geneid | 94160 |
---|---|
ensemblid | ENSG00000140798.17 |
hgncid | 14640 |
symbol | ABCC12 |
name | ATP binding cassette subfamily C member 12 |
refseq_nuc | NM_001393797.1 |
refseq_prot | NP_001380726.1 |
ensembl_nuc | ENST00000311303.8 |
ensembl_prot | ENSP00000311030.4 |
mane_status | MANE Select |
chr | chr16 |
start | 48080882 |
end | 48155993 |
strand | - |
ver | v1.2 |
region | chr16:48080882-48155993 |
region5000 | chr16:48075882-48160993 |
regionname0 | ABCC12_chr16_48080882_48155993 |
regionname5000 | ABCC12_chr16_48075882_48160993 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1359 | 36 | 11 | 7 | 9 | 1 | 8 | 2 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0002 | 1/0 | 1359 | 26 | 13 | 4 | 4 | 1 | 3 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0003 | 0/0 | 1359 | 9 | 5 | 0 | 3 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0004 | 0/0 | 1359 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0005 | 0/0 | 1359 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006 | 0/0 | 82 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0007 | 0/0 | 1359 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0008 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0009 | 0/0 | 1359 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0010 | 0/0 | 1359 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0011 | 0/1 | 1359 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0012 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0013 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0014 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0015 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0016 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0017 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0018 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0019 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0020 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0021 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0022 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0023 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0024 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4080 | 28 | 10 | 4 | 9 | 0 | 5 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0002 | 1/0 | 4080 | 26 | 13 | 4 | 4 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0003 | 0/0 | 4080 | 9 | 5 | 0 | 3 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0004 | 0/0 | 4080 | 8 | 1 | 3 | 0 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0005 | 0/0 | 4080 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0006 | 0/0 | 4080 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0007 | 0/0 | 4080 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0008 | 0/0 | 4080 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0009 | 0/0 | 4080 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0010 | 0/0 | 4078 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0011 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0012 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0013 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0014 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0015 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0016 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0017 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0018 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0019 | 0/1 | 4080 | 2 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0020 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0021 | 0/0 | 4078 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0022 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0023 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0024 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0025 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0026 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0027 | 0/0 | 4080 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0028 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0029 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
c0030 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3306 | 85 | 46 | 12 | 12 | 2 | 11 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0002 | 0/0 | 3306 | 8 | 7 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0003 | 0/0 | 3306 | 8 | 8 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0004 | 0/0 | 3306 | 7 | 4 | 0 | 3 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0005 | 0/0 | 3306 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0006 | 0/0 | 3306 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0007 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0008 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0009 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0010 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0011 | 0/0 | 3306 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0012 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0013 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0014 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0015 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0016 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0017 | 0/0 | 3306 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0018 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0019 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
t0020 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4080 | 28 | 10 | 4 | 9 | 0 | 5 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0001c0004 | 0/0 | 4080 | 8 | 1 | 3 | 0 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0002c0002 | 1/0 | 4080 | 26 | 13 | 4 | 4 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0003c0003 | 0/0 | 4080 | 9 | 5 | 0 | 3 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0004c0007 | 0/0 | 4080 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0004c0013 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0005c0005 | 0/0 | 4080 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0010 | 0/0 | 4078 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0021 | 0/0 | 4078 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0029 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0030 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0007c0006 | 0/0 | 4080 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0008c0008 | 0/0 | 4080 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0009c0009 | 0/0 | 4080 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0010c0018 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0010c0026 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0011c0019 | 0/1 | 4080 | 2 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0012c0020 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0013c0014 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0014c0016 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0015c0015 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0016c0017 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0017c0011 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0018c0012 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0019c0027 | 0/0 | 4080 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0020c0023 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0021c0024 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0022c0025 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0023c0022 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0024c0028 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7385 | 27 | 10 | 4 | 9 | 0 | 4 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0001c0001t0013 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0001c0004t0001 | 0/0 | 7385 | 7 | 1 | 2 | 0 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0001c0004t0017 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0002c0002t0001 | 1/0 | 7385 | 24 | 12 | 4 | 3 | 1 | 3 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0002c0002t0019 | 0/0 | 7385 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0002c0002t0020 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0003c0003t0001 | 0/0 | 7385 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0003c0003t0004 | 0/0 | 7385 | 7 | 4 | 0 | 3 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0003c0003t0014 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0004c0007t0003 | 0/0 | 7385 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0004c0013t0003 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0005c0005t0001 | 0/0 | 7385 | 7 | 7 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0010t0002 | 0/0 | 7383 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0021t0002 | 0/0 | 7383 | 2 | 1 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0029t0018 | 0/0 | 7383 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0006c0030t0001 | 0/0 | 7383 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0007c0006t0001 | 0/0 | 7385 | 6 | 6 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0008c0008t0009 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0008c0008t0010 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0008c0008t0015 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0009c0009t0001 | 0/0 | 7385 | 5 | 5 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0010c0018t0011 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0010c0026t0016 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0011c0019t0001 | 0/1 | 7385 | 2 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0012c0020t0005 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0013c0014t0001 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0014c0016t0005 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0015c0015t0008 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0016c0017t0002 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0017c0011t0006 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0018c0012t0007 | 0/0 | 7385 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0019c0027t0001 | 0/0 | 7385 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0020c0023t0006 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0021c0024t0001 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0022c0025t0001 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0023c0022t0012 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
