geneid | 129642 |
---|---|
ensemblid | ENSG00000143797.12 |
hgncid | 25193 |
symbol | MBOAT2 |
name | membrane bound O-acyltransferase domain containing 2 |
refseq_nuc | NM_138799.4 |
refseq_prot | NP_620154.2 |
ensembl_nuc | ENST00000305997.8 |
ensembl_prot | ENSP00000302177.3 |
mane_status | MANE Select |
chr | chr2 |
start | 8852690 |
end | 9003684 |
strand | - |
ver | v1.2 |
region | chr2:8852690-9003684 |
region5000 | chr2:8847690-9008684 |
regionname0 | MBOAT2_chr2_8852690_9003684 |
regionname5000 | MBOAT2_chr2_8847690_9008684 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 520 | 151 | 73 | 25 | 27 | 4 | 20 | 14 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002 | 0/0 | 520 | 7 | 4 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0003 | 0/0 | 520 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0004 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1563 | 150 | 72 | 25 | 27 | 4 | 20 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
c0002 | 0/0 | 1563 | 7 | 4 | 2 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
c0003 | 0/0 | 1563 | 3 | 0 | 1 | 0 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
c0004 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
c0005 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6060 | 27 | 19 | 3 | 4 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0002 | 0/1 | 6060 | 26 | 0 | 9 | 12 | 0 | 4 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0003 | 0/0 | 6065 | 10 | 1 | 3 | 0 | 0 | 6 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0004 | 0/0 | 6063 | 8 | 5 | 0 | 1 | 1 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0005 | 0/0 | 6058 | 7 | 6 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0006 | 0/0 | 6060 | 6 | 0 | 0 | 2 | 0 | 4 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0007 | 0/0 | 6060 | 5 | 4 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0008 | 0/0 | 6062 | 4 | 1 | 2 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0009 | 0/0 | 6060 | 3 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0010 | 0/0 | 6060 | 3 | 0 | 1 | 0 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0011 | 0/0 | 6055 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0012 | 0/0 | 6057 | 3 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0013 | 0/0 | 6063 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0014 | 0/0 | 6063 | 3 | 1 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0015 | 0/0 | 6062 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0016 | 1/0 | 6060 | 3 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0017 | 0/0 | 6057 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0018 | 0/0 | 6060 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0019 | 0/0 | 6057 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0020 | 0/0 | 6060 | 2 | 0 | 0 | 2 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0021 | 0/0 | 6063 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0022 | 0/0 | 6063 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0023 | 0/0 | 6062 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0024 | 0/0 | 6060 | 2 | 1 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0025 | 0/0 | 6060 | 2 | 0 | 0 | 0 | 1 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0026 | 0/0 | 6059 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0027 | 0/0 | 6060 | 2 | 0 | 1 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0028 | 0/0 | 6057 | 2 | 0 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0029 | 0/0 | 6062 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0030 | 0/0 | 6060 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0031 | 0/0 | 6057 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0032 | 0/0 | 6062 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0033 | 0/0 | 6065 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0034 | 0/0 | 6065 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0035 | 0/0 | 6063 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0036 | 0/0 | 6063 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0037 | 0/0 | 6060 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0038 | 0/0 | 6062 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0039 | 0/0 | 6060 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0040 | 0/0 | 6061 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0041 | 0/0 | 6060 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0042 | 0/0 | 6060 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0043 | 0/0 | 6060 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0044 | 0/0 | 6060 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0045 | 0/0 | 6058 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0046 | 0/0 | 6063 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0047 | 0/0 | 6060 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0048 | 0/0 | 6071 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
t0049 | 0/0 | 6057 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0002 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1563 | 150 | 72 | 25 | 27 | 4 | 20 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0004 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002c0002 | 0/0 | 1563 | 7 | 4 | 2 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0003c0003 | 0/0 | 1563 | 3 | 0 | 1 | 0 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0004c0005 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7622 | 27 | 19 | 3 | 4 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0002 | 0/1 | 7622 | 26 | 0 | 9 | 12 | 0 | 4 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0003 | 0/0 | 7627 | 10 | 1 | 3 | 0 | 0 | 6 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0004 | 0/0 | 7625 | 8 | 5 | 0 | 1 | 1 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0005 | 0/0 | 7620 | 7 | 6 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0006 | 0/0 | 7622 | 6 | 0 | 0 | 2 | 0 | 4 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0007 | 0/0 | 7622 | 5 | 4 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0008 | 0/0 | 7624 | 4 | 1 | 2 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0009 | 0/0 | 7622 | 3 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0011 | 0/0 | 7617 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0012 | 0/0 | 7619 | 3 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0013 | 0/0 | 7625 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0014 | 0/0 | 7625 | 3 | 1 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0015 | 0/0 | 7624 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0016 | 1/0 | 7622 | 3 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0018 | 0/0 | 7622 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0020 | 0/0 | 7622 | 2 | 0 | 0 | 2 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0021 | 0/0 | 7625 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0022 | 0/0 | 7625 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0023 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0024 | 0/0 | 7622 | 2 | 1 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0025 | 0/0 | 7622 | 2 | 0 | 0 | 0 | 1 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0026 | 0/0 | 7621 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0027 | 0/0 | 7622 | 2 | 0 | 1 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0029 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0030 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0032 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0034 | 0/0 | 7627 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0035 | 0/0 | 7625 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0036 | 0/0 | 7625 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0037 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0038 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0039 | 0/0 | 7622 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0040 | 0/0 | 7623 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0041 | 0/0 | 7622 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0042 | 0/0 | 7622 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0043 | 0/0 | 7622 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0044 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0045 | 0/0 | 7620 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0046 | 0/0 | 7625 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0047 | 0/0 | 7622 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0001t0048 | 0/0 | 7633 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0001c0004t0017 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002c0002t0017 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002c0002t0019 | 0/0 | 7619 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002c0002t0028 | 0/0 | 7619 | 2 | 0 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002c0002t0031 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0002c0002t0049 | 0/0 | 7619 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0003c0003t0010 | 0/0 | 7622 | 3 | 0 | 1 | 0 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
a0004c0005t0033 | 0/0 | 7627 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | copy fasta | chr2 | 8847690 | 9008684 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0008g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0012g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0014g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0014g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0015g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0016g0002 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0016g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0018g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0018g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0020g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0021g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0022g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0022g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0024g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0024g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0025g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0025g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0026g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0026g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0027g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0027g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0029g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0030g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0032g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0034g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0035g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0036g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0037g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0038g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0039g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0040g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0041g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0042g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0043g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0044g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0045g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0046g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0047g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0001t0048g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0001c0004t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0019g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0028g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0028g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0031g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0002c0002t0049g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0003c0003t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0003c0003t0010g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0003c0003t0010g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
a0004c0005t0033g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0043 | g0103 | EUR | GBR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00140 | hp2 | a0001 | c0001 | t0034 | g0095 | EUR | GBR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00558 | hp1 | a0001 | c0001 | t0020 | g0135 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00609 | hp2 | a0001 | c0001 | t0032 | g0003 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00642 | hp1 | a0003 | c0003 | t0010 | g0155 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0143 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00735 | hp2 | a0001 | c0001 | t0008 | g0126 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG00738 | hp2 | a0001 | c0001 | t0012 | g0052 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01070 | hp1 | a0001 | c0001 | t0014 | g0066 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01070 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01071 | hp1 | a0001 | c0001 | t0014 | g0067 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01071 | hp2 | a0001 | c0001 | t0027 | g0156 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01167 | hp2 | a0002 | c0002 | t0028 | g0159 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01169 | hp1 | a0002 | c0002 | t0028 | g0160 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01175 | hp2 | a0001 | c0001 | t0041 | g0042 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01884 | hp1 | a0001 | c0001 | t0029 | g0008 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0086 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0037 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02027 | hp1 | a0002 | c0002 | t0049 | g0158 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0002 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02055 | hp2 | a0001 | c0001 | t0014 | g0056 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02080 | hp2 | a0001 | c0001 | t0047 | g0129 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02083 | hp2 | a0001 | c0001 | t0024 | g0121 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0061 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02257 | hp1 | a0001 | c0001 | t0026 | g0083 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02257 | hp2 | a0002 | c0002 | t0017 | g0064 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02572 | hp1 | a0002 | c0002 | t0019 | g0012 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02622 | hp1 | a0001 | c0001 | t0016 | g0076 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02630 | hp2 | a0001 | c0001 | t0026 | g0084 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02647 | hp2 | a0002 | c0002 | t0019 | g0011 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0096 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0122 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02717 | hp2 | a0001 | c0001 | t0021 | g0025 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02809 | hp2 | a0001 | c0004 | t0017 | g0006 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02895 | hp2 | a0001 | c0001 | t0018 | g0009 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02896 | hp1 | a0001 | c0001 | t0018 | g0010 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02922 | hp2 | a0001 | c0001 | t0030 | g0005 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02976 | hp1 | a0001 | c0001 | t0022 | g0033 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02976 | hp2 | a0001 | c0001 | t0045 | g0038 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03017 | hp1 | a0001 | c0001 | t0042 | g0127 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03098 | hp1 | a0001 | c0001 | t0046 | g0111 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03130 | hp2 | a0001 | c0001 | t0015 | g0088 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03139 | hp2 | a0001 | c0001 | t0024 | g0082 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03195 | hp1 | a0001 | c0001 | t0023 | g0049 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0062 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0063 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03225 | hp2 | a0001 | c0001 | t0037 | g0022 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03453 | hp2 | a0001 | c0001 | t0048 | g0004 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03486 | hp2 | a0001 | c0001 | t0044 | g0112 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03490 | hp1 | a0001 | c0001 | t0025 | g0078 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03516 | hp1 | a0001 | c0001 | t0023 | g0048 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03654 | hp2 | a0003 | c0003 | t0010 | g0153 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03710 | hp1 | a0001 | c0001 | t0027 | g0157 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03710 | hp2 | a0003 | c0003 | t0010 | g0154 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | STU | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0092 | SAS | STU | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0050 | SAS | BEB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18522 | hp1 | a0001 | c0001 | t0022 | g0133 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0053 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18956 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18957 | hp1 | a0001 | c0001 | t0020 | g0134 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18982 | hp1 | a0001 | c0001 | t0038 | g0017 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19010 | hp1 | a0001 | c0001 | t0039 | g0094 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19030 | hp1 | a0001 | c0001 | t0036 | g0113 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19030 | hp2 | a0004 | c0005 | t0033 | g0013 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19043 | hp1 | a0001 | c0001 | t0021 | g0024 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19043 | hp2 | a0002 | c0002 | t0031 | g0036 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19063 | hp2 | a0001 | c0001 | t0040 | g0123 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0035 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0047 | EUR | TSI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA20752 | hp2 | a0001 | c0001 | t0025 | g0125 | EUR | TSI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | GIH | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0091 | SAS | GIH | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0031 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02486 | hp2 | a0001 | c0001 | t0015 | g0085 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG03471 | hp2 | a0001 | c0001 | t0035 | g0021 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | USA | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0105 | REF | REF | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0016 | g0002 | REF | REF | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:8858741
|
T | C | 1 | a0003 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
missense_variant | MODERATE | c.1501A>G | p.Thr501Ala | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1571/7622 | 1501/1563 | 501/520 | chr2 | 8858741 | ||
chr2:8860626
|
G | A | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1324C>T | p.Leu442Phe | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/13 | 1394/7622 | 1324/1563 | 442/520 | chr2 | 8860626 | ||
chr2:8873294
|
C | T | 1 | a0002 | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
missense_variant | MODERATE | c.697G>A | p.Val233Ile | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/13 | 767/7622 | 697/1563 | 233/520 | chr2 | 8873294 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:8858841
|
T | C | 2 | a0001c0004a0002c0002 | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
synonymous_variant | LOW | c.1401A>G | p.Lys467Lys | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1471/7622 | 1401/1563 | 467/520 | chr2 | 8858841 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:8852770
|
A | G | 1 | a0004c0005t0033 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5909T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5909 | chr2 | 8852770 | |||||
chr2:8853102
|
CA | C | 1 | a0001c0001t0023 | 2 | HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5576delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5576 | chr2 | 8853102 | |||||
chr2:8853209
|
G | A | 1 | a0001c0001t0030 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5470C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5470 | chr2 | 8853209 | |||||
chr2:8853212
|
C | T | 6 | a0001c0001t0004a0001c0001t0007a0001c0001t0014others(3): Show | 22 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5467G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5467 | chr2 | 8853212 | |||||
chr2:8853375
|
A | C | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(7): Show | 31 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5304T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5304 | chr2 | 8853375 | |||||
chr2:8853646
|
G | A | 1 | a0001c0001t0013 | 3 | HG02451.hp1 HG02486.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5033C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5033 | chr2 | 8853646 | |||||
chr2:8853664
|
G | T | 5 | a0001c0001t0011a0001c0004t0017a0002c0002t0017others(2): Show | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5015C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5015 | chr2 | 8853664 | |||||
chr2:8853879
|
T | C | 1 | a0001c0001t0042 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4800A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4800 | chr2 | 8853879 | |||||
chr2:8854078
|
G | A | 3 | a0001c0004t0017a0002c0002t0017a0002c0002t0028 | 4 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4601C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4601 | chr2 | 8854078 | |||||
chr2:8854080
|
T | C | 1 | a0001c0001t0043 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4599A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4599 | chr2 | 8854080 | |||||
chr2:8854172
|
C | G | 1 | a0001c0001t0012 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4507G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4507 | chr2 | 8854172 | |||||
chr2:8854172
|
CCT | C | 7 | a0001c0001t0011a0001c0004t0017a0002c0002t0017others(4): Show | 11 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4505_*4506delAG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4505 | chr2 | 8854172 | |||||
chr2:8854470
|
G | A | 1 | a0001c0001t0012 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4209C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4209 | chr2 | 8854470 | |||||
chr2:8855131
|
A | C | 1 | a0001c0001t0007 | 5 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3548T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3548 | chr2 | 8855131 | |||||
chr2:8855194
|
G | A | 1 | a0001c0001t0045 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3485C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3485 | chr2 | 8855194 | |||||
chr2:8855228
|
G | C | 1 | a0001c0001t0036 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3451C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3451 | chr2 | 8855228 | |||||
chr2:8855246
|
G | A | 1 | a0001c0001t0034 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3433C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3433 | chr2 | 8855246 | |||||
chr2:8855582
|
G | A | 3 | a0001c0001t0006a0001c0001t0039a0001c0001t0043 | 8 | HG00140.hp1 HG02698.hp2 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3097C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3097 | chr2 | 8855582 | |||||
chr2:8855589
|
A | T | 1 | a0001c0001t0039 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3090T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3090 | chr2 | 8855589 | |||||
chr2:8855855
|
T | C | 1 | a0001c0001t0044 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2824A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2824 | chr2 | 8855855 | |||||
chr2:8855961
|
CAGG | C | 1 | a0001c0001t0026 | 2 | HG02257.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2715_*2717delCCT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2715 | chr2 | 8855961 | |||||
chr2:8856033
|
T | A | 2 | a0001c0001t0007a0003c0003t0010 | 8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2646A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2646 | chr2 | 8856033 | |||||
chr2:8856110
|
C | CA | 2 | a0001c0001t0007a0003c0003t0010 | 8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2568dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2568 | chr2 | 8856110 | |||||
chr2:8856193
|
G | A | 16 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(13): Show | 38 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2486C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2486 | chr2 | 8856193 | |||||
chr2:8856196
|
C | T | 31 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(28): Show | 75 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2483G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2483 | chr2 | 8856196 | |||||
chr2:8856247
|
G | T | 6 | a0001c0004t0017a0002c0002t0017a0002c0002t0019others(3): Show | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2432C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2432 | chr2 | 8856247 | |||||
chr2:8856308
|
A | ACAC | 1 | a0001c0001t0022 | 2 | HG02976.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2370_*2371insGTG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2370 | chr2 | 8856308 | |||||
chr2:8856308
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0048 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2370_*2371insGTGT others(7): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2370 | chr2 | 8856308 | |||||
chr2:8856310
|
A | AC | 1 | a0001c0001t0018 | 2 | HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2368_*2369insG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2368 | chr2 | 8856310 | |||||
chr2:8856310
|
A | ACAC | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0021others(2): Show | 10 | HG01070.hp1 HG01071.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2368_*2369insGTG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2368 | chr2 | 8856310 | |||||
