geneid | 6519 |
---|---|
ensemblid | ENSG00000138079.14 |
hgncid | 11025 |
symbol | SLC3A1 |
name | solute carrier family 3 member 1 |
refseq_nuc | NM_000341.4 |
refseq_prot | NP_000332.2 |
ensembl_nuc | ENST00000260649.11 |
ensembl_prot | ENSP00000260649.6 |
mane_status | MANE Select |
chr | chr2 |
start | 44275480 |
end | 44321494 |
strand | + |
ver | v1.2 |
region | chr2:44275480-44321494 |
region5000 | chr2:44270480-44326494 |
regionname0 | SLC3A1_chr2_44275480_44321494 |
regionname5000 | SLC3A1_chr2_44270480_44326494 |
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 | 685 | 200 | 78 | 38 | 65 | 4 | 14 | 50 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002 | 0/1 | 685 | 143 | 16 | 34 | 61 | 10 | 21 | 48 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0003 | 0/0 | 685 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0004 | 0/0 | 685 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0005 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0006 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0007 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0008 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0009 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0010 | 0/0 | 685 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0011 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
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 | 0/1 | 2058 | 134 | 10 | 32 | 60 | 10 | 21 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0002 | 1/0 | 2058 | 103 | 13 | 26 | 57 | 1 | 5 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0003 | 0/0 | 2058 | 95 | 63 | 12 | 8 | 3 | 9 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0004 | 0/0 | 2058 | 6 | 4 | 1 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0005 | 0/0 | 2058 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0006 | 0/0 | 2058 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0007 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0008 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0009 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0010 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0011 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0012 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0013 | 0/0 | 2058 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0014 | 0/0 | 2058 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0015 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0016 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0017 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
c0018 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
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 | 912 | 190 | 54 | 39 | 64 | 11 | 21 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0002 | 1/0 | 912 | 103 | 7 | 21 | 67 | 2 | 5 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0003 | 0/0 | 912 | 28 | 7 | 9 | 2 | 1 | 9 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0004 | 0/0 | 912 | 20 | 19 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0005 | 0/0 | 912 | 4 | 2 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0006 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0007 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0008 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0009 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0010 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0011 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0012 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
t0013 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
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 | 1/0 | 6 | 1 | 0 | 4 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0002 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0004 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 2058 | 103 | 13 | 26 | 57 | 1 | 5 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003 | 0/0 | 2058 | 95 | 63 | 12 | 8 | 3 | 9 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0017 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0018 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0001 | 0/1 | 2058 | 134 | 10 | 32 | 60 | 10 | 21 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0004 | 0/0 | 2058 | 6 | 4 | 1 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0010 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0013 | 0/0 | 2058 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0016 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0003c0005 | 0/0 | 2058 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0004c0006 | 0/0 | 2058 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0005c0009 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0006c0008 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0007c0007 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0008c0011 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0009c0012 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0010c0014 | 0/0 | 2058 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0011c0015 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 2969 | 8 | 6 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0002t0002 | 1/0 | 2969 | 88 | 5 | 20 | 56 | 1 | 5 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0002t0003 | 0/0 | 2969 | 6 | 1 | 4 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0002t0009 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0001 | 0/0 | 2969 | 40 | 34 | 5 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0002 | 0/0 | 2969 | 10 | 2 | 1 | 6 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0003 | 0/0 | 2969 | 21 | 5 | 5 | 1 | 1 | 9 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0004 | 0/0 | 2969 | 19 | 18 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0006 | 0/0 | 2969 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0011 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0012 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0003t0013 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0017t0007 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0001c0018t0003 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0001t0001 | 0/1 | 2969 | 128 | 7 | 30 | 60 | 10 | 20 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0001t0005 | 0/0 | 2969 | 4 | 2 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0001t0008 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0001t0010 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0004t0001 | 0/0 | 2969 | 6 | 4 | 1 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0010t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0013t0001 | 0/0 | 2969 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0002c0016t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0003c0005t0002 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0004c0006t0001 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0005c0009t0002 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0006c0008t0002 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0007c0007t0002 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0008c0011t0004 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0009c0012t0001 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0010c0014t0001 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
a0011c0015t0001 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | copy fasta | chr2 | 44270480 | 44326494 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0001 | 1/0 | 6 | 1 | 0 | 4 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0002t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0011g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0003t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0017t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0001c0018t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0001t0010g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0010t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0013t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0002c0016t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0003c0005t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0003c0005t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0004c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0004c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0005c0009t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0006c0008t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0007c0007t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0008c0011t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0009c0012t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0010c0014t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
a0011c0015t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0269 | EUR | GBR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0071 | EUR | GBR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00280 | hp1 | a0001 | c0003 | t0003 | g0115 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00280 | hp2 | a0002 | c0001 | t0001 | g0092 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00323 | hp1 | a0002 | c0001 | t0001 | g0274 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0243 | EUR | FIN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00423 | hp1 | a0002 | c0001 | t0001 | g0056 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00597 | hp2 | a0002 | c0001 | t0001 | g0132 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0077 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00621 | hp2 | a0006 | c0008 | t0002 | g0192 | EAS | CHS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00639 | hp1 | a0001 | c0003 | t0003 | g0315 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0152 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00642 | hp2 | a0002 | c0001 | t0001 | g0303 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00733 | hp1 | a0002 | c0001 | t0001 | g0275 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0203 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00735 | hp2 | a0002 | c0001 | t0001 | g0034 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00738 | hp1 | a0001 | c0003 | t0003 | g0278 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG00741 | hp2 | a0001 | c0003 | t0003 | g0304 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01069 | hp1 | a0002 | c0001 | t0001 | g0100 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01069 | hp2 | a0002 | c0001 | t0001 | g0094 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01070 | hp1 | a0002 | c0001 | t0001 | g0271 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01070 | hp2 | a0001 | c0003 | t0003 | g0321 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01071 | hp1 | a0002 | c0001 | t0001 | g0273 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01071 | hp2 | a0002 | c0001 | t0001 | g0095 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0145 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01081 | hp2 | a0002 | c0001 | t0001 | g0101 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0276 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01109 | hp2 | a0001 | c0003 | t0004 | g0293 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01167 | hp1 | a0002 | c0001 | t0001 | g0139 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01168 | hp1 | a0002 | c0001 | t0005 | g0067 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0059 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01169 | hp1 | a0002 | c0001 | t0005 | g0068 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01192 | hp1 | a0001 | c0003 | t0003 | g0306 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0319 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01243 | hp2 | a0002 | c0004 | t0001 | g0171 | AMR | PUR | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01256 | hp1 | a0002 | c0001 | t0001 | g0120 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0119 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0118 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01258 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0035 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0176 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01358 | hp1 | a0002 | c0001 | t0001 | g0144 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01358 | hp2 | a0002 | c0001 | t0001 | g0117 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0261 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0075 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0116 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0260 | AMR | CLM | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0270 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0162 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0272 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01517 | hp2 | a0002 | c0001 | t0001 | g0004 | EUR | IBS | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01884 | hp1 | a0001 | c0003 | t0013 | g0286 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01884 | hp2 | a0001 | c0003 | t0004 | g0284 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01891 | hp1 | a0001 | c0003 | t0004 | g0282 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0018 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01934 | hp2 | a0002 | c0001 | t0001 | g0148 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01943 | hp1 | a0002 | c0001 | t0001 | g0053 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01952 | hp1 | a0002 | c0001 | t0001 | g0096 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01975 | hp2 | a0002 | c0001 | t0001 | g0083 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0242 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01993 | hp1 | a0002 | c0001 | t0001 | g0070 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG01993 | hp2 | a0002 | c0013 | t0001 | g0004 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02004 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02015 | hp1 | a0001 | c0003 | t0003 | g0309 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02040 | hp1 | a0001 | c0003 | t0002 | g0054 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02040 | hp2 | a0001 | c0003 | t0002 | g0123 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02055 | hp1 | a0001 | c0017 | t0007 | g0161 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02055 | hp2 | a0002 | c0001 | t0001 | g0069 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0156 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02074 | hp2 | a0005 | c0009 | t0002 | g0104 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0105 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02135 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02145 | hp1 | a0002 | c0001 | t0001 | g0060 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02145 | hp2 | a0001 | c0003 | t0004 | g0291 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0078 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02165 | hp2 | a0002 | c0001 | t0001 | g0063 | EAS | CDX | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0256 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02257 | hp2 | a0001 | c0003 | t0004 | g0295 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02258 | hp1 | a0001 | c0003 | t0003 | g0301 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0183 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02280 | hp1 | a0002 | c0001 | t0001 | g0091 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02293 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0207 | AMR | PEL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02451 | hp1 | a0008 | c0011 | t0004 | g0015 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02451 | hp2 | a0001 | c0003 | t0004 | g0300 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0141 | EAS | KHV | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02572 | hp1 | a0001 | c0003 | t0004 | g0057 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02572 | hp2 | a0001 | c0003 | t0004 | g0299 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0017 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02602 | hp2 | a0001 | c0003 | t0003 | g0310 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02615 | hp2 | a0001 | c0003 | t0002 | g0259 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0255 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02630 | hp2 | a0001 | c0003 | t0004 | g0281 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02647 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02683 | hp1 | a0001 | c0003 | t0003 | g0307 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0312 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02698 | hp2 | a0010 | c0014 | t0001 | g0320 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02717 | hp2 | a0002 | c0001 | t0001 | g0022 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0041 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02809 | hp2 | a0001 | c0003 | t0004 | g0292 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02886 | hp1 | a0002 | c0016 | t0001 | g0160 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02897 | hp1 | a0001 | c0003 | t0006 | g0267 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02922 | hp1 | a0001 | c0003 | t0012 | g0285 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0249 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02970 | hp1 | a0001 | c0003 | t0004 | g0298 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02970 | hp2 | a0002 | c0001 | t0001 | g0108 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02976 | hp1 | a0001 | c0003 | t0006 | g0289 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0150 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03017 | hp2 | a0001 | c0003 | t0003 | g0311 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03041 | hp1 | a0001 | c0003 | t0004 | g0279 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03041 | hp2 | a0001 | c0003 | t0003 | g0288 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0251 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03139 | hp2 | a0001 | c0003 | t0004 | g0297 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03195 | hp1 | a0011 | c0015 | t0001 | g0253 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0280 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03239 | hp1 | a0002 | c0001 | t0001 | g0318 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0149 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03453 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0165 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0254 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03486 | hp2 | a0002 | c0001 | t0001 | g0024 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03490 | hp1 | a0001 | c0003 | t0003 | g0314 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0097 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0241 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | ESN | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03540 | hp1 | a0002 | c0001 | t0008 | g0109 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03579 | hp1 | a0002 | c0004 | t0001 | g0172 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0294 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03654 | hp1 | a0002 | c0001 | t0001 | g0129 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0090 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0055 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03688 | hp2 | a0001 | c0003 | t0003 | g0316 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03704 | hp1 | a0001 | c0003 | t0003 | g0313 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03704 | hp2 | a0002 | c0001 | t0001 | g0137 | SAS | PJL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0140 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0099 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0037 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0302 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0153 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03942 | hp2 | a0002 | c0001 | t0010 | g0317 | SAS | BEB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04115 | hp1 | a0002 | c0001 | t0001 | g0038 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04115 | hp2 | a0002 | c0001 | t0001 | g0019 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0089 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04199 | hp2 | a0002 | c0001 | t0001 | g0021 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0194 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0237 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0147 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG04228 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | STU | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18522 | hp1 | a0001 | c0003 | t0003 | g0308 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0015 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | CHB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | CHB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0290 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18944 | hp1 | a0001 | c0003 | t0011 | g0122 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18945 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18951 | hp1 | a0007 | c0007 | t0002 | g0202 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18957 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18957 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18959 | hp2 | a0001 | c0003 | t0002 | g0113 