a0024c0028t0002 | 0/0 | 7385 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | copy fasta | chr16 | 48075882 | 48160993 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0001t0013g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0001c0004t0017g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0019g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0002c0002t0020g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0003c0003t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0007t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0007t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0007t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0007t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0007t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0007t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0013t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0004c0013t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0005c0005t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0005c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0005c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0005c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0005c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0005c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0010t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0010t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0010t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0021t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0021t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0029t0018g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0006c0030t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0007c0006t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0007c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0007c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0007c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0007c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0008c0008t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0008c0008t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0008c0008t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0008c0008t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0009c0009t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0009c0009t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0009c0009t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0009c0009t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0010c0018t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0010c0018t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0010c0026t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0011c0019t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0011c0019t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0012c0020t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0013c0014t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0013c0014t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0014c0016t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0015c0015t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0015c0015t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0016c0017t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0016c0017t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0017c0011t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0017c0011t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0018c0012t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0019c0027t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0020c0023t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0021c0024t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0022c0025t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0023c0022t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
a0024c0028t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00544 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00558 | hp1 | a0003 | c0003 | t0004 | g0045 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00741 | hp1 | a0011 | c0019 | t0001 | g0073 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0081 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0098 | AMR | PUR | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01256 | hp1 | a0019 | c0027 | t0001 | g0059 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01496 | hp2 | a0006 | c0021 | t0002 | g0026 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0010 | EUR | IBS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01884 | hp1 | a0014 | c0016 | t0005 | g0004 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01891 | hp1 | a0016 | c0017 | t0002 | g0109 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01891 | hp2 | a0004 | c0007 | t0003 | g0103 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02040 | hp1 | a0003 | c0003 | t0004 | g0061 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02055 | hp2 | a0004 | c0013 | t0003 | g0108 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02083 | hp1 | a0002 | c0002 | t0019 | g0050 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02129 | hp2 | a0003 | c0003 | t0004 | g0062 | EAS | KHV | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02257 | hp1 | a0007 | c0006 | t0001 | g0011 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02258 | hp1 | a0005 | c0005 | t0001 | g0042 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02258 | hp2 | a0004 | c0007 | t0003 | g0102 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02280 | hp1 | a0023 | c0022 | t0012 | g0028 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02572 | hp1 | a0018 | c0012 | t0007 | g0012 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02572 | hp2 | a0012 | c0020 | t0005 | g0007 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0099 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02615 | hp1 | a0015 | c0015 | t0008 | g0041 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02622 | hp2 | a0006 | c0021 | t0002 | g0025 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02630 | hp1 | a0009 | c0009 | t0001 | g0020 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02630 | hp2 | a0021 | c0024 | t0001 | g0092 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02647 | hp1 | a0006 | c0010 | t0002 | g0027 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02647 | hp2 | a0005 | c0005 | t0001 | g0064 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02717 | hp1 | a0007 | c0006 | t0001 | g0090 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02717 | hp2 | a0020 | c0023 | t0006 | g0037 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02723 | hp1 | a0010 | c0018 | t0011 | g0021 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02723 | hp2 | a0006 | c0010 | t0002 | g0024 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02809 | hp2 | a0009 | c0009 | t0001 | g0019 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02895 | hp1 | a0008 | c0008 | t0010 | g0014 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02895 | hp2 | a0012 | c0020 | t0005 | g0007 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02896 | hp1 | a0006 | c0029 | t0018 | g0029 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02896 | hp2 | a0005 | c0005 | t0001 | g0065 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02897 | hp1 | a0005 | c0005 | t0001 | g0031 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02897 | hp2 | a0008 | c0008 | t0010 | g0015 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02922 | hp1 | a0005 | c0005 | t0001 | g0009 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02965 | hp1 | a0016 | c0017 | t0002 | g0111 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02965 | hp2 | a0003 | c0003 | t0004 | g0008 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02970 | hp1 | a0022 | c0025 | t0001 | g0110 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02970 | hp2 | a0008 | c0008 | t0009 | g0005 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0088 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03041 | hp1 | a0017 | c0011 | t0006 | g0117 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03098 | hp1 | a0004 | c0007 | t0003 | g0101 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03098 | hp2 | a0002 | c0002 | t0020 | g0063 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03130 | hp1 | a0009 | c0009 | t0001 | g0003 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03130 | hp2 | a0004 | c0007 | t0003 | g0116 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03139 | hp2 | a0006 | c0010 | t0002 | g0023 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03195 | hp1 | a0013 | c0014 | t0001 | g0106 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0085 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03209 | hp1 | a0003 | c0003 | t0014 | g0068 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03209 | hp2 | a0008 | c0008 | t0015 | g0016 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03225 | hp1 | a0013 | c0014 | t0001 | g0107 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03225 | hp2 | a0005 | c0005 | t0001 | g0009 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03453 | hp1 | a0024 | c0028 | t0002 | g0018 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03453 | hp2 | a0008 | c0008 | t0009 | g0005 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03486 | hp1 | a0007 | c0006 | t0001 | g0091 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03486 | hp2 | a0015 | c0015 | t0008 | g0112 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0008 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03516 | hp2 | a0005 | c0005 | t0001 | g0066 | AFR | ESN | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03540 | hp2 | a0007 | c0006 | t0001 | g0011 | AFR | GWD | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03579 | hp1 | a0017 | c0011 | t0006 | g0115 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03579 | hp2 | a0003 | c0003 | t0004 | g0100 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03704 | hp2 | a0001 | c0004 | t0001 | g0035 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03710 | hp2 | a0001 | c0004 | t0001 | g0083 | SAS | PJL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | STU | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG04115 | hp2 | a0001 | c0001 | t0013 | g0079 | SAS | STU | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18522 | hp1 | a0010 | c0026 | t0016 | g0084 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18906 | hp2 | a0004 | c0013 | t0003 | g0114 | AFR | YRI | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA19030 | hp2 | a0007 | c0006 | t0001 | g0093 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA20129 | hp1 | a0014 | c0016 | t0005 | g0004 | AFR | ASW | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01123 | hp1 | a0001 | c0004 | t0017 | g0118 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02109 | hp1 | a0004 | c0007 | t0003 | g0104 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02109 | hp2 | a0009 | c0009 | t0001 | g0017 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02486 | hp2 | a0018 | c0012 | t0007 | g0012 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG02559 | hp2 | a0004 | c0007 | t0003 | g0105 | AFR | ACB | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG03471 | hp2 | a0010 | c0018 | t0011 | g0039 | AFR | MSL | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA20300 | hp1 | a0009 | c0009 | t0001 | g0003 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA20300 | hp2 | a0006 | c0030 | t0001 | g0119 | AFR | USA | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
NA21309 | hp2 | a0007 | c0006 | t0001 | g0094 | AFR | LWK | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
homoSapiens_chm13v2 | hp1 | a0011 | c0019 | t0001 | g0072 | REF | REF | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0057 | REF | REF | ABCC12_chr16_48075882_48160993 | ABCC12 | chr16 | 48075882 | 48160993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48087989
|
T | G | 3 | a0006a0023a0024 | 7 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.3572A>C | p.Glu1191Ala | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/31 | 4044/7385 | 3572/4080 | 1191/1359 | chr16 | 48087989 | ||
chr16:48088001
|
A | G | 7 | a0004a0006a0010others(4): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
missense_variant | MODERATE | c.3560T>C | p.Ile1187Thr | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/31 | 4032/7385 | 3560/4080 | 1187/1359 | chr16 | 48088001 | ||
chr16:48088076
|
G | A | 1 | a0018 | 2 | HG02486.hp2 HG02572.hp1 |
missense_variant | MODERATE | c.3485C>T | p.Ser1162Leu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/31 | 3957/7385 | 3485/4080 | 1162/1359 | chr16 | 48088076 | ||
chr16:48088545
|
C | T | 3 | a0012a0014a0015 | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.3475G>A | p.Gly1159Arg | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/31 | 3947/7385 | 3475/4080 | 1159/1359 | chr16 | 48088545 | ||
chr16:48088671
|
G | A | 4 | a0001a0006a0011others(1): Show | 40 | HG00544.hp1 HG00735.hp1 HG00741.hp1 others(37): Show |
missense_variant | MODERATE | c.3349C>T | p.Arg1117Cys | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/31 | 3821/7385 | 3349/4080 | 1117/1359 | chr16 | 48088671 | ||
chr16:48088694
|
G | T | 1 | a0022 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.3326C>A | p.Thr1109Asn | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/31 | 3798/7385 | 3326/4080 | 1109/1359 | chr16 | 48088694 | ||