chr2:8856310
|
A | ACACAC | 3 | a0001c0001t0003a0001c0001t0034a0004c0005t0033 | 12 | HG00140.hp2 HG01175.hp1 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2368_*2369insGTGT others(1): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2368 | chr2 | 8856310 | |||||
chr2:8856310
|
A | C | 2 | a0001c0001t0022a0001c0001t0048 | 3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2369T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2369 | chr2 | 8856310 | |||||
chr2:8856312
|
A | AAC | 5 | a0001c0001t0008a0001c0001t0015a0001c0001t0026others(2): Show | 11 | HG00609.hp2 HG00735.hp1 HG00735.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2365_*2366dupGT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2366 | chr2 | 8856312 | |||||
chr2:8856312
|
A | AC | 3 | a0001c0001t0009a0001c0001t0030a0001c0001t0040 | 5 | HG00639.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2367insG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2366 | chr2 | 8856312 | |||||
chr2:8856312
|
A | ACAC | 4 | a0001c0001t0004a0001c0001t0023a0001c0001t0029others(1): Show | 12 | HG01884.hp1 HG01891.hp1 HG03041.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2367insGTG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2366 | chr2 | 8856312 | |||||
chr2:8856312
|
A | C | 15 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(12): Show | 33 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2367T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2367 | chr2 | 8856312 | |||||
chr2:8856312
|
AAC | A | 4 | a0001c0001t0005a0001c0001t0011a0001c0001t0012others(1): Show | 14 | HG00738.hp2 HG01934.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2365_*2366delGT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2365 | chr2 | 8856312 | |||||
chr2:8856314
|
C | A | 2 | a0001c0001t0007a0003c0003t0010 | 8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2365G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2365 | chr2 | 8856314 | |||||
chr2:8856316
|
C | A | 4 | a0001c0001t0005a0001c0001t0011a0001c0001t0012others(1): Show | 14 | HG00738.hp2 HG01934.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2363G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2363 | chr2 | 8856316 | |||||
chr2:8856598
|
A | G | 5 | a0001c0001t0002a0001c0001t0020a0001c0001t0027others(2): Show | 32 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2081T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2081 | chr2 | 8856598 | |||||
chr2:8856616
|
A | G | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(23): Show | 60 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2063T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2063 | chr2 | 8856616 | |||||
chr2:8856744
|
G | A | 6 | a0001c0004t0017a0002c0002t0017a0002c0002t0019others(3): Show | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1935C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1935 | chr2 | 8856744 | |||||
chr2:8856748
|
A | T | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(25): Show | 66 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1931T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1931 | chr2 | 8856748 | |||||
chr2:8857175
|
A | G | 2 | a0001c0001t0013a0001c0001t0021 | 5 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1504T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1504 | chr2 | 8857175 | |||||
chr2:8857824
|
G | A | 1 | a0001c0001t0025 | 2 | HG03490.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*855C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 855 | chr2 | 8857824 | |||||
chr2:8857900
|
C | A | 1 | a0001c0001t0018 | 2 | HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*779G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 779 | chr2 | 8857900 | |||||
chr2:8858024
|
A | T | 2 | a0001c0001t0020a0001c0001t0032 | 3 | HG00558.hp1 HG00609.hp2 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 655 | chr2 | 8858024 | |||||
chr2:8858030
|
C | A | 2 | a0001c0001t0011a0001c0001t0012 | 6 | HG00738.hp2 HG02145.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*649G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 649 | chr2 | 8858030 | |||||
chr2:8858287
|
G | C | 1 | a0001c0001t0046 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 392 | chr2 | 8858287 | |||||
chr2:8858480
|
G | A | 1 | a0001c0001t0047 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 199 | chr2 | 8858480 | |||||
chr2:8858494
|
A | G | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | 154 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*185T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 185 | chr2 | 8858494 | |||||
chr2:8858540
|
T | A | 1 | a0002c0002t0019 | 2 | HG02572.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 139 | chr2 | 8858540 | |||||
chr2:8858556
|
T | C | 1 | a0001c0001t0048 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 123 | chr2 | 8858556 | |||||
chr2:8858645
|
CA | C | 14 | a0001c0001t0007a0001c0001t0009a0001c0001t0011others(11): Show | 29 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*33delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 33 | chr2 | 8858645 | |||||
chr2:9003634
|
G | C | 1 | a0001c0001t0027 | 2 | HG01071.hp2 HG03710.hp1 |
5_prime_UTR_variant | MODIFIER | c.-20C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/13 | 20 | chr2 | 9003634 | |||||
chr2:9003671
|
G | C | 2 | a0002c0002t0028a0002c0002t0049 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
5_prime_UTR_variant | MODIFIER | c.-57C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/13 | 57 | chr2 | 9003671 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:8858923
|
A | T | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1338-19T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8858923 | ||||||
chr2:8859912
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1337+701A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8859912 | ||||||
chr2:8860089
|
G | T | 1 | a0001c0001t0002g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1337+524C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860089 | ||||||
chr2:8860147
|
C | T | 1 | a0001c0001t0048g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1337+466G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860147 | ||||||
chr2:8860185
|
C | T | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337+428G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860185 | ||||||
chr2:8860224
|
ATAGCTGG others(64): Show |
A | 1 | a0001c0001t0024g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1337+318_1337+388d others(73): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860224 | ||||||
chr2:8860243
|
A | C | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337+370T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860243 | ||||||
chr2:8860318
|
A | C | 1 | a0001c0001t0004g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1337+295T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860318 | ||||||
chr2:8860407
|
T | C | 1 | a0001c0001t0024g0082 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1337+206A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860407 | ||||||
chr2:8861137
|
T | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-373A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861137 | ||||||
chr2:8861362
|
G | T | 42 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1186-598C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861362 | ||||||
chr2:8861659
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1186-895A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861659 | ||||||
chr2:8861662
|
A | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-898T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861662 | ||||||
chr2:8861749
|
C | T | 2 | a0001c0001t0022g0033a0001c0001t0022g0133 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1185+841G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861749 | ||||||
chr2:8861779
|
A | G | 31 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(28): Show | 31 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1185+811T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861779 | ||||||
chr2:8862015
|
C | T | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185+575G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862015 | ||||||
chr2:8862016
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1185+574C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862016 | ||||||
chr2:8862379
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1185+211G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862379 | ||||||
chr2:8862390
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1185+200G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862390 | ||||||
chr2:8862474
|
G | A | 10 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185+116C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862474 | ||||||
chr2:8862933
|
TTATTGGT others(14): Show |
T | 3 | a0001c0001t0006g0090a0001c0001t0006g0091a0001c0001t0006g0092 | 3 | HG02735.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1053-232_1053-212d others(23): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8862933 | ||||||
chr2:8863084
|
T | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1053-362A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863084 | ||||||
chr2:8863140
|
A | T | 1 | a0001c0001t0040g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1053-418T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863140 | ||||||
chr2:8863184
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1053-462A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863184 | ||||||
chr2:8863186
|
A | C | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1053-464T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863186 | ||||||
chr2:8863250
|
T | C | 1 | a0001c0001t0006g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1053-528A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863250 | ||||||
chr2:8863331
|
A | T | 1 | a0001c0001t0021g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1053-609T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863331 | ||||||
chr2:8863366
|
C | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1053-644G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863366 | ||||||
chr2:8863451
|
G | A | 159 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.1052+719C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863451 | ||||||
chr2:8863510
|
T | C | 9 | a0001c0001t0001g0043a0001c0001t0001g0097a0001c0001t0001g0098others(6): Show | 9 | HG00639.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1052+660A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863510 | ||||||
chr2:8863653
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1052+517A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863653 | ||||||
chr2:8863913
|
G | T | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1052+257C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863913 | ||||||
chr2:8864063
|
A | G | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1052+107T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8864063 | ||||||
chr2:8864140
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1052+30G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8864140 | ||||||
chr2:8864252
|
T | C | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.988-18A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864252 | ||||||
chr2:8864281
|
C | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0114 | 2 | HG01256.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.988-47G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864281 | ||||||
chr2:8864422
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.988-188A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864422 | ||||||
chr2:8864536
|
C | T | 22 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0093others(19): Show | 23 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.988-302G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864536 | ||||||
chr2:8864801
|
T | G | 2 | a0001c0001t0035g0021a0001c0001t0037g0022 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.988-567A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864801 | ||||||
chr2:8864818
|
C | T | 2 | a0001c0001t0027g0156a0001c0001t0027g0157 | 2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.988-584G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864818 | ||||||
chr2:8864902
|
G | T | 1 | a0001c0001t0035g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.988-668C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864902 | ||||||
chr2:8865246
|
G | A | 2 | a0001c0001t0048g0004a0004c0005t0033g0013 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.988-1012C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865246 | ||||||
chr2:8865607
|
A | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-1373T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865607 | ||||||
chr2:8865701
|
T | G | 1 | a0001c0001t0002g0071 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.988-1467A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865701 | ||||||
chr2:8865764
|
C | T | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.988-1530G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865764 | ||||||
chr2:8865894
|
G | A | 19 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(16): Show | 19 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.988-1660C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865894 | ||||||
chr2:8866000
|
G | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.988-1766C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866000 | ||||||
chr2:8866034
|
C | T | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.988-1800G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866034 | ||||||
chr2:8866036
|
C | A | 1 | a0001c0001t0044g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.988-1802G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | ||||||
chr2:8866036
|
C | CAAAT | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1806_988-1803d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | ||||||
chr2:8866036
|
C | CAAATAAA others(1): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0137 | 2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.988-1810_988-1803d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | ||||||
chr2:8866036
|
CAAAT | C | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | HG02735.hp2 HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.988-1806_988-1803d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | ||||||
chr2:8866351
|
T | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+2095A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866351 | ||||||
chr2:8866728
|
T | C | 1 | a0001c0001t0009g0007 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.987+1718A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866728 | ||||||
chr2:8866759
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.987+1687G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866759 | ||||||
chr2:8866761
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.987+1685A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866761 | ||||||
chr2:8866842
|
GA | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1603delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866842 | ||||||
chr2:8866875
|
C | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1571G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866875 | ||||||
chr2:8866908
|
C | T | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.987+1538G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866908 | ||||||
chr2:8866957
|
T | C | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.987+1489A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866957 | ||||||
chr2:8867047
|
A | C | 2 | a0001c0001t0022g0033a0001c0001t0022g0133 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.987+1399T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867047 | ||||||
chr2:8867268
|
T | C | 42 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.987+1178A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867268 | ||||||
chr2:8867274
|
A | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1172T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867274 | ||||||
chr2:8867444
|
T | G | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.987+1002A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867444 | ||||||
chr2:8867539
|
A | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+907T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867539 | ||||||
chr2:8867588
|
G | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.987+858C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867588 | ||||||
chr2:8867807
|
T | C | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.987+639A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867807 | ||||||
chr2:8868081
|
T | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+365A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8868081 | ||||||
chr2:8868278
|
G | C | 2 | a0001c0001t0003g0020a0001c0001t0046g0111 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+168C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8868278 | ||||||
chr2:8868372
|
T | C | 2 | a0001c0001t0027g0156a0001c0001t0027g0157 | 2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.987+74A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8868372 | ||||||
chr2:8868743
|
A | G | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.884-194T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8868743 | ||||||
chr2:8868774
|
A | G | 77 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0093others(74): Show | 78 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.884-225T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8868774 | ||||||
chr2:8869208
|
A | AT | 12 | a0001c0001t0002g0068a0001c0001t0002g0081a0001c0001t0004g0047others(9): Show | 12 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.884-660dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869208 | ||||||
chr2:8869208
|
AT | A | 20 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0001g0130others(17): Show | 20 | HG00735.hp2 HG01934.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.884-660delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869208 | ||||||
chr2:8869210
|
T | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-661A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869210 | ||||||
chr2:8869212
|
T | A | 5 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-663A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869212 | ||||||
chr2:8869304
|
C | G | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-755G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869304 | ||||||
chr2:8869366
|
C | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-817G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869366 | ||||||
chr2:8870429
|
T | C | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.884-1880A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8870429 | ||||||
chr2:8870607
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.884-2058G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8870607 | ||||||
chr2:8871002
|
A | AT | 6 | a0001c0001t0002g0015a0001c0001t0002g0093a0001c0001t0005g0037others(3): Show | 6 | HG01934.hp1 HG02135.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+2105dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8871002 | ||||||
chr2:8871756
|
A | C | 1 | a0001c0001t0029g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.883+1352T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8871756 | ||||||
chr2:8872187
|
C | T | 8 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.883+921G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872187 | ||||||
chr2:8872601
|
G | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.883+507C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872601 | ||||||
chr2:8872824
|
G | A | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.883+284C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872824 | ||||||
chr2:8872885
|
C | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0023 | 2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.883+223G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872885 | ||||||
chr2:8873005
|
T | G | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.883+103A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8873005 | ||||||
chr2:8873475
|
T | G | 2 | a0001c0001t0009g0007a0001c0004t0017g0006 | 2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.691-175A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873475 | ||||||
chr2:8873505
|
A | G | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.691-205T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873505 | ||||||
chr2:8873620
|
T | TA | 42 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.691-321dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873620 | ||||||
chr2:8873761
|
A | G | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.691-461T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873761 | ||||||
chr2:8874056
|
A | T | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.691-756T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874056 | ||||||
chr2:8874206
|
G | A | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-906C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874206 | ||||||
chr2:8874774
|
C | T | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.691-1474G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874774 | ||||||
chr2:8874817
|
T | C | 1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.691-1517A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874817 | ||||||
chr2:8875054
|
T | C | 10 | a0001c0001t0009g0007a0001c0001t0030g0005a0001c0004t0017g0006others(7): Show | 10 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.691-1754A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875054 | ||||||
chr2:8875122
|
C | A | 1 | a0001c0001t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.691-1822G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875122 | ||||||
chr2:8875142
|
G | A | 24 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0093others(21): Show | 25 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.691-1842C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875142 | ||||||
chr2:8875386
|
T | G | 42 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.690+1644A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875386 | ||||||
chr2:8875510
|
T | C | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.690+1520A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875510 | ||||||
chr2:8875555
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.690+1475A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875555 | ||||||
chr2:8875774
|
A | C | 8 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+1256T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875774 | ||||||
chr2:8875903
|
T | C | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.690+1127A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875903 | ||||||
chr2:8875952
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.690+1078T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875952 | ||||||
chr2:8876063
|
A | C | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.690+967T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876063 | ||||||
chr2:8876226
|
C | A | 68 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0093others(65): Show | 69 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.690+804G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876226 | ||||||
chr2:8876904
|
T | C | 98 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0075others(95): Show | 99 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.690+126A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876904 | ||||||
chr2:8876965
|
T | C | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+65A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876965 | ||||||
chr2:8877293
|
C | T | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.507-80G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877293 | ||||||
chr2:8877368
|
T | C | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.507-155A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877368 | ||||||
chr2:8877477
|
G | A | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.507-264C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877477 | ||||||
chr2:8877577
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.507-364G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877577 | ||||||
chr2:8877696
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.507-483C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877696 | ||||||
chr2:8877876
|
T | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.507-663A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877876 | ||||||
chr2:8878125
|
C | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-912G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878125 | ||||||
chr2:8878281
|
T | G | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.507-1068A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878281 | ||||||
chr2:8878350
|
C | T | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.507-1137G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878350 | ||||||
chr2:8878434
|
G | A | 2 | a0001c0001t0021g0024a0001c0001t0021g0025 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.507-1221C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878434 | ||||||
chr2:8878712
|
C | G | 2 | a0001c0001t0027g0156a0001c0001t0027g0157 | 2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.507-1499G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878712 | ||||||
chr2:8879075
|
C | CA | 6 | a0001c0001t0002g0072a0001c0001t0009g0034a0001c0001t0009g0035others(3): Show | 6 | HG03098.hp1 HG03098.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.507-1863dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879075 | ||||||
