geneid | 55102 |
---|---|
ensemblid | ENSG00000066739.12 |
hgncid | 20187 |
symbol | ATG2B |
name | autophagy related 2B |
refseq_nuc | NM_018036.7 |
refseq_prot | NP_060506.6 |
ensembl_nuc | ENST00000359933.6 |
ensembl_prot | ENSP00000353010.4 |
mane_status | MANE Select |
chr | chr14 |
start | 96279195 |
end | 96363341 |
strand | - |
ver | v1.2 |
region | chr14:96279195-96363341 |
region5000 | chr14:96274195-96368341 |
regionname0 | ATG2B_chr14_96279195_96363341 |
regionname5000 | ATG2B_chr14_96274195_96368341 |
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 | 0/0 | 2078 | 177 | 46 | 33 | 72 | 6 | 20 | 58 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002 | 0/1 | 2078 | 78 | 14 | 14 | 38 | 3 | 8 | 31 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003 | 1/0 | 2078 | 35 | 0 | 3 | 27 | 0 | 4 | 17 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0004 | 0/0 | 2078 | 12 | 0 | 0 | 8 | 0 | 4 | 5 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005 | 0/0 | 2078 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0006 | 0/0 | 2078 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0007 | 0/0 | 2078 | 6 | 0 | 5 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0008 | 0/0 | 2078 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0009 | 0/0 | 2078 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0010 | 0/0 | 2078 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0011 | 0/0 | 2078 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0012 | 0/0 | 2078 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0013 | 0/0 | 2078 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0014 | 0/0 | 2078 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0015 | 0/0 | 2078 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0016 | 0/0 | 2078 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0017 | 0/0 | 2078 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0018 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0019 | 0/0 | 2078 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0020 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0021 | 0/0 | 2078 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0022 | 0/0 | 2078 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0023 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0024 | 0/0 | 2078 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0025 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0026 | 0/0 | 2078 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0027 | 0/0 | 2078 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0028 | 0/0 | 2078 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
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 | 6237 | 78 | 14 | 14 | 38 | 3 | 8 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0002 | 0/0 | 6237 | 70 | 29 | 12 | 15 | 2 | 12 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0003 | 0/0 | 6237 | 59 | 8 | 11 | 28 | 4 | 8 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0004 | 1/0 | 6237 | 35 | 0 | 3 | 27 | 0 | 4 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0005 | 0/0 | 6237 | 33 | 1 | 5 | 27 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0006 | 0/0 | 6237 | 11 | 0 | 0 | 8 | 0 | 3 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0007 | 0/0 | 6237 | 8 | 8 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0008 | 0/0 | 6237 | 6 | 5 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0009 | 0/0 | 6237 | 6 | 0 | 5 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0010 | 0/0 | 6237 | 5 | 4 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0011 | 0/0 | 6237 | 3 | 0 | 3 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0012 | 0/0 | 6237 | 3 | 3 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0013 | 0/0 | 6237 | 3 | 2 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0014 | 0/0 | 6237 | 3 | 3 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0015 | 0/0 | 6237 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0016 | 0/0 | 6237 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0017 | 0/0 | 6237 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0018 | 0/0 | 6237 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0019 | 0/0 | 6237 | 2 | 1 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0020 | 0/0 | 6237 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0021 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0022 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0023 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0024 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0025 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0026 | 0/0 | 6237 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0027 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0028 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0029 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0030 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0031 | 0/0 | 6237 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0032 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0033 | 0/0 | 6237 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0034 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0035 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0036 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0037 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0038 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0039 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0040 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
c0041 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
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 | 0/0 | 6935 | 66 | 25 | 15 | 16 | 2 | 8 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0002 | 0/1 | 6935 | 47 | 1 | 16 | 22 | 2 | 5 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0003 | 1/0 | 6926 | 38 | 1 | 13 | 19 | 3 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0004 | 0/0 | 6935 | 34 | 2 | 3 | 23 | 0 | 6 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0005 | 0/0 | 6935 | 33 | 4 | 8 | 19 | 1 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0006 | 0/0 | 6935 | 22 | 12 | 5 | 0 | 1 | 4 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0007 | 0/0 | 6935 | 10 | 0 | 0 | 10 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0008 | 0/0 | 6935 | 9 | 9 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0009 | 0/0 | 6931 | 6 | 5 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0010 | 0/0 | 6925 | 6 | 0 | 0 | 3 | 0 | 3 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0011 | 0/0 | 6926 | 5 | 0 | 1 | 0 | 0 | 4 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0012 | 0/0 | 6931 | 5 | 5 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0013 | 0/0 | 6925 | 5 | 0 | 0 | 5 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0014 | 0/0 | 6935 | 4 | 0 | 0 | 4 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0015 | 0/0 | 6935 | 4 | 0 | 0 | 4 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0016 | 0/0 | 6926 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0017 | 0/0 | 6939 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0018 | 0/0 | 6935 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0019 | 0/0 | 6936 | 2 | 1 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0020 | 0/0 | 6926 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0021 | 0/0 | 6931 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0022 | 0/0 | 6935 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0023 | 0/0 | 6931 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0024 | 0/0 | 6935 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0025 | 0/0 | 6935 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0026 | 0/0 | 6931 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0027 | 0/0 | 6927 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0028 | 0/0 | 6936 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0029 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0030 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0031 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0032 | 0/0 | 6926 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0033 | 0/0 | 6926 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0034 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0035 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0036 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0037 | 0/0 | 6935 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0038 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0039 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0040 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0041 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0042 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0043 | 0/0 | 6935 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0044 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0045 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0046 | 0/0 | 6931 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0047 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0048 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0049 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0050 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0051 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0052 | 0/0 | 6926 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0053 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0054 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0055 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0056 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0057 | 0/0 | 6935 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0058 | 0/0 | 6935 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0059 | 0/0 | 6935 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0060 | 0/0 | 6935 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0061 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0062 | 0/0 | 6935 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
t0063 | 0/0 | 6929 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
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 | 0/0 | 6237 | 70 | 29 | 12 | 15 | 2 | 12 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003 | 0/0 | 6237 | 59 | 8 | 11 | 28 | 4 | 8 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0005 | 0/0 | 6237 | 33 | 1 | 5 | 27 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0011 | 0/0 | 6237 | 3 | 0 | 3 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0012 | 0/0 | 6237 | 3 | 3 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0013 | 0/0 | 6237 | 3 | 2 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0022 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0024 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0025 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0026 | 0/0 | 6237 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0032 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0035 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001 | 0/1 | 6237 | 78 | 14 | 14 | 38 | 3 | 8 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004 | 1/0 | 6237 | 35 | 0 | 3 | 27 | 0 | 4 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0004c0006 | 0/0 | 6237 | 11 | 0 | 0 | 8 | 0 | 3 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0004c0041 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0008 | 0/0 | 6237 | 6 | 5 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0010 | 0/0 | 6237 | 5 | 4 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0006c0007 | 0/0 | 6237 | 8 | 8 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0007c0009 | 0/0 | 6237 | 6 | 0 | 5 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0008c0014 | 0/0 | 6237 | 3 | 3 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0009c0018 | 0/0 | 6237 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0010c0016 | 0/0 | 6237 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0011c0017 | 0/0 | 6237 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0012c0020 | 0/0 | 6237 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0013c0015 | 0/0 | 6237 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0014c0019 | 0/0 | 6237 | 2 | 1 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0015c0021 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0016c0033 | 0/0 | 6237 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0017c0030 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0018c0023 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0019c0034 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0020c0029 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0021c0039 | 0/0 | 6237 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0022c0037 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0023c0036 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0024c0028 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0025c0027 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0026c0038 | 0/0 | 6237 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0027c0040 | 0/0 | 6237 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0028c0031 | 0/0 | 6237 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 13171 | 58 | 22 | 12 | 14 | 2 | 8 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0026 | 0/0 | 13167 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0051 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0052 | 0/0 | 13162 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0053 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0054 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0055 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0057 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0059 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0060 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0061 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0002t0062 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0002 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0003 | 0/0 | 13162 | 31 | 1 | 8 | 18 | 3 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0005 | 0/0 | 13171 | 6 | 0 | 1 | 3 | 1 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0011 | 0/0 | 13162 | 5 | 0 | 1 | 0 | 0 | 4 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0016 | 0/0 | 13162 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0020 | 0/0 | 13162 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0023 | 0/0 | 13167 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0027 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0031 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0032 | 0/0 | 13162 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0033 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0035 | 0/0 | 13167 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0037 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0044 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0045 | 0/0 | 13167 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0003t0046 | 0/0 | 13167 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0005t0005 | 0/0 | 13171 | 19 | 1 | 5 | 13 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0005t0007 | 0/0 | 13171 | 10 | 0 | 0 | 10 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0005t0018 | 0/0 | 13171 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0005t0038 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0005t0039 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0011t0003 | 0/0 | 13162 | 3 | 0 | 3 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0012t0024 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0012t0050 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0013t0005 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0013t0022 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0022t0015 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0024t0006 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0025t0001 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0026t0001 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0032t0056 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0001c0035t0034 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0002 | 0/1 | 13171 | 39 | 0 | 10 | 21 | 2 | 5 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0003 | 0/0 | 13162 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0004 | 0/0 | 13171 | 6 | 0 | 0 | 6 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0005 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0006 | 0/0 | 13171 | 17 | 10 | 3 | 0 | 1 | 3 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0014 | 0/0 | 13171 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0017 | 0/0 | 13175 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0019 | 0/0 | 13172 | 2 | 1 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0028 | 0/0 | 13172 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0040 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0041 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0042 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0047 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0002c0001t0048 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0003 | 1/0 | 13162 | 2 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0004 | 0/0 | 13171 | 23 | 0 | 3 | 16 | 0 | 4 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0005 | 0/0 | 13171 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0015 | 0/0 | 13171 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0025 | 0/0 | 13171 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0029 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0030 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0003c0004t0049 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0004c0006t0010 | 0/0 | 13161 | 6 | 0 | 0 | 3 | 0 | 3 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0004c0006t0013 | 0/0 | 13161 | 5 | 0 | 0 | 5 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0004c0041t0063 | 0/0 | 13165 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0008t0005 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0008t0012 | 0/0 | 13167 | 3 | 3 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0008t0021 | 0/0 | 13167 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0010t0009 | 0/0 | 13167 | 3 | 2 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0005c0010t0012 | 0/0 | 13167 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0006c0007t0008 | 0/0 | 13171 | 8 | 8 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0007c0009t0002 | 0/0 | 13171 | 6 | 0 | 5 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0008c0014t0009 | 0/0 | 13167 | 3 | 3 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0009c0018t0005 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0010c0016t0004 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0011c0017t0001 | 0/0 | 13171 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0012c0020t0006 | 0/0 | 13171 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0013c0015t0004 | 0/0 | 13171 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0014c0019t0001 | 0/0 | 13171 | 2 | 1 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0015c0021t0004 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0016c0033t0003 | 0/0 | 13162 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0017c0030t0018 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0018c0023t0036 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0019c0034t0014 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0020c0029t0001 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0021c0039t0005 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0022c0037t0043 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0023c0036t0002 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0024c0028t0058 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0025c0027t0008 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0026c0038t0006 | 0/0 | 13171 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0027c0040t0006 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
a0028c0031t0001 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | copy fasta | chr14 | 96274195 | 96368341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0026g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0051g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0052g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0053g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0054g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0055g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0057g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0059g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0060g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0061g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0002t0062g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0011g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0011g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0011g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0011g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0016g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0020g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0020g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0023g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0027g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0031g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0032g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0033g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0035g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0037g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0044g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0045g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0003t0046g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0018g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0018g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0038g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0005t0039g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0011t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0011t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0011t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0012t0024g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0012t0024g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0012t0050g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0013t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0013t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0013t0022g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0022t0015g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0024t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0025t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0026t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0032t0056g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0001c0035t0034g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0014g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0014g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0017g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0017g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0017g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0019g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0019g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0028g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0040g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0041g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0042g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0047g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0002c0001t0048g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0003g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0015g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0015g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0015g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0025g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0025g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0029g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0030g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0003c0004t0049g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0010g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0010g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0010g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0010g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0010g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0010g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0013g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0013g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0013g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0006t0013g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0004c0041t0063g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0008t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0008t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0008t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0008t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0008t0021g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0008t0021g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0010t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0010t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0010t0009g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0010t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0005c0010t0012g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0006c0007t0008g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0006c0007t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0006c0007t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0006c0007t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0006c0007t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0007c0009t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0007c0009t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0007c0009t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0007c0009t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0007c0009t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0007c0009t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0008c0014t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0008c0014t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0009c0018t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0009c0018t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0010c0016t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0010c0016t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0011c0017t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0011c0017t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0012c0020t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0012c0020t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0013c0015t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0013c0015t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0014c0019t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0014c0019t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0015c0021t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0016c0033t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0017c0030t0018g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0018c0023t0036g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0019c0034t0014g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0020c0029t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0021c0039t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0022c0037t0043g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0023c0036t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0024c0028t0058g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0025c0027t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0026c0038t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0027c0040t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
a0028c0031t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0005 | g0199 | EUR | GBR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00099 | hp2 | a0022 | c0037 | t0043 | g0173 | EUR | GBR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0288 | EUR | GBR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00140 | hp2 | a0002 | c0001 | t0006 | g0159 | EUR | GBR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0264 | EUR | FIN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00323 | hp2 | a0001 | c0003 | t0003 | g0225 | EUR | FIN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00408 | hp1 | a0003 | c0004 | t0004 | g0030 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00408 | hp2 | a0001 | c0003 | t0003 | g0234 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00438 | hp1 | a0007 | c0009 | t0002 | g0192 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00438 | hp2 | a0003 | c0004 | t0004 | g0041 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00558 | hp1 | a0002 | c0001 | t0004 | g0118 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00558 | hp2 | a0001 | c0005 | t0005 | g0032 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00597 | hp1 | a0019 | c0034 | t0014 | g0154 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00597 | hp2 | a0003 | c0004 | t0003 | g0033 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00609 | hp2 | a0002 | c0001 | t0002 | g0185 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00621 | hp1 | a0004 | c0006 | t0013 | g0013 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00621 | hp2 | a0002 | c0001 | t0004 | g0190 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00639 | hp1 | a0007 | c0009 | t0002 | g0128 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00639 | hp2 | a0014 | c0019 | t0001 | g0274 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00642 | hp1 | a0005 | c0008 | t0005 | g0098 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00642 | hp2 | a0001 | c0013 | t0005 | g0091 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00673 | hp2 | a0001 | c0005 | t0018 | g0255 | EAS | CHS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00735 | hp1 | a0002 | c0001 | t0002 | g0182 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00735 | hp2 | a0001 | c0005 | t0005 | g0076 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00738 | hp2 | a0002 | c0001 | t0006 | g0172 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00741 | hp1 | a0002 | c0001 | t0006 | g0170 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01069 | hp1 | a0012 | c0020 | t0006 | g0178 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01069 | hp2 | a0002 | c0001 | t0002 | g0183 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01070 | hp1 | a0002 | c0001 | t0002 | g0006 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01070 | hp2 | a0001 | c0005 | t0005 | g0075 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01071 | hp1 | a0012 | c0020 | t0006 | g0179 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01071 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0215 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01074 | hp2 | a0002 | c0001 | t0002 | g0134 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01081 | hp1 | a0007 | c0009 | t0002 | g0125 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01081 | hp2 | a0001 | c0005 | t0005 | g0072 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0321 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01099 | hp2 | a0001 | c0003 | t0005 | g0197 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01106 | hp2 | a0002 | c0001 | t0002 | g0126 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01109 | hp2 | a0002 | c0001 | t0002 | g0241 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01168 | hp1 | a0001 | c0003 | t0003 | g0008 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01168 | hp2 | a0001 | c0003 | t0011 | g0176 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01169 | hp1 | a0001 | c0003 | t0003 | g0008 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01169 | hp2 | a0028 | c0031 | t0001 | g0277 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01175 | hp2 | a0001 | c0003 | t0003 | g0239 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01192 | hp1 | a0001 | c0003 | t0003 | g0200 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0214 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01255 | hp2 | a0005 | c0010 | t0009 | g0107 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01256 | hp1 | a0003 | c0004 | t0004 | g0004 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01256 | hp2 | a0002 | c0001 | t0006 | g0113 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01257 | hp1 | a0007 | c0009 | t0002 | g0129 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01258 | hp2 | a0003 | c0004 | t0004 | g0004 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01261 | hp1 | a0001 | c0011 | t0003 | g0019 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01261 | hp2 | a0001 | c0026 | t0001 | g0269 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01346 | hp2 | a0002 | c0001 | t0002 | g0142 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0233 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01515 | hp1 | a0002 | c0001 | t0002 | g0186 | EUR | IBS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01515 | hp2 | a0001 | c0003 | t0003 | g0227 | EUR | IBS | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01891 | hp1 | a0020 | c0029 | t0001 | g0296 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01891 | hp2 | a0001 | c0024 | t0006 | g0092 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01928 | hp1 | a0001 | c0005 | t0005 | g0074 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01928 | hp2 | a0002 | c0001 | t0003 | g0123 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01952 | hp1 | a0001 | c0005 | t0005 | g0073 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0229 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01981 | hp2 | a0002 | c0001 | t0002 | g0155 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02015 | hp2 | a0003 | c0004 | t0015 | g0254 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02027 | hp1 | a0003 | c0004 | t0025 | g0251 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02027 | hp2 | a0001 | c0003 | t0003 | g0216 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02040 | hp1 | a0004 | c0006 | t0013 | g0338 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02040 | hp2 | a0021 | c0039 | t0005 | g0217 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02055 | hp1 | a0001 | c0002 | t0051 | g0257 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02055 | hp2 | a0002 | c0001 | t0019 | g0016 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02056 | hp1 | a0003 | c0004 | t0015 | g0256 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02056 | hp2 | a0001 | c0002 | t0062 | g0327 