chr16:48096870
|
C | T | 1 | a0019 | 1 | HG01256.hp1 | stop_gained | HIGH | c.3071G>A | p.Trp1024* | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/31 | 3543/7385 | 3071/4080 | 1024/1359 | chr16 | 48096870 | ||
chr16:48100873
|
A | G | 12 | a0004a0006a0008others(9): Show | 36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
missense_variant&splice_region_variant | MODERATE | c.3037T>C | p.Tyr1013His | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/31 | 3509/7385 | 3037/4080 | 1013/1359 | chr16 | 48100873 | ||
chr16:48100912
|
T | C | 2 | a0006a0024 | 3 | HG01496.hp2 HG02622.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.2998A>G | p.Ile1000Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/31 | 3470/7385 | 2998/4080 | 1000/1359 | chr16 | 48100912 | ||
chr16:48100945
|
T | A | 12 | a0004a0006a0008others(9): Show | 36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
missense_variant | MODERATE | c.2965A>T | p.Thr989Ser | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/31 | 3437/7385 | 2965/4080 | 989/1359 | chr16 | 48100945 | ||
chr16:48104361
|
T | A | 1 | a0005 | 7 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
missense_variant | MODERATE | c.2681A>T | p.Lys894Met | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/31 | 3153/7385 | 2681/4080 | 894/1359 | chr16 | 48104361 | ||
chr16:48105152
|
G | A | 1 | a0014 | 2 | HG01884.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.2660C>T | p.Thr887Met | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/31 | 3132/7385 | 2660/4080 | 887/1359 | chr16 | 48105152 | ||
chr16:48105263
|
A | G | 1 | a0011 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2549T>C | p.Val850Ala | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/31 | 3021/7385 | 2549/4080 | 850/1359 | chr16 | 48105263 | ||
chr16:48111793
|
G | A | 1 | a0006 | 1 | NA20300.hp2 | stop_gained | HIGH | c.2107C>T | p.Arg703* | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/31 | 2579/7385 | 2107/4080 | 703/1359 | chr16 | 48111793 | ||
chr16:48111831
|
T | A | 2 | a0003a0009 | 14 | HG00558.hp1 HG02040.hp1 HG02109.hp2 others(11): Show |
missense_variant | MODERATE | c.2069A>T | p.Glu690Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/31 | 2541/7385 | 2069/4080 | 690/1359 | chr16 | 48111831 | ||
chr16:48115458
|
G | A | 2 | a0016a0022 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.1946C>T | p.Thr649Met | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/31 | 2418/7385 | 1946/4080 | 649/1359 | chr16 | 48115458 | ||
chr16:48117287
|
T | A | 7 | a0007a0014a0015others(4): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
missense_variant | MODERATE | c.1759A>T | p.Asn587Tyr | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/31 | 2231/7385 | 1759/4080 | 587/1359 | chr16 | 48117287 | ||
chr16:48139215
|
C | A | 2 | a0016a0022 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.779G>T | p.Gly260Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/31 | 1251/7385 | 779/4080 | 260/1359 | chr16 | 48139215 | ||
chr16:48141324
|
G | T | 16 | a0004a0006a0007others(13): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
missense_variant | MODERATE | c.305C>A | p.Ala102Glu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 5/31 | 777/7385 | 305/4080 | 102/1359 | chr16 | 48141324 | ||
chr16:48143965
|
C | T | 1 | a0017 | 2 | HG03041.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.220G>A | p.Val74Ile | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/31 | 692/7385 | 220/4080 | 74/1359 | chr16 | 48143965 | ||
chr16:48143986
|
CTT | C | 1 | a0006 | 7 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
frameshift_variant | HIGH | c.197_198delAA | p.Lys66fs | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/31 | 670/7385 | 197/4080 | 66/1359 | chr16 | 48143986 | ||
chr16:48146349
|
C | T | 3 | a0017a0018a0023 | 5 | HG02280.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
missense_variant | MODERATE | c.76G>A | p.Asp26Asn | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/31 | 548/7385 | 76/4080 | 26/1359 | chr16 | 48146349 | ||
chr16:48146400
|
T | G | 4 | a0006a0008a0009others(1): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
missense_variant | MODERATE | c.25A>C | p.Ile9Leu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/31 | 497/7385 | 25/4080 | 9/1359 | chr16 | 48146400 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48083763
|
C | T | 1 | a0008c0008 | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.4032G>A | p.Lys1344Lys | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 4504/7385 | 4032/4080 | 1344/1359 | chr16 | 48083763 | ||
chr16:48086786
|
A | G | 16 | a0004c0007a0004c0013a0006c0010others(13): Show | 35 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(32): Show |
synonymous_variant | LOW | c.3669T>C | p.Asp1223Asp | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/31 | 4141/7385 | 3669/4080 | 1223/1359 | chr16 | 48086786 | ||
chr16:48104348
|
A | G | 17 | a0004c0007a0004c0013a0006c0010others(14): Show | 36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
synonymous_variant | LOW | c.2694T>C | p.Ser898Ser | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/31 | 3166/7385 | 2694/4080 | 898/1359 | chr16 | 48104348 | ||
chr16:48115556
|
A | G | 10 | a0004c0007a0007c0006a0008c0008others(7): Show | 29 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(26): Show |
synonymous_variant | LOW | c.1848T>C | p.Ala616Ala | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/31 | 2320/7385 | 1848/4080 | 616/1359 | chr16 | 48115556 | ||
chr16:48130866
|
T | C | 1 | a0001c0004 | 8 | HG00741.hp2 HG01074.hp2 HG01123.hp1 others(5): Show |
synonymous_variant | LOW | c.1158A>G | p.Val386Val | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/31 | 1630/7385 | 1158/4080 | 386/1359 | chr16 | 48130866 | ||
chr16:48138274
|
C | A | 1 | a0004c0007 | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
synonymous_variant | LOW | c.933G>T | p.Leu311Leu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/31 | 1405/7385 | 933/4080 | 311/1359 | chr16 | 48138274 | ||
chr16:48140828
|
G | T | 1 | a0010c0018 | 2 | HG02723.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.516C>A | p.Thr172Thr | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/31 | 988/7385 | 516/4080 | 172/1359 | chr16 | 48140828 | ||
chr16:48140855
|
A | G | 7 | a0006c0010a0006c0021a0006c0029others(4): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
synonymous_variant | LOW | c.489T>C | p.Ile163Ile | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/31 | 961/7385 | 489/4080 | 163/1359 | chr16 | 48140855 | ||
chr16:48144023
|
G | A | 4 | a0004c0007a0017c0011a0018c0012others(1): Show | 11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.162C>T | p.Phe54Phe | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/31 | 634/7385 | 162/4080 | 54/1359 | chr16 | 48144023 | ||
chr16:48146356
|
T | C | 7 | a0006c0010a0006c0021a0006c0029others(4): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
synonymous_variant | LOW | c.69A>G | p.Glu23Glu | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/31 | 541/7385 | 69/4080 | 23/1359 | chr16 | 48146356 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48080939
|
G | A | 1 | a0003c0003t0004 | 7 | HG00558.hp1 HG02040.hp1 HG02129.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2776C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2776 | chr16 | 48080939 | |||||
chr16:48081090
|
T | C | 19 | a0004c0007t0003a0004c0013t0003a0006c0010t0002others(16): Show | 37 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2625A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2625 | chr16 | 48081090 | |||||
chr16:48081255
|
T | C | 1 | a0023c0022t0012 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2460A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2460 | chr16 | 48081255 | |||||
chr16:48081326
|
G | A | 3 | a0008c0008t0009a0008c0008t0010a0008c0008t0015 | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2389C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2389 | chr16 | 48081326 | |||||
chr16:48081434
|
T | C | 1 | a0015c0015t0008 | 2 | HG02615.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2281A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2281 | chr16 | 48081434 | |||||
chr16:48081509
|
C | A | 3 | a0008c0008t0009a0008c0008t0010a0008c0008t0015 | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2206G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2206 | chr16 | 48081509 | |||||
chr16:48081579
|
T | A | 2 | a0004c0007t0003a0004c0013t0003 | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2136A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2136 | chr16 | 48081579 | |||||
chr16:48081660
|
C | T | 1 | a0010c0018t0011 | 2 | HG02723.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2055G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2055 | chr16 | 48081660 | |||||
chr16:48081670
|
G | A | 2 | a0006c0029t0018a0010c0018t0011 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2045C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 2045 | chr16 | 48081670 | |||||
chr16:48081879
|
T | C | 1 | a0008c0008t0010 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1836A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 1836 | chr16 | 48081879 | |||||
chr16:48082448
|
G | A | 1 | a0010c0026t0016 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 1267 | chr16 | 48082448 | |||||
chr16:48082498
|
C | T | 2 | a0017c0011t0006a0020c0023t0006 | 3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1217G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 1217 | chr16 | 48082498 | |||||
chr16:48082716
|
C | T | 1 | a0001c0004t0017 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 999 | chr16 | 48082716 | |||||
chr16:48082852
|
T | C | 3 | a0012c0020t0005a0014c0016t0005a0015c0015t0008 | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*863A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 863 | chr16 | 48082852 | |||||
chr16:48082854
|
A | G | 4 | a0008c0008t0009a0008c0008t0010a0008c0008t0015others(1): Show | 6 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*861T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 861 | chr16 | 48082854 | |||||
chr16:48083065
|
C | T | 2 | a0003c0003t0004a0003c0003t0014 | 8 | HG00558.hp1 HG02040.hp1 HG02129.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*650G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 650 | chr16 | 48083065 | |||||
chr16:48083178
|
A | T | 2 | a0001c0001t0013a0008c0008t0009 | 3 | HG02970.hp2 HG03453.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*537T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 537 | chr16 | 48083178 | |||||
chr16:48083185
|
T | A | 1 | a0002c0002t0019 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*530A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 530 | chr16 | 48083185 | |||||
chr16:48083269
|
G | A | 1 | a0002c0002t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 446 | chr16 | 48083269 | |||||
chr16:48083503
|
C | T | 4 | a0012c0020t0005a0014c0016t0005a0015c0015t0008others(1): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*212G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 212 | chr16 | 48083503 | |||||
chr16:48083505
|
G | A | 2 | a0004c0007t0003a0004c0013t0003 | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*210C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 210 | chr16 | 48083505 | |||||
chr16:48083712
|
C | T | 1 | a0023c0022t0012 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 31/31 | 3 | chr16 | 48083712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:48084125
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(115): Show | 133 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.3829-52G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084125 | ||||||
chr16:48084131
|
C | T | 23 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(20): Show | 26 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.3829-58G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084131 | ||||||