chr2:8879075
|
CA | C | 11 | a0001c0001t0001g0070a0001c0001t0001g0145a0001c0001t0001g0146others(8): Show | 11 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.507-1863delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879075 | ||||||
chr2:8879382
|
A | C | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.507-2169T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879382 | ||||||
chr2:8879475
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-2262G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879475 | ||||||
chr2:8879741
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.507-2528G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879741 | ||||||
chr2:8880071
|
T | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+2440A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880071 | ||||||
chr2:8880488
|
T | C | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2023A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880488 | ||||||
chr2:8880535
|
C | T | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.506+1976G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880535 | ||||||
chr2:8880536
|
G | A | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.506+1975C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880536 | ||||||
chr2:8880553
|
C | T | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0014g0066others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.506+1958G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880553 | ||||||
chr2:8880584
|
G | A | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.506+1927C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880584 | ||||||
chr2:8880680
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+1831C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880680 | ||||||
chr2:8880696
|
CAG | C | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.506+1813_506+1814d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880696 | ||||||
chr2:8880727
|
A | G | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+1784T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880727 | ||||||
chr2:8880831
|
G | A | 42 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.506+1680C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880831 | ||||||
chr2:8880952
|
C | T | 21 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(18): Show | 21 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.506+1559G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880952 | ||||||
chr2:8881012
|
G | A | 5 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.506+1499C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881012 | ||||||
chr2:8881024
|
G | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.506+1487C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881024 | ||||||
chr2:8881108
|
T | C | 2 | a0001c0001t0027g0156a0001c0001t0027g0157 | 2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.506+1403A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881108 | ||||||
chr2:8881159
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.506+1352G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881159 | ||||||
chr2:8881376
|
G | A | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+1135C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881376 | ||||||
chr2:8881616
|
G | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+895C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881616 | ||||||
chr2:8881971
|
T | G | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.506+540A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881971 | ||||||
chr2:8882764
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.452-199C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8882764 | ||||||
chr2:8883194
|
C | T | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.452-629G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883194 | ||||||
chr2:8883608
|
T | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1043A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883608 | ||||||
chr2:8883660
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.452-1095G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883660 | ||||||
chr2:8883681
|
C | G | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-1116G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883681 | ||||||
chr2:8883761
|
T | G | 2 | a0001c0001t0021g0024a0001c0001t0021g0025 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.452-1196A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883761 | ||||||
chr2:8883880
|
A | G | 2 | a0001c0001t0003g0018a0001c0001t0003g0023 | 2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.452-1315T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883880 | ||||||
chr2:8883993
|
C | T | 14 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-1428G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883993 | ||||||
chr2:8884014
|
G | C | 5 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(2): Show | 5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-1449C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884014 | ||||||
chr2:8884195
|
C | CA | 33 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0001g0139others(30): Show | 33 | HG01070.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.452-1631dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884195 | ||||||
chr2:8884195
|
C | CAA | 14 | a0001c0001t0004g0047a0001c0001t0004g0051a0001c0001t0005g0037others(11): Show | 14 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-1632_452-1631d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884195 | ||||||
chr2:8884367
|
C | G | 5 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(2): Show | 5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-1802G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884367 | ||||||
chr2:8884381
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-1816G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884381 | ||||||
chr2:8884390
|
A | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1825T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884390 | ||||||
chr2:8884485
|
T | TA | 118 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(115): Show | 119 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.452-1921dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884485 | ||||||
chr2:8884485
|
T | TAA | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1922_452-1921d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884485 | ||||||
chr2:8884721
|
C | T | 1 | a0001c0001t0020g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.452-2156G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884721 | ||||||
chr2:8885176
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-2611A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885176 | ||||||
chr2:8885219
|
G | C | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2654C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885219 | ||||||
chr2:8885258
|
G | T | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.452-2693C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885258 | ||||||
chr2:8885730
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451+2288A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885730 | ||||||
chr2:8885855
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.451+2163A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885855 | ||||||
chr2:8886019
|
C | A | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.451+1999G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886019 | ||||||
chr2:8886639
|
T | A | 1 | a0001c0001t0012g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.451+1379A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886639 | ||||||
chr2:8886794
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.451+1224T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886794 | ||||||
chr2:8886933
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.451+1085G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886933 | ||||||
chr2:8887119
|
C | A | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.451+899G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887119 | ||||||
chr2:8887303
|
T | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+715A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887303 | ||||||
chr2:8887336
|
CCT | C | 26 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(23): Show | 26 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+680_451+681del others(2): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887336 | ||||||
chr2:8887355
|
T | A | 26 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(23): Show | 26 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+663A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887355 | ||||||
chr2:8887613
|
A | G | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+405T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887613 | ||||||
chr2:8887622
|
G | T | 26 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(23): Show | 26 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+396C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887622 | ||||||
chr2:8887782
|
T | C | 1 | a0002c0002t0049g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.451+236A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887782 | ||||||
chr2:8888100
|
T | C | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-27A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888100 | ||||||
chr2:8888228
|
A | G | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.396-155T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888228 | ||||||
chr2:8888353
|
C | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.396-280G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888353 | ||||||
chr2:8888454
|
C | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-381G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888454 | ||||||
chr2:8888455
|
T | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-382A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888455 | ||||||
chr2:8888479
|
C | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-406G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888479 | ||||||
chr2:8888568
|
G | C | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-495C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888568 | ||||||
chr2:8888655
|
G | GA | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-583dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888655 | ||||||
chr2:8888807
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.396-734G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888807 | ||||||
chr2:8888992
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.396-919A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888992 | ||||||
chr2:8889092
|
G | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-1019C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889092 | ||||||
chr2:8889215
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.396-1142C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889215 | ||||||
chr2:8889300
|
T | A | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-1227A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889300 | ||||||
chr2:8889307
|
T | C | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.396-1234A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889307 | ||||||
chr2:8889472
|
T | A | 39 | a0001c0001t0001g0043a0001c0001t0001g0077a0001c0001t0001g0097others(36): Show | 39 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.396-1399A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889472 | ||||||
chr2:8889582
|
G | A | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-1509C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889582 | ||||||
chr2:8889692
|
T | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.396-1619A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889692 | ||||||
chr2:8889718
|
C | T | 1 | a0001c0001t0005g0037 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.396-1645G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889718 | ||||||
chr2:8890304
|
A | G | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.396-2231T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890304 | ||||||
chr2:8890306
|
G | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-2233C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890306 | ||||||
chr2:8890458
|
G | A | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.396-2385C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890458 | ||||||
chr2:8890466
|
C | T | 1 | a0001c0001t0039g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.396-2393G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890466 | ||||||
chr2:8890530
|
T | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-2457A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890530 | ||||||
chr2:8890810
|
C | T | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.396-2737G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890810 | ||||||
chr2:8890891
|
G | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-2818C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890891 | ||||||
chr2:8891124
|
T | A | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.396-3051A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891124 | ||||||
chr2:8891554
|
C | G | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-3481G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891554 | ||||||
chr2:8891555
|
A | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-3482T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891555 | ||||||
chr2:8891691
|
C | T | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.396-3618G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891691 | ||||||
chr2:8891816
|
G | A | 1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.396-3743C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891816 | ||||||
chr2:8891853
|
G | C | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.396-3780C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891853 | ||||||
chr2:8891977
|
A | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-3904T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891977 | ||||||
chr2:8892450
|
T | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-4377A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892450 | ||||||
chr2:8892619
|
A | G | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-4546T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892619 | ||||||
chr2:8892854
|
A | G | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-4781T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892854 | ||||||
chr2:8892924
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.396-4851C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892924 | ||||||
chr2:8893052
|
A | AGAGGCAG others(18): Show |
1 | a0001c0001t0002g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.396-5004_396-4980d others(27): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893052 | ||||||
chr2:8893411
|
G | T | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.396-5338C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893411 | ||||||
chr2:8893466
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.396-5393T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893466 | ||||||
chr2:8893588
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.396-5515A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893588 | ||||||
chr2:8893621
|
T | C | 1 | a0001c0001t0008g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.396-5548A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893621 | ||||||
chr2:8893996
|
G | T | 2 | a0001c0001t0005g0040a0001c0001t0045g0038 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.396-5923C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893996 | ||||||
chr2:8894016
|
T | C | 1 | a0001c0001t0006g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.396-5943A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894016 | ||||||
chr2:8894143
|
C | T | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.396-6070G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894143 | ||||||
chr2:8894390
|
A | G | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-6317T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894390 | ||||||
chr2:8894419
|
C | T | 2 | a0001c0001t0035g0021a0001c0001t0037g0022 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.396-6346G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894419 | ||||||
chr2:8894447
|
A | G | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396-6374T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894447 | ||||||
chr2:8894710
|
G | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-6637C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894710 | ||||||
chr2:8894878
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-6805A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894878 | ||||||
chr2:8894899
|
G | A | 2 | a0001c0001t0008g0089a0001c0001t0008g0143 | 2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.396-6826C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894899 | ||||||
chr2:8894991
|
T | C | 25 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(22): Show | 26 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.396-6918A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894991 | ||||||
chr2:8895071
|
G | A | 4 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0073others(1): Show | 4 | HG02083.hp1 NA18953.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-6998C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895071 | ||||||
chr2:8895164
|
T | G | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-7091A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895164 | ||||||
chr2:8895321
|
C | T | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-7248G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895321 | ||||||
chr2:8895429
|
T | C | 1 | a0001c0001t0034g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.396-7356A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895429 | ||||||
chr2:8895460
|
A | G | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-7387T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895460 | ||||||
chr2:8895684
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.396-7611G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895684 | ||||||
chr2:8895713
|
C | T | 9 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(6): Show | 9 | HG01175.hp2 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.396-7640G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895713 | ||||||
chr2:8895780
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.396-7707C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895780 | ||||||
chr2:8895959
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-7886G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895959 | ||||||
chr2:8896003
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0124a0001c0001t0001g0130 | 3 | HG00609.hp1 NA18957.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.396-7930G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896003 | ||||||
chr2:8896099
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0006g0016a0001c0001t0039g0094 | 3 | NA18956.hp1 NA18956.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.396-8026G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896099 | ||||||
chr2:8896234
|
G | A | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.396-8161C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896234 | ||||||
chr2:8896238
|
C | CA | 28 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0072others(25): Show | 29 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.396-8166dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896238 | ||||||
chr2:8896357
|
T | G | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.396-8284A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896357 | ||||||
chr2:8896440
|
C | CAA | 139 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(136): Show | 140 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.396-8368_396-8367i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896440 | ||||||
chr2:8896547
|
G | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-8474C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896547 | ||||||
chr2:8896908
|
C | CCT | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.396-8836_396-8835i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896908 | ||||||
chr2:8896952
|
C | T | 3 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0119 | 3 | HG02083.hp1 NA18953.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.396-8879G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896952 | ||||||
chr2:8896953
|
G | A | 2 | a0001c0001t0013g0014a0001c0001t0013g0032 | 2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.396-8880C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896953 | ||||||
chr2:8897227
|
T | TTC | 63 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(60): Show | 64 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.396-9156_396-9155d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897227 | ||||||
chr2:8897227
|
T | TTCTCTTT others(58): Show |
4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-9155_396-9154i others(67): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897227 | ||||||
chr2:8897260
|
T | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.396-9187A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897260 | ||||||
chr2:8897437
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.396-9364G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897437 | ||||||
chr2:8897589
|
G | A | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396-9516C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897589 | ||||||
chr2:8897638
|
ACTAACTA others(4): Show |
A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-9576_396-9566d others(13): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897638 | ||||||
chr2:8897658
|
C | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-9585G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897658 | ||||||
chr2:8897676
|
C | G | 2 | a0001c0001t0048g0004a0004c0005t0033g0013 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.396-9603G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897676 | ||||||
chr2:8898110
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.396-10037G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8898110 | ||||||
chr2:8898847
|
G | A | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.395+9774C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8898847 | ||||||
chr2:8898990
|
T | C | 1 | a0001c0001t0046g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+9631A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8898990 | ||||||
chr2:8899018
|
G | A | 9 | a0001c0001t0002g0079a0001c0001t0009g0007a0001c0001t0009g0034others(6): Show | 9 | HG00639.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.395+9603C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899018 | ||||||
chr2:8899264
|
C | T | 1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.395+9357G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899264 | ||||||
chr2:8899308
|
G | A | 3 | a0001c0001t0006g0090a0001c0001t0006g0091a0001c0001t0006g0092 | 3 | HG02735.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.395+9313C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899308 | ||||||
chr2:8899332
|
C | T | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+9289G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899332 | ||||||
chr2:8899341
|
A | T | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.395+9280T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899341 | ||||||
chr2:8899414
|
CA | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.395+9206delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899414 | ||||||
chr2:8899714
|
T | C | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.395+8907A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899714 | ||||||
chr2:8899813
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.395+8808A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899813 | ||||||
chr2:8899859
|
T | C | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.395+8762A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899859 | ||||||
chr2:8899961
|
G | A | 1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.395+8660C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899961 | ||||||
chr2:8900035
|
G | GC | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.395+8585dupG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900035 | ||||||
chr2:8900054
|
G | T | 1 | a0001c0001t0005g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.395+8567C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900054 | ||||||
chr2:8900171
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.395+8450C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900171 | ||||||
chr2:8900199
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.395+8422C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900199 | ||||||
chr2:8900243
|
G | A | 5 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(2): Show | 5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+8378C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900243 | ||||||
chr2:8900459
|
C | T | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+8162G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900459 | ||||||
chr2:8901154
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.395+7467A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901154 | ||||||
chr2:8901508
|
AAAG | A | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.395+7110_395+7112d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901508 | ||||||
chr2:8901821
|
G | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0114 | 2 | HG01256.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.395+6800C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901821 | ||||||
