|
C | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2838C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485819 | ||||||
chr2:190485852
|
C | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2805C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485852 | ||||||
chr2:190485855
|
A | T | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2802A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485855 | ||||||
chr2:190485856
|
A | T | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2801A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485856 | ||||||
chr2:190485857
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2800G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485857 | ||||||
chr2:190485858
|
A | G | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2799A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485858 | ||||||
chr2:190486251
|
G | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1631-2406G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486251 | ||||||
chr2:190486293
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1631-2364G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486293 | ||||||
chr2:190486410
|
C | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-2247C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486410 | ||||||
chr2:190486432
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1631-2225G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486432 | ||||||
chr2:190486969
|
T | A | 1 | a0002c0002t0001g0158 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1631-1688T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486969 | ||||||
chr2:190487015
|
T | C | 236 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(233): Show | 248 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1631-1642T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487015 | ||||||
chr2:190487172
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1631-1485C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487172 | ||||||
chr2:190487198
|
G | A | 9 | a0001c0001t0003g0036a0001c0001t0003g0042a0001c0001t0003g0044others(6): Show | 9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631-1459G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487198 | ||||||
chr2:190487209
|
C | G | 83 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(80): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1631-1448C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487209 | ||||||
chr2:190487209
|
C | T | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1631-1448C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487209 | ||||||
chr2:190487239
|
G | T | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1418G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487239 | ||||||
chr2:190487253
|
A | T | 1 | a0001c0001t0003g0028 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1631-1404A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487253 | ||||||
chr2:190487517
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1140G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487517 | ||||||
chr2:190487518
|
A | T | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1139A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487518 | ||||||
chr2:190487519
|
T | G | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1138T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487519 | ||||||
chr2:190487613
|
AAAG | A | 3 | a0002c0002t0001g0253a0002c0002t0001g0254a0002c0002t0001g0285 | 3 | NA18953.hp1 NA18967.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1631-1039_1631-103 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190487613 | |||||
chr2:190487903
|
AT | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-745delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190487903 | |||||
chr2:190487906
|
T | A | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-751T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487906 | ||||||
chr2:190487914
|
T | C | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-743T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487914 | ||||||
chr2:190487998
|
G | T | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-659G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487998 | ||||||
chr2:190488000
|
T | C | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-657T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488000 | ||||||
chr2:190488001
|
C | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-656C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488001 | ||||||
chr2:190488028
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-629G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488028 | ||||||
chr2:190488047
|
C | T | 2 | a0001c0007t0001g0043a0002c0002t0001g0188 | 2 | NA18986.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1631-610C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488047 | ||||||
chr2:190488059
|
C | T | 1 | a0001c0001t0003g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1631-598C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488059 | ||||||
chr2:190488128
|
C | A | 1 | a0002c0002t0001g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-529C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488128 | ||||||
chr2:190488148
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1631-509G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488148 | ||||||
chr2:190488162
|
A | C | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1631-495A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488162 | ||||||
chr2:190488190
|
T | C | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-467T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488190 | ||||||
chr2:190488240
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1631-417A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488240 | ||||||
chr2:190488282
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1631-375A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488282 | ||||||
chr2:190488403
|
A | G | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1631-254A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488403 | ||||||
chr2:190488501
|
C | T | 2 | a0003c0003t0010g0330a0003c0003t0010g0331 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-156C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488501 | ||||||
chr2:190488510
|
A | T | 1 | a0002c0002t0004g0213 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1631-147A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488510 | ||||||
chr2:190488646
|
T | C | 1 | a0002c0002t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1631-11T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488646 | ||||||
chr2:190489335
|
T | G | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1793-433T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489335 | ||||||
chr2:190489446
|
A | G | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1793-322A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489446 | ||||||
chr2:190489471
|
T | C | 1 | a0001c0001t0003g0045 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1793-297T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489471 | ||||||
chr2:190489499
|
A | T | 1 | a0002c0002t0008g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1793-269A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489499 | ||||||
chr2:190489574
|
T | C | 1 | a0001c0001t0012g0247 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1793-194T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489574 | ||||||
chr2:190489698
|
C | T | 6 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211others(3): Show | 6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793-70C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489698 | ||||||
chr2:190489703
|
G | A | 1 | a0002c0002t0001g0285 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1793-65G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489703 | ||||||
chr2:190489765
|
T | C | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
splice_region_variant&intron_variant | LOW | c.1793-3T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489765 | ||||||
chr2:190489932
|
C | CCT | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1891+66_1891+67ins others(2): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190489932 | ||||||
chr2:190490097
|
GTT | G | 54 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(51): Show | 54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1891+234_1891+235d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490097 | |||||