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18960 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18962 | hp2 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18964 | hp1 | a0002 | c0001 | t0001 | g0061 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18965 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18966 | hp2 | a0003 | c0005 | t0002 | g0199 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18967 | hp1 | a0003 | c0005 | t0002 | g0200 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18967 | hp2 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18969 | hp1 | a0004 | c0006 | t0001 | g0049 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18970 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18974 | hp2 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18980 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18983 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18984 | hp1 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18985 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18985 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18988 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0079 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18991 | hp2 | a0004 | c0006 | t0001 | g0051 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18993 | hp2 | a0002 | c0001 | t0001 | g0076 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18994 | hp2 | a0002 | c0001 | t0001 | g0080 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18998 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19004 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19006 | hp1 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19012 | hp1 | a0009 | c0012 | t0001 | g0082 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0287 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0066 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19057 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19058 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19059 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19059 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19060 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19063 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19064 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19068 | hp1 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19074 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19076 | hp1 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19076 | hp2 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19080 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19083 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19084 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19090 | hp2 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19091 | hp1 | a0002 | c0004 | t0001 | g0238 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19091 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19240 | hp1 | a0002 | c0001 | t0005 | g0048 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | YRI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20129 | hp1 | a0001 | c0003 | t0003 | g0322 | AFR | ASW | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20129 | hp2 | a0002 | c0001 | t0005 | g0065 | AFR | ASW | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0017 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0023 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0154 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0002 | EUR | TSI | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20905 | hp1 | a0001 | c0003 | t0003 | g0305 | SAS | GIH | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0081 | SAS | GIH | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02109 | hp1 | a0001 | c0003 | t0004 | g0277 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0283 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0296 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02486 | hp2 | a0002 | c0010 | t0001 | g0103 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0163 | AFR | ACB | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | MSL | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG06807 | hp1 | a0001 | c0018 | t0003 | g0033 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
HG06807 | hp2 | a0002 | c0004 | t0001 | g0169 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20300 | hp1 | a0001 | c0002 | t0009 | g0175 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | USA | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0268 | AFR | LWK | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0128 | REF | REF | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0001 | REF | REF | SLC3A1_chr2_44270480_44326494 | SLC3A1 | chr2 | 44270480 | 44326494 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44275792
|
G | A | 1 | a0005 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.257G>A | p.Arg86Gln | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 313/2969 | 257/2058 | 86/685 | chr2 | 44275792 | ||
chr2:44275848
|
A | G | 1 | a0004 | 2 | NA18969.hp1 NA18991.hp2 |
missense_variant | MODERATE | c.313A>G | p.Ile105Val | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 369/2969 | 313/2058 | 105/685 | chr2 | 44275848 | ||
chr2:44301022
|
C | T | 1 | a0006 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1031C>T | p.Ser344Leu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1087/2969 | 1031/2058 | 344/685 | chr2 | 44301022 | ||
chr2:44301054
|
G | A | 1 | a0007 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1063G>A | p.Val355Met | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1119/2969 | 1063/2058 | 355/685 | chr2 | 44301054 | ||
chr2:44301085
|
G | A | 1 | a0008 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1094G>A | p.Arg365Gln | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1150/2969 | 1094/2058 | 365/685 | chr2 | 44301085 | ||
chr2:44304276
|
G | C | 1 | a0009 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1270G>C | p.Val424Leu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/10 | 1326/2969 | 1270/2058 | 424/685 | chr2 | 44304276 | ||
chr2:44312587
|
T | C | 1 | a0003 | 2 | NA18966.hp2 NA18967.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1334T>C | p.Ile445Thr | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/10 | 1390/2969 | 1334/2058 | 445/685 | chr2 | 44312587 | ||
chr2:44312643
|
G | A | 1 | a0010 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1390G>A | p.Val464Met | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/10 | 1446/2969 | 1390/2058 | 464/685 | chr2 | 44312643 | ||
chr2:44320427
|
G | A | 1 | a0011 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1846G>A | p.Ala616Thr | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 1902/2969 | 1846/2058 | 616/685 | chr2 | 44320427 | ||
chr2:44320435
|
G | A | 4 | a0002a0004a0009others(1): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
missense_variant | MODERATE | c.1854G>A | p.Met618Ile | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 1910/2969 | 1854/2058 | 618/685 | chr2 | 44320435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44275649
|
A | C | 13 | a0001c0003a0001c0017a0001c0018others(10): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
synonymous_variant | LOW | c.114A>C | p.Gly38Gly | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 170/2969 | 114/2058 | 38/685 | chr2 | 44275649 | ||
chr2:44275835
|
C | T | 1 | a0001c0018 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.300C>T | p.Leu100Leu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/10 | 356/2969 | 300/2058 | 100/685 | chr2 | 44275835 | ||
chr2:44281448
|
A | G | 1 | a0001c0017 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.672A>G | p.Gln224Gln | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/10 | 728/2969 | 672/2058 | 224/685 | chr2 | 44281448 | ||
chr2:44301026
|
G | A | 1 | a0002c0010 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1035G>A | p.Glu345Glu | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/10 | 1091/2969 | 1035/2058 | 345/685 | chr2 | 44301026 | ||
chr2:44312618
|
G | A | 1 | a0002c0013 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.1365G>A | p.Ser455Ser | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/10 | 1421/2969 | 1365/2058 | 455/685 | chr2 | 44312618 | ||
chr2:44313906
|
C | T | 1 | a0002c0016 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1572C>T | p.Asn524Asn | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/10 | 1628/2969 | 1572/2058 | 524/685 | chr2 | 44313906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44320770
|
T | C | 17 | a0001c0002t0001a0001c0002t0009a0001c0003t0001others(14): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*131T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 131 | chr2 | 44320770 | |||||
chr2:44320865
|
C | T | 1 | a0002c0001t0010 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 226 | chr2 | 44320865 | |||||
chr2:44320958
|
G | T | 4 | a0001c0002t0009a0001c0003t0006a0001c0003t0012others(1): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*319G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 319 | chr2 | 44320958 | |||||
chr2:44321143
|
T | C | 24 | a0001c0002t0001a0001c0002t0003a0001c0002t0009others(21): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*504T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 504 | chr2 | 44321143 | |||||
chr2:44321235
|
C | T | 1 | a0002c0001t0005 | 4 | HG01168.hp1 HG01169.hp1 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*596C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 596 | chr2 | 44321235 | |||||
chr2:44321342
|
T | C | 1 | a0001c0017t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 703 | chr2 | 44321342 | |||||
chr2:44321418
|
C | T | 2 | a0001c0003t0013a0002c0001t0008 | 2 | HG01884.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*779C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 779 | chr2 | 44321418 | |||||
chr2:44321429
|
T | C | 1 | a0001c0002t0009 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*790T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 790 | chr2 | 44321429 | |||||
chr2:44321474
|
T | C | 18 | a0001c0002t0001a0001c0003t0001a0001c0003t0004others(15): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*835T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 10/10 | 835 | chr2 | 44321474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:44276040
|
A | G | 1 | a0001c0003t0003g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.430+75A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276040 | ||||||
chr2:44276291
|
C | A | 1 | a0001c0003t0002g0018 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+326C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276291 | ||||||
chr2:44276503
|
A | G | 22 | a0001c0003t0003g0301a0001c0003t0003g0302a0001c0003t0003g0304others(19): Show | 23 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.430+538A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276503 | ||||||
chr2:44276520
|
A | G | 1 | a0001c0002t0003g0016 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.430+555A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276520 | ||||||
chr2:44276611
|
AGCTACTT others(5): Show |
A | 49 | a0001c0003t0001g0006a0001c0003t0001g0287a0001c0003t0001g0296others(46): Show | 52 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.430+650_430+661del others(12): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44276611 | |||||
chr2:44276641
|
G | C | 1 | a0001c0003t0004g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+676G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276641 | ||||||
chr2:44276693
|
C | T | 4 | a0001c0003t0004g0297a0001c0003t0004g0298a0001c0003t0004g0299others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+728C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276693 | ||||||
chr2:44276990
|
G | T | 8 | a0002c0001t0001g0269a0002c0001t0001g0270a0002c0001t0001g0271others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1025G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276990 | ||||||
chr2:44276995
|
G | C | 7 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(4): Show | 7 | HG02717.hp2 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+1030G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44276995 | ||||||
chr2:44277030
|
C | A | 2 | a0001c0003t0003g0278a0001c0003t0003g0322 | 2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.430+1065C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277030 | ||||||
chr2:44277037
|
C | A | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1072C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277037 | ||||||
chr2:44277092
|
T | TTCTC | 190 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0009others(187): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.430+1133_430+1136d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277092 | |||||
chr2:44277097
|
T | G | 4 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1132T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277097 | ||||||
chr2:44277100
|
C | T | 1 | a0001c0002t0003g0016 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.430+1135C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277100 | ||||||
chr2:44277101
|
T | TC | 13 | a0001c0003t0001g0287a0001c0003t0004g0297a0001c0003t0004g0298others(10): Show | 13 | HG00099.hp1 HG01884.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+1136_430+1137i others(3): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277101 | ||||||
chr2:44277103
|
C | CT | 29 | a0001c0002t0002g0003a0001c0002t0002g0262a0001c0002t0002g0263others(26): Show | 34 | HG00438.hp2 HG00639.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.430+1159dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277103 | |||||
chr2:44277103
|
CT | C | 34 | a0001c0002t0002g0159a0001c0003t0001g0006a0001c0003t0001g0296others(31): Show | 37 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.430+1159delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277103 | |||||
chr2:44277104
|
T | TTC | 12 | a0001c0003t0001g0287a0001c0003t0004g0297a0001c0003t0004g0298others(9): Show | 12 | HG00099.hp1 HG01884.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1140_430+1141i others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44277104 | |||||
chr2:44277220
|
G | A | 1 | a0002c0001t0001g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.430+1255G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277220 | ||||||
chr2:44277326
|
C | T | 12 | a0001c0003t0001g0249a0001c0003t0001g0250a0001c0003t0001g0251others(9): Show | 12 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1361C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277326 | ||||||
chr2:44277356
|
C | A | 11 | a0001c0003t0001g0006a0001c0003t0004g0279a0001c0003t0004g0280others(8): Show | 13 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+1391C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277356 | ||||||
chr2:44277397
|
C | T | 1 | a0002c0001t0001g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.430+1432C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277397 | ||||||
chr2:44277419
|
G | A | 12 | a0001c0003t0001g0249a0001c0003t0001g0250a0001c0003t0001g0251others(9): Show | 12 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1454G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277419 | ||||||
chr2:44277448
|
A | G | 2 | a0001c0003t0003g0278a0001c0003t0003g0322 | 2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.430+1483A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277448 | ||||||
chr2:44277449
|
T | G | 1 | a0001c0017t0007g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430+1484T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277449 | ||||||
chr2:44277452
|
A | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.430+1487A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277452 | ||||||
chr2:44277532
|
C | T | 1 | a0001c0017t0007g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430+1567C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277532 | ||||||
chr2:44277666
|
G | T | 1 | a0002c0001t0001g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.430+1701G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277666 | ||||||
chr2:44277718
|
C | T | 29 | a0001c0003t0002g0018a0001c0003t0002g0123a0001c0003t0011g0122others(26): Show | 29 | HG00597.hp2 HG01167.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.430+1753C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277718 | ||||||
chr2:44277738
|
T | C | 211 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(208): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.430+1773T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277738 | ||||||
chr2:44277906
|
A | G | 4 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1941A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277906 | ||||||
chr2:44277925
|
A | C | 1 | a0002c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.430+1960A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277925 | ||||||
chr2:44277949
|
T | C | 1 | a0001c0002t0002g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+1984T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44277949 | ||||||
chr2:44278010
|
C | A | 1 | a0001c0003t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.430+2045C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278010 | ||||||
chr2:44278045
|
T | A | 1 | a0001c0003t0003g0302 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.430+2080T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278045 | ||||||
chr2:44278046
|
T | G | 236 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(233): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.430+2081T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278046 | ||||||
chr2:44278182
|
C | T | 6 | a0001c0003t0003g0115a0002c0001t0001g0116a0002c0001t0001g0117others(3): Show | 6 | HG00280.hp1 HG01256.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+2217C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278182 | ||||||
chr2:44278190
|
A | G | 3 | a0001c0003t0001g0255a0001c0003t0001g0256a0001c0003t0001g0257 | 3 | HG02257.hp1 HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.430+2225A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278190 | ||||||
chr2:44278318
|
G | C | 1 | a0001c0003t0002g0018 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+2353G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278318 | ||||||
chr2:44278371
|
C | A | 1 | a0001c0017t0007g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.431-2345C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278371 | ||||||
chr2:44278396
|
T | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.431-2320T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278396 | ||||||
chr2:44278435
|
G | A | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.431-2281G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278435 | ||||||
chr2:44278469
|
T | TAAATA | 2 | a0002c0001t0001g0017a0002c0001t0001g0303 | 3 | HG00642.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.431-2229_431-2225d others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44278469 | |||||
chr2:44278582
|
C | T | 1 | a0001c0003t0003g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-2134C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278582 | ||||||
chr2:44278740
|
G | A | 7 | a0001c0003t0001g0249a0001c0003t0001g0250a0001c0003t0001g0255others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1976G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278740 | ||||||
chr2:44278764
|
G | A | 1 | a0001c0002t0002g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.431-1952G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278764 | ||||||
chr2:44278950
|
T | C | 5 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0002t0002g0012others(2): Show | 6 | HG01074.hp1 HG01099.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1766T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44278950 | ||||||
chr2:44279006
|
T | A | 38 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0026others(35): Show | 41 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.431-1710T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279006 | ||||||
chr2:44279008
|
T | C | 1 | a0002c0001t0001g0036 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.431-1708T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279008 | ||||||
chr2:44279117
|
G | A | 24 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(21): Show | 24 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.431-1599G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279117 | ||||||
chr2:44279206
|
G | A | 155 | a0001c0003t0001g0006a0001c0003t0001g0009a0001c0003t0001g0010others(152): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.431-1510G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279206 | ||||||
chr2:44279229
|
A | T | 11 | a0001c0003t0001g0006a0001c0003t0004g0279a0001c0003t0004g0280others(8): Show | 13 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.431-1487A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279229 | ||||||
chr2:44279374
|
C | T | 1 | a0001c0002t0002g0248 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431-1342C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279374 | ||||||
chr2:44279429
|
G | T | 1 | a0002c0001t0001g0114 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.431-1287G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279429 | ||||||
chr2:44279485
|