chr2:8901930
|
G | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.395+6691C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901930 | ||||||
chr2:8901996
|
G | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+6625C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901996 | ||||||
chr2:8902037
|
G | A | 1 | a0001c0001t0038g0017 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.395+6584C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902037 | ||||||
chr2:8902332
|
C | T | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.395+6289G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902332 | ||||||
chr2:8902469
|
G | A | 1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.395+6152C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902469 | ||||||
chr2:8902570
|
G | A | 1 | a0001c0001t0006g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.395+6051C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902570 | ||||||
chr2:8902581
|
A | G | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.395+6040T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902581 | ||||||
chr2:8902780
|
G | A | 1 | a0001c0001t0030g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.395+5841C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902780 | ||||||
chr2:8902873
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.395+5748A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902873 | ||||||
chr2:8903214
|
C | T | 1 | a0002c0002t0049g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.395+5407G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8903214 | ||||||
chr2:8903476
|
A | AT | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+5144dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8903476 | ||||||
chr2:8903476
|
AT | A | 23 | a0001c0001t0001g0120a0001c0001t0002g0030a0001c0001t0003g0001others(20): Show | 24 | HG01175.hp1 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.395+5144delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8903476 | ||||||
chr2:8904018
|
C | A | 2 | a0001c0001t0005g0037a0001c0001t0005g0039 | 2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.395+4603G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904018 | ||||||
chr2:8904071
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+4550C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904071 | ||||||
chr2:8904313
|
T | A | 11 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(8): Show | 11 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.395+4308A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904313 | ||||||
chr2:8904316
|
A | T | 16 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(13): Show | 16 | HG00738.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.395+4305T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904316 | ||||||
chr2:8904316
|
AT | A | 66 | a0001c0001t0001g0098a0001c0001t0002g0030a0001c0001t0002g0106others(63): Show | 67 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.395+4304delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904316 | ||||||
chr2:8904317
|
T | A | 7 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+4304A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904317 | ||||||
chr2:8904415
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.395+4206C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904415 | ||||||
chr2:8904997
|
T | TAC | 2 | a0001c0001t0004g0051a0001c0001t0043g0103 | 2 | HG00140.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.395+3622_395+3623d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904997 | ||||||
chr2:8905010
|
A | G | 8 | a0001c0001t0027g0157a0002c0002t0017g0064a0002c0002t0019g0011others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+3611T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905010 | ||||||
chr2:8905012
|
G | A | 2 | a0001c0001t0018g0009a0001c0001t0018g0010 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.395+3609C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905012 | ||||||
chr2:8905014
|
G | A | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.395+3607C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905014 | ||||||
chr2:8905222
|
G | A | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+3399C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905222 | ||||||
chr2:8905750
|
C | T | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+2871G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905750 | ||||||
chr2:8905776
|
CACATGTA others(7): Show |
C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+2831_395+2844d others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905776 | ||||||
chr2:8906033
|
C | G | 1 | a0001c0001t0004g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.395+2588G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906033 | ||||||
chr2:8906039
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.395+2582G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906039 | ||||||
chr2:8906100
|
AGG | A | 26 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(23): Show | 27 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+2519_395+2520d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906100 | ||||||
chr2:8906108
|
G | A | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.395+2513C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906108 | ||||||
chr2:8906229
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395+2392T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906229 | ||||||
chr2:8906279
|
C | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.395+2342G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906279 | ||||||
chr2:8907056
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+1565A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907056 | ||||||
chr2:8907194
|
C | T | 1 | a0001c0001t0011g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.395+1427G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907194 | ||||||
chr2:8907308
|
C | T | 1 | a0003c0003t0010g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.395+1313G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907308 | ||||||
chr2:8907907
|
A | G | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.395+714T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907907 | ||||||
chr2:8908375
|
C | G | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.395+246G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8908375 | ||||||
chr2:8908434
|
T | G | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.395+187A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8908434 | ||||||
chr2:8909232
|
C | T | 2 | a0001c0001t0021g0024a0001c0001t0021g0025 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.300-516G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909232 | ||||||
chr2:8909266
|
A | G | 6 | a0001c0001t0009g0007a0001c0001t0018g0009a0001c0001t0018g0010others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-550T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909266 | ||||||
chr2:8909485
|
T | G | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-769A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909485 | ||||||
chr2:8909597
|
C | A | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.300-881G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909597 | ||||||
chr2:8910170
|
CAGAG | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-1458_300-1455d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8910170 | ||||||
chr2:8910314
|
A | G | 34 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(31): Show | 34 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.300-1598T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8910314 | ||||||
chr2:8910667
|
T | A | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-1951A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8910667 | ||||||
chr2:8911082
|
C | T | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300-2366G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911082 | ||||||
chr2:8911218
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-2502A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911218 | ||||||
chr2:8911274
|
T | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.300-2558A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911274 | ||||||
chr2:8911658
|
T | G | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-2942A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911658 | ||||||
chr2:8911659
|
G | T | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-2943C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911659 | ||||||
chr2:8911831
|
C | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-3115G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911831 | ||||||
chr2:8911975
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0044g0112 | 2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.300-3259T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911975 | ||||||
chr2:8912298
|
GA | G | 14 | a0001c0001t0002g0015a0001c0001t0004g0047a0001c0001t0004g0050others(11): Show | 14 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.300-3583delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912298 | ||||||
chr2:8912299
|
A | AAAAG | 13 | a0001c0001t0001g0116a0001c0001t0002g0030a0001c0001t0002g0071others(10): Show | 13 | HG01167.hp1 HG01256.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3587_300-3584d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
A | AAAAGAAA others(1): Show |
11 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0124others(8): Show | 11 | HG00609.hp1 HG02135.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.300-3591_300-3584d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
A | AAAAGAAA others(5): Show |
2 | a0001c0001t0002g0101a0001c0001t0042g0127 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.300-3595_300-3584d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
A | AAAAGAAA others(13): Show |
2 | a0001c0001t0001g0070a0001c0001t0001g0099 | 2 | HG03209.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.300-3603_300-3584d others(22): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
A | AAAAGAAA others(8): Show |
1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.300-3584_300-3583i others(17): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
A | AAAG | 19 | a0001c0001t0001g0137a0001c0001t0004g0055a0001c0001t0004g0058others(16): Show | 19 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.300-3584_300-3583i others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
AAAAG | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0115a0001c0001t0002g0105others(1): Show | 4 | HG02717.hp1 HG02735.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-3587_300-3584d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912299
|
AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0038g0017 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.300-3595_300-3584d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | ||||||
chr2:8912301
|
A | AGAAAGAA others(38): Show |
1 | a0001c0001t0011g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.300-3586_300-3585i others(47): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912301 | ||||||
chr2:8912303
|
G | A | 1 | a0001c0001t0011g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.300-3587C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912303 | ||||||
chr2:8912328
|
A | G | 1 | a0001c0001t0020g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.300-3612T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912328 | ||||||
chr2:8912329
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.300-3623_300-3614d others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912329 | ||||||
chr2:8912333
|
A | AAGAAAGA others(29): Show |
1 | a0001c0001t0005g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.300-3618_300-3617i others(38): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912333 | ||||||
chr2:8912337
|
AAGAAAGA others(7): Show |
A | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.300-3635_300-3622d others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912337 | ||||||
chr2:8912343
|
GAA | G | 2 | a0001c0001t0001g0120a0001c0001t0006g0016 | 2 | HG03704.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.300-3629_300-3628d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912343 | ||||||
chr2:8912345
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.300-3629T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912345 | ||||||
chr2:8912345
|
AAGAAAGA others(21): Show |
A | 1 | a0001c0001t0003g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.300-3657_300-3630d others(30): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912345 | ||||||
chr2:8912347
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.300-3631C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912347 | ||||||
chr2:8912348
|
A | AAAGAAAG others(3): Show |
1 | a0001c0001t0003g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.300-3633_300-3632i others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912348 | ||||||
chr2:8912349
|
A | G | 10 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0128others(7): Show | 10 | HG00639.hp1 HG00738.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.300-3633T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912349 | ||||||
chr2:8912349
|
AAG | A | 13 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0146others(10): Show | 13 | HG00609.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.300-3635_300-3634d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912349 | ||||||
chr2:8912351
|
G | A | 13 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0128others(10): Show | 13 | HG00639.hp1 HG00738.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3635C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAA | 17 | a0001c0001t0001g0110a0001c0001t0002g0081a0001c0001t0002g0104others(14): Show | 17 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.300-3636_300-3635i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAA | 7 | a0001c0001t0001g0075a0001c0001t0002g0102a0001c0001t0002g0114others(4): Show | 7 | HG00140.hp1 HG00642.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-3636_300-3635i others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAAA others(3): Show |
3 | a0001c0001t0002g0065a0001c0001t0002g0109a0001c0001t0035g0021 | 3 | HG00738.hp1 HG03471.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.300-3636_300-3635i others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAAA others(77): Show |
1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(86): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAAA others(7): Show |
2 | a0001c0001t0002g0144a0001c0001t0027g0156 | 2 | HG01071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.300-3636_300-3635i others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAAA others(12): Show |
1 | a0001c0001t0024g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(21): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAAA others(13): Show |
1 | a0001c0001t0025g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(22): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAAA others(31): Show |
1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(40): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912351
|
G | GAAAGAGA others(5): Show |
1 | a0001c0001t0008g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300-3636_300-3635i others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | ||||||
chr2:8912353
|
G | A | 24 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0141others(21): Show | 25 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.300-3637C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912353 | ||||||
chr2:8912355
|
A | AAG | 18 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0002g0081others(15): Show | 18 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.300-3641_300-3640d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912355 | ||||||
chr2:8912355
|
A | G | 23 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0140others(20): Show | 24 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.300-3639T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912355 | ||||||
chr2:8912357
|
G | A | 2 | a0001c0001t0044g0112a0003c0003t0010g0153 | 2 | HG03486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.300-3641C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912357 | ||||||
chr2:8912359
|
A | AAG | 6 | a0001c0001t0002g0065a0001c0001t0004g0047a0001c0001t0034g0095others(3): Show | 6 | HG00140.hp2 HG00738.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3645_300-3644d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912359 | ||||||
chr2:8912359
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.300-3653_300-3644d others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912359 | ||||||
chr2:8912359
|
A | G | 2 | a0001c0001t0044g0112a0003c0003t0010g0153 | 2 | HG03486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.300-3643T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912359 | ||||||
chr2:8912361
|
GAA | G | 3 | a0001c0001t0021g0025a0001c0001t0029g0008a0001c0004t0017g0006 | 3 | HG01884.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.300-3647_300-3646d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912361 | ||||||
chr2:8912363
|
A | AAG | 3 | a0001c0001t0004g0050a0001c0001t0007g0149a0001c0001t0009g0007 | 3 | HG00639.hp2 HG01070.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.300-3649_300-3648d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912363 | ||||||
chr2:8912367
|
A | AAG | 3 | a0001c0001t0001g0087a0001c0001t0003g0029a0001c0001t0013g0031 | 3 | HG02486.hp1 HG03453.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.300-3653_300-3652d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912367 | ||||||
chr2:8912367
|
A | G | 4 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0018g0009others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-3651T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912367 | ||||||
chr2:8912369
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0018g0009others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-3653C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912369 | ||||||
chr2:8912369
|
GAAAGAGA others(9): Show |
G | 1 | a0001c0001t0009g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.300-3669_300-3654d others(18): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912369 | ||||||
chr2:8912371
|
A | G | 13 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0146others(10): Show | 13 | HG00609.hp2 HG02080.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3655T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912371 | ||||||
chr2:8912371
|
AAG | A | 6 | a0001c0001t0002g0072a0001c0001t0007g0150a0001c0001t0007g0152others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3657_300-3656d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912371 | ||||||
chr2:8912373
|
G | A | 13 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0146others(10): Show | 13 | HG00609.hp2 HG02080.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3657C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAA | 12 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0128others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3658_300-3657i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(7): Show |
1 | a0001c0001t0006g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(63): Show |
1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(72): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(59): Show |
1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(68): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(71): Show |
1 | a0001c0001t0004g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.300-3658_300-3657i others(80): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(39): Show |
1 | a0001c0001t0011g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(48): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(51): Show |
2 | a0001c0001t0004g0057a0001c0001t0014g0056 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300-3658_300-3657i others(60): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(43): Show |
1 | a0001c0001t0012g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(52): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(39): Show |
1 | a0001c0001t0012g0052 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(48): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAA others(39): Show |
1 | a0001c0001t0004g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.300-3658_300-3657i others(48): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAAAGAAG others(38): Show |
1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(47): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAGAA | 14 | a0001c0001t0001g0097a0001c0001t0001g0116a0001c0001t0002g0101others(11): Show | 14 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.300-3661_300-3658d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAGAAAGA others(1): Show |
9 | a0001c0001t0001g0070a0001c0001t0001g0098a0001c0001t0001g0147others(6): Show | 9 | HG00735.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3665_300-3658d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
G | GAGAAAGA others(5): Show |
1 | a0001c0001t0008g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300-3669_300-3658d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
GAGAA | G | 6 | a0001c0001t0002g0105a0001c0001t0003g0020a0001c0001t0003g0028others(3): Show | 6 | HG02280.hp2 HG02735.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3661_300-3658d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
GAGAAAGA others(1): Show |
G | 11 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.300-3665_300-3658d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0009g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.300-3669_300-3658d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912373
|
GAGAAAGA others(9): Show |
G | 1 | a0001c0001t0020g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.300-3673_300-3658d others(18): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | ||||||
chr2:8912375
|
G | A | 43 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(40): Show | 44 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.300-3659C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912375 | ||||||
chr2:8912376
|
A | AG | 2 | a0001c0001t0002g0073a0001c0001t0043g0103 | 2 | HG00140.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.300-3661_300-3660i others(3): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912376 | ||||||
chr2:8912377
|
A | AAGAAAGA others(33): Show |
7 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0041others(4): Show | 7 | HG01934.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-3662_300-3661i others(42): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912377 | ||||||
chr2:8912377
|
A | G | 41 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(38): Show | 42 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.300-3661T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912377 | ||||||
chr2:8912379
|
G | A | 6 | a0001c0001t0004g0047a0001c0001t0009g0007a0001c0001t0044g0112others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3663C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912379 | ||||||
chr2:8912379
|
GAA | G | 3 | a0001c0001t0002g0072a0001c0001t0007g0150a0001c0001t0007g0152 | 3 | HG02559.hp2 HG03139.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.300-3665_300-3664d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912379 | ||||||
chr2:8912380
|
A | AAAGAAAG others(6): Show |
1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.300-3665_300-3664i others(15): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912380 | ||||||
chr2:8912381
|
A | AAG | 2 | a0001c0001t0004g0050a0001c0001t0007g0149 | 2 | HG01070.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.300-3667_300-3666d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912381 | ||||||
chr2:8912381
|
A | AAGAAAGA others(7): Show |
1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.300-3679_300-3666d others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912381 | ||||||
chr2:8912381
|
A | G | 6 | a0001c0001t0004g0047a0001c0001t0009g0007a0001c0001t0044g0112others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3665T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912381 | ||||||
chr2:8912383
|
GAA | G | 5 | a0001c0001t0003g0018a0001c0001t0018g0009a0001c0001t0018g0010others(2): Show | 5 | HG01175.hp1 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-3669_300-3668d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912383 | ||||||
chr2:8912413
|
A | C | 2 | a0001c0001t0048g0004a0004c0005t0033g0013 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.300-3697T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912413 | ||||||
chr2:8912416
|
A | G | 21 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(18): Show | 21 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.300-3700T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912416 | ||||||
chr2:8912417
|
C | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3701G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912417 | ||||||
chr2:8912420
|
G | A | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3704C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912420 | ||||||
chr2:8912421
|
C | A | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3705G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912421 | ||||||
chr2:8912422
|
C | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3706G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912422 | ||||||
chr2:8912559
|
C | T | 1 | a0002c0002t0049g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.300-3843G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912559 | ||||||
chr2:8912650
|
C | T | 1 | a0001c0001t0027g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.300-3934G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912650 | ||||||