chr16:48084232
|
C | T | 1 | a0003c0003t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3829-159G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084232 | ||||||
chr16:48084300
|
T | C | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3829-227A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084300 | ||||||
chr16:48084437
|
TA | T | 14 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(11): Show | 17 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.3829-365delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084437 | ||||||
chr16:48084456
|
A | G | 17 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(14): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3829-383T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084456 | ||||||
chr16:48084948
|
G | A | 3 | a0017c0011t0006g0115a0017c0011t0006g0117a0020c0023t0006g0037 | 3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3828+645C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084948 | ||||||
chr16:48084991
|
A | T | 2 | a0008c0008t0010g0014a0008c0008t0010g0015 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3828+602T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48084991 | ||||||
chr16:48085177
|
G | A | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3828+416C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085177 | ||||||
chr16:48085185
|
T | C | 8 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039others(5): Show | 11 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3828+408A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085185 | ||||||
chr16:48085214
|
A | G | 8 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0048others(5): Show | 8 | HG00544.hp2 HG00735.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.3828+379T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085214 | ||||||
chr16:48085363
|
G | A | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3828+230C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085363 | ||||||
chr16:48085374
|
A | C | 17 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(14): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3828+219T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085374 | ||||||
chr16:48085396
|
G | A | 6 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(3): Show | 6 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3828+197C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085396 | ||||||
chr16:48085514
|
C | T | 6 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(3): Show | 6 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3828+79G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 29/30 | chr16 | 48085514 | ||||||
chr16:48086003
|
A | G | 24 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(21): Show | 27 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.3715-297T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086003 | ||||||
chr16:48086057
|
T | G | 1 | a0007c0006t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3715-351A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086057 | ||||||
chr16:48086253
|
G | A | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3714+488C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086253 | ||||||
chr16:48086525
|
T | A | 2 | a0006c0010t0002g0023a0006c0010t0002g0024 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3714+216A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086525 | ||||||
chr16:48086615
|
C | T | 1 | a0001c0004t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3714+126G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086615 | ||||||
chr16:48086671
|
A | T | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3714+70T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 28/30 | chr16 | 48086671 | ||||||
chr16:48086875
|
G | T | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3636-56C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48086875 | ||||||
chr16:48087182
|
T | C | 15 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(12): Show | 18 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3636-363A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087182 | ||||||
chr16:48087538
|
C | T | 31 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(28): Show | 35 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.3635+388G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087538 | ||||||
chr16:48087722
|
T | C | 8 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3635+204A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087722 | ||||||
chr16:48087757
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3635+169C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087757 | ||||||
chr16:48087794
|
C | T | 8 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3635+132G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087794 | ||||||
chr16:48087796
|
C | G | 1 | a0009c0009t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3635+130G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 27/30 | chr16 | 48087796 | ||||||
chr16:48088116
|
C | G | 2 | a0008c0008t0010g0014a0008c0008t0010g0015 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3476-31G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/30 | chr16 | 48088116 | ||||||
chr16:48088538
|
T | C | 8 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.3475+7A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 26/30 | chr16 | 48088538 | ||||||
chr16:48088990
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3286-256C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48088990 | ||||||
chr16:48089009
|
T | C | 12 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3286-275A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089009 | ||||||
chr16:48089109
|
G | A | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3286-375C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089109 | ||||||
chr16:48089414
|
A | C | 7 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(4): Show | 8 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.3286-680T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089414 | ||||||
chr16:48089668
|
A | T | 1 | a0004c0013t0003g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3286-934T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089668 | ||||||
chr16:48089945
|
T | G | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3285+1175A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089945 | ||||||
chr16:48089956
|
CAAG | C | 8 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3285+1161_3285+116 others(7): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089956 | ||||||
chr16:48089994
|
T | TA | 17 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(14): Show | 20 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.3285+1125dupT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48089994 | ||||||
chr16:48090079
|
T | C | 1 | a0022c0025t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3285+1041A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090079 | ||||||
chr16:48090278
|
A | C | 1 | a0022c0025t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3285+842T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090278 | ||||||
chr16:48090401
|
C | CT | 9 | a0001c0001t0013g0079a0002c0002t0020g0063a0006c0029t0018g0029others(6): Show | 10 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.3285+718dupA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090401 | ||||||
chr16:48090401
|
CT | C | 18 | a0003c0003t0004g0061a0003c0003t0004g0062a0004c0007t0003g0101others(15): Show | 21 | HG01884.hp1 HG01891.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.3285+718delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090401 | ||||||
chr16:48090655
|
C | T | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3285+465G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 25/30 | chr16 | 48090655 | ||||||
chr16:48091395
|
C | A | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3196-186G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091395 | ||||||
chr16:48091677
|
T | C | 1 | a0015c0015t0008g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3196-468A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091677 | ||||||
chr16:48091885
|
T | C | 8 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039others(5): Show | 11 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3196-676A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091885 | ||||||
chr16:48091897
|
C | T | 29 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(26): Show | 33 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.3196-688G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48091897 | ||||||
chr16:48092239
|
C | T | 1 | a0006c0021t0002g0026 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3196-1030G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092239 | ||||||
chr16:48092240
|
G | A | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3196-1031C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092240 | ||||||
chr16:48092277
|
G | C | 3 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0060 | 3 | HG01884.hp2 HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3196-1068C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092277 | ||||||
chr16:48092313
|
C | T | 26 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(23): Show | 30 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3196-1104G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092313 | ||||||
chr16:48092348
|
C | T | 1 | a0002c0002t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3196-1139G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092348 | ||||||
chr16:48092493
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3196-1284G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092493 | ||||||
chr16:48092621
|
G | T | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3196-1412C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092621 | ||||||
chr16:48092764
|
G | A | 8 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3196-1555C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092764 | ||||||
chr16:48092800
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(115): Show | 133 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.3196-1591A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092800 | ||||||
chr16:48092924
|
C | T | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3196-1715G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48092924 | ||||||
chr16:48093369
|
T | C | 1 | a0002c0002t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3196-2160A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48093369 | ||||||
chr16:48093497
|
C | T | 1 | a0006c0010t0002g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3196-2288G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48093497 | ||||||
chr16:48094070
|
T | C | 7 | a0002c0002t0001g0040a0005c0005t0001g0009a0005c0005t0001g0031others(4): Show | 8 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3195+2676A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094070 | ||||||
chr16:48094710
|
GA | G | 5 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(2): Show | 5 | HG01496.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3195+2035delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094710 | ||||||
chr16:48094764
|
C | T | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3195+1982G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094764 | ||||||
chr16:48094793
|
A | G | 9 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3195+1953T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48094793 | ||||||
chr16:48095177
|
G | A | 1 | a0023c0022t0012g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3195+1569C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095177 | ||||||
chr16:48095252
|