G | A | 1 | a0001c0003t0003g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-1231G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279485 | ||||||
chr2:44279567
|
C | T | 1 | a0002c0001t0001g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.431-1149C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279567 | ||||||
chr2:44279588
|
G | A | 1 | a0002c0001t0001g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.431-1128G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279588 | ||||||
chr2:44279601
|
T | C | 26 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(23): Show | 26 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.431-1115T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279601 | ||||||
chr2:44279610
|
T | G | 6 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(3): Show | 7 | HG01243.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-1106T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279610 | ||||||
chr2:44279782
|
C | T | 156 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0009others(153): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.431-934C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279782 | ||||||
chr2:44279832
|
G | C | 156 | a0001c0003t0001g0006a0001c0003t0001g0009a0001c0003t0001g0010others(153): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.431-884G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279832 | ||||||
chr2:44279935
|
G | A | 1 | a0001c0003t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.431-781G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44279935 | ||||||
chr2:44280074
|
C | T | 143 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(140): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.431-642C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280074 | ||||||
chr2:44280214
|
T | G | 1 | a0001c0002t0002g0181 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.431-502T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280214 | ||||||
chr2:44280428
|
G | A | 1 | a0002c0001t0001g0038 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.431-288G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280428 | ||||||
chr2:44280459
|
G | A | 3 | a0001c0003t0001g0009a0001c0003t0001g0039a0001c0003t0001g0146 | 4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-257G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280459 | ||||||
chr2:44280534
|
G | A | 139 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(136): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.431-182G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280534 | ||||||
chr2:44280608
|
A | G | 1 | a0001c0003t0001g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431-108A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280608 | ||||||
chr2:44280654
|
A | AT | 4 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0108others(1): Show | 4 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-56dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 44280654 | |||||
chr2:44280670
|
C | A | 1 | a0001c0003t0011g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.431-46C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 1/9 | chr2 | 44280670 | ||||||
chr2:44280956
|
T | C | 6 | a0001c0003t0003g0020a0001c0018t0003g0033a0002c0001t0001g0019others(3): Show | 6 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.610+61T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44280956 | ||||||
chr2:44280990
|
A | G | 1 | a0002c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.610+95A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44280990 | ||||||
chr2:44281003
|
T | TTCCC | 49 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(46): Show | 54 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.610+122_610+125dup others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 44281003 | |||||
chr2:44281042
|
C | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+147C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281042 | ||||||
chr2:44281054
|
T | G | 19 | a0001c0003t0001g0008a0001c0003t0001g0009a0001c0003t0001g0010others(16): Show | 23 | HG00642.hp1 HG01099.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.610+159T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281054 | ||||||
chr2:44281061
|
C | T | 2 | a0001c0003t0002g0107a0002c0001t0001g0106 | 2 | NA18965.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.610+166C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281061 | ||||||
chr2:44281064
|
C | G | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+169C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | chr2 | 44281064 | ||||||
chr2:44281159
|
C | CT | 198 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(195): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.611-212dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 44281159 | |||||
chr2:44281159
|
C | CTT | 13 | a0001c0003t0002g0105a0001c0003t0003g0020a0001c0003t0003g0278others(10): Show | 13 | HG00738.hp1 HG02074.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.611-213_611-212dup others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 44281159 | |||||
chr2:44281377
|
T | TACTCATT others(228): Show |
1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.611-7_765+73dupTCA others(232): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 44281377 | |||||
chr2:44281696
|
G | A | 175 | a0001c0003t0001g0008a0001c0003t0001g0009a0001c0003t0001g0010others(172): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.765+155G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44281696 | ||||||
chr2:44281812
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.765+271C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44281812 | ||||||
chr2:44281826
|
TTCCATG | T | 7 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0026others(4): Show | 10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.765+289_765+294del others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 44281826 | |||||
chr2:44282016
|
C | T | 1 | a0001c0002t0002g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.765+475C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282016 | ||||||
chr2:44282021
|
G | A | 1 | a0002c0001t0001g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.765+480G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282021 | ||||||
chr2:44282185
|
T | A | 1 | a0001c0002t0002g0182 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.765+644T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282185 | ||||||
chr2:44282216
|
C | G | 1 | a0001c0003t0003g0278 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.765+675C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282216 | ||||||
chr2:44282223
|
T | C | 2 | a0001c0003t0001g0287a0001c0003t0001g0296 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.765+682T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282223 | ||||||
chr2:44282248
|
T | C | 1 | a0002c0001t0001g0029 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+707T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282248 | ||||||
chr2:44282425
|
C | A | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.765+884C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282425 | ||||||
chr2:44282432
|
G | A | 3 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0108 | 3 | HG02970.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.765+891G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282432 | ||||||
chr2:44282510
|
G | T | 1 | a0002c0001t0001g0029 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+969G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282510 | ||||||
chr2:44282514
|
C | G | 1 | a0001c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.765+973C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282514 | ||||||
chr2:44282623
|
C | T | 1 | a0002c0010t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.765+1082C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282623 | ||||||
chr2:44282639
|
T | A | 1 | a0002c0001t0001g0029 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+1098T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282639 | ||||||
chr2:44282744
|
G | A | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.765+1203G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282744 | ||||||
chr2:44282902
|
C | T | 1 | a0001c0003t0006g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.765+1361C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282902 | ||||||
chr2:44282921
|
G | C | 1 | a0002c0001t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.765+1380G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44282921 | ||||||
chr2:44283007
|
A | T | 190 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(187): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.765+1466A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283007 | ||||||
chr2:44283040
|
T | C | 215 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(212): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.765+1499T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283040 | ||||||
chr2:44283057
|
G | T | 25 | a0001c0003t0003g0020a0001c0003t0004g0015a0001c0003t0004g0277others(22): Show | 25 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.765+1516G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283057 | ||||||
chr2:44283268
|
G | A | 1 | a0001c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.765+1727G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283268 | ||||||
chr2:44283335
|
C | G | 1 | a0001c0002t0002g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.765+1794C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283335 | ||||||
chr2:44283439
|
C | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+1898C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283439 | ||||||
chr2:44283650
|
A | T | 1 | a0002c0001t0001g0029 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+2109A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283650 | ||||||
chr2:44283722
|
C | A | 1 | a0002c0001t0001g0038 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.765+2181C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283722 | ||||||
chr2:44283797
|
C | T | 16 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(13): Show | 16 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.766-2235C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283797 | ||||||
chr2:44283839
|
T | C | 1 | a0002c0001t0001g0029 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.766-2193T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44283839 | ||||||
chr2:44283858
|
T | TAGGTATA others(313): Show |
11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.766-2159_766-2158i others(322): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 44283858 | |||||
chr2:44284016
|
T | A | 1 | a0001c0003t0001g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.766-2016T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284016 | ||||||
chr2:44284076
|
C | T | 1 | a0001c0002t0009g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.766-1956C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284076 | ||||||
chr2:44284118
|
C | T | 1 | a0001c0003t0002g0018 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.766-1914C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284118 | ||||||
chr2:44284297
|
C | A | 1 | a0002c0001t0001g0114 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.766-1735C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284297 | ||||||
chr2:44284528
|
A | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-1504A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284528 | ||||||
chr2:44284648
|
G | T | 3 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0254 | 3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.766-1384G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284648 | ||||||
chr2:44284667
|
A | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(10): Show | 16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.766-1365A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284667 | ||||||
chr2:44284722
|
T | C | 215 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(212): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.766-1310T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284722 | ||||||
chr2:44284790
|
T | C | 179 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(176): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.766-1242T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284790 | ||||||
chr2:44284897
|
A | C | 1 | a0001c0003t0001g0047 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.766-1135A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44284897 | ||||||
chr2:44285149
|
C | T | 1 | a0002c0001t0001g0102 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.766-883C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285149 | ||||||
chr2:44285402
|
G | A | 1 | a0001c0003t0012g0285 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.766-630G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285402 | ||||||
chr2:44285440
|
C | T | 3 | a0001c0003t0003g0278a0001c0003t0003g0288a0001c0003t0003g0322 | 3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.766-592C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285440 | ||||||
chr2:44285696
|
C | G | 1 | a0001c0002t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.766-336C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285696 | ||||||
chr2:44285813
|
G | A | 4 | a0001c0002t0002g0184a0001c0002t0002g0185a0001c0002t0002g0186others(1): Show | 4 | HG01081.hp1 HG01106.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-219G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285813 | ||||||
chr2:44285831
|
C | T | 2 | a0001c0002t0002g0240a0001c0002t0002g0241 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.766-201C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285831 | ||||||
chr2:44285832
|
G | A | 212 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(209): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.766-200G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285832 | ||||||
chr2:44285948
|
G | A | 2 | a0001c0003t0012g0285a0001c0003t0013g0286 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.766-84G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285948 | ||||||
chr2:44285953
|
G | T | 1 | a0001c0002t0002g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.766-79G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285953 | ||||||
chr2:44285996
|
A | G | 3 | a0001c0003t0001g0009a0001c0003t0001g0039a0001c0003t0001g0146 | 4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-36A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 3/9 | chr2 | 44285996 | ||||||
chr2:44286497
|
ACGGTGCC others(17): Show |
A | 5 | a0001c0002t0002g0237a0001c0003t0001g0006a0001c0003t0001g0154others(2): Show | 7 | HG01106.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+418_891+441del others(24): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286497 | |||||
chr2:44286497
|
ACGGTGCC others(41): Show |
A | 156 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(153): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.891+394_891+441del others(48): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286497 | |||||
chr2:44286536
|
GTGAGCTG others(87): Show |
G | 1 | a0002c0001t0001g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.891+390_891+483del others(94): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286536 | |||||
chr2:44286551
|
C | T | 4 | a0002c0001t0001g0017a0002c0001t0001g0147a0002c0001t0001g0303others(1): Show | 5 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+394C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286551 | ||||||
chr2:44286551
|
CCTGTGAC others(41): Show |
C | 4 | a0001c0003t0004g0015a0001c0003t0004g0277a0001c0003t0004g0294others(1): Show | 4 | HG02109.hp1 HG02451.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+418_891+465del others(48): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286551 | |||||
chr2:44286575
|
C | T | 15 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(12): Show | 16 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+418C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286575 | ||||||
chr2:44286575
|
CCTGTGAC others(17): Show |
C | 5 | a0001c0003t0004g0057a0001c0003t0004g0291a0001c0003t0004g0292others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+450_891+473del others(24): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286575 | |||||
chr2:44286575
|
CCTGTGAC others(63): Show |
C | 1 | a0001c0003t0011g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.891+466_891+535del others(70): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286575 | |||||
chr2:44286582
|
CGG | C | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+426_891+427del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286582 | ||||||
chr2:44286584
|
GTGAGCTG others(39): Show |
G | 1 | a0002c0001t0001g0147 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.891+438_891+483del others(46): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286584 | |||||
chr2:44286591
|
G | GTGCGGTG others(129): Show |
7 | a0001c0003t0004g0281a0001c0003t0004g0283a0001c0003t0004g0284others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+449_891+450ins others(136): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286591 | |||||
chr2:44286595
|
G | A | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+438G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286595 | ||||||
chr2:44286596
|
G | C | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+439G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286596 | ||||||
chr2:44286596
|
G | GTGTCTGT others(15): Show |
4 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0282others(1): Show | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+449_891+450ins others(22): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286596 | |||||
chr2:44286620
|
GTGTCTGT others(15): Show |
G | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+474_891+495del others(22): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44286620 | |||||
chr2:44286623
|
T | C | 7 | a0001c0003t0004g0281a0001c0003t0004g0283a0001c0003t0004g0284others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+466T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286623 | ||||||
chr2:44286630
|
C | CGG | 7 | a0001c0003t0004g0281a0001c0003t0004g0283a0001c0003t0004g0284others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+473_891+474ins others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286630 | ||||||
chr2:44286630
|
C | CGGTGAGC others(109): Show |
4 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0282others(1): Show | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+473_891+474ins others(116): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286630 | ||||||
chr2:44286641
|
A | G | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+484A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286641 | ||||||
chr2:44286642
|
C | G | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+485C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286642 | ||||||
chr2:44286645
|
T | C | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+488T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286645 | ||||||
chr2:44286665
|
G | A | 1 | a0002c0001t0001g0058 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.891+508G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286665 | ||||||
chr2:44286669
|
T | C | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+512T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286669 | ||||||
chr2:44286676
|
CGG | C | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+520_891+521del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286676 | ||||||
chr2:44286693
|
C | T | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+536C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286693 | ||||||
chr2:44286711
|
G | A | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+554G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286711 | ||||||
chr2:44286715
|
T | C | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+558T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286715 | ||||||
chr2:44286733
|
A | G | 14 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(11): Show | 15 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+576A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286733 | ||||||
chr2:44286737
|
C | T | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+580C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286737 | ||||||
chr2:44286744
|
C | CGG | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+587_891+588ins others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286744 | ||||||
chr2:44286759
|
T | C | 3 | a0002c0001t0001g0017a0002c0001t0001g0303a0002c0001t0010g0317 | 4 | HG00642.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+602T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286759 | ||||||
chr2:44286838
|
T | C | 1 | a0001c0002t0002g0188 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.891+681T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286838 | ||||||
chr2:44286937
|
T | G | 1 | a0002c0001t0001g0148 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.891+780T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44286937 | ||||||
chr2:44287071
|
T | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+914T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287071 | ||||||
chr2:44287132
|