chr2:8912651
|
G | A | 8 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-3935C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912651 | ||||||
chr2:8912672
|
C | T | 8 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(5): Show | 8 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-3956G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912672 | ||||||
chr2:8912676
|
G | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3960C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912676 | ||||||
chr2:8912874
|
C | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-4158G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912874 | ||||||
chr2:8912975
|
G | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.300-4259C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912975 | ||||||
chr2:8913101
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.300-4385G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913101 | ||||||
chr2:8913169
|
T | G | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.300-4453A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913169 | ||||||
chr2:8913403
|
A | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-4687T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913403 | ||||||
chr2:8913475
|
A | C | 2 | a0001c0001t0008g0089a0001c0001t0008g0143 | 2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.300-4759T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913475 | ||||||
chr2:8913526
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300-4810A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913526 | ||||||
chr2:8913585
|
C | A | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-4869G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913585 | ||||||
chr2:8913675
|
A | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-4959T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913675 | ||||||
chr2:8913835
|
G | GA | 20 | a0001c0001t0001g0043a0001c0001t0001g0097a0001c0001t0001g0098others(17): Show | 20 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.300-5120dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913835 | ||||||
chr2:8914096
|
C | T | 2 | a0001c0001t0008g0089a0001c0001t0008g0143 | 2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.300-5380G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914096 | ||||||
chr2:8914169
|
G | C | 24 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(21): Show | 25 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.300-5453C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914169 | ||||||
chr2:8914415
|
C | T | 1 | a0001c0001t0042g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.300-5699G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914415 | ||||||
chr2:8914489
|
GA | G | 21 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(18): Show | 21 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.300-5774delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914489 | ||||||
chr2:8914934
|
C | CT | 43 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0115others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.300-6219dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914934 | ||||||
chr2:8914934
|
C | CTT | 10 | a0001c0001t0004g0057a0001c0001t0004g0058a0001c0001t0008g0126others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.300-6220_300-6219d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914934 | ||||||
chr2:8914934
|
CT | C | 32 | a0001c0001t0002g0030a0001c0001t0002g0093a0001c0001t0002g0132others(29): Show | 33 | HG00621.hp2 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-6219delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914934 | ||||||
chr2:8914939
|
T | C | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.300-6223A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914939 | ||||||
chr2:8914999
|
C | T | 44 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(41): Show | 45 | HG00621.hp2 HG00639.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.300-6283G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914999 | ||||||
chr2:8915007
|
C | T | 1 | a0002c0002t0049g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.300-6291G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915007 | ||||||
chr2:8915228
|
C | T | 1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.300-6512G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915228 | ||||||
chr2:8915289
|
T | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-6573A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915289 | ||||||
chr2:8915370
|
A | T | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.300-6654T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915370 | ||||||
chr2:8915622
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.300-6906C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915622 | ||||||
chr2:8916025
|
T | C | 1 | a0001c0001t0007g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.300-7309A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916025 | ||||||
chr2:8916112
|
T | C | 3 | a0001c0001t0018g0009a0001c0001t0018g0010a0001c0001t0029g0008 | 3 | HG01884.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.300-7396A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916112 | ||||||
chr2:8916117
|
T | G | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.300-7401A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916117 | ||||||
chr2:8916401
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0124 | 2 | HG00609.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.300-7685A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916401 | ||||||
chr2:8916639
|
G | C | 2 | a0002c0002t0028g0159a0002c0002t0028g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.300-7923C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916639 | ||||||
chr2:8916664
|
T | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-7948A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916664 | ||||||
chr2:8916679
|
T | C | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-7963A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916679 | ||||||
chr2:8916944
|
G | C | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.300-8228C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916944 | ||||||
chr2:8917999
|
A | G | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.300-9283T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8917999 | ||||||
chr2:8918169
|
A | C | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-9453T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918169 | ||||||
chr2:8918400
|
T | C | 1 | a0001c0001t0003g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.300-9684A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918400 | ||||||
chr2:8918570
|
G | A | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.300-9854C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918570 | ||||||
chr2:8918585
|
C | A | 1 | a0001c0001t0008g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300-9869G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918585 | ||||||
chr2:8918741
|
C | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-10025G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918741 | ||||||
chr2:8919002
|
A | G | 1 | a0001c0001t0007g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.300-10286T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919002 | ||||||
chr2:8919103
|
C | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-10387G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919103 | ||||||
chr2:8919643
|
C | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.300-10927G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919643 | ||||||
chr2:8919756
|
C | T | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11040G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919756 | ||||||
chr2:8920035
|
G | A | 9 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(6): Show | 9 | HG01175.hp2 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-11319C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920035 | ||||||
chr2:8920060
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11344A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920060 | ||||||
chr2:8920089
|
A | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11373T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920089 | ||||||
chr2:8920186
|
T | C | 1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.300-11470A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920186 | ||||||
chr2:8920481
|
A | T | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11765T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920481 | ||||||
chr2:8920560
|
C | CA | 41 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(38): Show | 41 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.300-11845dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920560 | ||||||
chr2:8920686
|
ATCT | A | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-11973_300-1197 others(7): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920686 | ||||||
chr2:8921179
|
T | TA | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300-12464dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921179 | ||||||
chr2:8921196
|
G | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.300-12480C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921196 | ||||||
chr2:8921489
|
A | G | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-12773T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921489 | ||||||
chr2:8921888
|
T | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-13172A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921888 | ||||||
chr2:8922257
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-13541A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922257 | ||||||
chr2:8922330
|
T | C | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-13614A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922330 | ||||||
chr2:8922497
|
T | G | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.300-13781A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922497 | ||||||
chr2:8922505
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-13789A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922505 | ||||||
chr2:8922548
|
T | A | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.300-13832A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922548 | ||||||
chr2:8922549
|
C | T | 1 | a0001c0001t0025g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.300-13833G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922549 | ||||||
chr2:8922668
|
G | C | 8 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-13952C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922668 | ||||||
chr2:8922785
|
T | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.300-14069A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922785 | ||||||
chr2:8922812
|
C | T | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-14096G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922812 | ||||||
chr2:8923001
|
G | A | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.300-14285C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923001 | ||||||
chr2:8923046
|
G | T | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.300-14330C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923046 | ||||||
chr2:8923105
|
A | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-14389T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923105 | ||||||
chr2:8923194
|
C | A | 1 | a0001c0001t0039g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.300-14478G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923194 | ||||||
chr2:8923367
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-14651A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923367 | ||||||
chr2:8923391
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.300-14675C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923391 | ||||||
chr2:8923499
|
G | T | 1 | a0001c0001t0008g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300-14783C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923499 | ||||||
chr2:8923590
|
C | G | 1 | a0001c0001t0008g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300-14874G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923590 | ||||||
chr2:8923634
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0116 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.300-14918C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923634 | ||||||
chr2:8923798
|
T | C | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-15082A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923798 | ||||||
chr2:8923981
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300-15265A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923981 | ||||||
chr2:8924030
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300-15314C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924030 | ||||||
chr2:8924061
|
A | G | 34 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(31): Show | 34 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.300-15345T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924061 | ||||||
chr2:8924109
|
CT | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-15394delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924109 | ||||||
chr2:8924159
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.300-15443G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924159 | ||||||
chr2:8924514
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.300-15798A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924514 | ||||||
chr2:8924515
|
C | T | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-15799G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924515 | ||||||
chr2:8924591
|
T | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-15875A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924591 | ||||||
chr2:8924706
|
CT | C | 42 | a0001c0001t0001g0075a0001c0001t0004g0047a0001c0001t0004g0050others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.300-15991delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924706 | ||||||
chr2:8924748
|
A | C | 34 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(31): Show | 34 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.300-16032T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924748 | ||||||
chr2:8924753
|
C | T | 2 | a0001c0001t0027g0156a0001c0001t0027g0157 | 2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.300-16037G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924753 | ||||||
chr2:8924922
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.300-16206G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924922 | ||||||
chr2:8925509
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0008g0126 | 2 | HG00735.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.300-16793C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8925509 | ||||||
chr2:8925726
|
T | C | 8 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-17010A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8925726 | ||||||
chr2:8925765
|
C | T | 1 | a0001c0001t0043g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.300-17049G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8925765 | ||||||
chr2:8926107
|
CTTTG | C | 2 | a0001c0001t0022g0033a0002c0002t0031g0036 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299+17076_299+1707 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926107 | ||||||
chr2:8926227
|
C | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+16960G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926227 | ||||||
chr2:8926229
|
A | G | 2 | a0001c0001t0009g0007a0001c0004t0017g0006 | 2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.299+16958T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926229 | ||||||
chr2:8926922
|
C | T | 8 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.299+16265G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926922 | ||||||
chr2:8926971
|
T | C | 21 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0075others(18): Show | 21 | HG00609.hp1 HG00735.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.299+16216A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926971 | ||||||
chr2:8927034
|
G | A | 1 | a0001c0001t0014g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299+16153C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927034 | ||||||
chr2:8927161
|
G | A | 1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.299+16026C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927161 | ||||||
chr2:8927307
|
G | A | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+15880C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927307 | ||||||
chr2:8927524
|
T | C | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299+15663A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927524 | ||||||
chr2:8927579
|
C | T | 1 | a0001c0001t0041g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.299+15608G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927579 | ||||||
chr2:8927637
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+15550C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927637 | ||||||
chr2:8927904
|
T | C | 1 | a0001c0001t0006g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.299+15283A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927904 | ||||||
chr2:8928462
|
A | G | 1 | a0001c0001t0004g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299+14725T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8928462 | ||||||
chr2:8928564
|
A | G | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+14623T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8928564 | ||||||
chr2:8928587
|
C | T | 2 | a0001c0001t0023g0048a0001c0001t0023g0049 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.299+14600G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8928587 | ||||||
chr2:8929131
|
C | A | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.299+14056G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929131 | ||||||
chr2:8929245
|
T | C | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299+13942A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929245 | ||||||
chr2:8929279
|
G | A | 1 | a0001c0001t0048g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299+13908C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929279 | ||||||
chr2:8929281
|
G | T | 14 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(11): Show | 14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.299+13906C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929281 | ||||||
chr2:8929330
|
G | GTTCA | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0002g0079others(3): Show | 6 | HG00642.hp2 HG01169.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+13853_299+1385 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929330 | ||||||
chr2:8929330
|
GTTCA | G | 29 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0002g0030others(26): Show | 29 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.299+13853_299+1385 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929330 | ||||||
chr2:8929330
|
GTTCATTC others(1): Show |
G | 8 | a0001c0001t0030g0005a0002c0002t0017g0064a0002c0002t0019g0011others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.299+13849_299+1385 others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929330 | ||||||
chr2:8929358
|
A | ATTCG | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+13828_299+1382 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929358 | ||||||
chr2:8929358
|
A | G | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+13829T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929358 | ||||||
chr2:8929436
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.299+13751G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929436 | ||||||
chr2:8929478
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299+13709T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929478 | ||||||
chr2:8929502
|
C | T | 1 | a0003c0003t0010g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.299+13685G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929502 | ||||||
chr2:8929580
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299+13607A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929580 | ||||||
chr2:8929581
|
G | C | 9 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(6): Show | 9 | HG01175.hp2 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299+13606C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929581 | ||||||
chr2:8929739
|
T | C | 42 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(39): Show | 42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.299+13448A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929739 | ||||||
chr2:8929942
|
A | G | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.299+13245T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929942 | ||||||
chr2:8930414
|
C | CT | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.299+12772dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930414 | ||||||
chr2:8930853
|
T | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+12334A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930853 | ||||||
chr2:8930859
|
T | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+12328A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930859 | ||||||
chr2:8930970
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299+12217C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930970 | ||||||
chr2:8931085
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.299+12102G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931085 | ||||||
chr2:8931102
|
C | T | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+12085G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931102 | ||||||
chr2:8931113
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.299+12074G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931113 | ||||||
chr2:8931132
|
A | G | 1 | a0001c0001t0025g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.299+12055T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931132 | ||||||
chr2:8931298
|
A | C | 78 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0101others(75): Show | 79 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.299+11889T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931298 | ||||||
chr2:8932128
|
T | TA | 9 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 9 | HG01109.hp1 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299+11058dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932128 | ||||||
chr2:8932551
|
C | A | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.299+10636G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932551 | ||||||
chr2:8932666
|
G | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.299+10521C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932666 | ||||||
chr2:8932885
|
A | G | 2 | a0001c0001t0035g0021a0001c0001t0037g0022 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299+10302T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932885 | ||||||
chr2:8933089
|
AT | A | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299+10097delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933089 | ||||||
chr2:8933116
|
T | C | 5 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(2): Show | 5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.299+10071A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933116 | ||||||
chr2:8933373
|
G | C | 2 | a0001c0001t0011g0061a0001c0001t0011g0063 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.299+9814C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933373 | ||||||
chr2:8933609
|
T | G | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299+9578A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933609 | ||||||
chr2:8933645
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0024g0082 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299+9542A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933645 | ||||||
chr2:8933866
|
C | T | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.299+9321G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933866 | ||||||
chr2:8933950
|
A | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.299+9237T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933950 | ||||||
chr2:8934095
|
C | T | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299+9092G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934095 | ||||||
chr2:8934218
|
A | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+8969T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934218 | ||||||
chr2:8934464
|
A | G | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+8723T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934464 | ||||||
chr2:8934975
|
T | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+8212A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934975 | ||||||
chr2:8934989
|
G | A | 1 | a0001c0001t0027g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299+8198C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934989 | ||||||
chr2:8935183
|
G | A | 2 | a0001c0001t0008g0089a0001c0001t0008g0143 | 2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.299+8004C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8935183 | ||||||
chr2:8935297
|
TAA | T | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+7888_299+7889d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8935297 | ||||||
chr2:8935906
|
TATC | T | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.299+7278_299+7280d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8935906 | ||||||
chr2:8936289
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299+6898G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936289 | ||||||
chr2:8936471
|
C | T | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299+6716G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936471 | ||||||
chr2:8936602
|
T | C | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+6585A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936602 | ||||||
chr2:8936664