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02074 | hp1 | a0001 | c0005 | t0005 | g0071 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02074 | hp2 | a0001 | c0003 | t0003 | g0228 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02080 | hp1 | a0003 | c0004 | t0004 | g0031 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02080 | hp2 | a0002 | c0001 | t0002 | g0132 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02083 | hp1 | a0003 | c0004 | t0049 | g0039 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02083 | hp2 | a0002 | c0001 | t0002 | g0151 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02145 | hp1 | a0006 | c0007 | t0008 | g0089 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02145 | hp2 | a0002 | c0001 | t0006 | g0167 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02148 | hp1 | a0007 | c0009 | t0002 | g0119 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02148 | hp2 | a0016 | c0033 | t0003 | g0211 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02155 | hp1 | a0002 | c0001 | t0014 | g0144 | EAS | CDX | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02155 | hp2 | a0003 | c0004 | t0004 | g0059 | EAS | CDX | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | CDX | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02165 | hp2 | a0003 | c0004 | t0005 | g0086 | EAS | CDX | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02257 | hp1 | a0002 | c0001 | t0042 | g0158 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02257 | hp2 | a0001 | c0003 | t0035 | g0247 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0272 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02258 | hp2 | a0005 | c0008 | t0021 | g0100 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02280 | hp2 | a0027 | c0040 | t0006 | g0168 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02293 | hp1 | a0002 | c0001 | t0002 | g0124 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02293 | hp2 | a0001 | c0003 | t0003 | g0213 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02300 | hp1 | a0001 | c0011 | t0003 | g0018 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02300 | hp2 | a0007 | c0009 | t0002 | g0131 | AMR | PEL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02451 | hp1 | a0010 | c0016 | t0004 | g0077 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02523 | hp2 | a0004 | c0006 | t0013 | g0332 | EAS | KHV | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02572 | hp1 | a0002 | c0001 | t0006 | g0187 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0316 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02602 | hp1 | a0002 | c0001 | t0006 | g0177 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02615 | hp1 | a0001 | c0003 | t0003 | g0209 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02622 | hp1 | a0001 | c0002 | t0053 | g0268 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0317 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02630 | hp2 | a0005 | c0010 | t0009 | g0106 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02647 | hp1 | a0002 | c0001 | t0006 | g0165 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02683 | hp1 | a0002 | c0001 | t0006 | g0169 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02683 | hp2 | a0001 | c0003 | t0003 | g0224 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02717 | hp1 | a0025 | c0027 | t0008 | g0079 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02717 | hp2 | a0002 | c0001 | t0006 | g0160 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02723 | hp1 | a0005 | c0010 | t0009 | g0105 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02723 | hp2 | a0002 | c0001 | t0006 | g0163 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02735 | hp1 | a0001 | c0002 | t0057 | g0267 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02735 | hp2 | a0004 | c0006 | t0010 | g0335 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02738 | hp1 | a0002 | c0001 | t0006 | g0171 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02738 | hp2 | a0002 | c0001 | t0002 | g0133 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02809 | hp1 | a0001 | c0002 | t0026 | g0010 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02809 | hp2 | a0001 | c0013 | t0022 | g0085 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02886 | hp2 | a0014 | c0019 | t0001 | g0273 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02895 | hp1 | a0005 | c0008 | t0012 | g0096 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02895 | hp2 | a0006 | c0007 | t0008 | g0001 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02896 | hp2 | a0006 | c0007 | t0008 | g0001 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02897 | hp1 | a0005 | c0008 | t0012 | g0097 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02922 | hp1 | a0001 | c0003 | t0044 | g0242 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02922 | hp2 | a0002 | c0001 | t0040 | g0166 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02965 | hp2 | a0006 | c0007 | t0008 | g0080 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02970 | hp1 | a0006 | c0007 | t0008 | g0082 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02970 | hp2 | a0001 | c0032 | t0056 | g0310 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02976 | hp1 | a0006 | c0007 | t0008 | g0001 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03017 | hp1 | a0003 | c0004 | t0004 | g0043 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03041 | hp1 | a0010 | c0016 | t0004 | g0078 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03041 | hp2 | a0001 | c0002 | t0026 | g0010 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03098 | hp1 | a0006 | c0007 | t0008 | g0081 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0315 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03130 | hp2 | a0001 | c0013 | t0022 | g0090 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03139 | hp1 | a0001 | c0003 | t0046 | g0244 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03139 | hp2 | a0006 | c0007 | t0008 | g0001 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03195 | hp1 | a0001 | c0002 | t0054 | g0306 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03195 | hp2 | a0001 | c0012 | t0024 | g0094 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03239 | hp1 | a0004 | c0006 | t0010 | g0339 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03239 | hp2 | a0001 | c0003 | t0011 | g0109 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03486 | hp2 | a0009 | c0018 | t0005 | g0083 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03490 | hp1 | a0013 | c0015 | t0004 | g0024 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03490 | hp2 | a0001 | c0003 | t0011 | g0007 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03491 | hp1 | a0001 | c0002 | t0060 | g0266 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03491 | hp2 | a0003 | c0004 | t0004 | g0003 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03492 | hp1 | a0003 | c0004 | t0004 | g0003 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03492 | hp2 | a0001 | c0003 | t0011 | g0007 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03516 | hp1 | a0005 | c0008 | t0021 | g0101 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03516 | hp2 | a0001 | c0003 | t0023 | g0243 | AFR | ESN | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03540 | hp2 | a0005 | c0010 | t0012 | g0236 | AFR | GWD | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03579 | hp1 | a0008 | c0014 | t0009 | g0005 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03579 | hp2 | a0001 | c0003 | t0033 | g0231 | AFR | MSL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03669 | hp1 | a0002 | c0001 | t0002 | g0181 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03669 | hp2 | a0013 | c0015 | t0004 | g0025 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03688 | hp1 | a0001 | c0003 | t0011 | g0226 | SAS | STU | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03688 | hp2 | a0004 | c0041 | t0063 | g0340 | SAS | STU | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03704 | hp1 | a0002 | c0001 | t0002 | g0122 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0313 | SAS | PJL | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03831 | hp1 | a0001 | c0002 | t0059 | g0259 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03831 | hp2 | a0001 | c0003 | t0005 | g0198 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03834 | hp1 | a0026 | c0038 | t0006 | g0174 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03927 | hp2 | a0002 | c0001 | t0002 | g0149 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03942 | hp1 | a0002 | c0001 | t0002 | g0146 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG03942 | hp2 | a0004 | c0006 | t0010 | g0336 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG04115 | hp1 | a0001 | c0003 | t0037 | g0196 | SAS | STU | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG04115 | hp2 | a0001 | c0002 | t0052 | g0330 | SAS | STU | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG04184 | hp1 | a0024 | c0028 | t0058 | g0326 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG04184 | hp2 | a0001 | c0003 | t0032 | g0195 | SAS | BEB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | STU | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | STU | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18522 | hp1 | a0001 | c0005 | t0005 | g0027 | AFR | YRI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18522 | hp2 | a0001 | c0012 | t0050 | g0095 | AFR | YRI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18612 | hp1 | a0001 | c0003 | t0016 | g0002 | EAS | CHB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18612 | hp2 | a0015 | c0021 | t0004 | g0026 | EAS | CHB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18747 | hp1 | a0001 | c0035 | t0034 | g0221 | EAS | CHB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18747 | hp2 | a0002 | c0001 | t0002 | g0135 | EAS | CHB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18906 | hp1 | a0002 | c0001 | t0006 | g0164 | AFR | YRI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | YRI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18939 | hp1 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18939 | hp2 | a0001 | c0005 | t0005 | g0045 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18940 | hp1 | a0003 | c0004 | t0004 | g0036 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18940 | hp2 | a0001 | c0003 | t0003 | g0219 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18941 | hp1 | a0001 | c0003 | t0020 | g0222 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18941 | hp2 | a0002 | c0001 | t0002 | g0120 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18942 | hp2 | a0001 | c0005 | t0007 | g0047 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18943 | hp1 | a0003 | c0004 | t0004 | g0103 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18943 | hp2 | a0002 | c0001 | t0014 | g0145 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18945 | hp1 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18945 | hp2 | a0003 | c0004 | t0029 | g0023 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18946 | hp1 | a0002 | c0001 | t0002 | g0150 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18946 | hp2 | a0001 | c0005 | t0005 | g0034 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18950 | hp1 | a0002 | c0001 | t0017 | g0138 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18950 | hp2 | a0001 | c0022 | t0015 | g0252 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18952 | hp1 | a0002 | c0001 | t0002 | g0148 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18952 | hp2 | a0003 | c0004 | t0004 | g0038 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18959 | hp1 | a0002 | c0001 | t0002 | g0235 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18959 | hp2 | a0003 | c0004 | t0004 | g0028 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18961 | hp1 | a0003 | c0004 | t0025 | g0249 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18961 | hp2 | a0001 | c0003 | t0005 | g0206 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18963 | hp1 | a0002 | c0001 | t0002 | g0137 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18965 | hp1 | a0001 | c0003 | t0003 | g0108 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18965 | hp2 | a0001 | c0005 | t0007 | g0049 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18968 | hp1 | a0001 | c0005 | t0038 | g0055 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18968 | hp2 | a0002 | c0001 | t0047 | g0188 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18970 | hp1 | a0002 | c0001 | t0002 | g0184 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18970 | hp2 | a0001 | c0003 | t0005 | g0207 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18974 | hp1 | a0002 | c0001 | t0002 | g0127 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18975 | hp1 | a0004 | c0006 | t0013 | g0013 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18975 | hp2 | a0001 | c0005 | t0007 | g0044 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18978 | hp1 | a0002 | c0001 | t0028 | g0015 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18978 | hp2 | a0001 | c0005 | t0007 | g0066 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18979 | hp1 | a0001 | c0003 | t0027 | g0017 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18979 | hp2 | a0002 | c0001 | t0002 | g0111 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18980 | hp1 | a0002 | c0001 | t0002 | g0139 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18980 | hp2 | a0001 | c0005 | t0007 | g0052 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18982 | hp2 | a0001 | c0003 | t0003 | g0218 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18983 | hp1 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18983 | hp2 | a0002 | c0001 | t0014 | g0121 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18984 | hp1 | a0001 | c0003 | t0020 | g0223 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18984 | hp2 | a0003 | c0004 | t0004 | g0029 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18985 | hp1 | a0001 | c0005 | t0005 | g0054 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18985 | hp2 | a0001 | c0003 | t0031 | g0240 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18986 | hp1 | a0004 | c0006 | t0013 | g0331 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18986 | hp2 | a0002 | c0001 | t0004 | g0117 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18987 | hp1 | a0002 | c0001 | t0002 | g0147 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18990 | hp1 | a0003 | c0004 | t0030 | g0062 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18990 | hp2 | a0002 | c0001 | t0004 | g0112 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18991 | hp1 | a0001 | c0005 | t0005 | g0087 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18991 | hp2 | a0002 | c0001 | t0002 | g0152 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18994 | hp1 | a0001 | c0005 | t0005 | g0056 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19001 | hp1 | a0001 | c0005 | t0007 | g0065 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19001 | hp2 | a0002 | c0001 | t0019 | g0014 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19002 | hp1 | a0002 | c0001 | t0004 | g0115 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19002 | hp2 | a0001 | c0005 | t0005 | g0053 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19005 | hp1 | a0003 | c0004 | t0004 | g0042 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19005 | hp2 | a0002 | c0001 | t0017 | g0140 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19007 | hp1 | a0004 | c0006 | t0010 | g0334 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19007 | hp2 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19009 | hp1 | a0004 | c0006 | t0010 | g0337 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19009 | hp2 | a0002 | c0001 | t0002 | g0110 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19011 | hp1 | a0001 | c0005 | t0007 | g0051 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19011 | hp2 | a0001 | c0003 | t0003 | g0205 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19012 | hp1 | a0002 | c0001 | t0004 | g0116 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19012 | hp2 | a0001 | c0005 | t0039 | g0050 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19030 | hp1 | a0001 | c0002 | t0055 | g0320 | AFR | LWK | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19030 | hp2 | a0009 | c0018 | t0005 | g0084 | AFR | LWK | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19043 | hp1 | a0001 | c0003 | t0045 | g0246 | AFR | LWK | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0318 | AFR | LWK | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19054 | hp1 | a0001 | c0005 | t0007 | g0067 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19054 | hp2 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19056 | hp1 | a0002 | c0001 | t0002 | g0153 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19056 | hp2 | a0003 | c0004 | t0004 | g0048 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19057 | hp1 | a0002 | c0001 | t0002 | g0143 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19057 | hp2 | a0004 | c0006 | t0010 | g0333 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19060 | hp1 | a0001 | c0005 | t0005 | g0058 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19060 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19063 | hp2 | a0003 | c0004 | t0004 | g0063 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19064 | hp1 | a0001 | c0005 | t0007 | g0102 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19066 | hp2 | a0001 | c0003 | t0003 | g0212 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19068 | hp1 | a0017 | c0030 | t0018 | g0248 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19068 | hp2 | a0003 | c0004 | t0004 | g0037 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19072 | hp1 | a0001 | c0005 | t0005 | g0061 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19072 | hp2 | a0002 | c0001 | t0017 | g0194 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19074 | hp1 | a0011 | c0017 | t0001 | g0289 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19074 | hp2 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19077 | hp1 | a0003 | c0004 | t0004 | g0021 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19077 | hp2 | a0001 | c0005 | t0018 | g0253 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19079 | hp1 | a0003 | c0004 | t0004 | g0070 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19079 | hp2 | a0001 | c0003 | t0005 | g0238 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19080 | hp1 | a0003 | c0004 | t0015 | g0250 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19080 | hp2 | a0011 | c0017 | t0001 | g0325 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19081 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19081 | hp2 | a0003 | c0004 | t0004 | g0064 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19083 | hp1 | a0002 | c0001 | t0048 | g0114 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19083 | hp2 | a0001 | c0003 | t0016 | g0002 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19084 | hp1 | a0002 | c0001 | t0002 | g0141 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19084 | hp2 | a0001 | c0005 | t0005 | g0057 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19085 | hp1 | a0001 | c0005 | t0005 | g0046 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19085 | hp2 | a0002 | c0001 | t0002 | g0136 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19086 | hp1 | a0003 | c0004 | t0005 | g0035 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19088 | hp1 | a0002 | c0001 | t0041 | g0189 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19088 | hp2 | a0001 | c0005 | t0005 | g0022 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19090 | hp1 | a0001 | c0005 | t0007 | g0060 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19090 | hp2 | a0002 | c0001 | t0002 | g0191 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19240 | hp1 | a0018 | c0023 | t0036 | g0088 | AFR | YRI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA19240 | hp2 | a0002 | c0001 | t0006 | g0162 | AFR | YRI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20129 | hp1 | a0001 | c0012 | t0024 | g0093 | AFR | ASW | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20129 | hp2 | a0008 | c0014 | t0009 | g0104 | AFR | ASW | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20805 | hp1 | a0002 | c0001 | t0002 | g0157 | EUR | TSI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20805 | hp2 | a0001 | c0003 | t0003 | g0220 | EUR | TSI | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0322 | SAS | GIH | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20905 | hp2 | a0003 | c0004 | t0004 | g0069 | SAS | GIH | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01123 | hp1 | a0001 | c0011 | t0003 | g0020 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG01123 | hp2 | a0003 | c0004 | t0004 | g0040 | AMR | CLM | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02109 | hp1 | a0005 | c0010 | t0012 | g0237 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02486 | hp1 | a0002 | c0001 | t0006 | g0193 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02486 | hp2 | a0001 | c0003 | t0023 | g0245 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02559 | hp1 | a0008 | c0014 | t0009 | g0005 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG02559 | hp2 | a0002 | c0001 | t0006 | g0161 | AFR | ACB | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG06807 | hp1 | a0005 | c0008 | t0012 | g0099 | AFR | USA | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
HG06807 | hp2 | a0002 | c0001 | t0005 | g0180 | AFR | USA | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA18955 | hp2 | a0001 | c0003 | t0016 | g0002 | EAS | JPT | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20300 | hp1 | a0001 | c0025 | t0001 | g0307 | AFR | USA | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA20300 | hp2 | a0023 | c0036 | t0002 | g0130 | AFR | USA | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA21309 | hp1 | a0002 | c0001 | t0006 | g0175 | AFR | LWK | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
NA21309 | hp2 | a0001 | c0002 | t0061 | g0276 | AFR | LWK | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0002 | g0156 | REF | REF | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
homoSapiens_grch38 | hp1 | a0003 | c0004 | t0003 | g0068 | REF | REF | ATG2B_chr14_96274195_96368341 | ATG2B | chr14 | 96274195 | 96368341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96289757
|
T | C | 1 | a0009 | 2 | HG03486.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.5905A>G | p.Ile1969Val | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/42 | 6270/13162 | 5905/6237 | 1969/2078 | chr14 | 96289757 | ||
chr14:96295108
|
T | C | 1 | a0025 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.5278A>G | p.Lys1760Glu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/42 | 5643/13162 | 5278/6237 | 1760/2078 | chr14 | 96295108 | ||
chr14:96295140
|
G | A | 1 | a0024 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.5246C>T | p.Thr1749Ile | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/42 | 5611/13162 | 5246/6237 | 1749/2078 | chr14 | 96295140 | ||
chr14:96295515
|
C | T | 1 | a0023 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.5185G>A | p.Glu1729Lys | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 35/42 | 5550/13162 | 5185/6237 | 1729/2078 | chr14 | 96295515 | ||
chr14:96302043
|
T | G | 2 | a0007a0023 | 7 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(4): Show |
missense_variant | MODERATE | c.5103A>C | p.Arg1701Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/42 | 5468/13162 | 5103/6237 | 1701/2078 | chr14 | 96302043 | ||
chr14:96305622
|
A | G | 24 | a0001a0002a0004others(21): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
missense_variant | MODERATE | c.4700T>C | p.Ile1567Thr | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/42 | 5065/13162 | 4700/6237 | 1567/2078 | chr14 | 96305622 | ||
chr14:96305722
|
T | A | 1 | a0022 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.4600A>T | p.Thr1534Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/42 | 4965/13162 | 4600/6237 | 1534/2078 | chr14 | 96305722 | ||
chr14:96306827
|
A | G | 1 | a0004 | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
missense_variant | MODERATE | c.4393T>C | p.Ser1465Pro | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/42 | 4758/13162 | 4393/6237 | 1465/2078 | chr14 | 96306827 | ||
chr14:96311131
|
G | C | 8 | a0002a0007a0012others(5): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
missense_variant | MODERATE | c.4147C>G | p.Gln1383Glu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/42 | 4512/13162 | 4147/6237 | 1383/2078 | chr14 | 96311131 | ||
chr14:96311552
|
T | A | 1 | a0026 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.3980A>T | p.Asp1327Val | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 27/42 | 4345/13162 | 3980/6237 | 1327/2078 | chr14 | 96311552 | ||
chr14:96313102
|
T | G | 1 | a0021 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.3805A>C | p.Ser1269Arg | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/42 | 4170/13162 | 3805/6237 | 1269/2078 | chr14 | 96313102 | ||
chr14:96313125
|
G | A | 1 | a0020 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.3782C>T | p.Thr1261Ile | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/42 | 4147/13162 | 3782/6237 | 1261/2078 | chr14 | 96313125 | ||
chr14:96315512
|
G | A | 1 | a0027 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.3433C>T | p.Pro1145Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 22/42 | 3798/13162 | 3433/6237 | 1145/2078 | chr14 | 96315512 | ||
chr14:96315529
|
C | T | 1 | a0019 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.3416G>A | p.Arg1139His | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 22/42 | 3781/13162 | 3416/6237 | 1139/2078 | chr14 | 96315529 | ||
chr14:96315575
|
T | C | 25 | a0001a0002a0004others(22): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
missense_variant | MODERATE | c.3370A>G | p.Asn1124Asp | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 22/42 | 3735/13162 | 3370/6237 | 1124/2078 | chr14 | 96315575 | ||
chr14:96316628
|
T | C | 1 | a0011 | 2 | NA19074.hp1 NA19080.hp2 |
missense_variant | MODERATE | c.3266A>G | p.Asn1089Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/42 | 3631/13162 | 3266/6237 | 1089/2078 | chr14 | 96316628 | ||
chr14:96325868
|
G | A | 1 | a0012 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.2218C>T | p.Arg740Trp | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/42 | 2583/13162 | 2218/6237 | 740/2078 | chr14 | 96325868 | ||
chr14:96328684
|
C | G | 1 | a0013 | 2 | HG03490.hp1 HG03669.hp2 |
missense_variant | MODERATE | c.1964G>C | p.Arg655Thr | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 13/42 | 2329/13162 | 1964/6237 | 655/2078 | chr14 | 96328684 | ||
chr14:96329606
|
A | G | 1 | a0018 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1759T>C | p.Tyr587His | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/42 | 2124/13162 | 1759/6237 | 587/2078 | chr14 | 96329606 | ||
chr14:96331530
|
G | C | 1 | a0004 | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
missense_variant | MODERATE | c.1576C>G | p.Pro526Ala | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/42 | 1941/13162 | 1576/6237 | 526/2078 | chr14 | 96331530 | ||
chr14:96332337
|
T | C | 2 | a0005a0008 | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.1436A>G | p.Asn479Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/42 | 1801/13162 | 1436/6237 | 479/2078 | chr14 | 96332337 | ||
chr14:96332343
|
G | A | 2 | a0006a0009 | 10 | HG02145.hp1 HG02895.hp2 HG02896.hp2 others(7): Show |
missense_variant | MODERATE | c.1430C>T | p.Pro477Leu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/42 | 1795/13162 | 1430/6237 | 477/2078 | chr14 | 96332343 | ||
chr14:96332368
|
G | C | 1 | a0017 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1405C>G | p.Gln469Glu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/42 | 1770/13162 | 1405/6237 | 469/2078 | chr14 | 96332368 | ||
chr14:96333724
|
A | G | 1 | a0016 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.1171T>C | p.Tyr391His | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 8/42 | 1536/13162 | 1171/6237 | 391/2078 | chr14 | 96333724 | ||
chr14:96341682
|
G | A | 1 | a0008 | 3 | HG02559.hp1 HG03579.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.764C>T | p.Ser255Leu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/42 | 1129/13162 | 764/6237 | 255/2078 | chr14 | 96341682 | ||
chr14:96343124
|
G | A | 1 | a0028 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.739C>T | p.Pro247Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/42 | 1104/13162 | 739/6237 | 247/2078 | chr14 | 96343124 | ||
chr14:96343210
|
T | C | 1 | a0014 | 2 | HG00639.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.653A>G | p.His218Arg | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/42 | 1018/13162 | 653/6237 | 218/2078 | chr14 | 96343210 | ||
chr14:96347184
|
C | T | 1 | a0015 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.320G>A | p.Arg107His | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/42 | 685/13162 | 320/6237 | 107/2078 | chr14 | 96347184 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96285824
|
G | A | 1 | a0001c0026 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.6168C>T | p.Gly2056Gly | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6533/13162 | 6168/6237 | 2056/2078 | chr14 | 96285824 | ||
chr14:96290487
|
C | T | 2 | a0001c0025a0001c0035 | 2 | NA18747.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.5805G>A | p.Ser1935Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 40/42 | 6170/13162 | 5805/6237 | 1935/2078 | chr14 | 96290487 | ||
chr14:96302088
|
G | A | 1 | a0004c0006 | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
synonymous_variant | LOW | c.5058C>T | p.His1686His | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/42 | 5423/13162 | 5058/6237 | 1686/2078 | chr14 | 96302088 | ||
chr14:96303199
|
G | A | 1 | a0001c0012 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.4899C>T | p.Leu1633Leu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/42 | 5264/13162 | 4899/6237 | 1633/2078 | chr14 | 96303199 | ||
chr14:96303229
|
C | T | 1 | a0001c0013 | 3 | HG00642.hp2 HG02809.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.4869G>A | p.Pro1623Pro | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/42 | 5234/13162 | 4869/6237 | 1623/2078 | chr14 | 96303229 | ||
chr14:96309559
|
T | C | 1 | a0001c0022 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.4197A>G | p.Pro1399Pro | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/42 | 4562/13162 | 4197/6237 | 1399/2078 | chr14 | 96309559 | ||
chr14:96317747
|
A | G | 2 | a0001c0013a0001c0024 | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.2988T>C | p.Asn996Asn | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 19/42 | 3353/13162 | 2988/6237 | 996/2078 | chr14 | 96317747 | ||
chr14:96331387
|
G | A | 34 | a0001c0002a0001c0003a0001c0011others(31): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
synonymous_variant | LOW | c.1719C>T | p.His573His | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/42 | 2084/13162 | 1719/6237 | 573/2078 | chr14 | 96331387 | ||
chr14:96343194
|
G | A | 1 | a0001c0032 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.669C>T | p.Leu223Leu | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/42 | 1034/13162 | 669/6237 | 223/2078 | chr14 | 96343194 | ||
chr14:96345249
|
A | G | 1 | a0001c0012 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.462T>C | p.Ala154Ala | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 3/42 | 827/13162 | 462/6237 | 154/2078 | chr14 | 96345249 | ||
chr14:96345327
|
T | C | 2 | a0004c0006a0004c0041 | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
synonymous_variant | LOW | c.384A>G | p.Ala128Ala | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 3/42 | 749/13162 | 384/6237 | 128/2078 | chr14 | 96345327 | ||
chr14:96362953
|
G | A | 17 | a0001c0003a0001c0011a0001c0035others(14): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
synonymous_variant | LOW | c.24C>T | p.Ser8Ser | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 389/13162 | 24/6237 | 8/2078 | chr14 | 96362953 | ||
chr14:96362965
|
C | T | 1 | a0001c0011 | 3 | HG01123.hp1 HG01261.hp1 HG02300.hp1 |
synonymous_variant | LOW | c.12G>A | p.Pro4Pro | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 377/13162 | 12/6237 | 4/2078 | chr14 | 96362965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96279224
|
T | C | 13 | a0001c0002t0051a0001c0002t0061a0001c0013t0022others(10): Show | 46 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*6531A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6531 | chr14 | 96279224 | |||||
chr14:96279393
|
G | A | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*6362C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6362 | chr14 | 96279393 | |||||
chr14:96279404
|
C | CTCAT | 10 | a0001c0002t0026a0001c0003t0023a0001c0003t0035others(7): Show | 20 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*6347_*6350dupATGA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6350 | chr14 | 96279404 | |||||
chr14:96279404
|
C | CTCATTCA others(1): Show |
71 | a0001c0002t0001a0001c0002t0051a0001c0002t0053others(68): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*6343_*6350dupATGA others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6350 | chr14 | 96279404 | |||||
chr14:96279404
|
C | CTCATTCA others(5): Show |
2 | a0002c0001t0017a0004c0041t0063 | 4 | HG03688.hp2 NA18950.hp1 NA19005.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6339_*6350dupATGA others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6350 | chr14 | 96279404 | |||||
chr14:96279477
|
C | T | 1 | a0001c0003t0045 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6278G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6278 | chr14 | 96279477 | |||||
chr14:96279546
|
G | A | 1 | a0002c0001t0042 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6209C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6209 | chr14 | 96279546 | |||||
chr14:96279564
|
TAACA | T | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6187_*6190delTGTT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6187 | chr14 | 96279564 | |||||
chr14:96279603
|
C | G | 1 | a0001c0032t0056 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6152G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6152 | chr14 | 96279603 | |||||
chr14:96279658
|
A | G | 79 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(76): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*6097T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6097 | chr14 | 96279658 | |||||