T | C | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3195+1494A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095252 | ||||||
chr16:48095290
|
A | C | 1 | a0001c0004t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3195+1456T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095290 | ||||||
chr16:48095341
|
GC | G | 20 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(17): Show | 25 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.3195+1404delG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095341 | ||||||
chr16:48095485
|
TA | T | 8 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0052others(5): Show | 8 | HG00544.hp1 HG00544.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.3195+1260delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48095485 | ||||||
chr16:48096391
|
A | C | 1 | a0002c0002t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3195+355T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 24/30 | chr16 | 48096391 | ||||||
chr16:48096913
|
C | T | 4 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(1): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3039-11G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48096913 | ||||||
chr16:48096923
|
C | T | 3 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0060 | 3 | HG01884.hp2 HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3039-21G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48096923 | ||||||
chr16:48097184
|
C | T | 1 | a0003c0003t0004g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3039-282G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097184 | ||||||
chr16:48097520
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3039-618C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097520 | ||||||
chr16:48097559
|
C | T | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3039-657G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097559 | ||||||
chr16:48097818
|
G | A | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3039-916C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097818 | ||||||
chr16:48097828
|
T | A | 9 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(6): Show | 11 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3039-926A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097828 | ||||||
chr16:48097930
|
G | C | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3039-1028C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097930 | ||||||
chr16:48097945
|
G | A | 1 | a0001c0004t0017g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3039-1043C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48097945 | ||||||
chr16:48098017
|
A | T | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3039-1115T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098017 | ||||||
chr16:48098090
|
G | GAC | 19 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0004t0001g0081others(16): Show | 20 | HG00558.hp1 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.3039-1190_3039-118 others(6): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | ||||||
chr16:48098090
|
G | GACACAC | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0018c0012t0007g0012 | 4 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3039-1194_3039-118 others(10): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | ||||||
chr16:48098090
|
GAC | G | 21 | a0001c0001t0001g0067a0001c0001t0001g0096a0002c0002t0001g0002others(18): Show | 24 | HG00735.hp2 HG01496.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.3039-1190_3039-118 others(6): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | ||||||
chr16:48098090
|
GACAC | G | 11 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0078others(8): Show | 11 | HG00544.hp1 HG00544.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3039-1192_3039-118 others(8): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | ||||||
chr16:48098090
|
GACACAC | G | 3 | a0001c0001t0001g0032a0008c0008t0010g0014a0008c0008t0010g0015 | 3 | HG02895.hp1 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3039-1194_3039-118 others(10): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | ||||||
chr16:48098090
|
GACACACA others(3): Show |
G | 1 | a0004c0007t0003g0104 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3039-1198_3039-118 others(14): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098090 | ||||||
chr16:48098130
|
CACACACA others(3): Show |
C | 1 | a0015c0015t0008g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3039-1238_3039-122 others(14): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098130 | ||||||
chr16:48098134
|
CACACAG | C | 1 | a0012c0020t0005g0007 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3039-1238_3039-123 others(10): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098134 | ||||||
chr16:48098140
|
G | C | 5 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039others(2): Show | 7 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3039-1238C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098140 | ||||||
chr16:48098340
|
C | G | 1 | a0011c0019t0001g0072 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3039-1438G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098340 | ||||||
chr16:48098494
|
C | G | 1 | a0001c0004t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3039-1592G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098494 | ||||||
chr16:48098538
|
CA | C | 2 | a0003c0003t0004g0061a0003c0003t0004g0062 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.3039-1637delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098538 | ||||||
chr16:48098936
|
C | T | 13 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(10): Show | 14 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3038+1936G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098936 | ||||||
chr16:48098960
|
T | A | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3038+1912A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48098960 | ||||||
chr16:48099008
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3038+1864C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099008 | ||||||
chr16:48099305
|
G | A | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3038+1567C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099305 | ||||||
chr16:48099464
|
T | G | 1 | a0001c0004t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3038+1408A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099464 | ||||||
chr16:48099831
|
C | A | 1 | a0002c0002t0001g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3038+1041G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099831 | ||||||
chr16:48099962
|
C | CT | 13 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(10): Show | 16 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3038+909dupA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48099962 | ||||||
chr16:48100148
|
T | C | 5 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(2): Show | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3038+724A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100148 | ||||||
chr16:48100351
|
G | T | 6 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(3): Show | 6 | HG01496.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3038+521C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100351 | ||||||
chr16:48100496
|
A | T | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3038+376T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100496 | ||||||
chr16:48100672
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3038+200G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 23/30 | chr16 | 48100672 | ||||||
chr16:48101154
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2901-145G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101154 | ||||||
chr16:48101210
|
G | C | 1 | a0002c0002t0001g0048 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2901-201C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101210 | ||||||
chr16:48101587
|
C | T | 5 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2901-578G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101587 | ||||||
chr16:48101755
|
A | T | 11 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(8): Show | 11 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2901-746T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48101755 | ||||||
chr16:48102068
|
A | T | 11 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(8): Show | 11 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2901-1059T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102068 | ||||||
chr16:48102094
|
C | T | 3 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027 | 3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2901-1085G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102094 | ||||||
chr16:48102117
|
A | G | 1 | a0008c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2901-1108T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102117 | ||||||
chr16:48102368
|
T | A | 2 | a0008c0008t0010g0014a0008c0008t0010g0015 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2901-1359A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102368 | ||||||
chr16:48102558
|
C | A | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2901-1549G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102558 | ||||||
chr16:48102562
|
G | A | 1 | a0002c0002t0019g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2901-1553C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102562 | ||||||
chr16:48102880
|
C | T | 1 | a0021c0024t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2900+1262G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102880 | ||||||
chr16:48102881
|
G | C | 3 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027 | 3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2900+1261C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48102881 | ||||||
chr16:48103208
|
C | T | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2900+934G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103208 | ||||||
chr16:48103337
|
G | C | 13 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(10): Show | 14 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2900+805C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103337 | ||||||
chr16:48103489
|
T | C | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2900+653A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103489 | ||||||
chr16:48103644
|
A | G | 34 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(31): Show | 38 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.2900+498T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103644 | ||||||
chr16:48103794
|
C | T | 4 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2900+348G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103794 | ||||||
chr16:48103811
|
C | A | 2 | a0010c0018t0011g0021a0010c0018t0011g0039 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2900+331G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103811 | ||||||
chr16:48103975
|
G | A | 4 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2900+167C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48103975 | ||||||
chr16:48104040
|
G | C | 1 | a0006c0021t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2900+102C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 22/30 | chr16 | 48104040 | ||||||
chr16:48104408
|
G | A | 2 | a0004c0007t0003g0102a0004c0007t0003g0103 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2674-40C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104408 | ||||||
chr16:48104445
|
T | C | 2 | a0001c0001t0001g0067a0003c0003t0014g0068 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2674-77A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104445 | ||||||
chr16:48104595
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0089 | 2 | HG01496.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2674-227G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104595 | ||||||
chr16:48104604