C | G | 3 | a0001c0003t0001g0009a0001c0003t0001g0039a0001c0003t0001g0146 | 4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+975C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287132 | ||||||
chr2:44287299
|
T | C | 13 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(10): Show | 16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+1142T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287299 | ||||||
chr2:44287364
|
G | A | 2 | a0001c0002t0002g0189a0001c0002t0002g0190 | 2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.891+1207G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287364 | ||||||
chr2:44287395
|
G | A | 7 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0026others(4): Show | 10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+1238G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287395 | ||||||
chr2:44287548
|
G | T | 1 | a0002c0001t0001g0102 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.891+1391G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287548 | ||||||
chr2:44287758
|
G | A | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+1601G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287758 | ||||||
chr2:44287896
|
C | G | 1 | a0001c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.891+1739C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287896 | ||||||
chr2:44287929
|
A | G | 10 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+1772A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287929 | ||||||
chr2:44287945
|
C | T | 23 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(20): Show | 23 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.891+1788C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287945 | ||||||
chr2:44287946
|
A | G | 5 | a0001c0003t0006g0267a0001c0003t0006g0289a0001c0003t0012g0285others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1789A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44287946 | ||||||
chr2:44288032
|
CT | C | 12 | a0001c0002t0002g0163a0001c0003t0001g0039a0001c0003t0004g0015others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.891+1890delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44288032 | |||||
chr2:44288118
|
C | T | 88 | a0001c0003t0002g0088a0001c0003t0002g0107a0001c0003t0002g0113others(85): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.891+1961C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288118 | ||||||
chr2:44288241
|
G | C | 1 | a0001c0003t0003g0321 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.891+2084G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288241 | ||||||
chr2:44288399
|
C | T | 3 | a0001c0003t0003g0278a0001c0003t0003g0288a0001c0003t0003g0322 | 3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2242C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288399 | ||||||
chr2:44288440
|
C | T | 3 | a0002c0001t0001g0147a0002c0001t0001g0149a0002c0001t0001g0150 | 3 | HG03017.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.891+2283C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288440 | ||||||
chr2:44288472
|
T | C | 1 | a0001c0003t0001g0010 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.891+2315T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288472 | ||||||
chr2:44288517
|
T | A | 3 | a0001c0003t0003g0278a0001c0003t0003g0288a0001c0003t0003g0322 | 3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.891+2360T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288517 | ||||||
chr2:44288529
|
C | T | 23 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(20): Show | 23 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.891+2372C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288529 | ||||||
chr2:44288680
|
A | G | 1 | a0001c0002t0002g0236 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.891+2523A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288680 | ||||||
chr2:44288712
|
C | T | 8 | a0002c0001t0001g0269a0002c0001t0001g0270a0002c0001t0001g0271others(5): Show | 8 | HG00099.hp1 HG00323.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+2555C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288712 | ||||||
chr2:44288861
|
G | T | 1 | a0001c0002t0002g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.891+2704G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288861 | ||||||
chr2:44288948
|
C | A | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(18): Show | 24 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.891+2791C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288948 | ||||||
chr2:44288949
|
C | A | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(18): Show | 24 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.891+2792C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44288949 | ||||||
chr2:44289021
|
GAT | G | 4 | a0001c0003t0006g0289a0001c0003t0012g0285a0001c0003t0013g0286others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+2865_891+2866d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289021 | ||||||
chr2:44289143
|
A | G | 222 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(219): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.891+2986A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289143 | ||||||
chr2:44289217
|
CT | C | 7 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0026others(4): Show | 10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+3071delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44289217 | |||||
chr2:44289334
|
C | A | 1 | a0002c0001t0001g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.891+3177C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289334 | ||||||
chr2:44289436
|
C | T | 1 | a0001c0003t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.891+3279C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289436 | ||||||
chr2:44289492
|
T | C | 9 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+3335T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289492 | ||||||
chr2:44289627
|
CTATT | C | 11 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(8): Show | 11 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+3480_891+3483d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44289627 | |||||
chr2:44289629
|
A | G | 7 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0026others(4): Show | 10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+3472A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289629 | ||||||
chr2:44289753
|
C | A | 13 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(10): Show | 16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+3596C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289753 | ||||||
chr2:44289777
|
C | T | 2 | a0002c0001t0001g0100a0002c0001t0001g0101 | 2 | HG01069.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.891+3620C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289777 | ||||||
chr2:44289808
|
T | G | 1 | a0001c0002t0002g0013 | 2 | NA18965.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.891+3651T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289808 | ||||||
chr2:44289822
|
C | T | 1 | a0002c0001t0001g0099 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.891+3665C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289822 | ||||||
chr2:44289858
|
T | G | 1 | a0001c0002t0002g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.891+3701T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289858 | ||||||
chr2:44289895
|
T | A | 1 | a0002c0001t0001g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.891+3738T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289895 | ||||||
chr2:44289897
|
C | G | 1 | a0002c0001t0001g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.891+3740C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289897 | ||||||
chr2:44289933
|
A | C | 174 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(171): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.891+3776A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44289933 | ||||||
chr2:44289941
|
A | AT | 16 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(13): Show | 16 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+3791dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44289941 | |||||
chr2:44290009
|
A | G | 25 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(22): Show | 25 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.891+3852A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290009 | ||||||
chr2:44290051
|
T | A | 20 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(17): Show | 23 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.891+3894T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290051 | ||||||
chr2:44290115
|
C | T | 2 | a0002c0001t0001g0141a0002c0001t0001g0142 | 2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.891+3958C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290115 | ||||||
chr2:44290123
|
C | CT | 163 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(160): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.891+3983dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290123 | |||||
chr2:44290123
|
C | CTT | 14 | a0001c0002t0001g0174a0001c0003t0001g0252a0001c0003t0004g0298others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.891+3982_891+3983d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290123 | |||||
chr2:44290123
|
CT | C | 31 | a0001c0002t0002g0163a0001c0002t0002g0193a0001c0003t0001g0009others(28): Show | 34 | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.891+3983delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290123 | |||||
chr2:44290337
|
T | G | 11 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(8): Show | 11 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+4180T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290337 | ||||||
chr2:44290420
|
G | A | 2 | a0001c0003t0003g0278a0001c0003t0003g0322 | 2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891+4263G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290420 | ||||||
chr2:44290523
|
T | C | 173 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(170): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.891+4366T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290523 | ||||||
chr2:44290583
|
G | A | 6 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(3): Show | 7 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+4426G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290583 | ||||||
chr2:44290613
|
G | A | 162 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(159): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.891+4456G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290613 | ||||||
chr2:44290620
|
T | C | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+4463T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290620 | ||||||
chr2:44290683
|
C | CT | 213 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(210): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.891+4539dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290683 | |||||
chr2:44290683
|
C | CTT | 15 | a0001c0002t0001g0174a0001c0003t0003g0278a0001c0003t0003g0322others(12): Show | 15 | HG00738.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.891+4538_891+4539d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44290683 | |||||
chr2:44290700
|
G | A | 216 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.891+4543G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44290700 | ||||||
chr2:44291199
|
G | C | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+5042G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291199 | ||||||
chr2:44291420
|
G | A | 17 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.891+5263G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291420 | ||||||
chr2:44291438
|
A | T | 1 | a0001c0002t0002g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.891+5281A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291438 | ||||||
chr2:44291439
|
T | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+5282T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291439 | ||||||
chr2:44291495
|
C | G | 1 | a0002c0001t0001g0022 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.891+5338C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291495 | ||||||
chr2:44291613
|
G | T | 8 | a0001c0003t0003g0316a0002c0001t0001g0037a0002c0001t0001g0089others(5): Show | 8 | HG00280.hp2 HG02280.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.891+5456G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291613 | ||||||
chr2:44291647
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.891+5490C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291647 | ||||||
chr2:44291661
|
G | T | 1 | a0002c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.891+5504G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291661 | ||||||
chr2:44291719
|
G | A | 1 | a0001c0003t0003g0302 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.891+5562G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291719 | ||||||
chr2:44291910
|
G | A | 7 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0026others(4): Show | 10 | HG01106.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+5753G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291910 | ||||||
chr2:44291934
|
T | C | 1 | a0001c0003t0003g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.891+5777T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44291934 | ||||||
chr2:44292003
|
A | G | 188 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(185): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.891+5846A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292003 | ||||||
chr2:44292151
|
C | T | 11 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(8): Show | 11 | HG00738.hp2 HG00741.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+5994C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292151 | ||||||
chr2:44292174
|
C | G | 1 | a0001c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+6017C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292174 | ||||||
chr2:44292205
|
A | C | 1 | a0001c0003t0004g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.891+6048A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292205 | ||||||
chr2:44292392
|
C | T | 1 | a0001c0002t0002g0231 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.891+6235C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292392 | ||||||
chr2:44292405
|
C | G | 13 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0011others(10): Show | 16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+6248C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292405 | ||||||
chr2:44292424
|
A | C | 1 | a0001c0002t0002g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.891+6267A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292424 | ||||||
chr2:44292475
|
G | T | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+6318G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292475 | ||||||
chr2:44292526
|
G | C | 1 | a0001c0002t0003g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.891+6369G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292526 | ||||||
chr2:44292551
|
C | T | 1 | a0002c0004t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.891+6394C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292551 | ||||||
chr2:44292574
|
C | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+6417C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292574 | ||||||
chr2:44292630
|
T | C | 3 | a0002c0001t0001g0147a0002c0001t0001g0149a0002c0001t0001g0150 | 3 | HG03017.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.891+6473T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44292630 | ||||||
chr2:44292766
|
GATAT | G | 10 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+6613_891+6616d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44292766 | |||||
chr2:44293146
|
G | C | 1 | a0002c0016t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.892-6825G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293146 | ||||||
chr2:44293362
|
C | G | 1 | a0002c0001t0001g0275 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.892-6609C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293362 | ||||||
chr2:44293444
|
G | A | 1 | a0001c0003t0003g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.892-6527G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293444 | ||||||
chr2:44293517
|
AG | A | 167 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(164): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.892-6448delG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44293517 | |||||
chr2:44293523
|
G | A | 54 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(51): Show | 59 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.892-6448G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293523 | ||||||
chr2:44293523
|
GA | G | 3 | a0001c0003t0001g0006a0001c0003t0002g0259a0011c0015t0001g0253 | 5 | HG01106.hp2 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-6438delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44293523 | |||||
chr2:44293525
|
A | G | 1 | a0001c0002t0002g0265 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.892-6446A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293525 | ||||||
chr2:44293547
|
G | A | 1 | a0002c0001t0001g0318 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.892-6424G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293547 | ||||||
chr2:44293577
|
A | G | 199 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(196): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.892-6394A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293577 | ||||||
chr2:44293764
|
G | C | 1 | a0001c0003t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892-6207G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293764 | ||||||
chr2:44293870
|
C | G | 1 | a0002c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.892-6101C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293870 | ||||||
chr2:44293959
|
T | TG | 231 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(228): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.892-6012_892-6011i others(3): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44293959 | ||||||
chr2:44294037
|
C | T | 2 | a0001c0002t0002g0240a0001c0002t0002g0241 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.892-5934C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294037 | ||||||
chr2:44294107
|
A | G | 231 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(228): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.892-5864A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294107 | ||||||
chr2:44294405
|
T | C | 226 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(223): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.892-5566T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294405 | ||||||
chr2:44294469
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.892-5502C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294469 | ||||||
chr2:44294502
|
CA | C | 14 | a0001c0002t0002g0193a0001c0002t0002g0227a0001c0002t0002g0228others(11): Show | 14 | HG00639.hp1 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.892-5451delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44294502 | |||||
chr2:44294625
|
A | G | 1 | a0002c0001t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.892-5346A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294625 | ||||||
chr2:44294959
|
G | T | 3 | a0001c0002t0002g0188a0001c0002t0002g0226a0001c0002t0002g0230 | 3 | NA18944.hp2 NA18946.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.892-5012G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44294959 | ||||||
chr2:44295032
|
C | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4939C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295032 | ||||||
chr2:44295141
|
G | A | 1 | a0002c0001t0001g0038 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-4830G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295141 | ||||||
chr2:44295186
|
AACTTGCT others(12): Show |
A | 1 | a0001c0003t0003g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.892-4776_892-4758d others(21): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44295186 | |||||
chr2:44295261
|
G | A | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4710G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295261 | ||||||
chr2:44295421
|
G | C | 1 | a0001c0002t0002g0194 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.892-4550G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295421 | ||||||
chr2:44295485
|
T | G | 1 | a0001c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.892-4486T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295485 | ||||||
chr2:44295602
|
A | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4369A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295602 | ||||||
chr2:44295614
|
C | T | 1 | a0002c0001t0001g0106 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.892-4357C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295614 | ||||||
chr2:44295666
|
C | T | 1 | a0001c0003t0004g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892-4305C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295666 | ||||||
chr2:44295683
|
G | A | 3 | a0001c0003t0003g0278a0001c0003t0003g0288a0001c0003t0003g0322 | 3 | HG00738.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.892-4288G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295683 | ||||||
chr2:44295689
|
T | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-4282T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295689 | ||||||
chr2:44295877
|