chr14:96279662
|
G | A | 19 | a0001c0003t0002a0001c0024t0006a0002c0001t0002others(16): Show | 84 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*6093C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 6093 | chr14 | 96279662 | |||||
chr14:96279786
|
G | T | 3 | a0003c0004t0049a0004c0006t0010a0004c0006t0013 | 12 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5969C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5969 | chr14 | 96279786 | |||||
chr14:96279837
|
C | A | 5 | a0001c0002t0026a0001c0003t0035a0005c0008t0012others(2): Show | 10 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5918G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5918 | chr14 | 96279837 | |||||
chr14:96279967
|
C | T | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5788G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5788 | chr14 | 96279967 | |||||
chr14:96279968
|
G | A | 1 | a0003c0004t0029 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5787C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5787 | chr14 | 96279968 | |||||
chr14:96280091
|
C | T | 1 | a0001c0005t0038 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5664G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5664 | chr14 | 96280091 | |||||
chr14:96280095
|
G | A | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*5660C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5660 | chr14 | 96280095 | |||||
chr14:96280140
|
C | G | 1 | a0001c0003t0033 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5615G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5615 | chr14 | 96280140 | |||||
chr14:96280143
|
G | A | 3 | a0001c0003t0023a0001c0003t0045a0001c0003t0046 | 4 | HG02486.hp2 HG03139.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5612C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5612 | chr14 | 96280143 | |||||
chr14:96280189
|
T | C | 1 | a0022c0037t0043 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5566A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5566 | chr14 | 96280189 | |||||
chr14:96280288
|
G | A | 1 | a0001c0003t0011 | 5 | HG01168.hp2 HG03239.hp2 HG03490.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5467C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5467 | chr14 | 96280288 | |||||
chr14:96280292
|
G | A | 2 | a0001c0002t0057a0001c0002t0060 | 2 | HG02735.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5463C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5463 | chr14 | 96280292 | |||||
chr14:96280365
|
C | A | 1 | a0001c0002t0051 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5390G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5390 | chr14 | 96280365 | |||||
chr14:96280466
|
C | T | 1 | a0001c0002t0051 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5289G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5289 | chr14 | 96280466 | |||||
chr14:96280511
|
AT | A | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5243delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5243 | chr14 | 96280511 | |||||
chr14:96280572
|
TTAAAG | T | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5178_*5182delCTTT others(1): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5178 | chr14 | 96280572 | |||||
chr14:96280615
|
C | T | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5140G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5140 | chr14 | 96280615 | |||||
chr14:96280616
|
G | A | 7 | a0001c0002t0026a0001c0003t0035a0005c0008t0012others(4): Show | 16 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5139C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5139 | chr14 | 96280616 | |||||
chr14:96280642
|
T | C | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*5113A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5113 | chr14 | 96280642 | |||||
chr14:96280735
|
T | A | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*5020A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 5020 | chr14 | 96280735 | |||||
chr14:96280897
|
T | C | 3 | a0001c0005t0007a0001c0005t0038a0001c0005t0039 | 12 | NA18942.hp2 NA18965.hp2 NA18968.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4858A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4858 | chr14 | 96280897 | |||||
chr14:96281001
|
G | T | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4754C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4754 | chr14 | 96281001 | |||||
chr14:96281012
|
T | A | 1 | a0001c0003t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4743A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4743 | chr14 | 96281012 | |||||
chr14:96281079
|
C | T | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4676G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4676 | chr14 | 96281079 | |||||
chr14:96281118
|
C | T | 1 | a0001c0003t0032 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4637G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4637 | chr14 | 96281118 | |||||
chr14:96281270
|
A | C | 8 | a0001c0024t0006a0002c0001t0006a0002c0001t0040others(5): Show | 25 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4485T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4485 | chr14 | 96281270 | |||||
chr14:96281594
|
T | C | 1 | a0001c0035t0034 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4161A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4161 | chr14 | 96281594 | |||||
chr14:96281607
|
C | T | 1 | a0001c0003t0020 | 2 | NA18941.hp1 NA18984.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4148G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4148 | chr14 | 96281607 | |||||
chr14:96281608
|
G | A | 1 | a0001c0003t0046 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4147C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4147 | chr14 | 96281608 | |||||
chr14:96281622
|
C | T | 1 | a0003c0004t0025 | 2 | HG02027.hp1 NA18961.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4133G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4133 | chr14 | 96281622 | |||||
chr14:96281629
|
A | C | 1 | a0001c0003t0031 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4126T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4126 | chr14 | 96281629 | |||||
chr14:96281649
|
T | C | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*4106A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4106 | chr14 | 96281649 | |||||
chr14:96281650
|
G | A | 7 | a0001c0002t0026a0001c0003t0035a0005c0008t0012others(4): Show | 16 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4105C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4105 | chr14 | 96281650 | |||||
chr14:96281727
|
T | A | 1 | a0024c0028t0058 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4028A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 4028 | chr14 | 96281727 | |||||
chr14:96281809
|
G | C | 1 | a0003c0004t0030 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3946C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3946 | chr14 | 96281809 | |||||
chr14:96281910
|
C | T | 22 | a0001c0002t0026a0001c0002t0051a0001c0002t0055others(19): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3845G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3845 | chr14 | 96281910 | |||||
chr14:96281918
|
G | A | 5 | a0001c0002t0026a0001c0003t0035a0005c0008t0012others(2): Show | 10 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3837C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3837 | chr14 | 96281918 | |||||
chr14:96281941
|
A | G | 1 | a0001c0002t0051 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3814T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3814 | chr14 | 96281941 | |||||
chr14:96281951
|
T | G | 79 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(76): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*3804A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3804 | chr14 | 96281951 | |||||
chr14:96282159
|
A | G | 1 | a0002c0001t0041 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3596T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3596 | chr14 | 96282159 | |||||
chr14:96282273
|
T | C | 78 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(75): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*3482A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3482 | chr14 | 96282273 | |||||
chr14:96282313
|
C | T | 2 | a0005c0010t0009a0008c0014t0009 | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3442G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3442 | chr14 | 96282313 | |||||
chr14:96282365
|
C | T | 1 | a0004c0041t0063 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3390G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3390 | chr14 | 96282365 | |||||
chr14:96282424
|
G | A | 2 | a0001c0012t0024a0001c0012t0050 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3331C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3331 | chr14 | 96282424 | |||||
chr14:96282465
|
C | T | 2 | a0001c0003t0016a0001c0003t0020 | 5 | NA18612.hp1 NA18941.hp1 NA18955.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3290G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3290 | chr14 | 96282465 | |||||
chr14:96282513
|
G | T | 3 | a0003c0004t0049a0004c0006t0010a0004c0006t0013 | 12 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3242C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3242 | chr14 | 96282513 | |||||
chr14:96282539
|
T | C | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*3216A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3216 | chr14 | 96282539 | |||||
chr14:96282599
|
T | C | 1 | a0001c0005t0039 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3156A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3156 | chr14 | 96282599 | |||||
chr14:96282654
|
A | G | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*3101T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 3101 | chr14 | 96282654 | |||||
chr14:96282759
|
A | T | 1 | a0001c0002t0053 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2996T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2996 | chr14 | 96282759 | |||||
chr14:96282973
|
A | T | 1 | a0001c0003t0037 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2782T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2782 | chr14 | 96282973 | |||||
chr14:96283033
|
T | A | 1 | a0001c0002t0059 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2722 | chr14 | 96283033 | |||||
chr14:96283044
|
A | T | 26 | a0001c0003t0002a0001c0003t0023a0001c0003t0044others(23): Show | 99 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2711T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2711 | chr14 | 96283044 | |||||
chr14:96283240
|
C | G | 1 | a0001c0002t0051 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2515G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2515 | chr14 | 96283240 | |||||
chr14:96283303
|
C | CA | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*2451dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2451 | chr14 | 96283303 | |||||
chr14:96283364
|
C | G | 1 | a0002c0001t0048 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2391G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2391 | chr14 | 96283364 | |||||
chr14:96283422
|
G | A | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*2333C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2333 | chr14 | 96283422 | |||||
chr14:96283509
|
T | C | 83 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(80): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*2246A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2246 | chr14 | 96283509 | |||||
chr14:96283516
|
G | C | 3 | a0001c0003t0023a0001c0003t0045a0001c0003t0046 | 4 | HG02486.hp2 HG03139.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2239C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2239 | chr14 | 96283516 | |||||
chr14:96283556
|
G | A | 1 | a0001c0002t0060 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2199C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2199 | chr14 | 96283556 | |||||
chr14:96283571
|
G | T | 2 | a0001c0012t0024a0001c0012t0050 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2184C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2184 | chr14 | 96283571 | |||||
chr14:96283614
|
T | C | 1 | a0004c0006t0010 | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2141A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2141 | chr14 | 96283614 | |||||
chr14:96283673
|
C | G | 1 | a0002c0001t0040 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2082G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2082 | chr14 | 96283673 | |||||
chr14:96283696
|
A | G | 32 | a0001c0002t0001a0001c0002t0053a0001c0002t0054others(29): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2059T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2059 | chr14 | 96283696 | |||||
chr14:96283721
|
G | A | 1 | a0001c0002t0061 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2034C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 2034 | chr14 | 96283721 | |||||
chr14:96283791
|
A | G | 3 | a0002c0001t0014a0002c0001t0028a0019c0034t0014 | 5 | HG00597.hp1 HG02155.hp1 NA18943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1964T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1964 | chr14 | 96283791 | |||||
chr14:96283813
|
C | T | 1 | a0018c0023t0036 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1942G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1942 | chr14 | 96283813 | |||||
chr14:96283878
|
C | T | 10 | a0001c0022t0015a0002c0001t0004a0003c0004t0004others(7): Show | 42 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1877G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1877 | chr14 | 96283878 | |||||
chr14:96284145
|
G | A | 2 | a0005c0010t0009a0008c0014t0009 | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1610C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1610 | chr14 | 96284145 | |||||
chr14:96284177
|
C | T | 1 | a0004c0041t0063 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1578G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1578 | chr14 | 96284177 | |||||
chr14:96284218
|
G | A | 1 | a0002c0001t0047 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1537 | chr14 | 96284218 | |||||
chr14:96284277
|
C | T | 1 | a0005c0008t0021 | 2 | HG02258.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1478G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1478 | chr14 | 96284277 | |||||
chr14:96284319
|
A | C | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1436T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1436 | chr14 | 96284319 | |||||
chr14:96284410
|
C | A | 1 | a0002c0001t0048 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1345 | chr14 | 96284410 | |||||
chr14:96284496
|
A | G | 2 | a0001c0002t0051a0001c0003t0035 | 2 | HG02055.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1259T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1259 | chr14 | 96284496 | |||||
chr14:96284672
|
G | C | 2 | a0001c0012t0024a0001c0012t0050 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1083C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1083 | chr14 | 96284672 | |||||
chr14:96284673
|
T | C | 73 | a0001c0002t0001a0001c0002t0026a0001c0002t0051others(70): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*1082A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 1082 | chr14 | 96284673 | |||||
chr14:96285021
|
T | C | 4 | a0003c0004t0049a0004c0006t0010a0004c0006t0013others(1): Show | 13 | HG00621.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*734A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 734 | chr14 | 96285021 | |||||
chr14:96285055
|
C | G | 2 | a0005c0010t0009a0008c0014t0009 | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*700G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 700 | chr14 | 96285055 | |||||
chr14:96285386
|
T | C | 1 | a0001c0012t0050 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*369A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 369 | chr14 | 96285386 | |||||
chr14:96285460
|
G | A | 1 | a0001c0002t0062 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 42/42 | 295 | chr14 | 96285460 | |||||
chr14:96363016
|
G | A | 5 | a0001c0005t0018a0001c0022t0015a0003c0004t0015others(2): Show | 9 | HG00673.hp2 HG02015.hp2 HG02027.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 40 | chr14 | 96363016 | |||||
chr14:96363032
|
C | CG | 3 | a0001c0003t0027a0002c0001t0019a0002c0001t0028 | 4 | HG02055.hp2 NA18978.hp1 NA18979.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-57dupC | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 57 | chr14 | 96363032 | |||||
chr14:96363180
|
G | C | 1 | a0001c0002t0051 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-204C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 204 | chr14 | 96363180 | |||||
chr14:96363218
|
G | C | 19 | a0001c0002t0001a0001c0002t0026a0001c0002t0052others(16): Show | 79 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-242C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 242 | chr14 | 96363218 | |||||
chr14:96363250
|
G | A | 3 | a0004c0006t0010a0004c0006t0013a0004c0041t0063 | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-274C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/42 | 274 | chr14 | 96363250 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96285990
|
G | A | 1 | a0004c0006t0010g0336 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.6007-5C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96285990 | ||||||
chr14:96286053
|
C | T | 17 | a0001c0002t0001g0275a0001c0002t0026g0010a0002c0001t0002g0120others(14): Show | 19 | HG00597.hp2 HG00621.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.6007-68G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286053 | ||||||
chr14:96286130
|
T | A | 4 | a0001c0002t0001g0272a0001c0003t0033g0231a0014c0019t0001g0273others(1): Show | 4 | HG00639.hp2 HG02258.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6007-145A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286130 | ||||||
chr14:96286218
|
C | T | 264 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(261): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.6007-233G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286218 | ||||||
chr14:96286247
|
G | A | 61 | a0001c0002t0052g0330a0001c0003t0002g0214a0001c0003t0003g0008others(58): Show | 67 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.6007-262C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286247 | ||||||
chr14:96286268
|
G | A | 39 | a0001c0022t0015g0252a0002c0001t0004g0190a0002c0001t0040g0166others(36): Show | 41 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.6007-283C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286268 | ||||||
chr14:96286450
|
A | G | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.6007-465T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286450 | ||||||
chr14:96286480
|
A | G | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6007-495T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286480 | ||||||
chr14:96286494
|
G | C | 3 | a0002c0001t0006g0161a0002c0001t0006g0175a0002c0001t0006g0187 | 3 | HG02559.hp2 HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.6007-509C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286494 | ||||||
chr14:96286666
|
C | T | 1 | a0001c0003t0045g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6007-681G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286666 | ||||||
chr14:96286682
|
A | G | 274 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(271): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.6007-697T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286682 | ||||||
chr14:96286713
|
A | C | 2 | a0001c0003t0023g0245a0001c0003t0045g0246 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6007-728T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286713 | ||||||
chr14:96286863
|
A | T | 286 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(283): Show | 297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.6007-878T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286863 | ||||||
chr14:96286864
|
A | C | 286 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(283): Show | 297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.6007-879T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286864 | ||||||
chr14:96286925
|
T | C | 1 | a0001c0012t0024g0093 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6007-940A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286925 | ||||||
chr14:96286975
|
G | T | 100 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0046g0244others(97): Show | 104 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.6007-990C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286975 | ||||||
chr14:96286983
|
C | T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6007-998G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96286983 | ||||||
chr14:96287065
|
C | T | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.6007-1080G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287065 | ||||||
chr14:96287124
|
A | G | 1 | a0001c0005t0007g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.6007-1139T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287124 | ||||||
chr14:96287202
|
C | T | 2 | a0002c0001t0002g0120a0002c0001t0002g0148 | 2 | NA18941.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.6007-1217G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287202 | ||||||
chr14:96287253
|
C | CA | 24 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0001g0261others(21): Show | 25 | HG00621.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.6007-1269dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287253 | ||||||
chr14:96287253
|
C | CAA | 130 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0262others(127): Show | 134 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.6007-1270_6007-126 others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287253 | ||||||
chr14:96287253
|
C | CAAA | 94 | a0001c0002t0055g0320a0001c0003t0046g0244a0001c0005t0007g0060others(91): Show | 100 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.6007-1271_6007-126 others(7): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287253 | ||||||
chr14:96287253
|
C | CAAAA | 38 | a0002c0001t0002g0110a0002c0001t0002g0120a0002c0001t0002g0126others(35): Show | 38 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.6007-1272_6007-126 others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287253 | ||||||
chr14:96287253
|
CA | C | 8 | a0001c0003t0003g0200a0001c0003t0003g0208a0001c0003t0003g0215others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.6007-1269delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287253 | ||||||
chr14:96287274
|
C | A | 116 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(113): Show | 119 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.6007-1289G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287274 | ||||||
chr14:96287438
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6007-1453C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287438 | ||||||
chr14:96287471
|
C | T | 3 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0337 | 3 | NA19007.hp1 NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.6007-1486G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287471 | ||||||
chr14:96287576
|
G | T | 1 | a0001c0002t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6007-1591C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287576 | ||||||
chr14:96287588
|
C | T | 273 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(270): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.6007-1603G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287588 | ||||||
chr14:96287627
|
G | A | 273 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(270): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.6007-1642C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287627 | ||||||
chr14:96287752
|
C | T | 1 | a0002c0001t0002g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.6007-1767G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287752 | ||||||
chr14:96287845
|
C | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6006+1811G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96287845 | ||||||
chr14:96288001
|
C | A | 7 | a0001c0003t0023g0243a0001c0003t0046g0244a0006c0007t0008g0001others(4): Show | 10 | HG02145.hp1 HG02895.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.6006+1655G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288001 | ||||||
chr14:96288012
|
CT | C | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.6006+1643delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288012 | ||||||
chr14:96288060
|
G | T | 15 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(12): Show | 16 | HG00621.hp1 HG00642.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.6006+1596C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288060 | ||||||
chr14:96288090
|
T | C | 1 | a0011c0017t0001g0325 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.6006+1566A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288090 | ||||||
chr14:96288286
|
A | G | 6 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(3): Show | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.6006+1370T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288286 | ||||||
chr14:96288528
|
T | C | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6006+1128A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288528 | ||||||
chr14:96288558
|
T | A | 1 | a0001c0003t0003g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.6006+1098A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288558 | ||||||
chr14:96288632
|
T | C | 1 | a0027c0040t0006g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6006+1024A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288632 | ||||||
chr14:96288656
|
C | T | 1 | a0004c0006t0010g0334 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6006+1000G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288656 | ||||||
chr14:96288750
|
T | C | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.6006+906A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288750 | ||||||
chr14:96288792
|
C | T | 1 | a0001c0002t0001g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6006+864G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288792 | ||||||
chr14:96288807
|
G | GA | 97 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.6006+848dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288807 | ||||||
chr14:96288845
|
G | T | 1 | a0001c0003t0011g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6006+811C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288845 | ||||||
chr14:96288943
|
G | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.6006+713C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288943 | ||||||
chr14:96288964
|
T | C | 1 | a0002c0001t0014g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.6006+692A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96288964 | ||||||
chr14:96289098
|
C | A | 1 | a0001c0002t0060g0266 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6006+558G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289098 | ||||||
chr14:96289128
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.6006+528G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289128 | ||||||
chr14:96289221
|
A | G | 275 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(272): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.6006+435T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289221 | ||||||
chr14:96289289
|
G | A | 275 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(272): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.6006+367C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289289 | ||||||
chr14:96289382
|
G | A | 281 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(278): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.6006+274C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289382 | ||||||
chr14:96289399
|
C | T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6006+257G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289399 | ||||||
chr14:96289411
|
T | G | 1 | a0003c0004t0004g0037 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6006+245A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289411 | ||||||
chr14:96289415
|
G | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.6006+241C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289415 | ||||||
chr14:96289472
|
A | G | 15 | a0001c0002t0001g0288a0001c0003t0035g0247a0005c0008t0005g0098others(12): Show | 16 | HG00140.hp1 HG00642.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.6006+184T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289472 | ||||||
chr14:96289613
|
C | T | 5 | a0002c0001t0014g0121a0002c0001t0014g0144a0002c0001t0014g0145others(2): Show | 5 | HG00597.hp1 HG02155.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.6006+43G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 41/41 | chr14 | 96289613 | ||||||
chr14:96289988
|
A | T | 6 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(3): Show | 9 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.5857-183T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 40/41 | chr14 | 96289988 | ||||||
chr14:96290121
|
T | G | 1 | a0001c0003t0003g0202 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5856+315A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 40/41 | chr14 | 96290121 | ||||||
chr14:96290289
|
T | A | 3 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0046g0244 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5856+147A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 40/41 | chr14 | 96290289 | ||||||
chr14:96290631
|
C | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5702-41G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 39/41 | chr14 | 96290631 | ||||||
chr14:96290636
|
T | C | 10 | a0001c0002t0001g0302a0001c0002t0001g0308a0001c0002t0001g0309others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.5702-46A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 39/41 | chr14 | 96290636 | ||||||
chr14:96290739
|
TA | T | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.5701+74delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 39/41 | chr14 | 96290739 | ||||||
chr14:96290781
|
C | G | 1 | a0002c0001t0019g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5701+33G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 39/41 | chr14 | 96290781 | ||||||
chr14:96290960
|
T | G | 1 | a0001c0002t0001g0290 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5580-25A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 38/41 | chr14 | 96290960 | ||||||
chr14:96290996
|
T | C | 1 | a0001c0003t0045g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5580-61A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 38/41 | chr14 | 96290996 | ||||||
chr14:96291002
|
G | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5580-67C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 38/41 | chr14 | 96291002 | ||||||
chr14:96291024
|
T | A | 272 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(269): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.5580-89A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 38/41 | chr14 | 96291024 | ||||||
chr14:96291570
|
C | T | 3 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0046g0244 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5579+30G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 38/41 | chr14 | 96291570 | ||||||
chr14:96291773
|
G | A | 1 | a0001c0003t0032g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5497-91C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 37/41 | chr14 | 96291773 | ||||||
chr14:96291823
|
C | T | 272 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(269): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.5497-141G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 37/41 | chr14 | 96291823 | ||||||
chr14:96291839
|
C | T | 1 | a0001c0003t0033g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5497-157G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 37/41 | chr14 | 96291839 | ||||||
chr14:96291893
|
AC | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5496+135delG | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 37/41 | chr14 | 96291893 | ||||||
chr14:96292328
|
G | A | 283 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(280): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.5427-230C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292328 | ||||||
chr14:96292647
|
G | A | 38 | a0001c0002t0051g0257a0003c0004t0003g0033a0003c0004t0004g0003others(35): Show | 40 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.5427-549C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292647 | ||||||
chr14:96292648
|
C | T | 38 | a0001c0002t0051g0257a0003c0004t0003g0033a0003c0004t0004g0003others(35): Show | 40 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.5427-550G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292648 | ||||||
chr14:96292719
|
G | A | 174 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(171): Show | 180 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.5427-621C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292719 | ||||||
chr14:96292742
|
G | A | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5427-644C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292742 | ||||||
chr14:96292761
|
C | T | 37 | a0003c0004t0003g0033a0003c0004t0004g0003a0003c0004t0004g0004others(34): Show | 39 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.5427-663G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292761 | ||||||
chr14:96292762
|
G | A | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5427-664C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292762 | ||||||
chr14:96292887
|
G | C | 8 | a0001c0003t0003g0108a0001c0003t0003g0201a0001c0003t0003g0202others(5): Show | 8 | NA18945.hp1 NA18965.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.5427-789C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96292887 | ||||||
chr14:96293212
|
C | G | 2 | a0001c0002t0001g0258a0001c0002t0059g0259 | 2 | HG01981.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.5427-1114G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293212 | ||||||
chr14:96293212
|
C | T | 1 | a0002c0001t0017g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5427-1114G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293212 | ||||||
chr14:96293250
|
C | G | 1 | a0001c0002t0052g0330 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5427-1152G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293250 | ||||||
chr14:96293348
|
C | CT | 118 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(115): Show | 121 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.5427-1251dupA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293348 | ||||||
chr14:96293483
|
T | G | 1 | a0005c0008t0021g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5427-1385A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293483 | ||||||