chr2:190490237
|
C | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(81): Show | 88 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1891+371C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490237 | ||||||
chr2:190490245
|
T | C | 1 | a0002c0002t0001g0291 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1891+379T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490245 | ||||||
chr2:190490257
|
A | G | 2 | a0001c0001t0002g0118a0001c0001t0016g0117 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1891+391A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490257 | ||||||
chr2:190490263
|
T | TA | 7 | a0002c0002t0001g0002a0002c0002t0001g0179a0002c0002t0001g0197others(4): Show | 9 | HG01884.hp2 HG02559.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891+411dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490263 | |||||
chr2:190490263
|
TA | T | 62 | a0001c0001t0001g0234a0001c0001t0002g0144a0001c0001t0003g0013others(59): Show | 62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1891+411delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490263 | |||||
chr2:190490307
|
T | C | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1891+441T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490307 | ||||||
chr2:190490334
|
C | T | 1 | a0002c0002t0001g0312 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1891+468C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490334 | ||||||
chr2:190490562
|
C | CA | 51 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(48): Show | 55 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1891+706dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490562 | |||||
chr2:190490655
|
C | A | 71 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0226others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1891+789C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490655 | ||||||
chr2:190490807
|
G | A | 9 | a0001c0001t0001g0148a0001c0001t0001g0231a0001c0001t0001g0232others(6): Show | 9 | HG01361.hp1 HG01496.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891+941G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490807 | ||||||
chr2:190490889
|
T | A | 3 | a0001c0001t0003g0030a0001c0001t0003g0045a0001c0001t0003g0051 | 3 | HG00544.hp1 NA18962.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1891+1023T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490889 | ||||||
chr2:190491574
|
C | T | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1891+1708C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190491574 | ||||||
chr2:190491940
|
A | G | 2 | a0002c0002t0001g0201a0002c0002t0001g0322 | 2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1891+2074A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190491940 | ||||||
chr2:190491994
|
C | T | 5 | a0002c0002t0005g0149a0002c0002t0005g0185a0002c0002t0005g0200others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891+2128C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190491994 | ||||||
chr2:190492017
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1891+2151C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492017 | ||||||
chr2:190492061
|
T | C | 1 | a0001c0001t0003g0054 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1891+2195T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492061 | ||||||
chr2:190492103
|
A | G | 6 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211others(3): Show | 6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891+2237A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492103 | ||||||
chr2:190492123
|
A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0015others(81): Show | 88 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1891+2257A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492123 | ||||||
chr2:190492561
|
A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1891+2695A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492561 | ||||||
chr2:190492762
|
C | CACTACCA others(16): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0250 | 2 | HG01192.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1891+2933_1891+295 others(27): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190492762 | |||||
chr2:190492822
|
A | C | 1 | a0002c0002t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1891+2956A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492822 | ||||||
chr2:190492826
|
A | C | 1 | a0002c0002t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1891+2960A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492826 | ||||||
chr2:190492968
|
A | T | 158 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(155): Show | 166 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1891+3102A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492968 | ||||||
chr2:190493036
|
C | T | 1 | a0002c0002t0001g0198 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1891+3170C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493036 | ||||||
chr2:190493074
|
A | C | 1 | a0002c0002t0001g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1891+3208A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493074 | ||||||
chr2:190493143
|
A | G | 235 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(232): Show | 247 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1891+3277A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493143 | ||||||
chr2:190493414
|
T | C | 6 | a0002c0002t0001g0008a0002c0002t0001g0182a0002c0002t0001g0192others(3): Show | 7 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1891+3548T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493414 | ||||||
chr2:190493441
|
G | A | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1891+3575G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493441 | ||||||
chr2:190493571
|
G | T | 2 | a0001c0001t0011g0041a0001c0001t0011g0046 | 2 | HG00408.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1891+3705G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493571 | ||||||
chr2:190493685
|
A | G | 3 | a0001c0001t0002g0126a0001c0001t0006g0003a0001c0001t0006g0004 | 5 | NA18982.hp1 NA19002.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1892-3754A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493685 | ||||||
chr2:190493720
|
C | A | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1892-3719C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493720 | ||||||
chr2:190493771
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1892-3668T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493771 | ||||||
chr2:190493787
|
A | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-3652A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493787 | ||||||
chr2:190493885
|
T | C | 68 | a0002c0002t0001g0005a0002c0002t0001g0010a0002c0002t0001g0125others(65): Show | 70 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1892-3554T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493885 | ||||||
chr2:190494010
|
G | C | 1 | a0003c0003t0022g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1892-3429G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494010 | ||||||
chr2:190494062
|
A | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1892-3377A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494062 | ||||||
chr2:190494198
|
C | T | 57 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1892-3241C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494198 | ||||||
chr2:190494253
|
C | G | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1892-3186C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494253 | ||||||
chr2:190494289
|
T | C | 68 | a0002c0002t0001g0005a0002c0002t0001g0010a0002c0002t0001g0125others(65): Show | 70 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1892-3150T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494289 | ||||||
chr2:190494425
|
GA | G | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-3012delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190494425 | |||||
chr2:190494829
|
C | T | 5 | a0002c0002t0001g0196a0002c0002t0001g0201a0002c0002t0001g0206others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1892-2610C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494829 | ||||||
chr2:190495018
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0229others(3): Show | 6 | HG01261.hp1 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1892-2421G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495018 | ||||||
chr2:190495063