|
C | G | 1 | a0006c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2674-236G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104604 | ||||||
chr16:48104655
|
C | T | 1 | a0006c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2674-287G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104655 | ||||||
chr16:48104806
|
G | A | 3 | a0001c0001t0001g0075a0001c0004t0001g0098a0001c0004t0001g0099 | 3 | HG01074.hp2 HG01255.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2673+333C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 21/30 | chr16 | 48104806 | ||||||
chr16:48105403
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2476-67C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105403 | ||||||
chr16:48105419
|
G | A | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476-83C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105419 | ||||||
chr16:48105615
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2476-279A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105615 | ||||||
chr16:48105617
|
C | T | 2 | a0011c0019t0001g0072a0011c0019t0001g0073 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2476-281G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105617 | ||||||
chr16:48105633
|
C | T | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476-297G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105633 | ||||||
chr16:48105916
|
G | A | 3 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027 | 3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2476-580C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48105916 | ||||||
chr16:48106140
|
T | A | 1 | a0002c0002t0019g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2476-804A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106140 | ||||||
chr16:48106326
|
G | A | 3 | a0017c0011t0006g0115a0017c0011t0006g0117a0020c0023t0006g0037 | 3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2476-990C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106326 | ||||||
chr16:48106343
|
T | C | 7 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(4): Show | 7 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2475+979A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106343 | ||||||
chr16:48106392
|
G | A | 3 | a0017c0011t0006g0115a0017c0011t0006g0117a0020c0023t0006g0037 | 3 | HG02717.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2475+930C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106392 | ||||||
chr16:48106712
|
C | T | 31 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(28): Show | 35 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.2475+610G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106712 | ||||||
chr16:48106778
|
A | G | 9 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(6): Show | 10 | HG01891.hp2 HG02258.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2475+544T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106778 | ||||||
chr16:48106917
|
A | T | 1 | a0001c0004t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2475+405T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106917 | ||||||
chr16:48106948
|
G | A | 3 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027 | 3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2475+374C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48106948 | ||||||
chr16:48107196
|
C | T | 2 | a0008c0008t0010g0014a0008c0008t0010g0015 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2475+126G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 20/30 | chr16 | 48107196 | ||||||
chr16:48107446
|
C | T | 1 | a0002c0002t0020g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2372-21G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48107446 | ||||||
chr16:48107578
|
T | A | 8 | a0012c0020t0005g0007a0014c0016t0005g0004a0015c0015t0008g0041others(5): Show | 11 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2372-153A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48107578 | ||||||
chr16:48108200
|
C | T | 2 | a0016c0017t0002g0109a0016c0017t0002g0111 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2371+240G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108200 | ||||||
chr16:48108245
|
T | A | 2 | a0002c0002t0001g0002a0002c0002t0001g0013 | 4 | HG02486.hp1 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371+195A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108245 | ||||||
chr16:48108282
|
C | T | 4 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371+158G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108282 | ||||||
chr16:48108366
|
C | T | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2371+74G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 19/30 | chr16 | 48108366 | ||||||
chr16:48108630
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2282-101C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108630 | ||||||
chr16:48108790
|
A | G | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2282-261T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108790 | ||||||
chr16:48108830
|
C | T | 7 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(4): Show | 7 | HG01496.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2282-301G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108830 | ||||||
chr16:48108863
|
T | C | 4 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2282-334A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48108863 | ||||||
chr16:48109493
|
C | T | 1 | a0002c0002t0001g0006 | 2 | HG01255.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2282-964G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109493 | ||||||
chr16:48109726
|
C | T | 1 | a0002c0002t0001g0058 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2282-1197G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109726 | ||||||
chr16:48109787
|
C | T | 4 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2282-1258G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109787 | ||||||
chr16:48109835
|
C | T | 2 | a0016c0017t0002g0109a0016c0017t0002g0111 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2282-1306G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109835 | ||||||
chr16:48109900
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2282-1371C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109900 | ||||||
chr16:48109927
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0013g0079 | 3 | HG03017.hp2 HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2282-1398C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109927 | ||||||
chr16:48109941
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2282-1412G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109941 | ||||||
chr16:48109942
|
G | A | 4 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2282-1413C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48109942 | ||||||
chr16:48110024
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2281+1412C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110024 | ||||||
chr16:48110027
|
G | T | 1 | a0017c0011t0006g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2281+1409C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110027 | ||||||
chr16:48110072
|
G | A | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2281+1364C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110072 | ||||||
chr16:48110175
|
G | A | 3 | a0002c0002t0001g0002a0002c0002t0001g0013a0002c0002t0001g0022 | 5 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2281+1261C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110175 | ||||||
chr16:48110233
|
TCTTTCCC others(1): Show |
T | 4 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2281+1195_2281+120 others(12): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110233 | ||||||
chr16:48110303
|
A | C | 1 | a0002c0002t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2281+1133T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110303 | ||||||
chr16:48110322
|
T | C | 2 | a0001c0001t0001g0067a0003c0003t0014g0068 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2281+1114A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110322 | ||||||
chr16:48110585
|
C | A | 8 | a0007c0006t0001g0011a0007c0006t0001g0091a0007c0006t0001g0093others(5): Show | 9 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2281+851G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110585 | ||||||
chr16:48110673
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2281+763G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110673 | ||||||
chr16:48110726
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(103): Show | 120 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.2281+710C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110726 | ||||||
chr16:48110770
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(114): Show | 132 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2281+666T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110770 | ||||||
chr16:48110778
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(74): Show | 87 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.2281+658A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110778 | ||||||
chr16:48110996
|
G | A | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2281+440C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48110996 | ||||||
chr16:48111089
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2281+347T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48111089 | ||||||
chr16:48111097
|
T | C | 1 | a0006c0010t0002g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2281+339A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48111097 | ||||||
chr16:48111113
|
T | A | 1 | a0001c0001t0013g0079 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2281+323A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 18/30 | chr16 | 48111113 | ||||||
chr16:48111674
|
A | G | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2125-12T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/30 | chr16 | 48111674 | ||||||
chr16:48111738
|
G | T | 38 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(35): Show | 42 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.2124+38C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 16/30 | chr16 | 48111738 | ||||||
chr16:48112049
|
A | T | 1 | a0006c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1990-139T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112049 | ||||||
chr16:48112088
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1990-178A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112088 | ||||||
chr16:48112118
|
C | T | 1 | a0006c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1990-208G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112118 | ||||||
chr16:48112350
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1990-440G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112350 | ||||||
chr16:48112376
|
A | G | 21 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(18): Show | 24 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1990-466T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112376 | ||||||
chr16:48112527
|
G | A | 2 | a0015c0015t0008g0041a0015c0015t0008g0112 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1990-617C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112527 | ||||||
chr16:48112604
|
A | C | 2 | a0002c0002t0001g0044a0010c0026t0016g0084 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1990-694T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112604 | ||||||
chr16:48112773
|
G | A | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1990-863C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112773 | ||||||
chr16:48112980
|
G | C | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1990-1070C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48112980 | ||||||
chr16:48113362
|
T | C | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1990-1452A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113362 | ||||||