chr14:96293509
|
T | C | 6 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(3): Show | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.5427-1411A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293509 | ||||||
chr14:96293516
|
A | C | 98 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(95): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5427-1418T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293516 | ||||||
chr14:96293602
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5426+1358A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293602 | ||||||
chr14:96293721
|
C | A | 1 | a0013c0015t0004g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5426+1239G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293721 | ||||||
chr14:96293732
|
C | G | 1 | a0003c0004t0004g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5426+1228G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96293732 | ||||||
chr14:96294015
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5426+945G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294015 | ||||||
chr14:96294025
|
C | T | 2 | a0001c0002t0057g0267a0001c0002t0060g0266 | 2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.5426+935G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294025 | ||||||
chr14:96294078
|
T | G | 5 | a0001c0003t0003g0215a0001c0003t0003g0220a0001c0003t0003g0224others(2): Show | 5 | HG00323.hp2 HG01074.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.5426+882A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294078 | ||||||
chr14:96294132
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5426+828C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294132 | ||||||
chr14:96294223
|
C | T | 2 | a0004c0006t0010g0335a0004c0006t0010g0336 | 2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.5426+737G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294223 | ||||||
chr14:96294226
|
G | A | 91 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.5426+734C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294226 | ||||||
chr14:96294288
|
G | C | 2 | a0002c0001t0002g0133a0002c0001t0002g0186 | 2 | HG01515.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.5426+672C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294288 | ||||||
chr14:96294346
|
C | A | 284 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(281): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.5426+614G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294346 | ||||||
chr14:96294413
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5426+547C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294413 | ||||||
chr14:96294419
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5426+541C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294419 | ||||||
chr14:96294574
|
A | C | 1 | a0001c0002t0061g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5426+386T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294574 | ||||||
chr14:96294597
|
T | C | 1 | a0016c0033t0003g0211 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5426+363A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294597 | ||||||
chr14:96294616
|
A | G | 1 | a0002c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5426+344T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294616 | ||||||
chr14:96294619
|
G | A | 1 | a0002c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5426+341C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294619 | ||||||
chr14:96294749
|
G | C | 273 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(270): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.5426+211C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294749 | ||||||
chr14:96294782
|
G | A | 1 | a0001c0002t0001g0293 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5426+178C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294782 | ||||||
chr14:96294871
|
A | G | 2 | a0010c0016t0004g0077a0010c0016t0004g0078 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.5426+89T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 36/41 | chr14 | 96294871 | ||||||
chr14:96295177
|
T | A | 117 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(114): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.5219-10A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 35/41 | chr14 | 96295177 | ||||||
chr14:96295220
|
A | C | 270 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(267): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.5219-53T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 35/41 | chr14 | 96295220 | ||||||
chr14:96295337
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5218+145A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 35/41 | chr14 | 96295337 | ||||||
chr14:96295434
|
T | A | 1 | a0002c0001t0002g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5218+48A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 35/41 | chr14 | 96295434 | ||||||
chr14:96295600
|
A | G | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.5140-40T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295600 | ||||||
chr14:96295609
|
T | C | 3 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090 | 3 | HG00642.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5140-49A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295609 | ||||||
chr14:96295653
|
C | T | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5140-93G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295653 | ||||||
chr14:96295727
|
C | CCACA | 3 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0046g0244 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5140-171_5140-168d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(1): Show |
29 | a0001c0002t0001g0302a0001c0003t0035g0247a0001c0025t0001g0307others(26): Show | 31 | HG00642.hp1 HG01255.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.5140-175_5140-168d others(10): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(3): Show |
30 | a0001c0002t0051g0257a0003c0004t0003g0033a0003c0004t0004g0004others(27): Show | 31 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.5140-177_5140-168d others(12): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(5): Show |
10 | a0001c0002t0001g0318a0001c0002t0001g0319a0001c0013t0005g0091others(7): Show | 10 | HG00621.hp2 HG00642.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.5140-179_5140-168d others(14): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(7): Show |
70 | a0001c0002t0001g0300a0001c0002t0001g0316a0001c0002t0001g0322others(67): Show | 75 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.5140-181_5140-168d others(16): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(9): Show |
56 | a0001c0002t0001g0012a0001c0002t0001g0260a0001c0002t0001g0261others(53): Show | 58 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.5140-183_5140-168d others(18): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(11): Show |
60 | a0001c0002t0001g0258a0001c0002t0001g0264a0001c0002t0001g0275others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.5140-185_5140-168d others(20): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(13): Show |
17 | a0001c0002t0001g0011a0001c0002t0001g0263a0001c0002t0001g0270others(14): Show | 18 | HG00609.hp1 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.5140-187_5140-168d others(22): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(15): Show |
8 | a0001c0002t0001g0262a0001c0002t0001g0278a0001c0002t0001g0284others(5): Show | 8 | HG00735.hp2 HG01070.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.5140-189_5140-168d others(24): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(17): Show |
4 | a0001c0002t0001g0265a0001c0002t0001g0299a0001c0026t0001g0269others(1): Show | 4 | HG01261.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.5140-191_5140-168d others(26): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295727
|
C | CCACACAC others(19): Show |
1 | a0001c0002t0001g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5140-193_5140-168d others(28): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295727 | ||||||
chr14:96295934
|
G | A | 65 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(62): Show | 66 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5140-374C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96295934 | ||||||
chr14:96296003
|
G | A | 1 | a0001c0002t0001g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5140-443C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296003 | ||||||
chr14:96296031
|
G | A | 1 | a0023c0036t0002g0130 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5140-471C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296031 | ||||||
chr14:96296211
|
T | C | 1 | a0002c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5140-651A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296211 | ||||||
chr14:96296231
|
C | T | 1 | a0010c0016t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5140-671G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296231 | ||||||
chr14:96296276
|
T | C | 1 | a0001c0003t0003g0205 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5140-716A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296276 | ||||||
chr14:96296320
|
T | C | 1 | a0003c0004t0004g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5140-760A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296320 | ||||||
chr14:96296364
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5140-804G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296364 | ||||||
chr14:96296388
|
T | C | 117 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(114): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.5140-828A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296388 | ||||||
chr14:96296484
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5140-924C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296484 | ||||||
chr14:96296538
|
G | A | 5 | a0002c0001t0006g0160a0002c0001t0006g0162a0002c0001t0006g0163others(2): Show | 5 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5140-978C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296538 | ||||||
chr14:96296543
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5140-983A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296543 | ||||||
chr14:96296552
|
G | C | 1 | a0001c0003t0003g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5140-992C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296552 | ||||||
chr14:96296703
|
G | C | 98 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(95): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5140-1143C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296703 | ||||||
chr14:96296747
|
C | A | 3 | a0004c0006t0013g0013a0004c0006t0013g0331a0004c0006t0013g0332 | 4 | HG00621.hp1 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.5140-1187G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296747 | ||||||
chr14:96296760
|
C | CA | 30 | a0001c0002t0001g0263a0001c0002t0001g0279a0001c0002t0051g0257others(27): Show | 31 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.5140-1201dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96296760 | ||||||
chr14:96297025
|
T | C | 66 | a0001c0002t0001g0012a0001c0002t0001g0262a0001c0002t0001g0265others(63): Show | 67 | HG00558.hp2 HG00673.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.5140-1465A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297025 | ||||||
chr14:96297255
|
C | CA | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5140-1696dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297255 | ||||||
chr14:96297293
|
TA | T | 7 | a0001c0002t0001g0280a0007c0009t0002g0119a0007c0009t0002g0125others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.5140-1734delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297293 | ||||||
chr14:96297446
|
G | A | 1 | a0003c0004t0029g0023 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5140-1886C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297446 | ||||||
chr14:96297649
|
G | A | 259 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(256): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.5140-2089C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297649 | ||||||
chr14:96297676
|
C | T | 3 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090 | 3 | HG00642.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5140-2116G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297676 | ||||||
chr14:96297814
|
G | A | 1 | a0001c0003t0044g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5140-2254C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96297814 | ||||||
chr14:96298246
|
C | T | 37 | a0003c0004t0003g0033a0003c0004t0004g0003a0003c0004t0004g0004others(34): Show | 39 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.5140-2686G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298246 | ||||||
chr14:96298394
|
T | C | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5140-2834A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298394 | ||||||
chr14:96298455
|
G | A | 4 | a0001c0002t0001g0263a0001c0002t0001g0285a0001c0012t0024g0094others(1): Show | 4 | HG03195.hp2 NA18522.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.5140-2895C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298455 | ||||||
chr14:96298560
|
C | T | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.5140-3000G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298560 | ||||||
chr14:96298664
|
A | C | 91 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.5140-3104T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298664 | ||||||
chr14:96298713
|
A | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5140-3153T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298713 | ||||||
chr14:96298747
|
G | A | 1 | a0001c0002t0001g0324 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5140-3187C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298747 | ||||||
chr14:96298779
|
G | A | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5140-3219C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298779 | ||||||
chr14:96298808
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+3199A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298808 | ||||||
chr14:96298919
|
A | ATGTT | 40 | a0001c0002t0001g0011a0001c0002t0001g0258a0001c0002t0001g0260others(37): Show | 42 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5139+3084_5139+308 others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96298919 | ||||||
chr14:96299015
|
G | A | 1 | a0001c0002t0026g0010 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5139+2992C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299015 | ||||||
chr14:96299015
|
GACTT | G | 7 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(4): Show | 10 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.5139+2988_5139+299 others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299015 | ||||||
chr14:96299032
|
G | T | 37 | a0003c0004t0003g0033a0003c0004t0004g0003a0003c0004t0004g0004others(34): Show | 39 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.5139+2975C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299032 | ||||||
chr14:96299171
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+2836C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299171 | ||||||
chr14:96299240
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+2767G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299240 | ||||||
chr14:96299378
|
G | A | 1 | a0001c0003t0044g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5139+2629C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299378 | ||||||
chr14:96299517
|
A | G | 259 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(256): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.5139+2490T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299517 | ||||||
chr14:96299546
|
C | T | 115 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(112): Show | 118 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.5139+2461G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299546 | ||||||
chr14:96299581
|
T | C | 270 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(267): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.5139+2426A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299581 | ||||||
chr14:96299692
|
C | T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5139+2315G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299692 | ||||||
chr14:96299800
|
C | T | 1 | a0001c0003t0033g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5139+2207G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299800 | ||||||
chr14:96299897
|
T | C | 1 | a0002c0001t0002g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5139+2110A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96299897 | ||||||
chr14:96300106
|
A | G | 270 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(267): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.5139+1901T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300106 | ||||||
chr14:96300159
|
T | C | 3 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090 | 3 | HG00642.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5139+1848A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300159 | ||||||
chr14:96300206
|
T | C | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5139+1801A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300206 | ||||||
chr14:96300222
|
C | T | 40 | a0001c0002t0001g0011a0001c0002t0001g0258a0001c0002t0001g0260others(37): Show | 42 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5139+1785G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300222 | ||||||
chr14:96300264
|
C | A | 9 | a0004c0006t0010g0333a0004c0006t0010g0335a0004c0006t0010g0337others(6): Show | 10 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.5139+1743G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300264 | ||||||
chr14:96300443
|
T | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5139+1564A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300443 | ||||||
chr14:96300543
|
T | C | 259 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(256): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.5139+1464A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300543 | ||||||
chr14:96300544
|
T | C | 16 | a0001c0002t0001g0263a0001c0002t0001g0264a0001c0002t0001g0278others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.5139+1463A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300544 | ||||||
chr14:96300581
|
T | A | 1 | a0013c0015t0004g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5139+1426A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300581 | ||||||
chr14:96300826
|
C | T | 1 | a0001c0003t0045g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5139+1181G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300826 | ||||||
chr14:96300975
|
C | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5139+1032G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96300975 | ||||||
chr14:96301105
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+902A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301105 | ||||||
chr14:96301158
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+849C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301158 | ||||||
chr14:96301291
|
T | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+716A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301291 | ||||||
chr14:96301304
|
A | G | 1 | a0001c0003t0003g0008 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5139+703T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301304 | ||||||
chr14:96301317
|
GCTACAGA others(1): Show |
G | 259 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(256): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.5139+682_5139+689d others(10): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301317 | ||||||
chr14:96301326
|
C | T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5139+681G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301326 | ||||||
chr14:96301339
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+668G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301339 | ||||||
chr14:96301340
|
C | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+667G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301340 | ||||||
chr14:96301368
|
G | A | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.5139+639C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301368 | ||||||
chr14:96301385
|
C | A | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5139+622G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301385 | ||||||
chr14:96301443
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+564T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301443 | ||||||
chr14:96301497
|
G | C | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.5139+510C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301497 | ||||||
chr14:96301560
|
A | G | 3 | a0001c0002t0001g0279a0011c0017t0001g0289a0011c0017t0001g0325 | 3 | HG03927.hp1 NA19074.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.5139+447T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301560 | ||||||
chr14:96301714
|
G | T | 5 | a0002c0001t0002g0120a0002c0001t0002g0148a0002c0001t0002g0235others(2): Show | 5 | NA18941.hp2 NA18952.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.5139+293C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301714 | ||||||
chr14:96301735
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+272C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301735 | ||||||
chr14:96301746
|
G | C | 1 | a0001c0002t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5139+261C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301746 | ||||||
chr14:96301789
|
C | G | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.5139+218G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301789 | ||||||
chr14:96301792
|
T | C | 1 | a0013c0015t0004g0025 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5139+215A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301792 | ||||||
chr14:96301814
|
C | CATCTAAT others(1): Show |
3 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090 | 3 | HG00642.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5139+185_5139+192d others(10): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301814 | ||||||
chr14:96301847
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+160A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301847 | ||||||
chr14:96301979
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5139+28G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301979 | ||||||
chr14:96301998
|
G | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5139+9C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 34/41 | chr14 | 96301998 | ||||||
chr14:96302142
|
C | G | 1 | a0028c0031t0001g0277 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.5038-34G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302142 | ||||||
chr14:96302144
|
A | G | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5038-36T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302144 | ||||||
chr14:96302153
|
T | C | 1 | a0003c0004t0025g0249 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5038-45A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302153 | ||||||
chr14:96302177
|
G | GA | 98 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(95): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.5038-70dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302177 | ||||||
chr14:96302316
|
G | A | 1 | a0001c0005t0005g0045 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5038-208C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302316 | ||||||
chr14:96302336
|
C | T | 7 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(4): Show | 10 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.5038-228G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302336 | ||||||
chr14:96302365
|
C | T | 3 | a0003c0004t0004g0063a0003c0004t0004g0064a0003c0004t0030g0062 | 3 | NA18990.hp1 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.5038-257G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302365 | ||||||
chr14:96302414
|
A | T | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.5038-306T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302414 | ||||||
chr14:96302474
|
C | T | 50 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(47): Show | 55 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.5038-366G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302474 | ||||||
chr14:96302579
|
G | A | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.5038-471C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302579 | ||||||
chr14:96302579
|
GA | G | 92 | a0001c0002t0001g0312a0001c0024t0006g0092a0002c0001t0002g0006others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.5038-472delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302579 | ||||||
chr14:96302896
|
A | G | 91 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.5037+165T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302896 | ||||||
chr14:96302938
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5037+123G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96302938 | ||||||
chr14:96303037
|
C | G | 2 | a0001c0003t0020g0222a0001c0003t0020g0223 | 2 | NA18941.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.5037+24G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96303037 | ||||||
chr14:96303043
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.5037+18C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 33/41 | chr14 | 96303043 | ||||||
chr14:96303264
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4843-9C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303264 | ||||||
chr14:96303269
|
G | GA | 3 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090 | 3 | HG00642.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4843-15dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303269 | ||||||
chr14:96303365
|
C | T | 1 | a0001c0002t0001g0308 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4843-110G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303365 | ||||||
chr14:96303391
|
A | C | 1 | a0002c0001t0002g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4843-136T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303391 | ||||||
chr14:96303581
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4843-326T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303581 | ||||||
chr14:96303593
|
TATTC | T | 3 | a0001c0024t0006g0092a0002c0001t0006g0164a0002c0001t0006g0165 | 3 | HG01891.hp2 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4843-342_4843-339d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303593 | ||||||
chr14:96303665
|
A | G | 61 | a0001c0002t0001g0012a0001c0002t0001g0262a0001c0002t0001g0265others(58): Show | 62 | HG00558.hp2 HG00673.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.4843-410T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303665 | ||||||
chr14:96303737
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4843-482A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303737 | ||||||
chr14:96303768
|
C | T | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4843-513G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303768 | ||||||
chr14:96303842
|
A | G | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.4843-587T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96303842 | ||||||
chr14:96304315
|
C | T | 8 | a0002c0001t0048g0114a0007c0009t0002g0119a0007c0009t0002g0125others(5): Show | 8 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.4842+180G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96304315 | ||||||
chr14:96304383
|
T | G | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.4842+112A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 32/41 | chr14 | 96304383 | ||||||
chr14:96304615
|
C | CA | 96 | a0001c0002t0001g0304a0001c0002t0001g0328a0001c0002t0052g0330others(93): Show | 97 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.4734-13dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304615 | ||||||
chr14:96304615
|
C | CAA | 7 | a0002c0001t0002g0142a0002c0001t0002g0146a0002c0001t0002g0149others(4): Show | 7 | HG00438.hp1 HG01346.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.4734-14_4734-13dup others(2): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304615 | ||||||
chr14:96304615
|
CAA | C | 68 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(65): Show | 74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.4734-14_4734-13del others(2): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304615 | ||||||
chr14:96304615
|
CAAA | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4734-15_4734-13del others(3): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304615 | ||||||
chr14:96304670
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4734-67T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304670 | ||||||
chr14:96304755
|
G | A | 1 | a0002c0001t0002g0155 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4734-152C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304755 | ||||||
chr14:96304793
|
C | T | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4734-190G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304793 | ||||||
chr14:96304995
|
T | TGGACGTG others(310): Show |
5 | a0004c0006t0010g0333a0004c0006t0010g0335a0004c0006t0010g0336others(2): Show | 5 | HG02735.hp2 HG03239.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.4734-393_4734-392i others(319): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304995 | ||||||
chr14:96304995
|
T | TGGACGTG others(311): Show |
1 | a0004c0006t0010g0334 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4734-393_4734-392i others(320): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96304995 | ||||||
chr14:96305013
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4734-410C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305013 | ||||||
chr14:96305044
|
G | A | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4734-441C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305044 | ||||||
chr14:96305085
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4734-482G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305085 | ||||||
chr14:96305097
|
G | A | 1 | a0001c0002t0001g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4733+492C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305097 | ||||||
chr14:96305115
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4733+474C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305115 | ||||||
chr14:96305133
|
T | TTC | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4733+454_4733+455d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305133 | ||||||
chr14:96305143
|
G | A | 1 | a0002c0001t0002g0183 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4733+446C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305143 | ||||||
chr14:96305166
|
A | G | 1 | a0004c0006t0013g0331 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4733+423T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305166 | ||||||
chr14:96305177
|
A | G | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4733+412T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305177 | ||||||
chr14:96305241
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4733+348G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305241 | ||||||
chr14:96305429
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4733+160T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305429 | ||||||
chr14:96305438
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4733+151T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 31/41 | chr14 | 96305438 | ||||||
chr14:96305836
|
A | G | 1 | a0002c0001t0002g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4507-21T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96305836 | ||||||
chr14:96305993
|
A | C | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.4507-178T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96305993 | ||||||
chr14:96306014
|
C | T | 1 | a0002c0001t0006g0169 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4507-199G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306014 | ||||||
chr14:96306054
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4507-239C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306054 | ||||||
chr14:96306166
|
G | A | 1 | a0001c0005t0005g0058 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4507-351C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306166 | ||||||
chr14:96306262
|
T | C | 1 | a0001c0002t0061g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4507-447A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306262 | ||||||
chr14:96306288
|
G | T | 1 | a0001c0003t0003g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4506+426C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306288 | ||||||
chr14:96306307
|
T | A | 1 | a0002c0001t0006g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4506+407A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306307 | ||||||
chr14:96306307
|
TAC | T | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4506+405_4506+406d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306307 | ||||||
chr14:96306320
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4506+394A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306320 | ||||||
chr14:96306322
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4506+392T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306322 | ||||||
chr14:96306534
|
T | TAGG | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4506+179_4506+180i others(5): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306534 | ||||||
chr14:96306570
|
C | A | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4506+144G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306570 | ||||||
chr14:96306588
|
TA | T | 30 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0035g0247others(27): Show | 32 | HG00621.hp1 HG00642.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.4506+125delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306588 | ||||||
chr14:96306588
|
TAA | T | 50 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(47): Show | 55 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.4506+124_4506+125d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306588 | ||||||
chr14:96306605
|
C | T | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4506+109G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306605 | ||||||
chr14:96306667
|
C | CA | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4506+46dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 30/41 | chr14 | 96306667 | ||||||
chr14:96307052
|
C | T | 91 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4304-136G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307052 | ||||||
chr14:96307098
|