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-2376G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495063 | ||||||
chr2:190495082
|
A | T | 3 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211 | 3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1892-2357A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495082 | ||||||
chr2:190495199
|
A | AC | 68 | a0002c0002t0001g0005a0002c0002t0001g0010a0002c0002t0001g0125others(65): Show | 70 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1892-2238dupC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190495199 | |||||
chr2:190495368
|
C | T | 242 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(239): Show | 254 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.1892-2071C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495368 | ||||||
chr2:190495426
|
A | C | 13 | a0002c0002t0001g0002a0002c0002t0001g0176a0002c0002t0001g0179others(10): Show | 15 | NA18941.hp2 NA18944.hp1 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.1892-2013A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495426 | ||||||
chr2:190495612
|
A | G | 4 | a0001c0001t0003g0038a0001c0001t0003g0040a0001c0001t0003g0049others(1): Show | 4 | NA18942.hp1 NA18944.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1892-1827A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495612 | ||||||
chr2:190495736
|
AG | A | 9 | a0001c0001t0003g0036a0001c0001t0003g0042a0001c0001t0003g0044others(6): Show | 9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1892-1698delG | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190495736 | |||||
chr2:190495745
|
G | A | 9 | a0001c0001t0003g0036a0001c0001t0003g0042a0001c0001t0003g0044others(6): Show | 9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1892-1694G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495745 | ||||||
chr2:190495826
|
G | T | 300 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.1892-1613G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495826 | ||||||
chr2:190495840
|
A | C | 59 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1892-1599A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495840 | ||||||
chr2:190495860
|
T | A | 1 | a0002c0002t0001g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1892-1579T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495860 | ||||||
chr2:190495916
|
T | C | 101 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0007t0001g0043others(98): Show | 105 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1892-1523T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495916 | ||||||
chr2:190495942
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1892-1497G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495942 | ||||||
chr2:190496028
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0090 | 3 | HG00423.hp1 HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1892-1411A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496028 | ||||||
chr2:190496122
|
C | G | 3 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211 | 3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1892-1317C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496122 | ||||||
chr2:190496143
|
GA | G | 8 | a0001c0001t0003g0038a0001c0001t0003g0040a0001c0001t0003g0049others(5): Show | 8 | HG03195.hp2 HG03453.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-1285delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190496143 | |||||
chr2:190496218
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1892-1221C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496218 | ||||||
chr2:190496231
|
A | G | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-1208A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496231 | ||||||
chr2:190496254
|
G | C | 1 | a0003c0003t0022g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1892-1185G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496254 | ||||||
chr2:190496522
|
C | T | 57 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1892-917C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496522 | ||||||
chr2:190496611
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1892-828A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496611 | ||||||
chr2:190496658
|
ATGTG | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-775_1892-772d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190496658 | |||||
chr2:190496678
|
G | GTA | 3 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211 | 3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1892-756_1892-755d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190496678 | |||||
chr2:190496779
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1892-660G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496779 | ||||||
chr2:190496824
|
A | G | 54 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(51): Show | 54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1892-615A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496824 | ||||||
chr2:190497018
|
C | T | 214 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0143others(211): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1892-421C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497018 | ||||||
chr2:190497071
|
A | T | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1892-368A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497071 | ||||||
chr2:190497107
|
G | A | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-332G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497107 | ||||||
chr2:190497132
|
T | C | 3 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0142 | 3 | HG02630.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1892-307T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497132 | ||||||
chr2:190497161
|
A | G | 1 | a0002c0002t0003g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1892-278A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497161 | ||||||
chr2:190497198
|
T | A | 1 | a0007c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1892-241T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497198 | ||||||
chr2:190497827
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2172+108G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190497827 | ||||||
chr2:190497862
|
T | G | 2 | a0002c0002t0008g0205a0002c0002t0008g0211 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2172+143T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190497862 | ||||||
chr2:190497931
|
C | T | 1 | a0002c0002t0001g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2172+212C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190497931 | ||||||
chr2:190498051
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0237 | 3 | HG01496.hp1 HG03942.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2172+332A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498051 | ||||||
chr2:190498266
|
T | G | 1 | a0001c0001t0003g0030 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2172+547T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498266 | ||||||
chr2:190498482
|
G | C | 2 | a0001c0001t0003g0037a0001c0001t0003g0066 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2172+763G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498482 | ||||||
chr2:190498770
|
T | C | 58 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.2172+1051T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498770 | ||||||
chr2:190498826
|
C | T | 1 | a0002c0002t0001g0271 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2172+1107C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498826 | ||||||
chr2:190499134
|
T | C | 6 | a0001c0001t0008g0332a0002c0002t0008g0205a0002c0002t0008g0211others(3): Show | 6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2173-881T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499134 | ||||||
chr2:190499583
|
C | T | 50 | a0001c0001t0001g0143a0002c0002t0001g0002a0002c0002t0001g0007others(47): Show | 54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2173-432C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499583 | ||||||
chr2:190499977
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2173-38T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499977 | ||||||
chr2:190499982
|
G | A | 57 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.2173-33G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499982 | ||||||
chr2:190500003
|
T | C | 3 | a0003c0003t0010g0330a0003c0003t0010g0331a0003c0003t0022g0207 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2173-12T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190500003 |