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.299+6523G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936664 | ||||||
chr2:8936711
|
C | T | 2 | a0001c0001t0018g0009a0001c0001t0018g0010 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.299+6476G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936711 | ||||||
chr2:8936735
|
C | G | 1 | a0001c0001t0036g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299+6452G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936735 | ||||||
chr2:8936786
|
C | CA | 11 | a0001c0001t0002g0069a0001c0001t0008g0096a0001c0001t0013g0014others(8): Show | 11 | HG02027.hp1 HG02135.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+6400dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936786 | ||||||
chr2:8936801
|
A | AG | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.299+6385_299+6386i others(3): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936801 | ||||||
chr2:8936822
|
GAAAA | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+6361_299+6364d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936822 | ||||||
chr2:8936828
|
A | AAAAG | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+6355_299+6358d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936828 | ||||||
chr2:8936828
|
AAAAG | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.299+6355_299+6358d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936828 | ||||||
chr2:8937104
|
G | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+6083C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937104 | ||||||
chr2:8937815
|
C | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.299+5372G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937815 | ||||||
chr2:8937922
|
G | A | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.299+5265C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937922 | ||||||
chr2:8937934
|
G | A | 1 | a0003c0003t0010g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299+5253C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937934 | ||||||
chr2:8938015
|
T | C | 7 | a0001c0001t0009g0007a0001c0001t0018g0009a0001c0001t0018g0010others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.299+5172A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938015 | ||||||
chr2:8938080
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+5107C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938080 | ||||||
chr2:8938548
|
G | A | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+4639C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938548 | ||||||
chr2:8938673
|
G | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.299+4514C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938673 | ||||||
chr2:8938927
|
C | T | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+4260G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938927 | ||||||
chr2:8939174
|
T | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+4013A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939174 | ||||||
chr2:8939194
|
T | C | 1 | a0001c0001t0008g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299+3993A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939194 | ||||||
chr2:8939396
|
T | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+3791A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939396 | ||||||
chr2:8939447
|
G | C | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.299+3740C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939447 | ||||||
chr2:8939548
|
G | A | 65 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(62): Show | 66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.299+3639C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939548 | ||||||
chr2:8939682
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299+3505C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939682 | ||||||
chr2:8939773
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0116 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.299+3414G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939773 | ||||||
chr2:8939781
|
A | G | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+3406T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939781 | ||||||
chr2:8940078
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.299+3109C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940078 | ||||||
chr2:8940078
|
G | GCTTA | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299+3105_299+3108d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940078 | ||||||
chr2:8940138
|
C | T | 1 | a0001c0001t0034g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299+3049G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940138 | ||||||
chr2:8940229
|
T | C | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299+2958A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940229 | ||||||
chr2:8940683
|
CAT | C | 25 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(22): Show | 26 | HG00621.hp2 HG00639.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.299+2502_299+2503d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940683 | ||||||
chr2:8940761
|
C | T | 8 | a0001c0001t0001g0146a0002c0002t0017g0064a0002c0002t0019g0011others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.299+2426G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940761 | ||||||
chr2:8940898
|
CGT | C | 2 | a0001c0001t0005g0040a0001c0001t0045g0038 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.299+2287_299+2288d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940898 | ||||||
chr2:8940899
|
G | A | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+2288C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940899 | ||||||
chr2:8941119
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0029 | 2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.299+2068A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941119 | ||||||
chr2:8941242
|
C | T | 1 | a0001c0001t0045g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299+1945G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941242 | ||||||
chr2:8941416
|
T | C | 1 | a0001c0001t0013g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.299+1771A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941416 | ||||||
chr2:8941493
|
G | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+1694C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941493 | ||||||
chr2:8941638
|
A | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0132a0001c0001t0006g0016others(1): Show | 4 | HG00621.hp2 HG02135.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.299+1549T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941638 | ||||||
chr2:8941654
|
GA | G | 6 | a0001c0001t0001g0043a0001c0001t0041g0042a0002c0002t0017g0064others(3): Show | 6 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+1532delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941654 | ||||||
chr2:8942005
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.299+1182T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942005 | ||||||
chr2:8942009
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+1178C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942009 | ||||||
chr2:8942038
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+1149A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942038 | ||||||
chr2:8942201
|
C | T | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.299+986G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942201 | ||||||
chr2:8942202
|
G | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.299+985C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942202 | ||||||
chr2:8942285
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0025g0078 | 2 | HG01258.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.299+902A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942285 | ||||||
chr2:8942532
|
T | C | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+655A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942532 | ||||||
chr2:8942544
|
A | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+643T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942544 | ||||||
chr2:8942563
|
T | G | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+624A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942563 | ||||||
chr2:8942636
|
G | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+551C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942636 | ||||||
chr2:8942693
|
C | T | 141 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(138): Show | 142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.299+494G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942693 | ||||||
chr2:8942987
|
C | CA | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+199dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942987 | ||||||
chr2:8943121
|
T | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+66A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8943121 | ||||||
chr2:8943294
|
G | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.222-30C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943294 | ||||||
chr2:8943329
|
T | G | 1 | a0001c0001t0005g0045 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.222-65A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943329 | ||||||
chr2:8943417
|
C | A | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.222-153G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943417 | ||||||
chr2:8943933
|
A | G | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-669T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943933 | ||||||
chr2:8943971
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-707G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943971 | ||||||
chr2:8944101
|
G | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-837C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944101 | ||||||
chr2:8944320
|
A | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-1056T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944320 | ||||||
chr2:8944353
|
G | A | 1 | a0001c0004t0017g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222-1089C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944353 | ||||||
chr2:8944480
|
T | G | 1 | a0001c0001t0046g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.222-1216A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944480 | ||||||
chr2:8944580
|
C | T | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-1316G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944580 | ||||||
chr2:8944605
|
A | C | 1 | a0001c0001t0044g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222-1341T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944605 | ||||||
chr2:8944648
|
G | GAC | 12 | a0001c0001t0001g0043a0001c0001t0001g0141a0001c0001t0001g0142others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-1386_222-1385d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | ||||||
chr2:8944648
|
G | GACAC | 32 | a0001c0001t0002g0015a0001c0001t0002g0132a0001c0001t0003g0001others(29): Show | 33 | HG00621.hp2 HG01070.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-1388_222-1385d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | ||||||
chr2:8944648
|
G | GACACACA others(1): Show |
2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.222-1392_222-1385d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | ||||||
chr2:8944648
|
G | GACACACA others(11): Show |
1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.222-1402_222-1385d others(20): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | ||||||
chr2:8944648
|
GAC | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1386_222-1385d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | ||||||
chr2:8944648
|
GACACACA others(3): Show |
G | 13 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(10): Show | 13 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.222-1394_222-1385d others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | ||||||
chr2:8944726
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.222-1462C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944726 | ||||||
chr2:8944878
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.222-1614C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944878 | ||||||
chr2:8944957
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-1693C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944957 | ||||||
chr2:8945009
|
T | C | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.222-1745A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945009 | ||||||
chr2:8945266
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.222-2002G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945266 | ||||||
chr2:8945497
|
T | A | 3 | a0001c0001t0002g0118a0001c0001t0020g0135a0001c0001t0032g0003 | 3 | HG00558.hp1 HG00609.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.222-2233A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945497 | ||||||
chr2:8945612
|
G | A | 1 | a0001c0001t0046g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.222-2348C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945612 | ||||||
chr2:8945726
|
T | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-2462A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945726 | ||||||
chr2:8946024
|
C | T | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-2760G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8946024 | ||||||
chr2:8946112
|
G | A | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.222-2848C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8946112 | ||||||
chr2:8946800
|
G | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.222-3536C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8946800 | ||||||
chr2:8947015
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.222-3751A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947015 | ||||||
chr2:8947137
|
C | T | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-3873G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947137 | ||||||
chr2:8947221
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-3957G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947221 | ||||||
chr2:8947252
|
T | C | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.222-3988A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947252 | ||||||
chr2:8947308
|
A | G | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-4044T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947308 | ||||||
chr2:8947315
|
T | C | 142 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(139): Show | 143 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.222-4051A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947315 | ||||||
chr2:8947454
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.222-4190T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947454 | ||||||
chr2:8947735
|
GA | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-4472delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947735 | ||||||
chr2:8948324
|
TAAC | T | 2 | a0002c0002t0028g0159a0002c0002t0028g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.222-5063_222-5061d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948324 | ||||||
chr2:8948482
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-5218C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948482 | ||||||
chr2:8948531
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-5267G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948531 | ||||||
chr2:8948670
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.222-5406T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948670 | ||||||
chr2:8948725
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.222-5461G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948725 | ||||||
chr2:8948875
|
G | A | 1 | a0001c0001t0013g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.222-5611C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948875 | ||||||
chr2:8948935
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-5671C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948935 | ||||||
chr2:8949144
|
T | A | 1 | a0001c0001t0005g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.222-5880A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8949144 | ||||||
chr2:8949942
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0006g0016 | 2 | HG02135.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.222-6678G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8949942 | ||||||
chr2:8950055
|
T | C | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.222-6791A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950055 | ||||||
chr2:8950084
|
C | T | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-6820G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950084 | ||||||
chr2:8950369
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.222-7105C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950369 | ||||||
chr2:8950488
|
C | T | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.222-7224G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950488 | ||||||
chr2:8950520
|
C | T | 5 | a0001c0001t0001g0120a0001c0001t0002g0131a0001c0001t0007g0149others(2): Show | 5 | HG01070.hp2 HG01258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-7256G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950520 | ||||||
chr2:8950618
|
G | A | 2 | a0001c0001t0042g0127a0002c0002t0049g0158 | 2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.222-7354C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950618 | ||||||
chr2:8951046
|
T | C | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+7451A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951046 | ||||||
chr2:8951085
|
C | T | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.221+7412G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951085 | ||||||
chr2:8951095
|
T | C | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221+7402A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951095 | ||||||
chr2:8951161
|
TCTC | T | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.221+7333_221+7335d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951161 | ||||||
chr2:8951207
|
CT | C | 64 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0030others(61): Show | 65 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.221+7289delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951207 | ||||||
chr2:8951355
|
T | C | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221+7142A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951355 | ||||||
chr2:8951358
|
C | T | 1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.221+7139G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951358 | ||||||
chr2:8951399
|
C | T | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+7098G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951399 | ||||||
chr2:8951989
|
T | C | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.221+6508A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951989 | ||||||
chr2:8952056
|
T | G | 1 | a0001c0001t0002g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.221+6441A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952056 | ||||||
chr2:8952384
|
T | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+6113A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952384 | ||||||
chr2:8952649
|
T | C | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.221+5848A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952649 | ||||||
chr2:8952734
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.221+5763G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952734 | ||||||
chr2:8952764
|
G | A | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+5733C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952764 | ||||||
chr2:8952837
|
A | G | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.221+5660T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952837 | ||||||
chr2:8952894
|
C | T | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+5603G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952894 | ||||||
chr2:8952905
|
G | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+5592C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952905 | ||||||
chr2:8953173
|
T | C | 1 | a0001c0001t0040g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.221+5324A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8953173 | ||||||
chr2:8953591
|
T | C | 1 | a0001c0001t0025g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.221+4906A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8953591 | ||||||
chr2:8953623
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.221+4874A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8953623 | ||||||
chr2:8954193
|
T | G | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+4304A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954193 | ||||||
chr2:8954293
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.221+4204G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954293 | ||||||
chr2:8954505
|
G | A | 5 | a0001c0001t0002g0109a0002c0002t0017g0064a0002c0002t0028g0159others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+3992C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954505 | ||||||
chr2:8954749
|
T | C | 2 | a0001c0001t0002g0068a0001c0001t0002g0081 | 2 | HG00621.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.221+3748A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954749 | ||||||
chr2:8954776
|
T | G | 46 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(43): Show | 46 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.221+3721A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954776 | ||||||
chr2:8954866
|
A | G | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+3631T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954866 | ||||||
chr2:8954907
|
A | G | 21 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(18): Show | 22 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.221+3590T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954907 | ||||||
chr2:8954938
|
T | G | 21 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(18): Show | 22 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.221+3559A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954938 | ||||||
chr2:8954985
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.221+3512C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954985 | ||||||
chr2:8954997
|
G | A | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+3500C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954997 | ||||||
chr2:8955117
|
C | G | 9 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+3380G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955117 | ||||||
chr2:8955365
|
C | A | 6 | a0001c0001t0009g0007a0001c0001t0018g0009a0001c0001t0018g0010others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+3132G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955365 | ||||||
chr2:8955736
|
C | G | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221+2761G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955736 | ||||||
chr2:8955997
|
A | T | 9 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+2500T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955997 | ||||||
chr2:8956131
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+2366A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956131 | ||||||
chr2:8956205
|
T | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0001g0115others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+2292A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956205 | ||||||
chr2:8956416
|
C | A | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.221+2081G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956416 | ||||||
chr2:8956456
|
T | C | 1 | a0001c0001t0008g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221+2041A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956456 | ||||||
chr2:8956658
|
C | G | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.221+1839G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956658 | ||||||
chr2:8956775
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.221+1722C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956775 | ||||||
chr2:8956820
|
C | T | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.221+1677G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956820 | ||||||
chr2:8956915
|
T | C | 141 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(138): Show | 142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.221+1582A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956915 | ||||||
chr2:8957141
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.221+1356C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957141 | ||||||
chr2:8957274
|
A | G | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+1223T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957274 | ||||||
chr2:8957475
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.221+1022A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957475 | ||||||
chr2:8957716
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.221+781C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957716 | ||||||
chr2:8957752
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+745G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957752 | ||||||
chr2:8957754
|
C | G | 2 | a0001c0001t0035g0021a0001c0001t0037g0022 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.221+743G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957754 | ||||||
chr2:8957755
|
G | C | 2 | a0001c0001t0035g0021a0001c0001t0037g0022 | 2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.221+742C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957755 | ||||||
chr2:8957778
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.221+719C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957778 | ||||||
chr2:8957844
|
T | C | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+653A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957844 | ||||||
chr2:8957922
|
C | T | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221+575G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957922 | ||||||