AAG | A | 91 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4304-184_4304-183d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307098 | ||||||
chr14:96307149
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-233A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307149 | ||||||
chr14:96307267
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-351G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307267 | ||||||
chr14:96307351
|
C | T | 1 | a0002c0001t0041g0189 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4304-435G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307351 | ||||||
chr14:96307412
|
A | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-496T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307412 | ||||||
chr14:96307412
|
AAAAC | A | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4304-500_4304-497d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307412 | ||||||
chr14:96307428
|
C | A | 68 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(65): Show | 74 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.4304-512G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307428 | ||||||
chr14:96307428
|
C | CA | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-513dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307428 | ||||||
chr14:96307435
|
C | A | 50 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(47): Show | 55 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.4304-519G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307435 | ||||||
chr14:96307482
|
C | T | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4304-566G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307482 | ||||||
chr14:96307512
|
T | C | 1 | a0002c0001t0019g0014 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4304-596A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307512 | ||||||
chr14:96307689
|
G | A | 3 | a0001c0002t0001g0315a0001c0002t0001g0316a0001c0002t0001g0317 | 3 | HG02572.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4304-773C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307689 | ||||||
chr14:96307777
|
G | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-861C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307777 | ||||||
chr14:96307800
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-884G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96307800 | ||||||
chr14:96308034
|
ACT | A | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.4304-1120_4304-111 others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308034 | ||||||
chr14:96308093
|
T | C | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.4304-1177A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308093 | ||||||
chr14:96308143
|
TAC | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-1229_4304-122 others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308143 | ||||||
chr14:96308151
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4304-1235G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308151 | ||||||
chr14:96308167
|
T | C | 1 | a0002c0001t0002g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4304-1251A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308167 | ||||||
chr14:96308169
|
AATATATA others(25): Show |
A | 1 | a0004c0006t0010g0336 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4303+1252_4304-125 others(36): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308169 | ||||||
chr14:96308191
|
TATATATA others(59): Show |
T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4303+1196_4303+126 others(70): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308191 | ||||||
chr14:96308197
|
TACATATA others(51): Show |
T | 4 | a0004c0006t0010g0333a0004c0006t0010g0335a0004c0006t0010g0339others(1): Show | 4 | HG02735.hp2 HG03239.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.4303+1198_4303+125 others(62): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308197 | ||||||
chr14:96308199
|
CATATATA others(53): Show |
C | 4 | a0004c0006t0013g0013a0004c0006t0013g0331a0004c0006t0013g0332others(1): Show | 5 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.4303+1194_4303+125 others(64): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308199 | ||||||
chr14:96308201
|
TATATATA others(49): Show |
T | 3 | a0004c0006t0010g0334a0004c0006t0010g0337a0025c0027t0008g0079 | 3 | HG02717.hp1 NA19007.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.4303+1196_4303+125 others(60): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308201 | ||||||
chr14:96308203
|
TATATATA others(47): Show |
T | 4 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0082others(1): Show | 7 | HG02145.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303+1196_4303+124 others(58): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308203 | ||||||
chr14:96308205
|
TATATAAA others(45): Show |
T | 1 | a0006c0007t0008g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4303+1196_4303+124 others(56): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308205 | ||||||
chr14:96308211
|
A | T | 1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4303+1242T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308211 | ||||||
chr14:96308215
|
C | T | 1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4303+1238G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308215 | ||||||
chr14:96308219
|
A | T | 1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4303+1234T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308219 | ||||||
chr14:96308219
|
AATATATA others(31): Show |
A | 4 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0045g0246others(1): Show | 4 | HG02922.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4303+1196_4303+123 others(42): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308219 | ||||||
chr14:96308219
|
AATATATA others(33): Show |
A | 4 | a0001c0003t0003g0009a0001c0003t0003g0210a0001c0003t0003g0225others(1): Show | 5 | HG00323.hp2 HG02486.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.4303+1194_4303+123 others(44): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308219 | ||||||
chr14:96308221
|
T | C | 1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4303+1232A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308221 | ||||||
chr14:96308225
|
TATATACA others(25): Show |
T | 1 | a0005c0010t0009g0105 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4303+1196_4303+122 others(36): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308225 | ||||||
chr14:96308227
|
TATACATA others(23): Show |
T | 1 | a0005c0010t0009g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4303+1196_4303+122 others(34): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308227 | ||||||
chr14:96308229
|
TACATATA others(19): Show |
T | 2 | a0001c0012t0024g0093a0001c0012t0050g0095 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4303+1198_4303+122 others(30): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308229 | ||||||
chr14:96308229
|
TACATATA others(21): Show |
T | 1 | a0005c0010t0009g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4303+1196_4303+122 others(32): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308229 | ||||||
chr14:96308231
|
C | CATATAT | 5 | a0002c0001t0002g0149a0002c0001t0006g0159a0002c0001t0042g0158others(2): Show | 5 | HG00099.hp2 HG00140.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.4303+1216_4303+122 others(10): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308231 | ||||||
chr14:96308231
|
C | T | 59 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0108others(56): Show | 64 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.4303+1222G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308231 | ||||||
chr14:96308231
|
CATATATA others(21): Show |
C | 1 | a0001c0012t0024g0094 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4303+1194_4303+122 others(32): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308231 | ||||||
chr14:96308231
|
CATATATA others(23): Show |
C | 2 | a0001c0002t0001g0281a0001c0002t0001g0318 | 2 | NA19043.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.4303+1192_4303+122 others(34): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308231 | ||||||
chr14:96308231
|
CATATATA others(27): Show |
C | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4303+1188_4303+122 others(38): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308231 | ||||||
chr14:96308231
|
CATATATA others(31): Show |
C | 1 | a0003c0004t0004g0004 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.4303+1184_4303+122 others(42): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308231 | ||||||
chr14:96308233
|
TATATATA others(17): Show |
T | 16 | a0001c0002t0001g0308a0001c0002t0060g0266a0001c0005t0005g0027others(13): Show | 16 | HG02109.hp2 HG03491.hp1 HG03942.hp2 others(13): Show |
intron_variant | MODIFIER | c.4303+1196_4303+121 others(28): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308233 | ||||||
chr14:96308235
|
TATATATA others(15): Show |
T | 65 | a0001c0002t0001g0012a0001c0002t0001g0258a0001c0002t0001g0261others(62): Show | 67 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.4303+1196_4303+121 others(26): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308235 | ||||||
chr14:96308237
|
TATATATA others(13): Show |
T | 8 | a0001c0002t0001g0011a0001c0002t0001g0272a0001c0002t0001g0282others(5): Show | 9 | HG02258.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.4303+1196_4303+121 others(24): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308237 | ||||||
chr14:96308239
|
TATATATA others(11): Show |
T | 14 | a0001c0002t0001g0263a0001c0002t0001g0271a0001c0002t0001g0278others(11): Show | 14 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.4303+1196_4303+121 others(22): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308239 | ||||||
chr14:96308239
|
TATATATA others(34): Show |
T | 1 | a0001c0003t0033g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4303+1173_4303+121 others(45): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308239 | ||||||
chr14:96308241
|
TATATATA others(9): Show |
T | 8 | a0001c0002t0001g0264a0001c0002t0001g0275a0001c0002t0001g0291others(5): Show | 8 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.4303+1196_4303+121 others(20): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308241 | ||||||
chr14:96308241
|
TATATATA others(32): Show |
T | 2 | a0001c0003t0003g0200a0001c0003t0003g0229 | 2 | HG01192.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.4303+1173_4303+121 others(43): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308241 | ||||||
chr14:96308243
|
TATATATA others(7): Show |
T | 4 | a0001c0002t0001g0270a0001c0002t0001g0287a0001c0002t0001g0292others(1): Show | 4 | HG00621.hp2 HG01496.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.4303+1196_4303+120 others(18): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308243 | ||||||
chr14:96308243
|
TATATATA others(30): Show |
T | 2 | a0001c0003t0005g0197a0001c0003t0005g0198 | 2 | HG01099.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.4303+1173_4303+120 others(41): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308243 | ||||||
chr14:96308243
|
TATATATA others(32): Show |
T | 29 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0108others(26): Show | 30 | HG01074.hp1 HG01123.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.4303+1171_4303+120 others(43): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308243 | ||||||
chr14:96308244
|
ATATATAT others(32): Show |
A | 3 | a0001c0003t0003g0232a0001c0003t0003g0234a0001c0003t0016g0002 | 5 | HG00408.hp2 NA18612.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.4303+1170_4303+120 others(43): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308244 | ||||||
chr14:96308245
|
T | C | 1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4303+1208A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308245 | ||||||
chr14:96308245
|
T | TATATACA others(17): Show |
1 | a0002c0001t0002g0186 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4303+1207_4303+120 others(28): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308245 | ||||||
chr14:96308245
|
T | TATATACA others(21): Show |
1 | a0002c0001t0002g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4303+1207_4303+120 others(32): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308245 | ||||||
chr14:96308245
|
TATATATA others(5): Show |
T | 1 | a0001c0002t0054g0306 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4303+1196_4303+120 others(16): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308245 | ||||||
chr14:96308245
|
TATATATA others(26): Show |
T | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4303+1175_4303+120 others(37): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308245 | ||||||
chr14:96308245
|
TATATATA others(30): Show |
T | 5 | a0001c0003t0005g0199a0001c0003t0011g0007a0001c0003t0011g0109others(2): Show | 6 | HG00099.hp1 HG01168.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.4303+1171_4303+120 others(41): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308245 | ||||||
chr14:96308246
|
ATATATAC others(30): Show |
A | 2 | a0001c0003t0037g0196a0001c0035t0034g0221 | 2 | HG04115.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.4303+1170_4303+120 others(41): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308246 | ||||||
chr14:96308246
|
ATATATAC others(33): Show |
A | 3 | a0001c0003t0020g0222a0005c0010t0012g0236a0005c0010t0012g0237 | 3 | HG02109.hp1 HG03540.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.4303+1167_4303+120 others(44): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308246 | ||||||
chr14:96308246
|
ATATATAC others(34): Show |
A | 6 | a0001c0003t0020g0223a0005c0008t0005g0098a0005c0008t0012g0096others(3): Show | 6 | HG00642.hp1 HG02258.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4303+1166_4303+120 others(45): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308246 | ||||||
chr14:96308246
|
ATATATAC others(35): Show |
A | 1 | a0005c0008t0012g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4303+1165_4303+120 others(46): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308246 | ||||||
chr14:96308247
|
TATATACA others(3): Show |
T | 1 | a0001c0002t0001g0283 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4303+1196_4303+120 others(14): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308247 | ||||||
chr14:96308247
|
TATATACA others(28): Show |
T | 1 | a0001c0011t0003g0018 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4303+1171_4303+120 others(39): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308247 | ||||||
chr14:96308248
|
ATATACAC others(29): Show |
A | 1 | a0001c0002t0001g0260 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4303+1169_4303+120 others(40): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308248 | ||||||
chr14:96308250
|
ATACACAC others(27): Show |
A | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4303+1169_4303+120 others(38): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308250 | ||||||
chr14:96308251
|
T | C | 2 | a0002c0001t0006g0170a0002c0001t0006g0171 | 2 | HG00741.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4303+1202A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308251 | ||||||
chr14:96308252
|
ACACACAT others(22): Show |
A | 1 | a0001c0002t0001g0319 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4303+1172_4303+120 others(33): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308252 | ||||||
chr14:96308252
|
ACACACAT others(26): Show |
A | 2 | a0008c0014t0009g0005a0008c0014t0009g0104 | 3 | HG02559.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4303+1168_4303+120 others(37): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308252 | ||||||
chr14:96308253
|
C | T | 60 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(57): Show | 61 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.4303+1200G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308253 | ||||||
chr14:96308255
|
C | T | 59 | a0001c0024t0006g0092a0002c0001t0002g0006a0002c0001t0002g0110others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.4303+1198G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308255 | ||||||
chr14:96308257
|
C | T | 68 | a0001c0024t0006g0092a0002c0001t0002g0110a0002c0001t0002g0122others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.4303+1196G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308257 | ||||||
chr14:96308259
|
T | C | 3 | a0003c0004t0004g0103a0003c0004t0025g0249a0003c0004t0025g0251 | 3 | HG02027.hp1 NA18943.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.4303+1194A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308259 | ||||||
chr14:96308265
|
T | C | 1 | a0001c0002t0001g0270 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4303+1188A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308265 | ||||||
chr14:96308267
|
T | C | 1 | a0002c0001t0002g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4303+1186A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308267 | ||||||
chr14:96308270
|
A | ACATATAT others(19): Show |
1 | a0002c0001t0002g0133 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4303+1182_4303+118 others(30): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308270 | ||||||
chr14:96308270
|
A | ATATATAT others(5): Show |
26 | a0002c0001t0002g0006a0002c0001t0002g0111a0002c0001t0002g0120others(23): Show | 27 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.4303+1182_4303+118 others(16): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308270 | ||||||
chr14:96308270
|
A | ATATATAT others(3): Show |
16 | a0002c0001t0002g0122a0002c0001t0002g0127a0002c0001t0002g0132others(13): Show | 16 | HG00558.hp1 HG00735.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.4303+1182_4303+118 others(14): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308270 | ||||||
chr14:96308270
|
A | ATATATAT others(1): Show |
12 | a0002c0001t0002g0184a0002c0001t0002g0185a0002c0001t0002g0235others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+1182_4303+118 others(12): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308270 | ||||||
chr14:96308270
|
A | G | 7 | a0002c0001t0002g0142a0002c0001t0002g0186a0002c0001t0004g0190others(4): Show | 7 | HG00438.hp1 HG00621.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303+1183T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308270 | ||||||
chr14:96308273
|
T | C | 1 | a0002c0001t0006g0170 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4303+1180A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308273 | ||||||
chr14:96308275
|
T | C | 1 | a0002c0001t0006g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4303+1178A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308275 | ||||||
chr14:96308276
|
A | G | 11 | a0001c0024t0006g0092a0002c0001t0006g0159a0002c0001t0006g0160others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4303+1177T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308276 | ||||||
chr14:96308276
|
A | T | 5 | a0004c0041t0063g0340a0006c0007t0008g0001a0006c0007t0008g0081others(2): Show | 8 | HG02717.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.4303+1177T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308276 | ||||||
chr14:96308277
|
T | C | 2 | a0002c0001t0006g0169a0026c0038t0006g0174 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.4303+1176A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308277 | ||||||
chr14:96308277
|
TA | T | 9 | a0001c0002t0001g0313a0001c0005t0007g0052a0004c0006t0010g0333others(6): Show | 9 | HG00639.hp2 HG02145.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.4303+1175delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308277 | ||||||
chr14:96308278
|
A | G | 9 | a0002c0001t0006g0113a0002c0001t0006g0162a0002c0001t0006g0164others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.4303+1175T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308278 | ||||||
chr14:96308278
|
A | T | 10 | a0001c0002t0001g0012a0001c0002t0001g0312a0001c0003t0023g0245others(7): Show | 14 | HG01257.hp2 HG01258.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.4303+1175T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308278 | ||||||
chr14:96308279
|
TA | T | 5 | a0001c0002t0001g0302a0001c0002t0060g0266a0013c0015t0004g0024others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.4303+1173delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308279 | ||||||
chr14:96308280
|
A | G | 2 | a0002c0001t0004g0117a0002c0001t0006g0163 | 2 | HG02723.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.4303+1173T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308280 | ||||||
chr14:96308280
|
A | T | 35 | a0001c0002t0001g0012a0001c0002t0001g0308a0001c0002t0001g0312others(32): Show | 40 | HG00621.hp1 HG00639.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.4303+1173T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308280 | ||||||
chr14:96308281
|
TA | T | 14 | a0001c0002t0001g0264a0001c0002t0001g0282a0001c0002t0001g0301others(11): Show | 14 | HG00323.hp1 HG02015.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.4303+1171delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308281 | ||||||
chr14:96308282
|
A | G | 1 | a0002c0001t0002g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4303+1171T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308282 | ||||||
chr14:96308282
|
A | T | 92 | a0001c0002t0001g0012a0001c0002t0001g0258a0001c0002t0001g0272others(89): Show | 97 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.4303+1171T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308282 | ||||||
chr14:96308282
|
AT | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0265a0001c0002t0001g0271others(8): Show | 12 | HG00738.hp1 HG01891.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.4303+1170delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308282 | ||||||
chr14:96308283
|
T | TATATATA | 11 | a0001c0024t0006g0092a0002c0001t0006g0159a0002c0001t0006g0160others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4303+1169_4303+117 others(11): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308283
|
T | TATATATA others(2): Show |
9 | a0002c0001t0006g0113a0002c0001t0006g0162a0002c0001t0006g0164others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.4303+1169_4303+117 others(13): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308283
|
T | TATATATA others(4): Show |
3 | a0002c0001t0002g0137a0002c0001t0004g0117a0002c0001t0006g0163 | 3 | HG02723.hp2 NA18963.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.4303+1169_4303+117 others(15): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308283
|
T | TATATATA others(24): Show |
2 | a0002c0001t0006g0169a0026c0038t0006g0174 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.4303+1169_4303+117 others(35): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308283
|
T | TATATATA others(22): Show |
1 | a0002c0001t0006g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4303+1169_4303+117 others(33): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308283
|
T | TATATATA others(20): Show |
1 | a0002c0001t0006g0170 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4303+1169_4303+117 others(31): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308283
|
T | TGTATATA others(6): Show |
1 | a0002c0001t0005g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4303+1169_4303+117 others(17): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308283 | ||||||
chr14:96308284
|
T | A | 68 | a0001c0002t0001g0315a0001c0002t0001g0316a0001c0002t0001g0317others(65): Show | 69 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.4303+1169A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308284 | ||||||
chr14:96308285
|
T | A | 23 | a0001c0024t0006g0092a0002c0001t0002g0137a0002c0001t0005g0180others(20): Show | 23 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.4303+1168A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308285 | ||||||
chr14:96308286
|
T | A | 3 | a0002c0001t0004g0115a0002c0001t0019g0016a0005c0010t0009g0106 | 3 | HG02055.hp2 HG02630.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4303+1167A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308286 | ||||||
chr14:96308287
|
T | A | 6 | a0002c0001t0006g0160a0002c0001t0006g0162a0002c0001t0006g0163others(3): Show | 6 | HG02145.hp2 HG02602.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4303+1166A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308287 | ||||||
chr14:96308321
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+1132T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308321 | ||||||
chr14:96308326
|
C | T | 1 | a0001c0003t0003g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4303+1127G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308326 | ||||||
chr14:96308341
|
G | A | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4303+1112C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308341 | ||||||
chr14:96308364
|
A | AACCTCCG others(12): Show |
11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+1070_4303+108 others(23): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308364 | ||||||
chr14:96308460
|
CT | C | 73 | a0001c0002t0001g0260a0001c0002t0051g0257a0001c0003t0002g0214others(70): Show | 79 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.4303+992delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308460 | ||||||
chr14:96308460
|
CTTTTT | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+988_4303+992d others(7): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308460 | ||||||
chr14:96308579
|
G | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+874C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308579 | ||||||
chr14:96308642
|
C | T | 5 | a0001c0002t0001g0012a0001c0002t0001g0312a0001c0002t0001g0313others(2): Show | 6 | HG01099.hp1 HG01192.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4303+811G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308642 | ||||||
chr14:96308896
|
T | C | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4303+557A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96308896 | ||||||
chr14:96309094
|
A | C | 1 | a0002c0001t0002g0141 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4303+359T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309094 | ||||||
chr14:96309105
|
C | T | 3 | a0001c0003t0003g0008a0001c0003t0003g0229a0001c0003t0003g0239 | 4 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.4303+348G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309105 | ||||||
chr14:96309140
|
G | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+313C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309140 | ||||||
chr14:96309276
|
G | T | 174 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(171): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.4303+177C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309276 | ||||||
chr14:96309367
|
A | T | 1 | a0002c0001t0002g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4303+86T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309367 | ||||||
chr14:96309387
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4303+66C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309387 | ||||||
chr14:96309401
|
A | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4303+52T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 29/41 | chr14 | 96309401 | ||||||
chr14:96309671
|
A | G | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4162-77T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96309671 | ||||||
chr14:96309709
|
AC | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4162-116delG | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96309709 | ||||||
chr14:96310084
|
C | G | 1 | a0002c0001t0002g0155 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4162-490G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310084 | ||||||
chr14:96310097
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4162-503T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310097 | ||||||
chr14:96310143
|
A | G | 80 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(77): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.4162-549T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310143 | ||||||
chr14:96310260
|
G | A | 117 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(114): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.4162-666C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310260 | ||||||
chr14:96310324
|
C | A | 1 | a0002c0001t0002g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4162-730G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310324 | ||||||
chr14:96310375
|
A | G | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.4161+742T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310375 | ||||||
chr14:96310755
|
C | T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4161+362G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310755 | ||||||
chr14:96310978
|
A | G | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4161+139T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96310978 | ||||||
chr14:96311071
|
T | C | 90 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4161+46A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 28/41 | chr14 | 96311071 | ||||||
chr14:96311405
|
A | G | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3991-118T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 27/41 | chr14 | 96311405 | ||||||
chr14:96311717
|
G | A | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3914-99C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 26/41 | chr14 | 96311717 | ||||||
chr14:96311758
|
T | G | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.3914-140A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 26/41 | chr14 | 96311758 | ||||||
chr14:96311876
|
T | C | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.3913+213A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 26/41 | chr14 | 96311876 | ||||||
chr14:96311912
|
T | C | 79 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(76): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.3913+177A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 26/41 | chr14 | 96311912 | ||||||
chr14:96312083
|
T | A | 3 | a0002c0001t0006g0162a0002c0001t0006g0167a0002c0001t0040g0166 | 3 | HG02145.hp2 HG02922.hp2 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.3913+6A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 26/41 | chr14 | 96312083 | ||||||
chr14:96312224
|
A | C | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3843-65T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312224 | ||||||
chr14:96312274
|
A | G | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3843-115T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312274 | ||||||
chr14:96312279
|
C | T | 1 | a0016c0033t0003g0211 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3843-120G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312279 | ||||||
chr14:96312401
|
C | T | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3843-242G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312401 | ||||||
chr14:96312442
|
T | C | 1 | a0002c0001t0002g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3843-283A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312442 | ||||||
chr14:96312615
|
A | T | 79 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(76): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.3842+450T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312615 | ||||||
chr14:96312623
|
G | A | 8 | a0001c0002t0051g0257a0006c0007t0008g0001a0006c0007t0008g0080others(5): Show | 11 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3842+442C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 25/41 | chr14 | 96312623 | ||||||
chr14:96313528
|
C | T | 65 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(62): Show | 72 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.3643-93G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96313528 | ||||||
chr14:96313545
|
T | C | 1 | a0001c0024t0006g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3643-110A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96313545 | ||||||
chr14:96313558
|
A | G | 90 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3643-123T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96313558 | ||||||
chr14:96313613
|
C | G | 1 | a0002c0001t0002g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3643-178G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96313613 | ||||||
chr14:96313681
|
A | AT | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.3643-247dupA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96313681 | ||||||
chr14:96313709
|
A | G | 117 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(114): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.3643-274T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96313709 | ||||||
chr14:96314125
|
C | T | 2 | a0001c0002t0001g0323a0001c0002t0053g0268 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3643-690G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314125 | ||||||
chr14:96314165
|
T | C | 302 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(299): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3643-730A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314165 | ||||||
chr14:96314211
|
C | T | 1 | a0002c0001t0006g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3643-776G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314211 | ||||||
chr14:96314443
|
T | G | 3 | a0001c0003t0002g0214a0001c0003t0003g0213a0016c0033t0003g0211 | 3 | HG01255.hp1 HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3642+711A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314443 | ||||||
chr14:96314497
|
A | T | 7 | a0001c0005t0007g0044a0001c0005t0007g0047a0001c0005t0007g0049others(4): Show | 7 | NA18942.hp2 NA18965.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3642+657T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314497 | ||||||
chr14:96314504
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3642+650G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314504 | ||||||
chr14:96314532
|
T | C | 2 | a0005c0008t0021g0100a0005c0008t0021g0101 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3642+622A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314532 | ||||||
chr14:96314596
|
AT | A | 90 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3642+557delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314596 | ||||||
chr14:96314670
|
CTGTTTTG others(3): Show |
C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3642+474_3642+483d others(12): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314670 | ||||||
chr14:96314670
|
CTGTTTTG others(8): Show |
C | 288 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(285): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.3642+469_3642+483d others(17): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314670 | ||||||
chr14:96314670
|
CTGTTTTG others(13): Show |