CTT | C | 3 | a0002c0001t0001g0032a0002c0001t0001g0124a0002c0001t0001g0125 | 3 | NA18948.hp1 NA18967.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.892-4091_892-4090d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44295877 | |||||
chr2:44295920
|
G | A | 1 | a0001c0003t0003g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.892-4051G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44295920 | ||||||
chr2:44296497
|
A | G | 3 | a0002c0001t0001g0110a0002c0001t0001g0111a0002c0001t0001g0112 | 3 | NA18999.hp2 NA19057.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.892-3474A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296497 | ||||||
chr2:44296769
|
A | T | 2 | a0001c0002t0002g0187a0002c0001t0001g0070 | 2 | HG01106.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.892-3202A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296769 | ||||||
chr2:44296789
|
C | T | 1 | a0001c0003t0004g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892-3182C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296789 | ||||||
chr2:44296832
|
G | T | 1 | a0001c0002t0002g0225 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.892-3139G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296832 | ||||||
chr2:44296922
|
C | T | 1 | a0001c0003t0004g0292 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.892-3049C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296922 | ||||||
chr2:44296925
|
G | A | 131 | a0001c0002t0002g0187a0001c0003t0001g0008a0001c0003t0001g0035others(128): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.892-3046G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296925 | ||||||
chr2:44296951
|
G | A | 1 | a0002c0001t0001g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.892-3020G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296951 | ||||||
chr2:44296953
|
C | T | 1 | a0001c0003t0003g0312 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.892-3018C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44296953 | ||||||
chr2:44297040
|
C | A | 1 | a0002c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.892-2931C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297040 | ||||||
chr2:44297130
|
G | A | 1 | a0004c0006t0001g0049 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.892-2841G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297130 | ||||||
chr2:44297244
|
C | T | 1 | a0001c0002t0002g0236 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.892-2727C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297244 | ||||||
chr2:44297436
|
T | C | 168 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(165): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.892-2535T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297436 | ||||||
chr2:44297491
|
T | A | 10 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892-2480T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297491 | ||||||
chr2:44297513
|
T | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-2458T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297513 | ||||||
chr2:44297626
|
C | T | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG02886.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-2345C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297626 | ||||||
chr2:44297636
|
G | A | 1 | a0002c0001t0001g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.892-2335G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297636 | ||||||
chr2:44297637
|
G | A | 1 | a0002c0001t0001g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.892-2334G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297637 | ||||||
chr2:44297652
|
C | T | 1 | a0001c0002t0002g0224 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.892-2319C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297652 | ||||||
chr2:44297723
|
G | A | 1 | a0002c0001t0001g0148 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.892-2248G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297723 | ||||||
chr2:44297758
|
C | T | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-2213C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297758 | ||||||
chr2:44297760
|
C | A | 2 | a0001c0003t0001g0008a0001c0003t0001g0035 | 3 | HG01346.hp1 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.892-2211C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297760 | ||||||
chr2:44297797
|
T | A | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-2174T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297797 | ||||||
chr2:44297806
|
C | T | 8 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(5): Show | 9 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-2165C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297806 | ||||||
chr2:44297808
|
G | A | 1 | a0001c0003t0004g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.892-2163G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297808 | ||||||
chr2:44297842
|
C | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-2129C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297842 | ||||||
chr2:44297861
|
T | C | 1 | a0001c0003t0003g0278 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.892-2110T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44297861 | ||||||
chr2:44298095
|
T | C | 1 | a0001c0003t0001g0255 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.892-1876T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298095 | ||||||
chr2:44298100
|
G | C | 1 | a0001c0003t0003g0306 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.892-1871G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298100 | ||||||
chr2:44298159
|
AC | A | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-1811delC | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298159 | ||||||
chr2:44298176
|
C | T | 1 | a0001c0003t0003g0278 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.892-1795C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298176 | ||||||
chr2:44298184
|
C | G | 4 | a0002c0001t0001g0138a0002c0001t0001g0155a0002c0001t0001g0156others(1): Show | 4 | HG02056.hp1 HG02071.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-1787C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298184 | ||||||
chr2:44298187
|
TA | T | 211 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(208): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.892-1776delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44298187 | |||||
chr2:44298216
|
T | C | 2 | a0001c0003t0003g0278a0001c0003t0003g0322 | 2 | HG00738.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.892-1755T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298216 | ||||||
chr2:44298239
|
G | A | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.892-1732G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298239 | ||||||
chr2:44298259
|
C | G | 1 | a0001c0002t0002g0229 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.892-1712C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298259 | ||||||
chr2:44298345
|
C | T | 4 | a0002c0001t0001g0318a0002c0001t0001g0319a0002c0001t0010g0317others(1): Show | 4 | HG01192.hp2 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-1626C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298345 | ||||||
chr2:44298370
|
A | G | 3 | a0002c0001t0001g0147a0002c0001t0001g0149a0002c0001t0001g0150 | 3 | HG03017.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.892-1601A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298370 | ||||||
chr2:44298384
|
C | CT | 42 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(39): Show | 45 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.892-1578dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44298384 | |||||
chr2:44298501
|
C | T | 1 | a0002c0016t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.892-1470C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298501 | ||||||
chr2:44298526
|
T | C | 22 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(19): Show | 24 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.892-1445T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298526 | ||||||
chr2:44298665
|
G | A | 35 | a0001c0002t0002g0003a0001c0002t0002g0013a0001c0002t0002g0014others(32): Show | 41 | HG00438.hp2 HG00733.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.892-1306G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298665 | ||||||
chr2:44298871
|
G | A | 170 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(167): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.892-1100G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44298871 | ||||||
chr2:44299031
|
C | CT | 30 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(27): Show | 33 | HG00621.hp2 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.892-918dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | |||||
chr2:44299031
|
CT | C | 143 | a0001c0002t0002g0177a0001c0002t0002g0187a0001c0002t0002g0196others(140): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.892-918delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | |||||
chr2:44299031
|
CTT | C | 21 | a0001c0003t0003g0020a0001c0003t0003g0322a0001c0003t0004g0300others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.892-919_892-918del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | |||||
chr2:44299031
|
CTTTTTTT | C | 12 | a0001c0002t0001g0180a0001c0002t0002g0013a0001c0002t0002g0014others(9): Show | 14 | HG02040.hp1 HG02040.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.892-924_892-918del others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299031 | |||||
chr2:44299032
|
T | C | 1 | a0001c0002t0002g0225 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.892-939T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299032 | ||||||
chr2:44299033
|
T | C | 1 | a0001c0002t0002g0210 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.892-938T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299033 | ||||||
chr2:44299052
|
TTA | T | 10 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892-918_892-917del others(2): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299052 | ||||||
chr2:44299145
|
T | TCACCTG | 3 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168 | 3 | HG00738.hp2 HG00741.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892-825_892-824ins others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 44299145 | |||||
chr2:44299197
|
C | T | 20 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(17): Show | 22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-774C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299197 | ||||||
chr2:44299392
|
T | C | 35 | a0001c0002t0002g0003a0001c0002t0002g0013a0001c0002t0002g0014others(32): Show | 41 | HG00438.hp2 HG00733.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.892-579T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299392 | ||||||
chr2:44299405
|
G | A | 5 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(2): Show | 6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-566G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299405 | ||||||
chr2:44299411
|
A | G | 1 | a0002c0001t0001g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.892-560A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299411 | ||||||
chr2:44299479
|
C | A | 1 | a0001c0003t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.892-492C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299479 | ||||||
chr2:44299582
|
T | C | 3 | a0001c0002t0002g0159a0001c0002t0002g0213a0001c0002t0002g0227 | 3 | NA18947.hp2 NA18960.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.892-389T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299582 | ||||||
chr2:44299954
|
T | G | 2 | a0001c0003t0003g0313a0001c0003t0003g0314 | 2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.892-17T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299954 | ||||||
chr2:44299965
|
C | G | 1 | a0002c0016t0001g0160 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.892-6C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 4/9 | chr2 | 44299965 | ||||||
chr2:44300282
|
T | A | 10 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1011+192T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300282 | ||||||
chr2:44300293
|
C | T | 17 | a0001c0002t0003g0016a0001c0002t0003g0260a0001c0002t0003g0261others(14): Show | 19 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1011+203C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300293 | ||||||
chr2:44300525
|
C | A | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1011+435C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300525 | ||||||
chr2:44300562
|
C | T | 1 | a0001c0003t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012-441C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300562 | ||||||
chr2:44300716
|
A | T | 1 | a0001c0003t0001g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1012-287A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300716 | ||||||
chr2:44300960
|
A | T | 1 | a0002c0001t0001g0058 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1012-43A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300960 | ||||||
chr2:44300972
|
G | A | 4 | a0001c0002t0002g0163a0001c0003t0004g0057a0001c0003t0004g0291others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012-31G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300972 | ||||||
chr2:44300980
|
C | T | 1 | a0001c0003t0003g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1012-23C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 5/9 | chr2 | 44300980 | ||||||
chr2:44301128
|
GT | G | 40 | a0001c0002t0002g0163a0001c0002t0003g0016a0001c0002t0003g0183others(37): Show | 42 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.1136+3delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301128 | |||||
chr2:44301432
|
T | A | 15 | a0001c0002t0001g0164a0001c0002t0001g0174a0001c0003t0001g0009others(12): Show | 18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136+305T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301432 | ||||||
chr2:44301463
|
G | A | 10 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+336G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301463 | ||||||
chr2:44301542
|
C | G | 17 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(14): Show | 17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136+415C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301542 | ||||||
chr2:44301547
|
T | A | 2 | a0002c0001t0005g0067a0002c0001t0005g0068 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1136+420T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301547 | ||||||
chr2:44301558
|
G | A | 9 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+431G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301558 | ||||||
chr2:44301693
|
T | G | 1 | a0011c0015t0001g0253 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1136+566T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301693 | ||||||
chr2:44301738
|
C | CA | 41 | a0001c0002t0002g0163a0001c0002t0002g0184a0001c0003t0001g0007others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1136+629dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301738 | |||||
chr2:44301738
|
C | CAA | 158 | a0001c0002t0001g0164a0001c0002t0001g0173a0001c0002t0001g0180others(155): Show | 174 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1136+628_1136+629d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301738 | |||||
chr2:44301738
|
C | CAAA | 10 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(7): Show | 10 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1136+627_1136+629d others(5): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301738 | |||||
chr2:44301783
|
C | G | 279 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(276): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1136+656C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301783 | ||||||
chr2:44301798
|
T | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1136+671T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301798 | ||||||
chr2:44301895
|
A | ACT | 3 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0254 | 3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1136+769_1136+770d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44301895 | |||||
chr2:44301978
|
C | T | 1 | a0002c0001t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1136+851C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44301978 | ||||||
chr2:44302013
|
C | G | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+886C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302013 | ||||||
chr2:44302104
|
ATT | A | 17 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(14): Show | 17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136+978_1136+979d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302104 | ||||||
chr2:44302115
|
A | G | 1 | a0001c0002t0001g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1136+988A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302115 | ||||||
chr2:44302234
|
C | T | 1 | a0001c0002t0002g0212 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1136+1107C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302234 | ||||||
chr2:44302285
|
A | G | 2 | a0001c0003t0001g0287a0001c0018t0003g0033 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1136+1158A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302285 | ||||||
chr2:44302289
|
C | T | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+1162C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302289 | ||||||
chr2:44302290
|
C | T | 1 | a0001c0002t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1136+1163C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302290 | ||||||
chr2:44302309
|
GATTAA | G | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+1187_1136+119 others(9): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44302309 | |||||
chr2:44302367
|
A | G | 1 | a0001c0002t0002g0182 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1136+1240A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302367 | ||||||
chr2:44302454
|
C | T | 1 | a0001c0003t0002g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1136+1327C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302454 | ||||||
chr2:44302566
|
A | G | 11 | a0001c0002t0002g0163a0001c0003t0004g0015a0001c0003t0004g0057others(8): Show | 11 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1136+1439A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302566 | ||||||
chr2:44302576
|
C | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136+1449C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302576 | ||||||
chr2:44302583
|
C | T | 7 | a0001c0002t0009g0175a0001c0003t0001g0047a0001c0003t0006g0267others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1136+1456C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302583 | ||||||
chr2:44302650
|
T | C | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-1493T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302650 | ||||||
chr2:44302674
|
A | G | 1 | a0001c0002t0003g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1137-1469A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302674 | ||||||
chr2:44302701
|
A | G | 1 | a0001c0002t0003g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1137-1442A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302701 | ||||||
chr2:44302731
|
G | A | 1 | a0002c0001t0001g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1137-1412G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302731 | ||||||
chr2:44302775
|
A | C | 5 | a0001c0003t0004g0015a0001c0003t0004g0277a0001c0003t0004g0290others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-1368A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302775 | ||||||
chr2:44302822
|
A | C | 1 | a0001c0002t0002g0232 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1137-1321A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302822 | ||||||
chr2:44302834
|
G | A | 17 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(14): Show | 17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1137-1309G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302834 | ||||||
chr2:44302889
|
G | A | 1 | a0001c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1137-1254G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302889 | ||||||
chr2:44302918
|
GCTTGGTG others(14): Show |
G | 1 | a0001c0002t0002g0223 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1137-1224_1137-120 others(25): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302918 | ||||||
chr2:44302945
|
T | A | 20 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(17): Show | 22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1137-1198T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44302945 | ||||||
chr2:44303062
|
G | A | 1 | a0004c0006t0001g0051 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1137-1081G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303062 | ||||||
chr2:44303093
|
C | T | 1 | a0001c0002t0009g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1137-1050C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303093 | ||||||
chr2:44303128
|
G | T | 1 | a0002c0001t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1137-1015G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303128 | ||||||
chr2:44303181
|
ATAAGAG | A | 20 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(17): Show | 22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1137-958_1137-953d others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303181 | |||||
chr2:44303245
|
A | AT | 45 | a0001c0002t0002g0196a0001c0002t0002g0207a0001c0002t0002g0208others(42): Show | 47 | HG00280.hp1 HG01069.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1137-881dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303245 | |||||