chr2:8957923
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0008g0126 | 2 | HG00735.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.221+574C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957923 | ||||||
chr2:8958288
|
A | C | 2 | a0001c0001t0001g0077a0001c0001t0044g0112 | 2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.221+209T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8958288 | ||||||
chr2:8958862
|
G | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-220C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958862 | ||||||
chr2:8958903
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.76-261G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958903 | ||||||
chr2:8958917
|
A | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-275T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958917 | ||||||
chr2:8958985
|
G | T | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-343C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958985 | ||||||
chr2:8959185
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-543A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959185 | ||||||
chr2:8959376
|
C | G | 13 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(10): Show | 14 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-734G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959376 | ||||||
chr2:8959464
|
C | CT | 15 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(12): Show | 16 | HG00621.hp2 HG00738.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.76-823dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959464 | ||||||
chr2:8959713
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-1071A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959713 | ||||||
chr2:8959727
|
T | C | 1 | a0001c0001t0044g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.76-1085A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959727 | ||||||
chr2:8959837
|
A | G | 3 | a0001c0001t0002g0093a0001c0001t0039g0094a0001c0001t0040g0123 | 3 | NA18956.hp1 NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.76-1195T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959837 | ||||||
chr2:8960007
|
C | T | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-1365G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960007 | ||||||
chr2:8960008
|
A | G | 76 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0030others(73): Show | 77 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.76-1366T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960008 | ||||||
chr2:8960565
|
C | A | 18 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0055others(15): Show | 18 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-1923G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960565 | ||||||
chr2:8960728
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-2086G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960728 | ||||||
chr2:8961590
|
GA | G | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-2949delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961590 | ||||||
chr2:8961592
|
A | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-2950T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961592 | ||||||
chr2:8961692
|
G | A | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-3050C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961692 | ||||||
chr2:8961802
|
G | C | 65 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(62): Show | 66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-3160C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961802 | ||||||
chr2:8961829
|
C | G | 1 | a0001c0001t0032g0003 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.76-3187G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961829 | ||||||
chr2:8961844
|
T | G | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-3202A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961844 | ||||||
chr2:8962070
|
C | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-3428G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962070 | ||||||
chr2:8962566
|
C | A | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-3924G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962566 | ||||||
chr2:8962603
|
C | T | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.76-3961G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962603 | ||||||
chr2:8962724
|
T | C | 1 | a0001c0001t0004g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.76-4082A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962724 | ||||||
chr2:8962810
|
C | A | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-4168G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962810 | ||||||
chr2:8962969
|
G | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-4327C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962969 | ||||||
chr2:8963142
|
G | A | 1 | a0001c0001t0025g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.76-4500C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963142 | ||||||
chr2:8963194
|
C | T | 1 | a0001c0001t0029g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-4552G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963194 | ||||||
chr2:8963221
|
G | A | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-4579C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963221 | ||||||
chr2:8963287
|
C | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-4645G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963287 | ||||||
chr2:8963288
|
G | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-4646C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963288 | ||||||
chr2:8963352
|
A | G | 1 | a0003c0003t0010g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-4710T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963352 | ||||||
chr2:8963353
|
G | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-4711C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963353 | ||||||
chr2:8963365
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.76-4723T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963365 | ||||||
chr2:8963366
|
C | T | 2 | a0002c0002t0028g0159a0002c0002t0028g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.76-4724G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963366 | ||||||
chr2:8963397
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-4755C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963397 | ||||||
chr2:8963554
|
T | C | 32 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(29): Show | 33 | HG00621.hp2 HG00639.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-4912A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963554 | ||||||
chr2:8963594
|
C | T | 1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.76-4952G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963594 | ||||||
chr2:8963898
|
G | A | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-5256C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963898 | ||||||
chr2:8964218
|
G | A | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-5576C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964218 | ||||||
chr2:8964306
|
G | A | 1 | a0001c0001t0048g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76-5664C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964306 | ||||||
chr2:8964403
|
T | C | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-5761A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964403 | ||||||
chr2:8964411
|
T | G | 2 | a0002c0002t0028g0159a0002c0002t0028g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.76-5769A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964411 | ||||||
chr2:8964840
|
C | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-6198G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964840 | ||||||
chr2:8964902
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-6260T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964902 | ||||||
chr2:8965001
|
C | G | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-6359G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965001 | ||||||
chr2:8965113
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-6471C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965113 | ||||||
chr2:8965126
|
C | T | 2 | a0001c0001t0048g0004a0004c0005t0033g0013 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76-6484G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965126 | ||||||
chr2:8965264
|
T | C | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-6622A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965264 | ||||||
chr2:8965371
|
G | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-6729C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965371 | ||||||
chr2:8965382
|
T | C | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.76-6740A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965382 | ||||||
chr2:8965803
|
G | A | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-7161C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965803 | ||||||
chr2:8965879
|
T | G | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-7237A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965879 | ||||||
chr2:8966130
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-7488C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966130 | ||||||
chr2:8966165
|
T | C | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-7523A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966165 | ||||||
chr2:8966199
|
A | G | 1 | a0001c0001t0006g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.76-7557T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966199 | ||||||
chr2:8966336
|
G | T | 6 | a0001c0001t0009g0007a0001c0001t0018g0009a0001c0001t0018g0010others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-7694C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966336 | ||||||
chr2:8966378
|
C | T | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-7736G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966378 | ||||||
chr2:8966544
|
G | A | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-7902C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966544 | ||||||
chr2:8966722
|
T | C | 1 | a0004c0005t0033g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-8080A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966722 | ||||||
chr2:8966906
|
G | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-8264C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966906 | ||||||
chr2:8967015
|
T | C | 1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.76-8373A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967015 | ||||||
chr2:8967041
|
T | A | 65 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(62): Show | 66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-8399A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967041 | ||||||
chr2:8967426
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-8784A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967426 | ||||||
chr2:8967585
|
TA | T | 23 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(20): Show | 24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-8944delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967585 | ||||||
chr2:8967761
|
T | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-9119A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967761 | ||||||
chr2:8968041
|
G | C | 14 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-9399C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968041 | ||||||
chr2:8968193
|
C | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-9551G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968193 | ||||||
chr2:8968492
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-9850C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968492 | ||||||
chr2:8968800
|
G | T | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-10158C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968800 | ||||||
chr2:8968810
|
G | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-10168C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968810 | ||||||
chr2:8968847
|
C | T | 1 | a0003c0003t0010g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-10205G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968847 | ||||||
chr2:8968977
|
T | G | 1 | a0001c0001t0024g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-10335A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968977 | ||||||
chr2:8969135
|
T | C | 65 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(62): Show | 66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-10493A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969135 | ||||||
chr2:8969197
|
A | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-10555T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969197 | ||||||
chr2:8969401
|
T | C | 142 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(139): Show | 143 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.76-10759A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969401 | ||||||
chr2:8969557
|
T | A | 72 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0030others(69): Show | 73 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.76-10915A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969557 | ||||||
chr2:8969580
|
T | C | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-10938A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969580 | ||||||
chr2:8969729
|
G | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-11087C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969729 | ||||||
chr2:8969796
|
G | A | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-11154C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969796 | ||||||
chr2:8969814
|
A | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-11172T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969814 | ||||||
chr2:8970180
|
A | C | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.76-11538T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970180 | ||||||
chr2:8970236
|
A | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-11594T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970236 | ||||||
chr2:8970778
|
T | C | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-12136A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970778 | ||||||
chr2:8970791
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-12149G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970791 | ||||||
chr2:8970910
|
C | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-12268G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970910 | ||||||
chr2:8970951
|
G | C | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-12309C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970951 | ||||||
chr2:8971100
|
C | T | 2 | a0001c0001t0007g0151a0001c0001t0007g0152 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-12458G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971100 | ||||||
chr2:8971135
|
G | T | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.76-12493C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971135 | ||||||
chr2:8971256
|
C | T | 6 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-12614G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971256 | ||||||
chr2:8971277
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-12635G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971277 | ||||||
chr2:8971375
|
TAA | T | 3 | a0001c0001t0018g0009a0001c0001t0018g0010a0001c0001t0029g0008 | 3 | HG01884.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.76-12735_76-12734d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971375 | ||||||
chr2:8971473
|
G | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-12831C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971473 | ||||||
chr2:8971477
|
C | T | 1 | a0001c0001t0020g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.76-12835G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971477 | ||||||
chr2:8971595
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.76-12953G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971595 | ||||||
chr2:8971600
|
T | C | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-12958A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971600 | ||||||
chr2:8971856
|
C | T | 5 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(2): Show | 5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-13214G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971856 | ||||||
chr2:8972004
|
T | C | 2 | a0001c0001t0009g0034a0001c0001t0009g0035 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-13362A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972004 | ||||||
chr2:8972902
|
C | A | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-14260G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972902 | ||||||
chr2:8972918
|
A | G | 2 | a0001c0001t0026g0083a0001c0001t0026g0084 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.76-14276T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972918 | ||||||
chr2:8972978
|
C | A | 1 | a0001c0001t0024g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-14336G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972978 | ||||||
chr2:8973079
|
C | T | 142 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(139): Show | 143 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.76-14437G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973079 | ||||||
chr2:8973289
|
T | C | 9 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-14647A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973289 | ||||||
chr2:8973375
|
G | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-14733C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973375 | ||||||
chr2:8973444
|
A | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-14802T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973444 | ||||||
chr2:8973552
|
TA | T | 61 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(58): Show | 62 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-14911delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973552 | ||||||
chr2:8973562
|
A | G | 3 | a0001c0001t0006g0090a0001c0001t0006g0091a0001c0001t0006g0092 | 3 | HG02735.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.76-14920T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973562 | ||||||
chr2:8973614
|
G | T | 142 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(139): Show | 143 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.76-14972C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973614 | ||||||
chr2:8973750
|
C | T | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.76-15108G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973750 | ||||||
chr2:8973894
|
T | G | 14 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-15252A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973894 | ||||||
chr2:8973909
|
T | C | 23 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(20): Show | 24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-15267A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973909 | ||||||
chr2:8974129
|
A | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-15487T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974129 | ||||||
chr2:8974378
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.76-15736G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974378 | ||||||
chr2:8974414
|
C | T | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-15772G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974414 | ||||||
chr2:8974635
|
T | G | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-15993A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974635 | ||||||
chr2:8974663
|
A | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-16021T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974663 | ||||||
chr2:8974918
|
G | A | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-16276C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974918 | ||||||
chr2:8975303
|
C | A | 5 | a0001c0001t0005g0037a0001c0001t0005g0039a0001c0001t0005g0040others(2): Show | 5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-16661G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975303 | ||||||
chr2:8975462
|
C | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.76-16820G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975462 | ||||||
chr2:8975788
|
T | G | 1 | a0001c0001t0029g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-17146A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975788 | ||||||
chr2:8975797
|
C | CA | 61 | a0001c0001t0001g0128a0001c0001t0001g0145a0001c0001t0001g0146others(58): Show | 62 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.76-17156dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975797 | ||||||
chr2:8975797
|
C | CAA | 6 | a0001c0001t0003g0023a0001c0001t0007g0151a0001c0001t0011g0061others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-17157_76-17156d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975797 | ||||||
chr2:8975849
|
T | C | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-17207A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975849 | ||||||
chr2:8975909
|
C | A | 1 | a0001c0001t0003g0026 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.76-17267G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975909 | ||||||
chr2:8976695
|
G | A | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-18053C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8976695 | ||||||
chr2:8976789
|
C | T | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-18147G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8976789 | ||||||
chr2:8977010
|
C | T | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-18368G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977010 | ||||||
chr2:8977050
|
A | T | 1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.76-18408T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977050 | ||||||
chr2:8977299
|
T | C | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-18657A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977299 | ||||||
chr2:8977461
|
A | G | 1 | a0001c0001t0006g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.76-18819T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977461 | ||||||
chr2:8977558
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0041g0042 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-18916A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977558 | ||||||
chr2:8977581
|
C | T | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-18939G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977581 | ||||||
chr2:8977829
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.76-19187A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977829 | ||||||
chr2:8977841
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-19199G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977841 | ||||||
chr2:8977945
|
C | T | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.76-19303G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977945 | ||||||
chr2:8978086
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-19444A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978086 | ||||||
chr2:8978308
|
T | C | 33 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(30): Show | 33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-19666A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978308 | ||||||
chr2:8978610
|
T | C | 32 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(29): Show | 32 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.76-19968A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978610 | ||||||
chr2:8978686
|
A | G | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-20044T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978686 | ||||||
chr2:8978756
|
C | G | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-20114G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978756 | ||||||
chr2:8978853
|
TA | T | 65 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(62): Show | 66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-20212delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978853 | ||||||
chr2:8978854
|
A | T | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.76-20212T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978854 | ||||||
chr2:8979251
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-20609C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979251 | ||||||
chr2:8979449
|
C | T | 2 | a0001c0001t0009g0007a0001c0004t0017g0006 | 2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.76-20807G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979449 | ||||||
chr2:8979564
|
T | G | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-20922A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979564 | ||||||
chr2:8979605
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-20963C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979605 | ||||||
chr2:8979916
|
G | A | 23 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(20): Show | 24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-21274C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979916 | ||||||
chr2:8980069
|
T | C | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.76-21427A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980069 | ||||||
chr2:8980254
|
A | AG | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.76-21613dupC | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980254 | ||||||
chr2:8980356
|
CA | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0029 | 2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.76-21715delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980356 | ||||||
chr2:8980418
|
T | C | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | HG02735.hp2 HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.76-21776A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980418 | ||||||
chr2:8980925
|
A | T | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-22283T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980925 | ||||||
chr2:8981007
|
T | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-22365A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981007 | ||||||
chr2:8981041
|
AAGAT | A | 9 | a0001c0001t0001g0043a0001c0001t0005g0039a0001c0001t0005g0040others(6): Show | 9 | HG00639.hp1 HG01175.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-22403_76-22400d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981041 | ||||||
chr2:8981049
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.76-22407A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981049 | ||||||
chr2:8981207
|
G | T | 1 | a0001c0001t0024g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.75+22333C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981207 | ||||||
chr2:8981215
|
C | T | 14 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+22325G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981215 | ||||||
chr2:8981436
|
T | TGTCGCCC others(34): Show |
1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.75+22063_75+22103d others(43): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981436 | ||||||
chr2:8981682
|
G | T | 2 | a0001c0001t0009g0007a0001c0004t0017g0006 | 2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.75+21858C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981682 | ||||||
chr2:8982030
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+21510G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982030 | ||||||
chr2:8982102
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.75+21438G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982102 | ||||||
chr2:8982164
|
A | T | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+21376T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982164 | ||||||
chr2:8982289
|
C | T | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+21251G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982289 | ||||||
chr2:8982932
|
C | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+20608G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982932 | ||||||
chr2:8982994
|
A | G | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+20546T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982994 | ||||||
chr2:8983031
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+20509C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983031 | ||||||
chr2:8983274
|
T | A | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+20266A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983274 | ||||||
chr2:8983363
|
A | G | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+20177T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983363 | ||||||
chr2:8983393
|
A | C | 9 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+20147T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983393 | ||||||
chr2:8983425
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+20115G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983425 | ||||||
chr2:8984043
|
T | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+19497A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984043 | ||||||
chr2:8984189
|
G | A | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.75+19351C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984189 | ||||||
chr2:8984202
|
C | G | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+19338G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984202 | ||||||
chr2:8984349
|
G | C | 1 | a0001c0001t0048g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+19191C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984349 | ||||||
chr2:8984417
|
G | C | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+19123C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984417 | ||||||
chr2:8984469
|
G | C | 2 | a0002c0002t0028g0159a0002c0002t0028g0160 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.75+19071C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984469 | ||||||
chr2:8984539
|
G | GTGAAAGC others(10): Show |
1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.75+19000_75+19001i others(19): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984539 | ||||||
chr2:8984541
|
G | C | 1 | a0001c0001t0047g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.75+18999C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984541 | ||||||
chr2:8984602
|
C | A | 6 | a0001c0001t0002g0118a0001c0001t0020g0134a0001c0001t0020g0135others(3): Show | 6 | HG00558.hp1 HG00609.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+18938G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984602 | ||||||
chr2:8984663
|
A | G | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+18877T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984663 | ||||||
chr2:8984683
|
G | GA | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+18856dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984683 | ||||||
chr2:8984779
|
G | A | 1 | a0002c0002t0031g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.75+18761C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984779 | ||||||
chr2:8985033
|
C | T | 2 | a0001c0001t0002g0068a0001c0001t0002g0081 | 2 | HG00621.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.75+18507G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985033 | ||||||
chr2:8985084
|
GA | G | 8 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(5): Show | 8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+18455delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985084 | ||||||
chr2:8985118
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.75+18422G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985118 | ||||||
chr2:8985246
|
G | A | 1 | a0001c0001t0022g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.75+18294C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985246 | ||||||
chr2:8985561
|
A | G | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+17979T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985561 | ||||||
chr2:8985829
|
T | C | 1 | a0001c0001t0003g0029 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+17711A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985829 | ||||||
chr2:8985895
|
C | T | 23 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(20): Show | 24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+17645G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985895 | ||||||
chr2:8985991
|
A | G | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+17549T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985991 | ||||||
chr2:8986114
|
A | T | 15 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0128others(12): Show | 15 | HG00609.hp1 HG00735.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+17426T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986114 | ||||||
chr2:8986207
|
CA | C | 5 | a0001c0001t0001g0120a0001c0001t0002g0119a0001c0001t0006g0090others(2): Show | 5 | HG02735.hp1 HG02895.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+17332delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986207 | ||||||
chr2:8986378
|
A | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+17162T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986378 | ||||||
chr2:8986565
|
T | TA | 8 | a0001c0001t0002g0093a0001c0001t0006g0090a0001c0001t0006g0091others(5): Show | 8 | HG00140.hp2 HG02698.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+16974dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986565 | ||||||
chr2:8986811
|
G | A | 11 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+16729C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986811 | ||||||
chr2:8987016
|
C | A | 12 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(9): Show | 12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+16524G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987016 | ||||||
chr2:8987063
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+16477C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987063 | ||||||
chr2:8987079
|
T | C | 15 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0128others(12): Show | 15 | HG00609.hp1 HG00735.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+16461A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987079 | ||||||
chr2:8987095
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+16445T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987095 | ||||||
chr2:8987122
|
T | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+16418A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987122 | ||||||
chr2:8987213
|
C | T | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+16327G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987213 | ||||||
chr2:8987422
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.75+16118A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987422 | ||||||
chr2:8987591
|
C | A | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.75+15949G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987591 | ||||||
chr2:8987591
|
C | G | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+15949G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987591 | ||||||
chr2:8987692
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+15848G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987692 | ||||||
chr2:8987766
|
G | A | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.75+15774C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987766 | ||||||
chr2:8988301
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+15239C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988301 | ||||||
chr2:8988563
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0025g0078 | 2 | HG01258.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.75+14977A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988563 | ||||||
chr2:8988905
|
G | A | 65 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0132others(62): Show | 66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.75+14635C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988905 | ||||||
chr2:8988995
|
G | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+14545C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988995 | ||||||
chr2:8989196
|
T | C | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+14344A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989196 | ||||||
chr2:8989523
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+14017A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989523 | ||||||
chr2:8989953
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.75+13587C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989953 | ||||||
chr2:8989999
|
A | G | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+13541T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989999 | ||||||
chr2:8990053
|
G | A | 14 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+13487C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990053 | ||||||
chr2:8990417
|
T | C | 142 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(139): Show | 143 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.75+13123A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990417 | ||||||
chr2:8990773
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.75+12767A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990773 | ||||||
chr2:8990902
|
A | C | 14 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(11): Show | 14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+12638T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990902 | ||||||
chr2:8991051
|
A | T | 1 | a0001c0001t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.75+12489T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8991051 | ||||||
chr2:8991510
|
G | A | 6 | a0001c0001t0009g0007a0001c0001t0018g0009a0001c0001t0018g0010others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+12030C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8991510 | ||||||
chr2:8992309
|
G | A | 1 | a0001c0001t0022g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+11231C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8992309 | ||||||
chr2:8992705
|
C | T | 1 | a0001c0001t0025g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75+10835G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8992705 | ||||||
chr2:8992879
|
C | T | 1 | a0001c0001t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75+10661G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8992879 | ||||||
chr2:8993440
|
G | A | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+10100C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993440 | ||||||
chr2:8993595
|
C | T | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+9945G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993595 | ||||||
chr2:8993680
|
T | C | 3 | a0002c0002t0028g0159a0002c0002t0028g0160a0002c0002t0049g0158 | 3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.75+9860A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993680 | ||||||
chr2:8993839
|
C | G | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+9701G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993839 | ||||||
chr2:8994151
|
T | C | 3 | a0002c0002t0019g0011a0002c0002t0019g0012a0002c0002t0031g0036 | 3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+9389A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994151 | ||||||
chr2:8994240
|
CA | C | 7 | a0002c0002t0017g0064a0002c0002t0019g0011a0002c0002t0019g0012others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+9299delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994240 | ||||||
chr2:8994483
|
T | C | 3 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0001t0005g0046 | 3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.75+9057A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994483 | ||||||
chr2:8994530
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+9010G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994530 | ||||||
chr2:8994795
|
A | G | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+8745T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994795 | ||||||
chr2:8994803
|
T | C | 1 | a0001c0001t0022g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.75+8737A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994803 | ||||||
chr2:8994988
|
T | A | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+8552A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994988 | ||||||
chr2:8995011
|
C | T | 1 | a0001c0001t0014g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.75+8529G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995011 | ||||||
chr2:8995302
|
T | C | 74 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0030others(71): Show | 75 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.75+8238A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995302 | ||||||
chr2:8995589
|
C | CT | 3 | a0001c0001t0009g0007a0001c0001t0030g0005a0001c0004t0017g0006 | 3 | HG00639.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.75+7950_75+7951ins others(1): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995589 | ||||||
chr2:8995590
|
A | AT | 58 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0068others(55): Show | 59 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.75+7949dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995590 | ||||||
chr2:8995590
|
A | T | 3 | a0001c0001t0009g0007a0001c0001t0030g0005a0001c0004t0017g0006 | 3 | HG00639.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.75+7950T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995590 | ||||||
chr2:8995645
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+7895A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995645 | ||||||
chr2:8995652
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+7888T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995652 | ||||||
chr2:8995653
|
C | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+7887G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995653 | ||||||
chr2:8995673
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+7867G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995673 | ||||||
chr2:8995689
|
C | T | 1 | a0001c0001t0025g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75+7851G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995689 | ||||||
chr2:8995768
|
G | T | 2 | a0001c0001t0020g0134a0001c0001t0022g0033 | 2 | HG02976.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.75+7772C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995768 | ||||||
chr2:8995804
|
A | G | 77 | a0001c0001t0001g0043a0001c0001t0001g0074a0001c0001t0001g0075others(74): Show | 78 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.75+7736T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995804 | ||||||
chr2:8995879
|
T | C | 158 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0074others(155): Show | 159 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.75+7661A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995879 | ||||||
chr2:8995886
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.75+7654G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995886 | ||||||
chr2:8996348
|
TGACAACA | T | 4 | a0001c0001t0001g0070a0001c0001t0002g0071a0001c0001t0002g0072others(1): Show | 4 | HG02083.hp1 NA18953.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+7185_75+7191del others(7): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996348 | ||||||
chr2:8996361
|
T | C | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+7179A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996361 | ||||||
chr2:8996531
|
G | A | 2 | a0001c0001t0018g0009a0001c0001t0018g0010 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.75+7009C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996531 | ||||||
chr2:8996557
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+6983G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996557 | ||||||
chr2:8996666
|
G | A | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.75+6874C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996666 | ||||||
chr2:8996843
|
T | C | 3 | a0001c0001t0020g0134a0001c0001t0020g0135a0001c0001t0032g0003 | 3 | HG00558.hp1 HG00609.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.75+6697A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996843 | ||||||
chr2:8996901
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.75+6639G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996901 | ||||||
chr2:8997017
|
C | T | 2 | a0001c0001t0013g0014a0001c0001t0013g0032 | 2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.75+6523G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8997017 | ||||||
chr2:8997512
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.75+6028G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8997512 | ||||||
chr2:8997831
|
T | A | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+5709A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8997831 | ||||||
chr2:8998015
|
C | T | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.75+5525G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998015 | ||||||
chr2:8998093
|
A | T | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+5447T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998093 | ||||||
chr2:8998131
|
T | G | 29 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0003g0001others(26): Show | 30 | HG00639.hp2 HG01175.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.75+5409A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998131 | ||||||
chr2:8998179
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.75+5361G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998179 | ||||||
chr2:8998277
|
C | A | 1 | a0001c0001t0006g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.75+5263G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998277 | ||||||
chr2:8998358
|
T | C | 3 | a0001c0001t0012g0052a0001c0001t0012g0053a0001c0001t0012g0054 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+5182A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998358 | ||||||
chr2:8998609
|
C | T | 22 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0003g0001others(19): Show | 23 | HG01175.hp1 HG01256.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+4931G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998609 | ||||||
chr2:8998624
|
G | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4916C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998624 | ||||||
chr2:8998905
|
G | C | 1 | a0002c0002t0017g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75+4635C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998905 | ||||||
chr2:8998921
|
G | A | 1 | a0001c0001t0011g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4619C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998921 | ||||||
chr2:8999159
|
A | G | 17 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(14): Show | 17 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.75+4381T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999159 | ||||||
chr2:8999188
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.75+4352G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999188 | ||||||
chr2:8999454
|
G | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+4086C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999454 | ||||||
chr2:8999526
|
T | C | 19 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(16): Show | 19 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+4014A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999526 | ||||||
chr2:8999731
|
A | G | 1 | a0002c0002t0049g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.75+3809T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999731 | ||||||
chr2:8999818
|
G | C | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3722C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999818 | ||||||
chr2:8999839
|
T | C | 9 | a0001c0001t0004g0055a0001c0001t0004g0057a0001c0001t0004g0058others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+3701A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999839 | ||||||
chr2:8999867
|
T | C | 1 | a0001c0001t0013g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.75+3673A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999867 | ||||||
chr2:9000041
|
C | T | 1 | a0001c0001t0030g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+3499G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000041 | ||||||
chr2:9000156
|
C | T | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+3384G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000156 | ||||||
chr2:9000192
|
T | A | 1 | a0001c0001t0008g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.75+3348A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000192 | ||||||
chr2:9000320
|
T | G | 9 | a0001c0001t0009g0007a0001c0001t0009g0034a0001c0001t0009g0035others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+3220A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000320 | ||||||
chr2:9000358
|
C | T | 61 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0003g0001others(58): Show | 62 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.75+3182G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000358 | ||||||
chr2:9000560
|
G | A | 17 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(14): Show | 17 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.75+2980C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000560 | ||||||
chr2:9000785
|
C | T | 2 | a0002c0002t0019g0011a0002c0002t0019g0012 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+2755G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000785 | ||||||
chr2:9000889
|
A | G | 6 | a0001c0001t0009g0007a0001c0001t0018g0009a0001c0001t0018g0010others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+2651T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000889 | ||||||
chr2:9000987
|
A | G | 1 | a0001c0001t0048g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+2553T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000987 | ||||||
chr2:9001054
|
T | C | 4 | a0002c0002t0017g0064a0002c0002t0028g0159a0002c0002t0028g0160others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+2486A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9001054 | ||||||
chr2:9002045
|
CAT | C | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1493_75+1494del others(2): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002045 | ||||||
chr2:9002053
|
G | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1487C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002053 | ||||||
chr2:9002054
|
C | T | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1486G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002054 | ||||||
chr2:9002055
|
ACACCAGT others(31): Show |
A | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1447_75+1484del others(38): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002055 | ||||||
chr2:9002094
|
C | G | 4 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(1): Show | 4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1446G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002094 | ||||||
chr2:9002419
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.75+1121C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002419 | ||||||
chr2:9002430
|
T | C | 3 | a0003c0003t0010g0153a0003c0003t0010g0154a0003c0003t0010g0155 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+1110A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002430 | ||||||
chr2:9002883
|
A | T | 72 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0030others(69): Show | 73 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.75+657T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002883 | ||||||
chr2:9002928
|
C | G | 2 | a0001c0001t0007g0149a0001c0001t0007g0150 | 2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.75+612G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002928 | ||||||
chr2:9002993
|
C | T | 1 | a0001c0001t0032g0003 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.75+547G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002993 | ||||||
chr2:9003366
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+174C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9003366 | ||||||
chr2:9003515
|
C | A | 7 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+25G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9003515 |