C | 3 | a0002c0001t0002g0006a0002c0001t0002g0126a0002c0001t0002g0146 | 4 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3642+464_3642+483d others(22): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314670 | ||||||
chr14:96314824
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3642+330A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314824 | ||||||
chr14:96314826
|
C | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3642+328G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314826 | ||||||
chr14:96314917
|
C | T | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.3642+237G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314917 | ||||||
chr14:96314946
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3642+208A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314946 | ||||||
chr14:96314954
|
G | A | 6 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(3): Show | 9 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3642+200C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314954 | ||||||
chr14:96314981
|
G | T | 3 | a0002c0001t0002g0006a0002c0001t0002g0126a0002c0001t0002g0146 | 4 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3642+173C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96314981 | ||||||
chr14:96315069
|
T | A | 2 | a0001c0003t0023g0243a0001c0003t0046g0244 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3642+85A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 23/41 | chr14 | 96315069 | ||||||
chr14:96315587
|
G | C | 7 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(4): Show | 10 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.3362-4C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96315587 | ||||||
chr14:96315767
|
C | T | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.3362-184G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96315767 | ||||||
chr14:96315836
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3362-253A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96315836 | ||||||
chr14:96316257
|
T | C | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.3361+276A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96316257 | ||||||
chr14:96316269
|
C | T | 1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.3361+264G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96316269 | ||||||
chr14:96316270
|
A | G | 1 | a0001c0003t0033g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3361+263T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96316270 | ||||||
chr14:96316271
|
T | C | 84 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(81): Show | 91 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.3361+262A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96316271 | ||||||
chr14:96316336
|
T | C | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3361+197A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96316336 | ||||||
chr14:96316426
|
G | A | 1 | a0001c0002t0061g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3361+107C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 21/41 | chr14 | 96316426 | ||||||
chr14:96316971
|
G | A | 90 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.3210+174C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 20/41 | chr14 | 96316971 | ||||||
chr14:96317079
|
G | A | 2 | a0002c0001t0002g0133a0002c0001t0002g0186 | 2 | HG01515.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3210+66C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 20/41 | chr14 | 96317079 | ||||||
chr14:96317127
|
C | T | 117 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(114): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.3210+18G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 20/41 | chr14 | 96317127 | ||||||
chr14:96317342
|
C | T | 1 | a0001c0003t0003g0200 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3038-25G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 19/41 | chr14 | 96317342 | ||||||
chr14:96317390
|
A | T | 117 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(114): Show | 120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.3038-73T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 19/41 | chr14 | 96317390 | ||||||
chr14:96317860
|
A | G | 1 | a0001c0002t0001g0323 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.2880-5T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96317860 | ||||||
chr14:96317883
|
T | C | 8 | a0001c0002t0051g0257a0006c0007t0008g0001a0006c0007t0008g0080others(5): Show | 11 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2880-28A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96317883 | ||||||
chr14:96318116
|
T | C | 1 | a0001c0002t0001g0264 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2880-261A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318116 | ||||||
chr14:96318123
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2880-268T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318123 | ||||||
chr14:96318303
|
G | A | 1 | a0002c0001t0002g0133 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2880-448C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318303 | ||||||
chr14:96318346
|
G | A | 1 | a0001c0003t0003g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2880-491C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318346 | ||||||
chr14:96318376
|
C | T | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.2880-521G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318376 | ||||||
chr14:96318510
|
A | G | 66 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(63): Show | 67 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.2880-655T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318510 | ||||||
chr14:96318815
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2880-960G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318815 | ||||||
chr14:96318943
|
G | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2880-1088C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96318943 | ||||||
chr14:96319073
|
G | C | 1 | a0014c0019t0001g0274 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2880-1218C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319073 | ||||||
chr14:96319275
|
C | T | 1 | a0002c0001t0006g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2880-1420G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319275 | ||||||
chr14:96319296
|
A | C | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2880-1441T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319296 | ||||||
chr14:96319540
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2880-1685A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319540 | ||||||
chr14:96319911
|
G | A | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2880-2056C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319911 | ||||||
chr14:96319946
|
A | C | 1 | a0001c0002t0001g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2880-2091T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319946 | ||||||
chr14:96319948
|
G | C | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2880-2093C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96319948 | ||||||
chr14:96320205
|
C | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2879+1907G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320205 | ||||||
chr14:96320228
|
T | C | 1 | a0001c0002t0001g0279 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2879+1884A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320228 | ||||||
chr14:96320251
|
T | C | 1 | a0001c0002t0001g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2879+1861A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320251 | ||||||
chr14:96320253
|
T | C | 2 | a0001c0002t0001g0280a0024c0028t0058g0326 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2879+1859A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320253 | ||||||
chr14:96320335
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2879+1777G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320335 | ||||||
chr14:96320415
|
T | A | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2879+1697A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320415 | ||||||
chr14:96320453
|
C | T | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2879+1659G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320453 | ||||||
chr14:96320511
|
C | T | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.2879+1601G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320511 | ||||||
chr14:96320536
|
A | T | 1 | a0001c0003t0003g0008 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2879+1576T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320536 | ||||||
chr14:96320610
|
G | C | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2879+1502C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320610 | ||||||
chr14:96320941
|
T | C | 2 | a0002c0001t0002g0122a0002c0001t0002g0134 | 2 | HG01074.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2879+1171A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320941 | ||||||
chr14:96320975
|
T | C | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.2879+1137A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96320975 | ||||||
chr14:96321389
|
C | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2879+723G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321389 | ||||||
chr14:96321410
|
T | C | 13 | a0002c0001t0006g0113a0002c0001t0006g0159a0002c0001t0006g0169others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2879+702A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321410 | ||||||
chr14:96321462
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2879+650G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321462 | ||||||
chr14:96321810
|
G | A | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2879+302C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321810 | ||||||
chr14:96321845
|
G | A | 1 | a0005c0008t0021g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2879+267C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321845 | ||||||
chr14:96321918
|
G | A | 2 | a0011c0017t0001g0289a0011c0017t0001g0325 | 2 | NA19074.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2879+194C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321918 | ||||||
chr14:96321927
|
C | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2879+185G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 18/41 | chr14 | 96321927 | ||||||
chr14:96322331
|
T | C | 4 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(1): Show | 4 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2737-77A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 17/41 | chr14 | 96322331 | ||||||
chr14:96322413
|
A | C | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2736+127T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 17/41 | chr14 | 96322413 | ||||||
chr14:96322868
|
T | C | 4 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(1): Show | 4 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2541-133A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96322868 | ||||||
chr14:96323093
|
T | C | 1 | a0001c0002t0001g0264 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2541-358A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323093 | ||||||
chr14:96323217
|
T | C | 1 | a0001c0002t0001g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2541-482A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323217 | ||||||
chr14:96323581
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2540+315G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323581 | ||||||
chr14:96323586
|
T | C | 1 | a0002c0001t0002g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2540+310A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323586 | ||||||
chr14:96323588
|
A | G | 2 | a0001c0002t0001g0301a0001c0002t0001g0328 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2540+308T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323588 | ||||||
chr14:96323610
|
C | T | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2540+286G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323610 | ||||||
chr14:96323652
|
T | G | 1 | a0001c0002t0001g0290 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2540+244A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323652 | ||||||
chr14:96323753
|
C | T | 9 | a0001c0002t0051g0257a0001c0003t0045g0246a0006c0007t0008g0001others(6): Show | 12 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2540+143G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323753 | ||||||
chr14:96323836
|
A | T | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2540+60T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 16/41 | chr14 | 96323836 | ||||||
chr14:96324000
|
T | TA | 118 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(115): Show | 121 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.2438-3dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324000 | ||||||
chr14:96324079
|
A | G | 1 | a0003c0004t0004g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2438-81T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324079 | ||||||
chr14:96324315
|
C | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2438-317G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324315 | ||||||
chr14:96324403
|
G | A | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2438-405C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324403 | ||||||
chr14:96324411
|
C | T | 21 | a0001c0002t0001g0302a0001c0002t0001g0308a0001c0002t0001g0309others(18): Show | 22 | HG00621.hp1 HG02040.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2438-413G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324411 | ||||||
chr14:96324445
|
G | A | 1 | a0002c0001t0019g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2438-447C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324445 | ||||||
chr14:96324467
|
C | A | 1 | a0001c0003t0003g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2438-469G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324467 | ||||||
chr14:96324648
|
G | A | 6 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(3): Show | 6 | HG00642.hp1 HG02258.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2438-650C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324648 | ||||||
chr14:96324851
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437+798G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324851 | ||||||
chr14:96324860
|
G | A | 1 | a0003c0004t0004g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2437+789C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324860 | ||||||
chr14:96324902
|
G | C | 1 | a0001c0005t0005g0046 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2437+747C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324902 | ||||||
chr14:96324917
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437+732A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324917 | ||||||
chr14:96324951
|
G | A | 1 | a0001c0002t0001g0329 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2437+698C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324951 | ||||||
chr14:96324961
|
C | T | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2437+688G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96324961 | ||||||
chr14:96325043
|
A | G | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437+606T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325043 | ||||||
chr14:96325317
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437+332A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325317 | ||||||
chr14:96325337
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437+312T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325337 | ||||||
chr14:96325371
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2437+278C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325371 | ||||||
chr14:96325459
|
A | G | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2437+190T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325459 | ||||||
chr14:96325554
|
T | A | 1 | a0001c0003t0045g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2437+95A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325554 | ||||||
chr14:96325626
|
T | C | 1 | a0013c0015t0004g0024 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2437+23A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 15/41 | chr14 | 96325626 | ||||||
chr14:96325967
|
T | C | 1 | a0004c0006t0010g0334 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2164-45A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96325967 | ||||||
chr14:96326108
|
T | C | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2164-186A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96326108 | ||||||
chr14:96326239
|
G | C | 52 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.2164-317C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96326239 | ||||||
chr14:96327008
|
A | G | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2164-1086T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327008 | ||||||
chr14:96327230
|
CAAT | C | 86 | a0001c0002t0001g0321a0001c0002t0001g0323a0001c0005t0005g0022others(83): Show | 89 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.2163+1114_2163+111 others(7): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327230 | ||||||
chr14:96327230
|
CAATAAT | C | 248 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(245): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2163+1111_2163+111 others(10): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327230 | ||||||
chr14:96327230
|
CAATAATA others(5): Show |
C | 1 | a0002c0001t0005g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2163+1105_2163+111 others(16): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327230 | ||||||
chr14:96327383
|
T | G | 10 | a0001c0002t0051g0257a0006c0007t0008g0001a0006c0007t0008g0080others(7): Show | 13 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.2163+964A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327383 | ||||||
chr14:96327855
|
C | T | 1 | a0017c0030t0018g0248 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2163+492G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327855 | ||||||
chr14:96327997
|
T | C | 3 | a0001c0005t0005g0022a0001c0005t0005g0057a0001c0005t0005g0058 | 3 | NA19060.hp1 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2163+350A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96327997 | ||||||
chr14:96328014
|
C | T | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163+333G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96328014 | ||||||
chr14:96328204
|
G | A | 6 | a0002c0001t0004g0112a0002c0001t0004g0115a0002c0001t0004g0116others(3): Show | 6 | HG00558.hp1 HG00621.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.2163+143C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96328204 | ||||||
chr14:96328301
|
A | C | 1 | a0018c0023t0036g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2163+46T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 14/41 | chr14 | 96328301 | ||||||
chr14:96328845
|
G | C | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1882-79C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96328845 | ||||||
chr14:96328925
|
C | T | 1 | a0001c0003t0003g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1882-159G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96328925 | ||||||
chr14:96328957
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1882-191C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96328957 | ||||||
chr14:96329016
|
T | C | 1 | a0003c0004t0004g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1882-250A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96329016 | ||||||
chr14:96329048
|
GT | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1882-283delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96329048 | ||||||
chr14:96329163
|
T | A | 1 | a0004c0006t0013g0338 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1881+321A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96329163 | ||||||
chr14:96329339
|
A | G | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1881+145T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96329339 | ||||||
chr14:96329345
|
C | G | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1881+139G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 12/41 | chr14 | 96329345 | ||||||
chr14:96329648
|
T | C | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-14A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96329648 | ||||||
chr14:96329660
|
G | C | 79 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(76): Show | 82 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1731-26C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96329660 | ||||||
chr14:96329821
|
T | G | 52 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1731-187A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96329821 | ||||||
chr14:96329844
|
G | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1731-210C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96329844 | ||||||
chr14:96330026
|
A | G | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-392T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330026 | ||||||
chr14:96330051
|
G | GA | 59 | a0001c0002t0001g0011a0001c0002t0001g0260a0001c0002t0001g0261others(56): Show | 61 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1731-418dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330051 | ||||||
chr14:96330051
|
G | GAA | 34 | a0001c0002t0001g0012a0001c0002t0001g0258a0001c0002t0001g0262others(31): Show | 35 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1731-419_1731-418d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330051 | ||||||
chr14:96330142
|
G | A | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-508C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330142 | ||||||
chr14:96330173
|
A | G | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1731-539T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330173 | ||||||
chr14:96330213
|
G | A | 2 | a0001c0003t0003g0216a0001c0003t0031g0240 | 2 | HG02027.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1731-579C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330213 | ||||||
chr14:96330403
|
A | G | 1 | a0001c0003t0037g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1731-769T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330403 | ||||||
chr14:96330717
|
T | C | 3 | a0002c0001t0017g0138a0002c0001t0017g0140a0002c0001t0017g0194 | 3 | NA18950.hp1 NA19005.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1730+659A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330717 | ||||||
chr14:96330817
|
T | C | 52 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1730+559A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96330817 | ||||||
chr14:96331027
|
G | C | 1 | a0002c0001t0004g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1730+349C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331027 | ||||||
chr14:96331136
|
T | C | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1730+240A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331136 | ||||||
chr14:96331164
|
T | C | 79 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(76): Show | 82 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1730+212A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331164 | ||||||
chr14:96331209
|
C | G | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1730+167G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331209 | ||||||
chr14:96331264
|
A | T | 1 | a0003c0004t0004g0036 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1730+112T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331264 | ||||||
chr14:96331267
|
A | T | 1 | a0003c0004t0004g0036 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1730+109T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331267 | ||||||
chr14:96331297
|
T | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1730+79A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 11/41 | chr14 | 96331297 | ||||||
chr14:96331648
|
A | G | 1 | a0001c0005t0005g0032 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1469-11T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/41 | chr14 | 96331648 | ||||||
chr14:96331762
|
A | G | 1 | a0001c0005t0018g0253 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1469-125T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/41 | chr14 | 96331762 | ||||||
chr14:96331858
|
T | C | 1 | a0003c0004t0004g0021 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1469-221A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/41 | chr14 | 96331858 | ||||||
chr14:96332095
|
T | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468+210A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/41 | chr14 | 96332095 | ||||||
chr14:96332214
|
G | GA | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468+90dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 10/41 | chr14 | 96332214 | ||||||
chr14:96332797
|
T | A | 2 | a0002c0001t0004g0112a0002c0001t0004g0190 | 2 | HG00621.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1208-142A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 8/41 | chr14 | 96332797 | ||||||
chr14:96333070
|
T | C | 1 | a0001c0003t0003g0203 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1208-415A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 8/41 | chr14 | 96333070 | ||||||
chr14:96333222
|
G | C | 1 | a0001c0002t0001g0316 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+466C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 8/41 | chr14 | 96333222 | ||||||
chr14:96333473
|
C | A | 1 | a0001c0003t0023g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1207+215G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 8/41 | chr14 | 96333473 | ||||||
chr14:96333473
|
C | CA | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1207+214dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 8/41 | chr14 | 96333473 | ||||||
chr14:96334002
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1022-129C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 7/41 | chr14 | 96334002 | ||||||
chr14:96334126
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1022-253A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 7/41 | chr14 | 96334126 | ||||||
chr14:96334229
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021+176A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 7/41 | chr14 | 96334229 | ||||||
chr14:96334250
|
C | A | 13 | a0001c0002t0051g0257a0001c0012t0024g0093a0001c0012t0024g0094others(10): Show | 16 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1021+155G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 7/41 | chr14 | 96334250 | ||||||
chr14:96334735
|
G | A | 2 | a0010c0016t0004g0077a0010c0016t0004g0078 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.925-234C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96334735 | ||||||
chr14:96334919
|
A | G | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.925-418T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96334919 | ||||||
chr14:96334954
|
A | G | 2 | a0001c0003t0023g0245a0001c0003t0045g0246 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.925-453T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96334954 | ||||||
chr14:96335010
|
C | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.925-509G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335010 | ||||||
chr14:96335043
|
C | T | 261 | a0001c0002t0001g0012a0001c0002t0001g0258a0001c0002t0001g0260others(258): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.925-542G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335043 | ||||||
chr14:96335054
|
G | A | 3 | a0001c0002t0001g0272a0014c0019t0001g0273a0014c0019t0001g0274 | 3 | HG00639.hp2 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.925-553C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335054 | ||||||
chr14:96335061
|
C | T | 3 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0046g0244 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.925-560G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335061 | ||||||
chr14:96335188
|
T | C | 1 | a0001c0003t0005g0238 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.925-687A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335188 | ||||||
chr14:96335195
|
T | C | 3 | a0001c0002t0001g0272a0014c0019t0001g0273a0014c0019t0001g0274 | 3 | HG00639.hp2 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.925-694A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335195 | ||||||
chr14:96335263
|
T | C | 84 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(81): Show | 88 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.925-762A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335263 | ||||||
chr14:96335265
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.925-764A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335265 | ||||||
chr14:96335434
|
T | C | 1 | a0001c0002t0001g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.925-933A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335434 | ||||||
chr14:96335465
|
T | C | 1 | a0001c0003t0033g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.925-964A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335465 | ||||||
chr14:96335477
|
G | C | 13 | a0002c0001t0006g0113a0002c0001t0006g0159a0002c0001t0006g0169others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.925-976C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335477 | ||||||
chr14:96335502
|
T | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.925-1001A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335502 | ||||||
chr14:96335537
|
A | C | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.925-1036T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335537 | ||||||
chr14:96335771
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.925-1270G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96335771 | ||||||
chr14:96336016
|
C | G | 1 | a0001c0002t0001g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.925-1515G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336016 | ||||||
chr14:96336123
|
A | G | 10 | a0003c0004t0004g0028a0003c0004t0004g0031a0003c0004t0004g0036others(7): Show | 10 | HG02080.hp1 HG02165.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.925-1622T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336123 | ||||||
chr14:96336153
|
T | TAA | 7 | a0006c0007t0008g0001a0006c0007t0008g0081a0006c0007t0008g0082others(4): Show | 10 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.925-1654_925-1653d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336153 | ||||||
chr14:96336153
|
TA | T | 9 | a0001c0002t0001g0294a0001c0003t0023g0243a0001c0003t0023g0245others(6): Show | 9 | HG02165.hp1 HG02486.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.925-1653delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336153 | ||||||
chr14:96336153
|
TAA | T | 12 | a0001c0003t0045g0246a0004c0006t0010g0333a0004c0006t0010g0334others(9): Show | 13 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.925-1654_925-1653d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336153 | ||||||
chr14:96336190
|
T | G | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.925-1689A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336190 | ||||||
chr14:96336274
|
G | T | 65 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(62): Show | 66 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.925-1773C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336274 | ||||||
chr14:96336328
|
C | T | 5 | a0002c0001t0006g0160a0002c0001t0006g0162a0002c0001t0006g0163others(2): Show | 5 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-1827G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336328 | ||||||
chr14:96336512
|
A | G | 3 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0337 | 3 | NA19007.hp1 NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.925-2011T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336512 | ||||||
chr14:96336530
|
T | A | 1 | a0003c0004t0004g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.925-2029A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336530 | ||||||
chr14:96336873
|
G | C | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.925-2372C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96336873 | ||||||
chr14:96337279
|
G | A | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.925-2778C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337279 | ||||||
chr14:96337329
|
C | T | 1 | a0004c0006t0010g0337 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.925-2828G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337329 | ||||||
chr14:96337378
|
A | G | 6 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(3): Show | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.925-2877T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337378 | ||||||
chr14:96337443
|
A | G | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.925-2942T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337443 | ||||||
chr14:96337482
|
T | C | 1 | a0002c0001t0006g0170 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.925-2981A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337482 | ||||||
chr14:96337484
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.925-2983C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337484 | ||||||
chr14:96337758
|
G | A | 1 | a0002c0001t0014g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.925-3257C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337758 | ||||||
chr14:96337785
|
T | C | 3 | a0001c0003t0003g0224a0001c0003t0003g0225a0001c0003t0003g0227 | 3 | HG00323.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.925-3284A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337785 | ||||||
chr14:96337888
|
C | T | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.925-3387G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337888 | ||||||
chr14:96337909
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.925-3408A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96337909 | ||||||
chr14:96338038
|
A | T | 1 | a0018c0023t0036g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.924+3484T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338038 | ||||||
chr14:96338043
|
C | A | 1 | a0001c0003t0003g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.924+3479G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338043 | ||||||
chr14:96338063
|
G | C | 1 | a0002c0001t0048g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.924+3459C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338063 | ||||||
chr14:96338100
|
T | C | 1 | a0001c0003t0023g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.924+3422A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338100 | ||||||
chr14:96338185
|
T | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+3337A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338185 | ||||||
chr14:96338456
|
A | G | 2 | a0002c0001t0002g0122a0002c0001t0002g0134 | 2 | HG01074.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.924+3066T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338456 | ||||||