chr2:44303245
|
A | ATT | 154 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(151): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1137-882_1137-881d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303245 | |||||
chr2:44303245
|
AT | A | 9 | a0001c0002t0002g0178a0001c0002t0002g0185a0001c0002t0002g0198others(6): Show | 9 | HG01167.hp2 HG01975.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-881delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303245 | |||||
chr2:44303269
|
A | C | 1 | a0001c0003t0003g0304 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1137-874A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303269 | ||||||
chr2:44303284
|
C | T | 190 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(187): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1137-859C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303284 | ||||||
chr2:44303466
|
A | T | 29 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(26): Show | 31 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1137-677A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303466 | ||||||
chr2:44303484
|
G | A | 17 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(14): Show | 17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1137-659G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303484 | ||||||
chr2:44303489
|
G | T | 2 | a0001c0002t0002g0205a0001c0002t0002g0206 | 2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1137-654G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303489 | ||||||
chr2:44303542
|
ATG | A | 9 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1137-597_1137-596d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303542 | |||||
chr2:44303559
|
T | TG | 20 | a0001c0002t0002g0012a0001c0002t0002g0178a0001c0002t0003g0234others(17): Show | 21 | HG00639.hp1 HG00741.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1137-576dupG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303559 | |||||
chr2:44303559
|
TG | T | 210 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(207): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1137-576delG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 44303559 | |||||
chr2:44303622
|
G | A | 2 | a0001c0002t0002g0210a0001c0002t0002g0225 | 2 | NA18959.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.1137-521G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303622 | ||||||
chr2:44303688
|
G | A | 3 | a0001c0003t0004g0057a0001c0003t0004g0291a0001c0003t0004g0295 | 3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1137-455G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303688 | ||||||
chr2:44303755
|
G | A | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-388G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303755 | ||||||
chr2:44303790
|
C | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1137-353C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303790 | ||||||
chr2:44303801
|
A | T | 15 | a0001c0002t0001g0164a0001c0002t0001g0174a0001c0003t0001g0009others(12): Show | 18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-342A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303801 | ||||||
chr2:44303809
|
C | T | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-334C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303809 | ||||||
chr2:44303826
|
C | T | 19 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(16): Show | 21 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1137-317C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303826 | ||||||
chr2:44303942
|
G | T | 128 | a0001c0003t0002g0113a0002c0001t0001g0002a0002c0001t0001g0004others(125): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1137-201G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44303942 | ||||||
chr2:44304075
|
C | A | 1 | a0001c0002t0002g0223 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1137-68C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 6/9 | chr2 | 44304075 | ||||||
chr2:44304345
|
C | T | 169 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(166): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
splice_region_variant&intron_variant | LOW | c.1332+7C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304345 | ||||||
chr2:44304360
|
G | T | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1332+22G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304360 | ||||||
chr2:44304494
|
G | C | 1 | a0002c0001t0010g0317 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1332+156G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304494 | ||||||
chr2:44304496
|
T | C | 35 | a0001c0002t0002g0003a0001c0002t0002g0013a0001c0002t0002g0014others(32): Show | 41 | HG00438.hp2 HG00733.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1332+158T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304496 | ||||||
chr2:44304564
|
C | T | 4 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0108others(1): Show | 4 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+226C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304564 | ||||||
chr2:44304768
|
C | T | 5 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(2): Show | 6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332+430C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304768 | ||||||
chr2:44304813
|
A | AT | 78 | a0001c0002t0002g0012a0001c0002t0002g0163a0001c0002t0002g0176others(75): Show | 81 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1332+502dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
A | ATT | 75 | a0001c0002t0002g0222a0001c0003t0001g0154a0001c0003t0001g0268others(72): Show | 83 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1332+501_1332+502d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
A | ATTT | 20 | a0001c0003t0001g0287a0001c0003t0003g0306a0001c0003t0006g0267others(17): Show | 20 | HG00323.hp1 HG00642.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1332+500_1332+502d others(5): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
AT | A | 37 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(34): Show | 42 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1332+502delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
ATT | A | 11 | a0001c0002t0001g0174a0001c0002t0003g0016a0001c0002t0003g0183others(8): Show | 12 | HG00280.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1332+501_1332+502d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
ATTTT | A | 11 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(8): Show | 12 | HG01109.hp2 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332+499_1332+502d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
ATTTTTTT | A | 6 | a0001c0002t0002g0003a0001c0002t0002g0193a0001c0002t0002g0229others(3): Show | 10 | NA18946.hp2 NA18962.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+496_1332+502d others(9): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304813
|
ATTTTTTT others(6): Show |
A | 1 | a0002c0001t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1332+490_1332+502d others(15): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44304813 | |||||
chr2:44304906
|
C | T | 1 | a0001c0003t0002g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1332+568C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44304906 | ||||||
chr2:44305000
|
T | G | 1 | a0002c0016t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1332+662T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305000 | ||||||
chr2:44305166
|
T | G | 1 | a0001c0003t0003g0316 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1332+828T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305166 | ||||||
chr2:44305187
|
C | T | 25 | a0001c0003t0003g0020a0001c0003t0004g0015a0001c0003t0004g0057others(22): Show | 25 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1332+849C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305187 | ||||||
chr2:44305328
|
T | C | 1 | a0001c0003t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1332+990T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305328 | ||||||
chr2:44305413
|
CCTTT | C | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1332+1080_1332+108 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305413 | |||||
chr2:44305427
|
C | CT | 9 | a0001c0002t0002g0184a0001c0002t0002g0185a0001c0002t0002g0186others(6): Show | 9 | HG01081.hp1 HG01106.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1332+1108dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | |||||
chr2:44305427
|
CT | C | 27 | a0001c0002t0001g0164a0001c0002t0002g0214a0001c0002t0002g0216others(24): Show | 30 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1332+1108delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | |||||
chr2:44305427
|
CTT | C | 177 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1332+1107_1332+110 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | |||||
chr2:44305427
|
CTTT | C | 14 | a0001c0002t0009g0175a0001c0003t0004g0015a0001c0003t0004g0057others(11): Show | 14 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1332+1106_1332+110 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44305427 | |||||
chr2:44305429
|
T | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+1091T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305429 | ||||||
chr2:44305488
|
C | T | 6 | a0001c0003t0003g0020a0001c0018t0003g0033a0002c0001t0001g0019others(3): Show | 6 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332+1150C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305488 | ||||||
chr2:44305699
|
G | A | 15 | a0001c0002t0001g0164a0001c0002t0001g0174a0001c0003t0001g0009others(12): Show | 18 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1332+1361G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305699 | ||||||
chr2:44305711
|
G | C | 1 | a0001c0003t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1332+1373G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305711 | ||||||
chr2:44305808
|
C | G | 1 | a0002c0016t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1332+1470C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305808 | ||||||
chr2:44305907
|
C | T | 1 | a0001c0003t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1332+1569C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305907 | ||||||
chr2:44305985
|
G | C | 3 | a0001c0003t0004g0057a0001c0003t0004g0291a0001c0003t0004g0295 | 3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1332+1647G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44305985 | ||||||
chr2:44306071
|
T | G | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+1733T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306071 | ||||||
chr2:44306140
|
G | T | 10 | a0001c0002t0001g0174a0001c0003t0004g0015a0001c0003t0004g0277others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+1802G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306140 | ||||||
chr2:44306205
|
T | C | 1 | a0001c0003t0004g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1332+1867T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306205 | ||||||
chr2:44306258
|
G | A | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+1920G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306258 | ||||||
chr2:44306524
|
C | T | 10 | a0001c0003t0002g0259a0001c0003t0004g0015a0001c0003t0004g0057others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+2186C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306524 | ||||||
chr2:44306550
|
C | CT | 46 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(43): Show | 52 | HG00323.hp2 HG00438.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1332+2234dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | |||||
chr2:44306550
|
C | T | 1 | a0001c0002t0002g0229 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1332+2212C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306550 | ||||||
chr2:44306550
|
CT | C | 144 | a0001c0002t0001g0180a0001c0002t0002g0228a0001c0002t0009g0175others(141): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1332+2234delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | |||||
chr2:44306550
|
CTT | C | 8 | a0001c0002t0001g0174a0001c0003t0001g0287a0001c0003t0003g0020others(5): Show | 8 | HG02257.hp2 HG02970.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332+2233_1332+223 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | |||||
chr2:44306550
|
CTTT | C | 23 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(20): Show | 23 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1332+2232_1332+223 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44306550 | |||||
chr2:44306586
|
G | C | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+2248G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306586 | ||||||
chr2:44306594
|
C | T | 10 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+2256C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306594 | ||||||
chr2:44306807
|
T | C | 14 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(11): Show | 16 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332+2469T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306807 | ||||||
chr2:44306858
|
A | C | 1 | a0001c0002t0001g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1332+2520A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306858 | ||||||
chr2:44306873
|
A | C | 133 | a0001c0003t0002g0113a0002c0001t0001g0002a0002c0001t0001g0004others(130): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1332+2535A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44306873 | ||||||
chr2:44307021
|
G | C | 2 | a0002c0001t0001g0094a0002c0001t0001g0095 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1332+2683G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307021 | ||||||
chr2:44307048
|
C | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332+2710C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307048 | ||||||
chr2:44307128
|
C | T | 1 | a0001c0003t0001g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1332+2790C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307128 | ||||||
chr2:44307182
|
C | A | 91 | a0001c0003t0002g0113a0002c0001t0001g0002a0002c0001t0001g0004others(88): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1332+2844C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307182 | ||||||
chr2:44307220
|
C | A | 26 | a0001c0003t0003g0020a0001c0003t0004g0015a0001c0003t0004g0057others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1332+2882C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307220 | ||||||
chr2:44307275
|
T | C | 8 | a0001c0002t0001g0180a0001c0003t0001g0006a0001c0003t0001g0249others(5): Show | 10 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+2937T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307275 | ||||||
chr2:44307278
|
C | T | 234 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(231): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1332+2940C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307278 | ||||||
chr2:44307333
|
A | C | 184 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(181): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1332+2995A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307333 | ||||||
chr2:44307363
|
T | C | 4 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0108others(1): Show | 4 | HG02970.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+3025T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307363 | ||||||
chr2:44307425
|
C | A | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1332+3087C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307425 | ||||||
chr2:44307564
|
AT | A | 168 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(165): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1332+3243delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44307564 | |||||
chr2:44307564
|
ATT | A | 18 | a0001c0003t0001g0044a0001c0003t0001g0287a0001c0003t0003g0020others(15): Show | 18 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1332+3242_1332+324 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44307564 | |||||
chr2:44307895
|
T | C | 10 | a0001c0003t0004g0280a0001c0003t0004g0281a0001c0003t0004g0282others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1332+3557T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44307895 | ||||||
chr2:44308139
|
A | G | 1 | a0001c0003t0003g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1332+3801A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308139 | ||||||
chr2:44308149
|
C | G | 2 | a0001c0003t0001g0043a0001c0003t0001g0045 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1332+3811C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308149 | ||||||
chr2:44308208
|
A | G | 4 | a0001c0003t0001g0066a0001c0003t0001g0251a0001c0003t0001g0252others(1): Show | 4 | HG03130.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+3870A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308208 | ||||||
chr2:44308274
|
G | A | 1 | a0002c0001t0001g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1332+3936G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308274 | ||||||
chr2:44308315
|
T | A | 1 | a0001c0003t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1332+3977T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308315 | ||||||
chr2:44308380
|
G | C | 87 | a0001c0003t0002g0113a0002c0001t0001g0002a0002c0001t0001g0004others(84): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1332+4042G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308380 | ||||||
chr2:44308547
|
G | A | 216 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1333-4039G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308547 | ||||||
chr2:44308555
|
C | T | 8 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(5): Show | 9 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1333-4031C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308555 | ||||||
chr2:44308573
|
T | C | 1 | a0001c0003t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1333-4013T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308573 | ||||||
chr2:44308599
|
G | T | 25 | a0001c0003t0003g0020a0001c0003t0004g0015a0001c0003t0004g0057others(22): Show | 25 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1333-3987G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308599 | ||||||
chr2:44308732
|
A | AT | 7 | a0001c0002t0002g0223a0001c0002t0003g0016a0001c0002t0003g0183others(4): Show | 8 | HG00280.hp1 HG01070.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333-3841dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44308732 | |||||
chr2:44308798
|
TCTCAG | T | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333-3783_1333-377 others(9): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44308798 | |||||
chr2:44308819
|
G | A | 24 | a0001c0003t0003g0020a0001c0003t0004g0015a0001c0003t0004g0057others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1333-3767G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308819 | ||||||
chr2:44308836
|
C | T | 3 | a0002c0001t0001g0019a0002c0001t0001g0021a0002c0001t0001g0023 | 3 | HG04115.hp2 HG04199.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1333-3750C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308836 | ||||||
chr2:44308845
|
G | C | 1 | a0001c0002t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1333-3741G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308845 | ||||||
chr2:44308922
|
C | T | 1 | a0001c0003t0002g0088 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1333-3664C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308922 | ||||||
chr2:44308933
|
C | T | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1333-3653C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44308933 | ||||||
chr2:44309110
|
A | G | 142 | a0001c0003t0001g0008a0001c0003t0001g0035a0001c0003t0001g0066others(139): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1333-3476A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309110 | ||||||
chr2:44309223
|
C | A | 15 | a0001c0002t0003g0234a0001c0003t0002g0105a0001c0003t0003g0302others(12): Show | 15 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1333-3363C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309223 | ||||||
chr2:44309233
|
C | G | 5 | a0001c0002t0009g0175a0001c0003t0004g0293a0001c0003t0006g0267others(2): Show | 5 | HG01109.hp2 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-3353C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309233 | ||||||
chr2:44309407
|
T | C | 179 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(176): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1333-3179T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309407 | ||||||
chr2:44309494
|
TG | T | 15 | a0001c0002t0002g0223a0001c0002t0003g0016a0001c0002t0003g0183others(12): Show | 17 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1333-3090delG | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44309494 | |||||
chr2:44309538
|
C | T | 5 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(2): Show | 5 | HG00738.hp2 HG00741.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-3048C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309538 | ||||||
chr2:44309567
|
C | T | 6 | a0001c0002t0009g0175a0001c0003t0004g0293a0001c0003t0006g0267others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-3019C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309567 | ||||||
chr2:44309577
|
G | T | 1 | a0001c0002t0002g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1333-3009G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309577 | ||||||
chr2:44309682
|