chr16:48113377
|
C | A | 1 | a0006c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1990-1467G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113377 | ||||||
chr16:48113444
|
T | C | 2 | a0017c0011t0006g0115a0017c0011t0006g0117 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1990-1534A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113444 | ||||||
chr16:48113491
|
C | T | 4 | a0002c0002t0020g0063a0013c0014t0001g0106a0013c0014t0001g0107others(1): Show | 4 | HG02717.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1990-1581G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113491 | ||||||
chr16:48113530
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1990-1620A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113530 | ||||||
chr16:48113608
|
G | A | 2 | a0017c0011t0006g0115a0017c0011t0006g0117 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1990-1698C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113608 | ||||||
chr16:48113815
|
C | T | 2 | a0017c0011t0006g0115a0017c0011t0006g0117 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1989+1600G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113815 | ||||||
chr16:48113941
|
C | A | 1 | a0006c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1989+1474G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48113941 | ||||||
chr16:48114479
|
A | G | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989+936T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114479 | ||||||
chr16:48114588
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1989+827C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114588 | ||||||
chr16:48114647
|
C | G | 3 | a0006c0021t0002g0025a0006c0021t0002g0026a0024c0028t0002g0018 | 3 | HG01496.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1989+768G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114647 | ||||||
chr16:48114857
|
A | G | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989+558T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48114857 | ||||||
chr16:48115345
|
A | G | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989+70T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 15/30 | chr16 | 48115345 | ||||||
chr16:48115702
|
A | T | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1786-84T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115702 | ||||||
chr16:48115803
|
T | C | 1 | a0002c0002t0020g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1786-185A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115803 | ||||||
chr16:48115859
|
C | T | 2 | a0016c0017t0002g0109a0022c0025t0001g0110 | 2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1786-241G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115859 | ||||||
chr16:48115874
|
T | G | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1786-256A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48115874 | ||||||
chr16:48116172
|
A | C | 4 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786-554T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116172 | ||||||
chr16:48116328
|
G | A | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786-710C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116328 | ||||||
chr16:48116400
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(115): Show | 133 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.1786-782C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116400 | ||||||
chr16:48116642
|
T | G | 6 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(3): Show | 7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+619A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116642 | ||||||
chr16:48116733
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1785+528T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116733 | ||||||
chr16:48116756
|
A | G | 6 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(3): Show | 7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+505T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48116756 | ||||||
chr16:48117075
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1785+186C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117075 | ||||||
chr16:48117123
|
T | C | 38 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(35): Show | 42 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1785+138A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117123 | ||||||
chr16:48117149
|
C | T | 6 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(3): Show | 7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+112G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117149 | ||||||
chr16:48117219
|
T | C | 6 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(3): Show | 7 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+42A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117219 | ||||||
chr16:48117254
|
C | T | 2 | a0004c0007t0003g0104a0004c0007t0003g0105 | 2 | HG02109.hp1 HG02559.hp2 |
splice_region_variant&intron_variant | LOW | c.1785+7G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 14/30 | chr16 | 48117254 | ||||||
chr16:48117374
|
C | T | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1713-41G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117374 | ||||||
chr16:48117452
|
T | C | 25 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(22): Show | 29 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713-119A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117452 | ||||||
chr16:48117552
|
G | C | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1713-219C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117552 | ||||||
chr16:48117578
|
T | C | 27 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(24): Show | 31 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1713-245A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117578 | ||||||
chr16:48117639
|
G | C | 30 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(27): Show | 34 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1713-306C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117639 | ||||||
chr16:48117694
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1713-361C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117694 | ||||||
chr16:48117877
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1713-544A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48117877 | ||||||
chr16:48118108
|
C | T | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1713-775G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118108 | ||||||
chr16:48118173
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1713-840G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118173 | ||||||
chr16:48118223
|
G | T | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1713-890C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118223 | ||||||
chr16:48118334
|
C | A | 2 | a0010c0018t0011g0021a0010c0018t0011g0039 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1713-1001G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118334 | ||||||
chr16:48118842
|
G | C | 2 | a0006c0021t0002g0025a0006c0021t0002g0026 | 2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1713-1509C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48118842 | ||||||
chr16:48119297
|
T | C | 2 | a0001c0001t0001g0053a0002c0002t0001g0006 | 3 | HG01255.hp1 HG01256.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1713-1964A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48119297 | ||||||
chr16:48119664
|
C | T | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1712+2052G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48119664 | ||||||
chr16:48120136
|
T | C | 1 | a0008c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1712+1580A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120136 | ||||||
chr16:48120551
|
G | T | 1 | a0008c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1712+1165C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120551 | ||||||
chr16:48120558
|
GT | G | 39 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(36): Show | 43 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1712+1157delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120558 | ||||||
chr16:48120587
|
G | T | 2 | a0015c0015t0008g0041a0015c0015t0008g0112 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1712+1129C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120587 | ||||||
chr16:48120833
|
C | T | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1712+883G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48120833 | ||||||
chr16:48121017
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1712+699G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121017 | ||||||
chr16:48121224
|
T | C | 3 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027 | 3 | HG02647.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1712+492A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121224 | ||||||
chr16:48121489
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1712+227G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121489 | ||||||
chr16:48121534
|
C | T | 32 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(29): Show | 36 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1712+182G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121534 | ||||||
chr16:48121535
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1712+181C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121535 | ||||||
chr16:48121636
|
T | A | 1 | a0006c0021t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1712+80A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 13/30 | chr16 | 48121636 | ||||||
chr16:48122380
|
C | T | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1588-540G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122380 | ||||||
chr16:48122381
|
A | T | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1588-541T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122381 | ||||||
chr16:48122522
|
G | A | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1588-682C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122522 | ||||||
chr16:48122531
|
C | T | 2 | a0001c0001t0001g0053a0002c0002t0001g0006 | 3 | HG01255.hp1 HG01256.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1588-691G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122531 | ||||||
chr16:48122568
|
A | C | 3 | a0006c0029t0018g0029a0010c0018t0011g0021a0010c0018t0011g0039 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1588-728T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122568 | ||||||
chr16:48122605
|
C | T | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-765G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122605 | ||||||
chr16:48122943
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1588-1103C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48122943 | ||||||
chr16:48123082
|
C | T | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1587+1131G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123082 | ||||||
chr16:48123225
|
A | G | 19 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(16): Show | 22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1587+988T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123225 | ||||||
chr16:48123304
|
C | T | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1587+909G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123304 | ||||||
chr16:48123591
|
G | T | 2 | a0001c0001t0001g0067a0003c0003t0014g0068 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1587+622C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 12/30 | chr16 | 48123591 | ||||||
chr16:48124352
|
GC | G | 2 | a0004c0007t0003g0104a0004c0007t0003g0105 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1516-69delG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48124352 | ||||||
chr16:48125370
|
C | T | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1516-1086G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48125370 | ||||||
chr16:48125388
|