chr14:96338933
|
G | C | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.924+2589C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96338933 | ||||||
chr14:96339120
|
A | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+2402T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339120 | ||||||
chr14:96339145
|
A | G | 11 | a0001c0002t0001g0012a0001c0002t0001g0312a0001c0002t0001g0313others(8): Show | 12 | HG01099.hp1 HG01192.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+2377T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339145 | ||||||
chr14:96339209
|
A | G | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.924+2313T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339209 | ||||||
chr14:96339237
|
A | G | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.924+2285T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339237 | ||||||
chr14:96339271
|
A | AGT | 9 | a0001c0005t0007g0047a0002c0001t0002g0150a0002c0001t0019g0014others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.924+2249_924+2250d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339271 | ||||||
chr14:96339271
|
AGT | A | 29 | a0001c0002t0001g0012a0001c0002t0001g0279a0001c0002t0001g0312others(26): Show | 32 | HG00621.hp1 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.924+2249_924+2250d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339271 | ||||||
chr14:96339271
|
AGTGT | A | 130 | a0001c0002t0001g0011a0001c0002t0001g0258a0001c0002t0001g0260others(127): Show | 137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.924+2247_924+2250d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339271 | ||||||
chr14:96339271
|
AGTGTGT | A | 13 | a0001c0003t0005g0199a0001c0013t0005g0091a0001c0013t0022g0085others(10): Show | 16 | HG00099.hp1 HG00642.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.924+2245_924+2250d others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339271 | ||||||
chr14:96339353
|
T | C | 1 | a0001c0002t0053g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.924+2169A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339353 | ||||||
chr14:96339388
|
C | T | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.924+2134G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339388 | ||||||
chr14:96339414
|
G | A | 90 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.924+2108C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339414 | ||||||
chr14:96339418
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+2104T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339418 | ||||||
chr14:96339436
|
T | C | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+2086A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339436 | ||||||
chr14:96339585
|
A | G | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.924+1937T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339585 | ||||||
chr14:96339641
|
A | G | 65 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(62): Show | 66 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.924+1881T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339641 | ||||||
chr14:96339686
|
A | C | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+1836T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339686 | ||||||
chr14:96339769
|
G | A | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.924+1753C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339769 | ||||||
chr14:96339853
|
C | G | 1 | a0003c0004t0004g0004 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.924+1669G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339853 | ||||||
chr14:96339853
|
C | T | 5 | a0001c0002t0001g0012a0001c0002t0001g0312a0001c0002t0001g0313others(2): Show | 6 | HG01099.hp1 HG01192.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.924+1669G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96339853 | ||||||
chr14:96340069
|
T | TAG | 5 | a0001c0003t0023g0243a0001c0003t0046g0244a0002c0001t0006g0161others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1452_924+1453i others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340069 | ||||||
chr14:96340070
|
G | A | 5 | a0001c0003t0023g0243a0001c0003t0046g0244a0002c0001t0006g0161others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1452C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340070 | ||||||
chr14:96340071
|
T | A | 5 | a0001c0003t0023g0243a0001c0003t0046g0244a0002c0001t0006g0161others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1451A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340071 | ||||||
chr14:96340072
|
G | T | 5 | a0001c0003t0023g0243a0001c0003t0046g0244a0002c0001t0006g0161others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1450C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340072 | ||||||
chr14:96340090
|
ATATGC | A | 68 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(65): Show | 69 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.924+1427_924+1431d others(7): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340090 | ||||||
chr14:96340093
|
T | TATATCAT others(824): Show |
1 | a0001c0003t0046g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.924+1428_924+1429i others(833): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340093 | ||||||
chr14:96340094
|
G | A | 1 | a0001c0003t0046g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.924+1428C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340094 | ||||||
chr14:96340095
|
C | A | 1 | a0001c0003t0046g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.924+1427G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340095 | ||||||
chr14:96340095
|
C | CTATATAG others(21): Show |
1 | a0001c0003t0023g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.924+1399_924+1426d others(30): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340095 | ||||||
chr14:96340095
|
C | CTATATAT others(105): Show |
1 | a0001c0005t0005g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.924+1426_924+1427i others(114): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340095 | ||||||
chr14:96340095
|
C | CTATATAT others(273): Show |
2 | a0003c0004t0004g0028a0015c0021t0004g0026 | 2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.924+1426_924+1427i others(282): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340095 | ||||||
chr14:96340102
|
G | T | 72 | a0001c0003t0046g0244a0001c0005t0005g0072a0002c0001t0002g0006others(69): Show | 73 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.924+1420C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340102 | ||||||
chr14:96340103
|
A | AATATATG others(49): Show |
13 | a0001c0005t0005g0022a0001c0005t0005g0061a0001c0005t0007g0060others(10): Show | 13 | HG03490.hp1 NA18978.hp2 NA18990.hp1 others(10): Show |
intron_variant | MODIFIER | c.924+1363_924+1418d others(58): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(77): Show |
15 | a0001c0005t0005g0053a0001c0005t0005g0054a0001c0005t0005g0056others(12): Show | 15 | HG02155.hp2 HG03669.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.924+1418_924+1419i others(86): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(105): Show |
18 | a0001c0005t0005g0045a0001c0005t0005g0046a0001c0005t0005g0071others(15): Show | 19 | HG00438.hp2 HG00735.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.924+1418_924+1419i others(114): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(133): Show |
14 | a0001c0005t0005g0032a0001c0005t0005g0034a0001c0005t0005g0073others(11): Show | 15 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.924+1418_924+1419i others(142): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(161): Show |
5 | a0001c0005t0005g0027a0001c0022t0015g0252a0003c0004t0004g0030others(2): Show | 5 | HG00408.hp1 HG02027.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1418_924+1419i others(170): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(189): Show |
1 | a0003c0004t0004g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.924+1418_924+1419i others(198): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(217): Show |
1 | a0003c0004t0025g0249 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.924+1418_924+1419i others(226): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(245): Show |
1 | a0010c0016t0004g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.924+1418_924+1419i others(254): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(273): Show |
1 | a0010c0016t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924+1418_924+1419i others(282): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(497): Show |
1 | a0001c0003t0044g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.924+1418_924+1419i others(506): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(581): Show |
2 | a0001c0003t0023g0245a0001c0003t0045g0246 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.924+1418_924+1419i others(590): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | AATATATG others(913): Show |
1 | a0001c0003t0023g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.924+1418_924+1419i others(922): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
A | C | 72 | a0001c0003t0046g0244a0001c0005t0005g0072a0002c0001t0002g0006others(69): Show | 73 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.924+1419T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340103
|
AATATATG others(21): Show |
A | 169 | a0001c0002t0001g0012a0001c0002t0001g0258a0001c0002t0001g0260others(166): Show | 180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.924+1391_924+1418d others(30): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340103 | ||||||
chr14:96340120
|
AATATATA others(23): Show |
A | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.924+1372_924+1401d others(32): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340120 | ||||||
chr14:96340131
|
CATATATG others(23): Show |
C | 1 | a0001c0002t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.924+1361_924+1390d others(32): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340131 | ||||||
chr14:96340148
|
A | AATATATA others(334): Show |
1 | a0002c0001t0006g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(343): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(315): Show |
1 | a0002c0001t0002g0183 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(324): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(287): Show |
3 | a0002c0001t0002g0149a0002c0001t0002g0182a0002c0001t0047g0188 | 3 | HG00735.hp1 HG03927.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.924+1373_924+1374i others(296): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(316): Show |
1 | a0022c0037t0043g0173 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(325): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(315): Show |
3 | a0002c0001t0002g0133a0002c0001t0002g0146a0002c0001t0002g0184 | 3 | HG02738.hp2 HG03942.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.924+1373_924+1374i others(324): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(317): Show |
1 | a0002c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(326): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(343): Show |
1 | a0002c0001t0002g0139 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(352): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(338): Show |
1 | a0002c0001t0006g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(347): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(344): Show |
1 | a0002c0001t0006g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(353): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(344): Show |
3 | a0002c0001t0006g0172a0012c0020t0006g0178a0012c0020t0006g0179 | 3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.924+1373_924+1374i others(353): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(372): Show |
1 | a0002c0001t0005g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(381): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(343): Show |
6 | a0002c0001t0002g0132a0002c0001t0002g0150a0002c0001t0002g0185others(3): Show | 6 | HG00558.hp1 HG00609.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.924+1373_924+1374i others(352): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(373): Show |
1 | a0002c0001t0017g0194 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(382): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(381): Show |
1 | a0002c0001t0014g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(390): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(371): Show |
1 | a0002c0001t0017g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(380): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(399): Show |
1 | a0002c0001t0002g0153 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(408): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(371): Show |
8 | a0002c0001t0002g0111a0002c0001t0002g0135a0002c0001t0002g0136others(5): Show | 8 | HG02083.hp2 NA18747.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.924+1373_924+1374i others(380): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(379): Show |
1 | a0002c0001t0014g0121 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(388): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(394): Show |
2 | a0002c0001t0006g0169a0002c0001t0006g0170 | 2 | HG00741.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.924+1373_924+1374i others(403): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(373): Show |
1 | a0002c0001t0041g0189 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(382): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(343): Show |
1 | a0007c0009t0002g0125 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(352): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(371): Show |
7 | a0002c0001t0004g0116a0002c0001t0004g0117a0002c0001t0019g0014others(4): Show | 7 | HG00639.hp1 HG01257.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+1373_924+1374i others(380): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(373): Show |
1 | a0002c0001t0004g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(382): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(371): Show |
1 | a0002c0001t0002g0148 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(380): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(399): Show |
1 | a0002c0001t0002g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(408): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(235): Show |
1 | a0026c0038t0006g0174 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(244): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(399): Show |
3 | a0002c0001t0002g0127a0002c0001t0002g0235a0002c0001t0004g0115 | 3 | NA18959.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.924+1373_924+1374i others(408): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(425): Show |
1 | a0019c0034t0014g0154 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(434): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(235): Show |
1 | a0002c0001t0006g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(244): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(594): Show |
1 | a0002c0001t0002g0141 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(603): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(344): Show |
1 | a0002c0001t0040g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(353): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(316): Show |
1 | a0002c0001t0006g0162 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(325): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(313): Show |
1 | a0002c0001t0006g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(322): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(288): Show |
1 | a0002c0001t0006g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(297): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(287): Show |
1 | a0002c0001t0006g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(296): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(368): Show |
1 | a0002c0001t0014g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(377): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(260): Show |
1 | a0027c0040t0006g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(269): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(344): Show |
1 | a0002c0001t0006g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(353): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(260): Show |
1 | a0002c0001t0006g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(269): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(405): Show |
1 | a0002c0001t0028g0015 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(414): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(234): Show |
1 | a0002c0001t0006g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(243): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(343): Show |
1 | a0002c0001t0002g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(352): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(341): Show |
1 | a0002c0001t0002g0152 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(350): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(313): Show |
4 | a0002c0001t0002g0142a0002c0001t0002g0143a0002c0001t0002g0155others(1): Show | 4 | HG01346.hp2 HG01928.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.924+1373_924+1374i others(322): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(340): Show |
1 | a0002c0001t0002g0126 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(349): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(204): Show |
1 | a0002c0001t0006g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(213): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(150): Show |
1 | a0002c0001t0006g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(159): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(396): Show |
1 | a0002c0001t0002g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(405): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(341): Show |
1 | a0002c0001t0002g0156 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(350): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(397): Show |
2 | a0002c0001t0002g0157a0002c0001t0019g0016 | 2 | HG02055.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.924+1373_924+1374i others(406): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(257): Show |
1 | a0002c0001t0002g0124 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(266): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(362): Show |
1 | a0002c0001t0002g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(371): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(369): Show |
1 | a0002c0001t0002g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(378): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(341): Show |
1 | a0002c0001t0002g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(350): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(342): Show |
1 | a0002c0001t0006g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.924+1373_924+1374i others(351): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(370): Show |
1 | a0002c0001t0042g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(379): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340148
|
A | AATATATA others(259): Show |
1 | a0002c0001t0002g0186 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.924+1373_924+1374i others(268): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340148 | ||||||
chr14:96340150
|
T | TATATATA others(143): Show |
1 | a0007c0009t0002g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.924+1371_924+1372i others(152): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340150 | ||||||
chr14:96340157
|
A | ATCATATA others(343): Show |
1 | a0002c0001t0002g0006 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.924+1364_924+1365i others(352): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340157 | ||||||
chr14:96340209
|
T | TTG | 18 | a0001c0025t0001g0307a0002c0001t0002g0146a0002c0001t0002g0147others(15): Show | 19 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.924+1311_924+1312d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340209 | ||||||
chr14:96340209
|
TTG | T | 12 | a0001c0002t0001g0328a0001c0002t0055g0320a0004c0006t0010g0333others(9): Show | 13 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.924+1311_924+1312d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340209 | ||||||
chr14:96340209
|
TTGTG | T | 3 | a0002c0001t0005g0180a0012c0020t0006g0178a0012c0020t0006g0179 | 3 | HG01069.hp1 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.924+1309_924+1312d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340209 | ||||||
chr14:96340209
|
TTGTGTG | T | 6 | a0002c0001t0004g0112a0002c0001t0004g0115a0002c0001t0004g0116others(3): Show | 6 | HG00558.hp1 HG00621.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.924+1307_924+1312d others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340209 | ||||||
chr14:96340209
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.924+1305_924+1312d others(10): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340209 | ||||||
chr14:96340246
|
T | C | 5 | a0002c0001t0002g0120a0002c0001t0002g0148a0002c0001t0002g0235others(2): Show | 5 | NA18941.hp2 NA18952.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+1276A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340246 | ||||||
chr14:96340302
|
T | C | 1 | a0013c0015t0004g0025 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.924+1220A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340302 | ||||||
chr14:96340346
|
A | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+1176T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340346 | ||||||
chr14:96340532
|
A | G | 3 | a0002c0001t0002g0124a0002c0001t0002g0155a0002c0001t0003g0123 | 3 | HG01928.hp2 HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.924+990T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340532 | ||||||
chr14:96340605
|
T | C | 1 | a0002c0001t0006g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.924+917A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340605 | ||||||
chr14:96340631
|
G | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+891C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340631 | ||||||
chr14:96340641
|
G | A | 1 | a0002c0001t0002g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.924+881C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340641 | ||||||
chr14:96340886
|
C | T | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.924+636G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340886 | ||||||
chr14:96340925
|
C | CA | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.924+596_924+597ins others(1): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340925 | ||||||
chr14:96340926
|
G | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.924+596C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340926 | ||||||
chr14:96340926
|
G | GA | 164 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(161): Show | 172 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.924+595dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340926 | ||||||
chr14:96340926
|
G | GAA | 30 | a0001c0002t0052g0330a0001c0002t0062g0327a0002c0001t0002g0150others(27): Show | 30 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.924+594_924+595dup others(2): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96340926 | ||||||
chr14:96341060
|
C | T | 1 | a0018c0023t0036g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.924+462G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96341060 | ||||||
chr14:96341141
|
A | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.924+381T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96341141 | ||||||
chr14:96341446
|
G | A | 3 | a0002c0001t0002g0151a0002c0001t0002g0152a0002c0001t0002g0153 | 3 | HG02083.hp2 NA18991.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.924+76C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 6/41 | chr14 | 96341446 | ||||||
chr14:96341980
|
T | C | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.745-279A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96341980 | ||||||
chr14:96342092
|
T | C | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-391A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342092 | ||||||
chr14:96342101
|
T | C | 8 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(5): Show | 11 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.745-400A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342101 | ||||||
chr14:96342123
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.745-422T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342123 | ||||||
chr14:96342162
|
C | A | 1 | a0005c0010t0012g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.745-461G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342162 | ||||||
chr14:96342192
|
TA | T | 29 | a0001c0003t0002g0214a0001c0003t0003g0210a0001c0003t0003g0212others(26): Show | 33 | HG00621.hp1 HG01069.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.745-492delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342192 | ||||||
chr14:96342413
|
G | A | 90 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.744+706C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342413 | ||||||
chr14:96342448
|
G | A | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+671C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342448 | ||||||
chr14:96342450
|
G | A | 1 | a0019c0034t0014g0154 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.744+669C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342450 | ||||||
chr14:96342488
|
G | A | 1 | a0001c0003t0011g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.744+631C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342488 | ||||||
chr14:96342578
|
C | T | 2 | a0002c0001t0006g0159a0002c0001t0042g0158 | 2 | HG00140.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.744+541G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342578 | ||||||
chr14:96342620
|
G | T | 10 | a0001c0002t0051g0257a0006c0007t0008g0001a0006c0007t0008g0080others(7): Show | 13 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.744+499C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342620 | ||||||
chr14:96342670
|
C | T | 1 | a0002c0001t0002g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.744+449G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342670 | ||||||
chr14:96342700
|
C | T | 3 | a0001c0003t0023g0243a0001c0003t0044g0242a0001c0003t0046g0244 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.744+419G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342700 | ||||||
chr14:96342717
|
C | CA | 8 | a0002c0001t0002g0155a0002c0001t0019g0016a0003c0004t0004g0069others(5): Show | 9 | HG01255.hp2 HG01981.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+401dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342717 | ||||||
chr14:96342717
|
CA | C | 120 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(117): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.744+401delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342717 | ||||||
chr14:96342730
|
A | AC | 7 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(4): Show | 7 | HG00642.hp1 HG02258.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.744+388_744+389ins others(1): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342730 | ||||||
chr14:96342730
|
A | C | 1 | a0017c0030t0018g0248 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.744+389T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342730 | ||||||
chr14:96342737
|
A | G | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.744+382T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342737 | ||||||
chr14:96342754
|
G | A | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.744+365C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342754 | ||||||
chr14:96342781
|
T | C | 1 | a0001c0005t0018g0255 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.744+338A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342781 | ||||||
chr14:96342893
|
A | G | 1 | a0001c0002t0001g0278 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.744+226T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 5/41 | chr14 | 96342893 | ||||||
chr14:96343401
|
T | A | 1 | a0003c0004t0004g0004 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.582-120A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96343401 | ||||||
chr14:96343735
|
G | A | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.582-454C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96343735 | ||||||
chr14:96343950
|
T | G | 5 | a0001c0002t0001g0012a0001c0002t0001g0312a0001c0002t0001g0313others(2): Show | 6 | HG01099.hp1 HG01192.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.582-669A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96343950 | ||||||
chr14:96344156
|
G | A | 6 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0315others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.581+498C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96344156 | ||||||
chr14:96344237
|
C | T | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.581+417G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96344237 | ||||||
chr14:96344270
|
C | T | 1 | a0001c0002t0001g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.581+384G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96344270 | ||||||
chr14:96344491
|
G | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.581+163C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96344491 | ||||||
chr14:96344612
|
G | A | 1 | a0001c0003t0003g0227 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.581+42C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 4/41 | chr14 | 96344612 | ||||||
chr14:96344797
|
T | C | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.479-41A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 3/41 | chr14 | 96344797 | ||||||
chr14:96344994
|
A | G | 270 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(267): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.479-238T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 3/41 | chr14 | 96344994 | ||||||
chr14:96345136
|
C | T | 1 | a0001c0013t0022g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.478+97G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 3/41 | chr14 | 96345136 | ||||||
chr14:96345506
|
A | G | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.326-121T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96345506 | ||||||
chr14:96346170
|
A | C | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.326-785T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346170 | ||||||
chr14:96346302
|
G | A | 43 | a0001c0002t0001g0012a0001c0002t0001g0262a0001c0002t0001g0265others(40): Show | 44 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.325+877C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346302 | ||||||
chr14:96346343
|
C | A | 1 | a0018c0023t0036g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.325+836G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346343 | ||||||
chr14:96346482
|
C | T | 4 | a0001c0003t0003g0209a0001c0011t0003g0018a0001c0011t0003g0019others(1): Show | 4 | HG01123.hp1 HG01261.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+697G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346482 | ||||||
chr14:96346483
|
A | C | 91 | a0001c0003t0011g0109a0001c0003t0011g0176a0002c0001t0002g0006others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.325+696T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346483 | ||||||
chr14:96346567
|
T | A | 79 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(76): Show | 82 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.325+612A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346567 | ||||||
chr14:96346836
|
T | C | 91 | a0001c0003t0011g0109a0001c0003t0011g0176a0002c0001t0002g0006others(88): Show | 92 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.325+343A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346836 | ||||||
chr14:96346854
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.325+325A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346854 | ||||||
chr14:96346996
|
C | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.325+183G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 2/41 | chr14 | 96346996 | ||||||
chr14:96347366
|
A | T | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.163-25T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96347366 | ||||||
chr14:96347380
|
C | G | 10 | a0001c0002t0051g0257a0006c0007t0008g0001a0006c0007t0008g0080others(7): Show | 13 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-39G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96347380 | ||||||
chr14:96347411
|
G | A | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.163-70C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96347411 | ||||||
chr14:96347589
|
C | T | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.163-248G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96347589 | ||||||
chr14:96348012
|
T | G | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.163-671A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348012 | ||||||
chr14:96348120
|
T | C | 2 | a0002c0001t0002g0156a0002c0001t0002g0157 | 2 | NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.163-779A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348120 | ||||||
chr14:96348183
|
A | G | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-842T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348183 | ||||||
chr14:96348263
|
T | A | 1 | a0001c0003t0003g0205 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.163-922A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348263 | ||||||
chr14:96348355
|
G | T | 3 | a0001c0002t0001g0270a0001c0002t0001g0275a0001c0026t0001g0269 | 3 | HG01261.hp2 HG01496.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.163-1014C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348355 | ||||||
chr14:96348407
|
G | A | 1 | a0003c0004t0004g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.163-1066C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348407 | ||||||
chr14:96348433
|
G | A | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.163-1092C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348433 | ||||||
chr14:96348454
|
G | A | 79 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(76): Show | 82 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.163-1113C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348454 | ||||||
chr14:96348458
|
A | G | 65 | a0002c0001t0002g0006a0002c0001t0002g0110a0002c0001t0002g0111others(62): Show | 66 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.163-1117T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348458 | ||||||
chr14:96348510
|
C | A | 2 | a0001c0002t0001g0318a0001c0002t0001g0319 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.163-1169G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348510 | ||||||
chr14:96348650
|