C | G | 6 | a0001c0002t0009g0175a0001c0003t0004g0293a0001c0003t0006g0267others(3): Show | 6 | HG01109.hp2 HG01884.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-2904C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309682 | ||||||
chr2:44309721
|
C | G | 1 | a0002c0001t0001g0079 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1333-2865C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309721 | ||||||
chr2:44309789
|
G | T | 17 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(14): Show | 17 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1333-2797G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309789 | ||||||
chr2:44309889
|
T | G | 2 | a0002c0001t0001g0270a0002c0001t0001g0272 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1333-2697T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44309889 | ||||||
chr2:44309897
|
C | CT | 22 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0174others(19): Show | 23 | HG00741.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1333-2680dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44309897 | |||||
chr2:44310162
|
G | A | 2 | a0004c0006t0001g0049a0004c0006t0001g0051 | 2 | NA18969.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1333-2424G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310162 | ||||||
chr2:44310224
|
G | T | 1 | a0009c0012t0001g0082 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1333-2362G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310224 | ||||||
chr2:44310258
|
G | A | 1 | a0002c0001t0001g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1333-2328G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310258 | ||||||
chr2:44310283
|
C | T | 2 | a0001c0003t0003g0305a0001c0003t0003g0310 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1333-2303C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310283 | ||||||
chr2:44310337
|
A | G | 1 | a0002c0001t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1333-2249A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310337 | ||||||
chr2:44310428
|
GTTCT | G | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1333-2150_1333-214 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44310428 | |||||
chr2:44310603
|
G | A | 1 | a0001c0002t0002g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1333-1983G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310603 | ||||||
chr2:44310631
|
G | C | 1 | a0001c0002t0002g0222 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1333-1955G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310631 | ||||||
chr2:44310652
|
C | T | 1 | a0001c0002t0002g0201 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1333-1934C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310652 | ||||||
chr2:44310682
|
G | A | 1 | a0002c0001t0010g0317 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1333-1904G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310682 | ||||||
chr2:44310689
|
G | T | 1 | a0001c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1333-1897G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310689 | ||||||
chr2:44310690
|
C | A | 1 | a0001c0003t0001g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1333-1896C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310690 | ||||||
chr2:44310692
|
A | AT | 10 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(7): Show | 10 | HG01256.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333-1884dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44310692 | |||||
chr2:44310805
|
G | GT | 17 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(14): Show | 19 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1333-1770dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44310805 | |||||
chr2:44310839
|
C | T | 1 | a0002c0001t0001g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1333-1747C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310839 | ||||||
chr2:44310941
|
C | T | 20 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(17): Show | 22 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1333-1645C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44310941 | ||||||
chr2:44311097
|
ATTC | A | 6 | a0001c0002t0009g0175a0001c0003t0004g0293a0001c0003t0006g0267others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-1483_1333-148 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44311097 | |||||
chr2:44311107
|
T | G | 1 | a0001c0017t0007g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1333-1479T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311107 | ||||||
chr2:44311302
|
C | A | 1 | a0002c0001t0001g0075 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1333-1284C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311302 | ||||||
chr2:44311345
|
A | G | 218 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(215): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1333-1241A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311345 | ||||||
chr2:44311394
|
A | G | 1 | a0001c0002t0002g0265 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1333-1192A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311394 | ||||||
chr2:44311594
|
G | A | 3 | a0001c0003t0004g0057a0001c0003t0004g0291a0001c0003t0004g0295 | 3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1333-992G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311594 | ||||||
chr2:44311602
|
A | G | 1 | a0010c0014t0001g0320 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1333-984A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311602 | ||||||
chr2:44311723
|
T | TA | 172 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(169): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1333-850dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44311723 | |||||
chr2:44311723
|
T | TAA | 16 | a0001c0003t0004g0057a0001c0003t0004g0280a0001c0003t0004g0281others(13): Show | 16 | HG00735.hp2 HG01433.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1333-851_1333-850d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44311723 | |||||
chr2:44311723
|
T | TTA | 3 | a0002c0004t0001g0169a0002c0004t0001g0170a0002c0004t0001g0172 | 3 | HG02647.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1333-863_1333-862i others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311723 | ||||||
chr2:44311737
|
C | A | 18 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1333-849C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311737 | ||||||
chr2:44311790
|
G | T | 1 | a0001c0003t0004g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1333-796G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311790 | ||||||
chr2:44311793
|
C | T | 7 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1333-793C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311793 | ||||||
chr2:44311797
|
C | T | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-789C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311797 | ||||||
chr2:44311824
|
G | A | 17 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(14): Show | 19 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1333-762G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311824 | ||||||
chr2:44311870
|
C | T | 214 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(211): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1333-716C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311870 | ||||||
chr2:44311900
|
G | A | 1 | a0002c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1333-686G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311900 | ||||||
chr2:44311902
|
A | G | 177 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(174): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1333-684A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44311902 | ||||||
chr2:44312007
|
G | GATTTAAA others(23): Show |
1 | a0002c0001t0001g0076 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1333-568_1333-539d others(32): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 44312007 | |||||
chr2:44312039
|
T | G | 1 | a0001c0003t0004g0292 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1333-547T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312039 | ||||||
chr2:44312148
|
T | G | 11 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1333-438T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312148 | ||||||
chr2:44312167
|
T | C | 27 | a0001c0002t0002g0003a0001c0002t0002g0013a0001c0002t0002g0014others(24): Show | 33 | HG00438.hp2 HG00733.hp2 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333-419T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312167 | ||||||
chr2:44312279
|
T | G | 1 | a0001c0002t0003g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1333-307T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312279 | ||||||
chr2:44312280
|
G | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1333-306G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312280 | ||||||
chr2:44312361
|
T | C | 1 | a0001c0002t0002g0182 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1333-225T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312361 | ||||||
chr2:44312375
|
C | T | 1 | a0001c0003t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1333-211C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312375 | ||||||
chr2:44312504
|
G | A | 1 | a0001c0003t0002g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1333-82G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312504 | ||||||
chr2:44312564
|
C | G | 2 | a0002c0001t0001g0136a0002c0001t0001g0157 | 2 | NA18985.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1333-22C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312564 | ||||||
chr2:44312574
|
T | A | 1 | a0001c0002t0001g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1333-12T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 7/9 | chr2 | 44312574 | ||||||
chr2:44312774
|
C | CAGCTATA others(8): Show |
10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+21_1500+22ins others(15): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312774 | ||||||
chr2:44312779
|
C | T | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+26C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312779 | ||||||
chr2:44312781
|
T | TACTA | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+28_1500+29ins others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312781 | ||||||
chr2:44312782
|
C | T | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+29C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312782 | ||||||
chr2:44312831
|
A | C | 1 | a0001c0003t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1500+78A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44312831 | ||||||
chr2:44313041
|
G | C | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500+288G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313041 | ||||||
chr2:44313080
|
G | A | 11 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(8): Show | 12 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1500+327G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313080 | ||||||
chr2:44313102
|
C | T | 211 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(208): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1500+349C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313102 | ||||||
chr2:44313261
|
C | T | 1 | a0002c0004t0001g0170 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1500+508C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313261 | ||||||
chr2:44313266
|
G | C | 8 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(5): Show | 9 | HG00280.hp1 HG01070.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1500+513G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313266 | ||||||
chr2:44313293
|
C | T | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1500+540C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313293 | ||||||
chr2:44313316
|
C | A | 1 | a0001c0003t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1501-519C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313316 | ||||||
chr2:44313320
|
G | C | 1 | a0001c0002t0009g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1501-515G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313320 | ||||||
chr2:44313409
|
G | A | 9 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501-426G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313409 | ||||||
chr2:44313442
|
C | T | 5 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0168others(2): Show | 5 | HG00738.hp2 HG00741.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1501-393C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313442 | ||||||
chr2:44313470
|
T | C | 1 | a0001c0002t0001g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1501-365T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313470 | ||||||
chr2:44313598
|
T | C | 1 | a0002c0001t0001g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1501-237T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313598 | ||||||
chr2:44313735
|
G | C | 1 | a0001c0003t0003g0307 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1501-100G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 8/9 | chr2 | 44313735 | ||||||
chr2:44314009
|
G | C | 1 | a0002c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1617+58G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314009 | ||||||
chr2:44314118
|
T | C | 1 | a0001c0003t0001g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1617+167T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314118 | ||||||
chr2:44314203
|
C | G | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+252C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314203 | ||||||
chr2:44314291
|
G | GAGA | 5 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(2): Show | 6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+341_1617+343d others(5): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314291 | |||||
chr2:44314332
|
G | GATCA | 4 | a0002c0001t0001g0138a0002c0001t0001g0155a0002c0001t0001g0156others(1): Show | 4 | HG02056.hp1 HG02071.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617+391_1617+394d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314332 | |||||
chr2:44314373
|
C | T | 11 | a0001c0002t0009g0175a0001c0003t0001g0007a0001c0003t0001g0026others(8): Show | 12 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1617+422C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314373 | ||||||
chr2:44314549
|
A | G | 3 | a0001c0003t0004g0057a0001c0003t0004g0291a0001c0003t0004g0295 | 3 | HG02145.hp2 HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1617+598A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314549 | ||||||
chr2:44314560
|
G | A | 1 | a0001c0002t0002g0233 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1617+609G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314560 | ||||||
chr2:44314567
|
G | C | 217 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(214): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1617+616G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314567 | ||||||
chr2:44314586
|
C | T | 170 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(167): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1617+635C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314586 | ||||||
chr2:44314592
|
C | CCA | 175 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(172): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1617+657_1617+658d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314592 | |||||
chr2:44314592
|
C | CCACA | 3 | a0001c0003t0001g0249a0001c0017t0007g0161a0002c0001t0001g0136 | 3 | HG02055.hp1 HG02922.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1617+655_1617+658d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314592 | |||||
chr2:44314592
|
CCA | C | 30 | a0001c0002t0009g0175a0001c0003t0001g0007a0001c0003t0001g0026others(27): Show | 31 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1617+657_1617+658d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314592 | |||||
chr2:44314612
|
T | A | 5 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(2): Show | 6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+661T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314612 | ||||||
chr2:44314665
|
A | G | 1 | a0001c0003t0013g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1617+714A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314665 | ||||||
chr2:44314718
|
C | G | 16 | a0001c0002t0003g0234a0001c0003t0001g0154a0001c0003t0003g0301others(13): Show | 16 | HG00639.hp1 HG00741.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1617+767C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314718 | ||||||
chr2:44314757
|
T | C | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+806T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314757 | ||||||
chr2:44314778
|
AAT | A | 172 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(169): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1617+834_1617+835d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314778 | |||||
chr2:44314858
|
T | G | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+907T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314858 | ||||||
chr2:44314900
|
G | A | 5 | a0001c0003t0004g0015a0001c0003t0004g0277a0001c0003t0004g0290others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+949G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314900 | ||||||
chr2:44314905
|
T | C | 1 | a0001c0003t0001g0287 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1617+954T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44314905 | ||||||
chr2:44314922
|
A | AT | 178 | a0001c0002t0002g0003a0001c0002t0002g0013a0001c0002t0002g0014others(175): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1617+997dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | |||||
chr2:44314922
|
A | ATT | 46 | a0001c0002t0002g0212a0001c0002t0002g0233a0001c0002t0002g0243others(43): Show | 49 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1617+996_1617+997d others(4): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | |||||
chr2:44314922
|
AT | A | 6 | a0001c0002t0001g0180a0001c0002t0002g0211a0001c0002t0009g0175others(3): Show | 6 | HG01257.hp1 HG02818.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+997delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | |||||
chr2:44314922
|
ATTTTTTT others(5): Show |
A | 17 | a0001c0002t0001g0164a0001c0002t0001g0174a0001c0003t0001g0009others(14): Show | 20 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617+986_1617+997d others(14): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44314922 | |||||
chr2:44315008
|
C | T | 13 | a0001c0002t0001g0164a0001c0003t0001g0009a0001c0003t0001g0010others(10): Show | 16 | HG00642.hp1 HG01099.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1617+1057C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315008 | ||||||
chr2:44315022
|
C | G | 7 | a0001c0002t0001g0180a0001c0003t0001g0006a0001c0003t0001g0249others(4): Show | 9 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1617+1071C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315022 | ||||||
chr2:44315051
|
C | T | 5 | a0001c0003t0001g0007a0001c0003t0001g0026a0001c0003t0001g0027others(2): Show | 6 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+1100C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315051 | ||||||
chr2:44315080
|
C | T | 9 | a0001c0002t0001g0180a0001c0003t0001g0006a0001c0003t0001g0249others(6): Show | 11 | HG01106.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1617+1129C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315080 | ||||||
chr2:44315145
|
G | A | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG02886.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617+1194G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315145 | ||||||
chr2:44315184
|
C | T | 1 | a0001c0002t0002g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1617+1233C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315184 | ||||||
chr2:44315194
|
C | T | 1 | a0001c0003t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1617+1243C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315194 | ||||||
chr2:44315379
|
T | C | 1 | a0002c0001t0001g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1617+1428T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315379 | ||||||
chr2:44315455
|
C | T | 1 | a0001c0003t0003g0315 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1617+1504C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315455 | ||||||
chr2:44315500
|
C | T | 1 | a0001c0002t0002g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1617+1549C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315500 | ||||||
chr2:44315501
|
G | A | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+1550G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315501 | ||||||
chr2:44315503
|
C | CA | 33 | a0001c0002t0002g0159a0001c0002t0002g0184a0001c0002t0002g0185others(30): Show | 33 | HG01081.hp1 HG01106.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1617+1567dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315503 | |||||
chr2:44315503
|
CA | C | 210 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(207): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1617+1567delA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315503 | |||||
chr2:44315509
|
A | G | 1 | a0001c0002t0002g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1617+1558A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315509 | ||||||
chr2:44315598
|
G | C | 1 | a0002c0001t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1617+1647G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315598 | ||||||