C | G | 2 | a0013c0015t0004g0024a0013c0015t0004g0025 | 2 | HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.163-1309G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348650 | ||||||
chr14:96348655
|
G | A | 48 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(45): Show | 53 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.163-1314C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348655 | ||||||
chr14:96348668
|
C | CAA | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-1329_163-1328d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348668 | ||||||
chr14:96348680
|
AAAAT | A | 63 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(60): Show | 69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.163-1343_163-1340d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348680 | ||||||
chr14:96348771
|
T | A | 2 | a0012c0020t0006g0178a0012c0020t0006g0179 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.163-1430A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348771 | ||||||
chr14:96348849
|
T | C | 1 | a0001c0003t0045g0246 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-1508A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348849 | ||||||
chr14:96348872
|
G | A | 1 | a0001c0002t0053g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.163-1531C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96348872 | ||||||
chr14:96349017
|
G | C | 83 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(80): Show | 86 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.163-1676C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349017 | ||||||
chr14:96349051
|
C | T | 3 | a0001c0003t0005g0206a0001c0003t0005g0207a0001c0003t0005g0238 | 3 | NA18961.hp2 NA18970.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.163-1710G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349051 | ||||||
chr14:96349056
|
T | G | 3 | a0001c0003t0005g0206a0001c0003t0005g0207a0001c0003t0005g0238 | 3 | NA18961.hp2 NA18970.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.163-1715A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349056 | ||||||
chr14:96349128
|
C | T | 1 | a0003c0004t0029g0023 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.163-1787G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349128 | ||||||
chr14:96349194
|
A | G | 5 | a0001c0002t0001g0295a0001c0002t0001g0300a0001c0002t0001g0311others(2): Show | 5 | HG01891.hp1 HG02523.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-1853T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349194 | ||||||
chr14:96349299
|
G | C | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-1958C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349299 | ||||||
chr14:96349306
|
G | C | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-1965C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349306 | ||||||
chr14:96349386
|
T | C | 52 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.163-2045A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349386 | ||||||
chr14:96349552
|
G | C | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-2211C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349552 | ||||||
chr14:96349572
|
T | G | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-2231A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349572 | ||||||
chr14:96349600
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2259C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349600 | ||||||
chr14:96349850
|
C | G | 1 | a0025c0027t0008g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163-2509G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349850 | ||||||
chr14:96349924
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2583T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349924 | ||||||
chr14:96349933
|
G | A | 1 | a0001c0003t0003g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.163-2592C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349933 | ||||||
chr14:96349951
|
T | G | 1 | a0001c0005t0005g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.163-2610A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96349951 | ||||||
chr14:96350203
|
C | T | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.163-2862G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350203 | ||||||
chr14:96350240
|
A | G | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2899T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350240 | ||||||
chr14:96350353
|
T | C | 8 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(5): Show | 11 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-3012A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350353 | ||||||
chr14:96350503
|
A | G | 6 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(3): Show | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-3162T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350503 | ||||||
chr14:96350545
|
A | G | 1 | a0001c0002t0001g0292 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.163-3204T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350545 | ||||||
chr14:96350619
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-3278G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350619 | ||||||
chr14:96350773
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-3432G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96350773 | ||||||
chr14:96351180
|
A | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-3839T>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351180 | ||||||
chr14:96351380
|
T | C | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-4039A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351380 | ||||||
chr14:96351382
|
G | A | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.163-4041C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351382 | ||||||
chr14:96351584
|
G | A | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.163-4243C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351584 | ||||||
chr14:96351608
|
C | T | 1 | a0025c0027t0008g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163-4267G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351608 | ||||||
chr14:96351629
|
G | A | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-4288C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351629 | ||||||
chr14:96351677
|
C | T | 1 | a0001c0003t0005g0197 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163-4336G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351677 | ||||||
chr14:96351678
|
G | A | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-4337C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351678 | ||||||
chr14:96351692
|
C | T | 1 | a0001c0005t0005g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.163-4351G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351692 | ||||||
chr14:96351714
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.163-4373G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351714 | ||||||
chr14:96351735
|
CA | C | 93 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(90): Show | 98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.163-4395delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351735 | ||||||
chr14:96351901
|
C | CA | 177 | a0001c0002t0051g0257a0001c0003t0002g0214a0001c0003t0003g0008others(174): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.163-4561dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351901 | ||||||
chr14:96351901
|
C | CAA | 75 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(72): Show | 78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.163-4562_163-4561d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351901 | ||||||
chr14:96351901
|
CA | C | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-4561delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351901 | ||||||
chr14:96351926
|
T | A | 6 | a0001c0002t0001g0275a0001c0003t0023g0243a0001c0003t0023g0245others(3): Show | 6 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-4585A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96351926 | ||||||
chr14:96352128
|
T | C | 1 | a0024c0028t0058g0326 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163-4787A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352128 | ||||||
chr14:96352158
|
A | G | 1 | a0001c0002t0053g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.163-4817T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352158 | ||||||
chr14:96352321
|
C | T | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.163-4980G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352321 | ||||||
chr14:96352548
|
C | T | 1 | a0001c0003t0037g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.163-5207G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352548 | ||||||
chr14:96352577
|
T | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-5236A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352577 | ||||||
chr14:96352583
|
G | A | 4 | a0004c0006t0013g0013a0004c0006t0013g0331a0004c0006t0013g0332others(1): Show | 5 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-5242C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352583 | ||||||
chr14:96352614
|
TA | T | 12 | a0001c0013t0022g0085a0004c0006t0010g0333a0004c0006t0010g0334others(9): Show | 13 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-5274delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352614 | ||||||
chr14:96352662
|
TAAAGAA | T | 10 | a0001c0002t0051g0257a0006c0007t0008g0001a0006c0007t0008g0080others(7): Show | 13 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-5327_163-5322d others(8): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352662 | ||||||
chr14:96352713
|
T | G | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.163-5372A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352713 | ||||||
chr14:96352791
|
T | C | 52 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.163-5450A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352791 | ||||||
chr14:96352792
|
G | GA | 11 | a0005c0008t0005g0098a0005c0008t0012g0099a0005c0008t0021g0100others(8): Show | 12 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-5452dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352792 | ||||||
chr14:96352792
|
GA | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-5452delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352792 | ||||||
chr14:96352802
|
AG | A | 5 | a0001c0005t0005g0072a0001c0005t0005g0073a0001c0005t0005g0074others(2): Show | 5 | HG00735.hp2 HG01070.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-5462delC | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352802 | ||||||
chr14:96352853
|
C | T | 1 | a0007c0009t0002g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.163-5512G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352853 | ||||||
chr14:96352890
|
C | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-5549G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96352890 | ||||||
chr14:96353033
|
A | G | 8 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-5692T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353033 | ||||||
chr14:96353143
|
T | C | 13 | a0001c0002t0051g0257a0001c0012t0024g0093a0001c0012t0024g0094others(10): Show | 16 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.163-5802A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353143 | ||||||
chr14:96353170
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.163-5829C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353170 | ||||||
chr14:96353470
|
C | CA | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-6130dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353470 | ||||||
chr14:96353518
|
C | T | 1 | a0025c0027t0008g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163-6177G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353518 | ||||||
chr14:96353584
|
C | T | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-6243G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353584 | ||||||
chr14:96353587
|
C | T | 1 | a0004c0006t0013g0332 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.163-6246G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353587 | ||||||
chr14:96353609
|
CAGTG | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-6272_163-6269d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353609 | ||||||
chr14:96353642
|
T | TTA | 17 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0293others(14): Show | 19 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-6303_163-6302d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353642 | ||||||
chr14:96353642
|
TTA | T | 12 | a0002c0001t0002g0182a0002c0001t0002g0183a0004c0006t0010g0333others(9): Show | 13 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-6303_163-6302d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353642 | ||||||
chr14:96353659
|
T | A | 2 | a0002c0001t0002g0182a0002c0001t0002g0183 | 2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.163-6318A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353659 | ||||||
chr14:96353659
|
T | TAA | 90 | a0001c0003t0011g0109a0001c0003t0011g0176a0002c0001t0002g0006others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.163-6320_163-6319d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353659 | ||||||
chr14:96353679
|
A | G | 1 | a0001c0003t0003g0208 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.163-6338T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353679 | ||||||
chr14:96353860
|
G | A | 1 | a0002c0001t0002g0235 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.163-6519C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353860 | ||||||
chr14:96353962
|
G | A | 1 | a0005c0010t0009g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.163-6621C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96353962 | ||||||
chr14:96354005
|
T | C | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-6664A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354005 | ||||||
chr14:96354010
|
T | C | 1 | a0001c0002t0001g0261 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.163-6669A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354010 | ||||||
chr14:96354054
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-6713T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354054 | ||||||
chr14:96354085
|
T | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-6744A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354085 | ||||||
chr14:96354109
|
G | A | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-6768C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354109 | ||||||
chr14:96354116
|
G | T | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.163-6775C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354116 | ||||||
chr14:96354191
|
C | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-6850G>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354191 | ||||||
chr14:96354239
|
A | AG | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-6899dupC | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354239 | ||||||
chr14:96354265
|
A | G | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-6924T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354265 | ||||||
chr14:96354299
|
C | T | 1 | a0003c0004t0004g0021 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.163-6958G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354299 | ||||||
chr14:96354440
|
G | A | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-7099C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354440 | ||||||
chr14:96354489
|
T | G | 1 | a0001c0002t0001g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163-7148A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354489 | ||||||
chr14:96354546
|
G | A | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.163-7205C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354546 | ||||||
chr14:96354615
|
T | C | 1 | a0001c0003t0003g0229 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.163-7274A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354615 | ||||||
chr14:96354664
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-7323A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354664 | ||||||
chr14:96354712
|
T | C | 49 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(46): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-7371A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354712 | ||||||
chr14:96354750
|
G | A | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.163-7409C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354750 | ||||||
chr14:96354794
|
TTTG | T | 7 | a0001c0003t0003g0108a0001c0003t0003g0201a0001c0003t0003g0202others(4): Show | 7 | NA18945.hp1 NA18965.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-7456_163-7454d others(5): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354794 | ||||||
chr14:96354802
|
T | A | 1 | a0001c0003t0003g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.163-7461A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354802 | ||||||
chr14:96354806
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-7465C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354806 | ||||||
chr14:96354896
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.163-7555C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96354896 | ||||||
chr14:96355052
|
C | T | 1 | a0003c0004t0004g0103 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.163-7711G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355052 | ||||||
chr14:96355059
|
C | T | 92 | a0001c0003t0011g0109a0001c0003t0011g0176a0002c0001t0002g0006others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.163-7718G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355059 | ||||||
chr14:96355110
|
G | C | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.162+7705C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355110 | ||||||
chr14:96355172
|
G | A | 80 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(77): Show | 83 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+7643C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355172 | ||||||
chr14:96355173
|
C | A | 80 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(77): Show | 83 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+7642G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355173 | ||||||
chr14:96355291
|
T | A | 1 | a0028c0031t0001g0277 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.162+7524A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355291 | ||||||
chr14:96355561
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+7254A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355561 | ||||||
chr14:96355592
|
A | T | 1 | a0003c0004t0015g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.162+7223T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355592 | ||||||
chr14:96355725
|
A | G | 1 | a0001c0003t0003g0200 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.162+7090T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355725 | ||||||
chr14:96355789
|
T | C | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.162+7026A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355789 | ||||||
chr14:96355962
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6853C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96355962 | ||||||
chr14:96356032
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6783C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356032 | ||||||
chr14:96356035
|
G | A | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+6780C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356035 | ||||||
chr14:96356037
|
G | A | 4 | a0001c0013t0005g0091a0001c0013t0022g0085a0001c0013t0022g0090others(1): Show | 4 | HG00642.hp2 HG01891.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+6778C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356037 | ||||||
chr14:96356098
|
G | A | 1 | a0002c0001t0005g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.162+6717C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356098 | ||||||
chr14:96356148
|
G | A | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+6667C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356148 | ||||||
chr14:96356170
|
CA | C | 252 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(249): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.162+6644delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356170 | ||||||
chr14:96356271
|
C | T | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162+6544G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356271 | ||||||
chr14:96356272
|
A | T | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6543T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356272 | ||||||
chr14:96356302
|
G | A | 3 | a0001c0002t0001g0315a0001c0002t0001g0316a0001c0002t0001g0317 | 3 | HG02572.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.162+6513C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356302 | ||||||
chr14:96356317
|
G | A | 9 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(6): Show | 12 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6498C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356317 | ||||||
chr14:96356393
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0001g0319 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+6422G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356393 | ||||||
chr14:96356400
|
C | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6415G>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356400 | ||||||
chr14:96356435
|
T | C | 1 | a0001c0003t0003g0232 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.162+6380A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356435 | ||||||
chr14:96356473
|
CATA | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6339_162+6341d others(5): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356473 | ||||||
chr14:96356488
|
C | T | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.162+6327G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356488 | ||||||
chr14:96356632
|
C | T | 6 | a0002c0001t0004g0112a0002c0001t0004g0115a0002c0001t0004g0116others(3): Show | 6 | HG00558.hp1 HG00621.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+6183G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356632 | ||||||
chr14:96356652
|
G | T | 1 | a0001c0002t0001g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.162+6163C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356652 | ||||||
chr14:96356697
|
T | C | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+6118A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356697 | ||||||
chr14:96356776
|
A | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+6039T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356776 | ||||||
chr14:96356897
|
T | G | 1 | a0001c0003t0003g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.162+5918A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96356897 | ||||||
chr14:96357000
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+5815A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357000 | ||||||
chr14:96357110
|
CA | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+5704delT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357110 | ||||||
chr14:96357241
|
T | G | 4 | a0004c0006t0013g0013a0004c0006t0013g0331a0004c0006t0013g0332others(1): Show | 5 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+5574A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357241 | ||||||
chr14:96357299
|
T | C | 2 | a0001c0002t0001g0318a0001c0002t0001g0319 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+5516A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357299 | ||||||
chr14:96357330
|
T | A | 1 | a0001c0002t0055g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162+5485A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357330 | ||||||
chr14:96357373
|
T | G | 13 | a0005c0008t0005g0098a0005c0008t0012g0096a0005c0008t0012g0097others(10): Show | 14 | HG00642.hp1 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+5442A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357373 | ||||||
chr14:96357390
|
A | G | 4 | a0001c0002t0001g0265a0001c0002t0001g0297a0001c0002t0001g0298others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+5425T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357390 | ||||||
chr14:96357402
|
C | T | 52 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(49): Show | 57 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.162+5413G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357402 | ||||||
chr14:96357618
|
C | T | 1 | a0001c0002t0051g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.162+5197G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357618 | ||||||
chr14:96357684
|
G | GT | 53 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(50): Show | 58 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.162+5130dupA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357684 | ||||||
chr14:96357916
|
T | C | 1 | a0002c0001t0002g0181 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.162+4899A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96357916 | ||||||
chr14:96358060
|
T | G | 3 | a0001c0012t0024g0093a0001c0012t0024g0094a0001c0012t0050g0095 | 3 | HG03195.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+4755A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358060 | ||||||
chr14:96358063
|
C | CT | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+4751_162+4752i others(3): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358063 | ||||||
chr14:96358162
|
C | T | 2 | a0001c0002t0001g0011a0002c0001t0048g0114 | 3 | HG02896.hp1 HG02897.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.162+4653G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358162 | ||||||
chr14:96358194
|
G | C | 1 | a0001c0002t0001g0321 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.162+4621C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358194 | ||||||
chr14:96358194
|
G | T | 2 | a0001c0002t0001g0295a0001c0003t0005g0238 | 2 | HG02630.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.162+4621C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358194 | ||||||
chr14:96358256
|
T | A | 2 | a0002c0001t0002g0182a0002c0001t0002g0183 | 2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.162+4559A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358256 | ||||||
chr14:96358326
|
T | C | 27 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0001g0261others(24): Show | 27 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.162+4489A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358326 | ||||||
chr14:96358352
|
G | A | 2 | a0002c0001t0002g0184a0002c0001t0002g0185 | 2 | HG00609.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.162+4463C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358352 | ||||||
chr14:96358389
|
C | T | 4 | a0001c0003t0005g0197a0001c0003t0005g0198a0001c0003t0005g0199others(1): Show | 4 | HG00099.hp1 HG01099.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+4426G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358389 | ||||||
chr14:96358507
|
T | A | 8 | a0006c0007t0008g0001a0006c0007t0008g0080a0006c0007t0008g0081others(5): Show | 11 | HG02145.hp1 HG02717.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+4308A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358507 | ||||||
chr14:96358595
|
A | G | 1 | a0004c0006t0013g0331 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.162+4220T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358595 | ||||||
chr14:96358709
|
C | T | 1 | a0001c0003t0032g0195 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.162+4106G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358709 | ||||||
chr14:96358759
|
AT | A | 69 | a0001c0003t0002g0214a0001c0003t0003g0008a0001c0003t0003g0009others(66): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.162+4055delA | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358759 | ||||||
chr14:96358775
|
T | C | 1 | a0001c0003t0003g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.162+4040A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358775 | ||||||
chr14:96358928
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+3887C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358928 | ||||||
chr14:96358933
|
T | C | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+3882A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358933 | ||||||
chr14:96358969
|
G | C | 1 | a0001c0002t0001g0322 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162+3846C>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96358969 | ||||||
chr14:96359192
|
C | T | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+3623G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359192 | ||||||
chr14:96359244
|
C | T | 39 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0001g0261others(36): Show | 40 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.162+3571G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359244 | ||||||
chr14:96359480
|
C | T | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+3335G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359480 | ||||||
chr14:96359550
|
C | T | 1 | a0002c0001t0006g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.162+3265G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359550 | ||||||
chr14:96359618
|
C | T | 1 | a0001c0003t0023g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+3197G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359618 | ||||||
chr14:96359767
|
G | A | 1 | a0004c0041t0063g0340 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.162+3048C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359767 | ||||||
chr14:96359795
|
T | C | 1 | a0004c0006t0010g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.162+3020A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359795 | ||||||
chr14:96359944
|
T | G | 3 | a0002c0001t0002g0235a0002c0001t0041g0189a0002c0001t0047g0188 | 3 | NA18959.hp1 NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.162+2871A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96359944 | ||||||
chr14:96360163
|
G | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+2652C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360163 | ||||||
chr14:96360755
|
G | A | 267 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(264): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.162+2060C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360755 | ||||||
chr14:96360834
|
C | T | 1 | a0002c0001t0004g0112 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.162+1981G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360834 | ||||||
chr14:96360910
|
A | T | 92 | a0001c0003t0011g0109a0001c0003t0011g0176a0002c0001t0002g0006others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.162+1905T>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360910 | ||||||
chr14:96360933
|
C | CA | 16 | a0001c0002t0001g0263a0001c0002t0001g0264a0001c0002t0001g0265others(13): Show | 16 | HG00323.hp1 HG02056.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.162+1881dupT | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360933 | ||||||
chr14:96360933
|
C | CAA | 155 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0258others(152): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.162+1880_162+1881d others(4): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360933 | ||||||
chr14:96360933
|
C | CAAA | 68 | a0001c0002t0001g0323a0001c0002t0001g0324a0001c0002t0001g0328others(65): Show | 74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.162+1879_162+1881d others(5): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360933 | ||||||
chr14:96360933
|
C | CAAAA | 20 | a0001c0003t0003g0239a0001c0003t0005g0238a0001c0003t0031g0240others(17): Show | 20 | HG00642.hp1 HG01123.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+1878_162+1881d others(6): Show |
ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96360933 | ||||||
chr14:96361169
|
T | A | 1 | a0002c0001t0002g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.162+1646A>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361169 | ||||||
chr14:96361247
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.162+1568G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361247 | ||||||
chr14:96361309
|
G | T | 1 | a0001c0002t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.162+1506C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361309 | ||||||
chr14:96361498
|
A | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+1317T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361498 | ||||||
chr14:96361517
|
T | C | 5 | a0001c0003t0023g0243a0001c0003t0023g0245a0001c0003t0044g0242others(2): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+1298A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361517 | ||||||
chr14:96361724
|
G | A | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+1091C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361724 | ||||||
chr14:96361934
|
T | G | 1 | a0001c0003t0035g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.162+881A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96361934 | ||||||
chr14:96362000
|
C | T | 3 | a0001c0011t0003g0018a0001c0011t0003g0019a0001c0011t0003g0020 | 3 | HG01123.hp1 HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.162+815G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362000 | ||||||
chr14:96362214
|
T | C | 1 | a0001c0005t0007g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.162+601A>G | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362214 | ||||||
chr14:96362217
|
G | T | 4 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0001g0261others(1): Show | 4 | HG00741.hp2 HG01981.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+598C>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362217 | ||||||
chr14:96362415
|
G | A | 1 | a0003c0004t0004g0103 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.162+400C>T | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362415 | ||||||
chr14:96362459
|
A | G | 10 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(7): Show | 11 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+356T>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362459 | ||||||
chr14:96362468
|
T | G | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+347A>C | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362468 | ||||||
chr14:96362484
|
C | T | 1 | a0001c0003t0003g0108 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.162+331G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362484 | ||||||
chr14:96362525
|
C | T | 11 | a0004c0006t0010g0333a0004c0006t0010g0334a0004c0006t0010g0335others(8): Show | 12 | HG00621.hp1 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+290G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362525 | ||||||
chr14:96362615
|
C | T | 5 | a0005c0010t0009g0105a0005c0010t0009g0106a0005c0010t0009g0107others(2): Show | 6 | HG01255.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+200G>A | ATG2B | ENSG00000066739.12 | transcript | ENST00000359933.6 | protein_coding | 1/41 | chr14 | 96362615 |