chr2:44315653
|
C | CA | 78 | a0001c0002t0001g0166a0001c0002t0001g0168a0001c0002t0001g0174others(75): Show | 82 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1617+1724dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315653 | |||||
chr2:44315653
|
C | CAA | 106 | a0001c0002t0001g0167a0001c0002t0003g0016a0001c0002t0003g0183others(103): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1617+1723_1617+172 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315653 | |||||
chr2:44315653
|
C | CAAA | 13 | a0001c0002t0003g0261a0001c0003t0003g0322a0001c0003t0004g0291others(10): Show | 13 | HG00423.hp1 HG01109.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1617+1722_1617+172 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315653 | |||||
chr2:44315698
|
TAAAACAT others(20): Show |
T | 1 | a0001c0002t0009g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1617+1749_1617+177 others(31): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44315698 | |||||
chr2:44315724
|
T | G | 1 | a0002c0001t0001g0097 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1617+1773T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315724 | ||||||
chr2:44315884
|
G | C | 9 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+1933G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315884 | ||||||
chr2:44315958
|
C | A | 3 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0254 | 3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1617+2007C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315958 | ||||||
chr2:44315986
|
C | G | 216 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1617+2035C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44315986 | ||||||
chr2:44316104
|
G | A | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1617+2153G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316104 | ||||||
chr2:44316164
|
C | G | 10 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+2213C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316164 | ||||||
chr2:44316178
|
C | T | 215 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(212): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1617+2227C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316178 | ||||||
chr2:44316250
|
T | A | 136 | a0001c0003t0001g0008a0001c0003t0001g0035a0001c0003t0003g0321others(133): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1617+2299T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316250 | ||||||
chr2:44316252
|
T | C | 1 | a0001c0003t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1617+2301T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316252 | ||||||
chr2:44316273
|
A | T | 1 | a0001c0003t0004g0281 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1617+2322A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316273 | ||||||
chr2:44316295
|
G | C | 1 | a0001c0002t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1617+2344G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316295 | ||||||
chr2:44316345
|
C | T | 1 | a0001c0003t0006g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1617+2394C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316345 | ||||||
chr2:44316455
|
CAAAG | C | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+2507_1617+251 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44316455 | |||||
chr2:44316851
|
C | T | 1 | a0001c0003t0003g0304 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1617+2900C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316851 | ||||||
chr2:44316880
|
A | G | 1 | a0001c0003t0002g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1617+2929A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316880 | ||||||
chr2:44316885
|
A | G | 1 | a0001c0003t0013g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1617+2934A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316885 | ||||||
chr2:44316900
|
G | T | 1 | a0002c0001t0001g0059 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1617+2949G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316900 | ||||||
chr2:44316902
|
T | C | 1 | a0002c0001t0001g0059 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1617+2951T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316902 | ||||||
chr2:44316976
|
T | A | 24 | a0001c0002t0002g0159a0001c0002t0002g0184a0001c0002t0002g0185others(21): Show | 24 | HG01081.hp1 HG01106.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.1617+3025T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316976 | ||||||
chr2:44316983
|
C | G | 1 | a0002c0001t0001g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1617+3032C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44316983 | ||||||
chr2:44317035
|
G | A | 10 | a0001c0003t0004g0279a0001c0003t0004g0280a0001c0003t0004g0281others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1617+3084G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317035 | ||||||
chr2:44317073
|
G | C | 1 | a0002c0001t0001g0138 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1617+3122G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317073 | ||||||
chr2:44317091
|
A | G | 3 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0254 | 3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1618-3108A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317091 | ||||||
chr2:44317125
|
C | G | 11 | a0001c0003t0001g0258a0001c0003t0004g0279a0001c0003t0004g0280others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618-3074C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317125 | ||||||
chr2:44317187
|
G | T | 1 | a0002c0001t0001g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1618-3012G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317187 | ||||||
chr2:44317201
|
G | A | 5 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(2): Show | 5 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618-2998G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317201 | ||||||
chr2:44317339
|
G | T | 7 | a0001c0002t0001g0180a0001c0003t0001g0006a0001c0003t0001g0249others(4): Show | 9 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-2860G>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317339 | ||||||
chr2:44317459
|
C | CA | 57 | a0001c0002t0002g0221a0001c0002t0002g0225a0001c0002t0002g0236others(54): Show | 58 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1618-2724dupA | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317459 | |||||
chr2:44317459
|
C | CAA | 170 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(167): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1618-2725_1618-272 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317459 | |||||
chr2:44317459
|
C | CAAA | 7 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0254others(4): Show | 7 | HG00735.hp2 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618-2726_1618-272 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317459 | |||||
chr2:44317567
|
T | G | 1 | a0001c0003t0004g0057 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1618-2632T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317567 | ||||||
chr2:44317646
|
T | A | 3 | a0002c0004t0001g0169a0002c0004t0001g0170a0002c0004t0001g0172 | 3 | HG02647.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1618-2553T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317646 | ||||||
chr2:44317667
|
TATTTTCA others(34): Show |
T | 1 | a0001c0003t0004g0291 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1618-2519_1618-247 others(45): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317667 | |||||
chr2:44317775
|
A | C | 30 | a0002c0001t0001g0032a0002c0001t0001g0060a0002c0001t0001g0061others(27): Show | 30 | HG00597.hp2 HG01358.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.1618-2424A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317775 | ||||||
chr2:44317797
|
C | T | 1 | a0001c0002t0002g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1618-2402C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317797 | ||||||
chr2:44317810
|
G | A | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-2389G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317810 | ||||||
chr2:44317816
|
G | A | 174 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(171): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1618-2383G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317816 | ||||||
chr2:44317892
|
A | G | 1 | a0002c0001t0001g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1618-2307A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317892 | ||||||
chr2:44317953
|
G | C | 1 | a0001c0002t0002g0264 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1618-2246G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317953 | ||||||
chr2:44317959
|
AAAT | A | 7 | a0001c0002t0001g0180a0001c0003t0001g0006a0001c0003t0001g0249others(4): Show | 9 | HG01106.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-2235_1618-223 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44317959 | |||||
chr2:44317973
|
T | G | 5 | a0002c0001t0001g0024a0002c0001t0001g0025a0002c0001t0001g0069others(2): Show | 5 | HG02055.hp2 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-2226T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317973 | ||||||
chr2:44317987
|
T | C | 2 | a0001c0002t0002g0003a0001c0002t0002g0262 | 6 | NA18962.hp1 NA18979.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618-2212T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44317987 | ||||||
chr2:44318093
|
CTG | C | 19 | a0001c0003t0004g0015a0001c0003t0004g0277a0001c0003t0004g0279others(16): Show | 19 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1618-2104_1618-210 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318093 | |||||
chr2:44318095
|
G | GT | 7 | a0001c0002t0002g0216a0001c0002t0002g0242a0001c0002t0002g0248others(4): Show | 7 | HG01978.hp1 HG02004.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1618-2089dupT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | |||||
chr2:44318095
|
GT | G | 152 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0003t0001g0006others(149): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1618-2089delT | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | |||||
chr2:44318095
|
GTT | G | 25 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(22): Show | 28 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1618-2090_1618-208 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | |||||
chr2:44318095
|
GTTT | G | 11 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0261others(8): Show | 12 | HG00280.hp1 HG00738.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1618-2091_1618-208 others(7): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318095 | |||||
chr2:44318159
|
C | T | 9 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0261others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1618-2040C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318159 | ||||||
chr2:44318252
|
G | A | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-1947G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318252 | ||||||
chr2:44318282
|
G | A | 1 | a0002c0004t0001g0171 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1618-1917G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318282 | ||||||
chr2:44318312
|
G | C | 4 | a0001c0002t0002g0012a0001c0002t0002g0177a0001c0002t0002g0178others(1): Show | 5 | HG01074.hp1 HG01099.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-1887G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318312 | ||||||
chr2:44318345
|
C | A | 1 | a0001c0002t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1618-1854C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318345 | ||||||
chr2:44318356
|
G | C | 3 | a0002c0001t0001g0110a0002c0001t0001g0111a0002c0001t0001g0112 | 3 | NA18999.hp2 NA19057.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1618-1843G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318356 | ||||||
chr2:44318403
|
T | G | 1 | a0011c0015t0001g0253 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1618-1796T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318403 | ||||||
chr2:44318406
|
T | G | 10 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1618-1793T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318406 | ||||||
chr2:44318437
|
T | C | 189 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(186): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1618-1762T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318437 | ||||||
chr2:44318566
|
C | G | 1 | a0001c0002t0002g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1618-1633C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318566 | ||||||
chr2:44318573
|
T | G | 2 | a0002c0001t0001g0019a0002c0001t0001g0021 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1618-1626T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318573 | ||||||
chr2:44318596
|
A | ATG | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1602_1618-160 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318596 | |||||
chr2:44318598
|
A | T | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1601A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318598 | ||||||
chr2:44318601
|
A | C | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1598A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318601 | ||||||
chr2:44318601
|
A | T | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1598A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318601 | ||||||
chr2:44318602
|
A | T | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1597A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318602 | ||||||
chr2:44318603
|
A | T | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1596A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318603 | ||||||
chr2:44318604
|
T | A | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1595T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318604 | ||||||
chr2:44318604
|
T | G | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1595T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318604 | ||||||
chr2:44318605
|
G | C | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1594G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318605 | ||||||
chr2:44318606
|
A | G | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1593A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318606 | ||||||
chr2:44318607
|
T | C | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1592T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318607 | ||||||
chr2:44318609
|
C | G | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1590C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318609 | ||||||
chr2:44318610
|
A | G | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1589A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318610 | ||||||
chr2:44318611
|
T | C | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1588T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318611 | ||||||
chr2:44318611
|
T | G | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1588T>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318611 | ||||||
chr2:44318612
|
T | A | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1587T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318612 | ||||||
chr2:44318613
|
C | A | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1586C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318613 | ||||||
chr2:44318614
|
T | A | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1585T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318614 | ||||||
chr2:44318615
|
GTGCC | G | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1582_1618-157 others(8): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44318615 | |||||
chr2:44318616
|
T | A | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1583T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318616 | ||||||
chr2:44318617
|
G | A | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1582G>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318617 | ||||||
chr2:44318618
|
C | T | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1581C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318618 | ||||||
chr2:44318619
|
C | G | 203 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-1580C>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318619 | ||||||
chr2:44318623
|
G | C | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1576G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318623 | ||||||
chr2:44318624
|
C | A | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1575C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318624 | ||||||
chr2:44318625
|
A | T | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1574A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318625 | ||||||
chr2:44318626
|
A | T | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1573A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318626 | ||||||
chr2:44318627
|
A | T | 207 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1618-1572A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318627 | ||||||
chr2:44318637
|
C | A | 4 | a0001c0003t0003g0020a0002c0001t0001g0019a0002c0001t0001g0021others(1): Show | 4 | HG02717.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618-1562C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318637 | ||||||
chr2:44318713
|
T | C | 1 | a0002c0001t0001g0059 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1618-1486T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318713 | ||||||
chr2:44318737
|
T | C | 1 | a0001c0003t0012g0285 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1618-1462T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318737 | ||||||
chr2:44318877
|
C | T | 211 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(208): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1618-1322C>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318877 | ||||||
chr2:44318945
|
A | C | 1 | a0001c0002t0002g0221 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1618-1254A>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44318945 | ||||||
chr2:44319036
|
CAT | C | 3 | a0001c0003t0001g0251a0001c0003t0001g0252a0001c0003t0001g0254 | 3 | HG03130.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1618-1162_1618-116 others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319036 | ||||||
chr2:44319040
|
T | C | 1 | a0001c0003t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1618-1159T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319040 | ||||||
chr2:44319264
|
T | A | 3 | a0001c0003t0001g0009a0001c0003t0001g0039a0001c0003t0001g0146 | 4 | HG02647.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618-935T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319264 | ||||||
chr2:44319287
|
A | T | 1 | a0002c0001t0001g0149 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1618-912A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319287 | ||||||
chr2:44319367
|
T | C | 1 | a0001c0003t0003g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1618-832T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319367 | ||||||
chr2:44319454
|
G | C | 1 | a0001c0018t0003g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1618-745G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319454 | ||||||
chr2:44319462
|
C | A | 5 | a0001c0002t0009g0175a0001c0003t0006g0267a0001c0003t0006g0289others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-737C>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319462 | ||||||
chr2:44319493
|
CATTT | C | 27 | a0002c0001t0001g0032a0002c0001t0001g0061a0002c0001t0001g0062others(24): Show | 27 | HG00597.hp2 HG01358.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.1618-703_1618-700d others(6): Show |
SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 44319493 | |||||
chr2:44319562
|
T | C | 1 | a0001c0002t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1618-637T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319562 | ||||||
chr2:44319602
|
T | C | 138 | a0001c0017t0007g0161a0002c0001t0001g0002a0002c0001t0001g0004others(135): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1618-597T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319602 | ||||||
chr2:44319634
|
T | A | 1 | a0001c0003t0003g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1618-565T>A | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319634 | ||||||
chr2:44319694
|
T | C | 4 | a0001c0002t0002g0013a0001c0002t0002g0189a0001c0002t0002g0239others(1): Show | 5 | HG02040.hp2 HG02155.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618-505T>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319694 | ||||||
chr2:44319992
|
A | G | 190 | a0001c0002t0001g0164a0001c0002t0001g0166a0001c0002t0001g0167others(187): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1618-207A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44319992 | ||||||
chr2:44320003
|
A | G | 10 | a0001c0002t0003g0016a0001c0002t0003g0183a0001c0002t0003g0260others(7): Show | 11 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618-196A>G | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44320003 | ||||||
chr2:44320057
|
A | T | 1 | a0002c0001t0001g0134 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1618-142A>T | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44320057 | ||||||
chr2:44320097
|
G | C | 20 | a0001c0003t0004g0015a0001c0003t0004g0057a0001c0003t0004g0277others(17): Show | 20 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1618-102G>C | SLC3A1 | ENSG00000138079.14 | transcript | ENST00000260649.11 | protein_coding | 9/9 | chr2 | 44320097 |