T | C | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1516-1104A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48125388 | ||||||
chr16:48125540
|
C | G | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1516-1256G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48125540 | ||||||
chr16:48126231
|
C | T | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1516-1947G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126231 | ||||||
chr16:48126260
|
T | C | 1 | a0002c0002t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1516-1976A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126260 | ||||||
chr16:48126499
|
C | T | 19 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(16): Show | 22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515+1960G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126499 | ||||||
chr16:48126517
|
G | A | 1 | a0001c0004t0017g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1515+1942C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126517 | ||||||
chr16:48126525
|
T | A | 13 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(10): Show | 14 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1515+1934A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126525 | ||||||
chr16:48126749
|
C | G | 2 | a0002c0002t0001g0055a0002c0002t0001g0056 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1515+1710G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126749 | ||||||
chr16:48126754
|
G | C | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+1705C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126754 | ||||||
chr16:48126919
|
C | A | 2 | a0015c0015t0008g0041a0015c0015t0008g0112 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1515+1540G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48126919 | ||||||
chr16:48127008
|
T | C | 19 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(16): Show | 22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515+1451A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127008 | ||||||
chr16:48127064
|
T | C | 9 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(6): Show | 9 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515+1395A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127064 | ||||||
chr16:48127143
|
C | G | 6 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(3): Show | 7 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515+1316G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127143 | ||||||
chr16:48127245
|
C | T | 1 | a0023c0022t0012g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1515+1214G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127245 | ||||||
chr16:48127360
|
C | T | 1 | a0006c0021t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1515+1099G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127360 | ||||||
chr16:48127731
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1515+728T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127731 | ||||||
chr16:48127806
|
T | C | 1 | a0008c0008t0009g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1515+653A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127806 | ||||||
chr16:48127997
|
T | C | 13 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1515+462A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48127997 | ||||||
chr16:48128160
|
C | G | 19 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(16): Show | 22 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1515+299G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 11/30 | chr16 | 48128160 | ||||||
chr16:48128889
|
G | T | 2 | a0006c0021t0002g0025a0006c0021t0002g0026 | 2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1237-152C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48128889 | ||||||
chr16:48128921
|
A | G | 13 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(10): Show | 14 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1237-184T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48128921 | ||||||
chr16:48129348
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1237-611G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129348 | ||||||
chr16:48129624
|
G | A | 10 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(7): Show | 11 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237-887C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129624 | ||||||
chr16:48129625
|
T | C | 1 | a0005c0005t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1237-888A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129625 | ||||||
chr16:48129895
|
T | C | 5 | a0004c0013t0003g0108a0004c0013t0003g0114a0016c0017t0002g0109others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+893A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48129895 | ||||||
chr16:48130062
|
G | A | 16 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(13): Show | 19 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1236+726C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130062 | ||||||
chr16:48130093
|
A | G | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1236+695T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130093 | ||||||
chr16:48130465
|
T | C | 1 | a0002c0002t0001g0038 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1236+323A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130465 | ||||||
chr16:48130553
|
A | G | 2 | a0010c0018t0011g0021a0010c0018t0011g0039 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1236+235T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130553 | ||||||
chr16:48130573
|
T | C | 22 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(19): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1236+215A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 10/30 | chr16 | 48130573 | ||||||
chr16:48131003
|
G | A | 22 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(19): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129-108C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131003 | ||||||
chr16:48131093
|
T | C | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1129-198A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131093 | ||||||
chr16:48131457
|
A | G | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1129-562T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131457 | ||||||
chr16:48131594
|
A | G | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1129-699T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131594 | ||||||
chr16:48131667
|
A | G | 22 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(19): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129-772T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131667 | ||||||
chr16:48131778
|
C | G | 17 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(14): Show | 18 | HG01496.hp2 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1129-883G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131778 | ||||||
chr16:48131936
|
C | T | 11 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(8): Show | 12 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1129-1041G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48131936 | ||||||
chr16:48132140
|
T | C | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1129-1245A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132140 | ||||||
chr16:48132345
|
A | T | 2 | a0004c0013t0003g0108a0004c0013t0003g0114 | 2 | HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1128+1342T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132345 | ||||||
chr16:48132515
|
TTCTC | T | 1 | a0014c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+1168_1128+117 others(8): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132515 | ||||||
chr16:48132716
|
C | T | 2 | a0017c0011t0006g0115a0017c0011t0006g0117 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1128+971G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132716 | ||||||
chr16:48132766
|
G | A | 22 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(19): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1128+921C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132766 | ||||||
chr16:48132793
|
A | G | 1 | a0014c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+894T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48132793 | ||||||
chr16:48133357
|
T | C | 9 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0091others(6): Show | 10 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1128+330A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133357 | ||||||
chr16:48133482
|
C | T | 22 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(19): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1128+205G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133482 | ||||||
chr16:48133527
|
G | GA | 10 | a0007c0006t0001g0011a0007c0006t0001g0090a0007c0006t0001g0093others(7): Show | 13 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1128+159dupT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133527 | ||||||
chr16:48133527
|
GA | G | 5 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+159delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133527 | ||||||
chr16:48133663
|
C | G | 22 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(19): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1128+24G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 9/30 | chr16 | 48133663 | ||||||
chr16:48133933
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0040 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.980-98G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48133933 | ||||||
chr16:48134058
|
T | G | 3 | a0001c0001t0001g0049a0002c0002t0001g0051a0002c0002t0019g0050 | 3 | HG00544.hp2 HG02083.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.980-223A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134058 | ||||||
chr16:48134295
|
C | T | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.980-460G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134295 | ||||||
chr16:48134324
|
T | A | 1 | a0023c0022t0012g0028 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.980-489A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134324 | ||||||
chr16:48134659
|
G | A | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-824C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134659 | ||||||
chr16:48134747
|
C | G | 1 | a0024c0028t0002g0018 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980-912G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134747 | ||||||
chr16:48134890
|
A | C | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1055T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134890 | ||||||
chr16:48134926
|
C | A | 6 | a0005c0005t0001g0009a0005c0005t0001g0031a0005c0005t0001g0042others(3): Show | 7 | HG02258.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.980-1091G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48134926 | ||||||
chr16:48135023
|
G | A | 2 | a0006c0021t0002g0025a0006c0021t0002g0026 | 2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.980-1188C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135023 | ||||||
chr16:48135049
|
C | CA | 4 | a0001c0001t0001g0082a0008c0008t0009g0005a0008c0008t0010g0015others(1): Show | 5 | HG00735.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-1215dupT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135049 | ||||||
chr16:48135283
|
C | T | 1 | a0014c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.980-1448G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135283 | ||||||
chr16:48135543
|
G | T | 1 | a0010c0026t0016g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.980-1708C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135543 | ||||||
chr16:48135609
|
T | C | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1774A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135609 | ||||||
chr16:48135611
|
T | C | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.980-1776A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135611 | ||||||
chr16:48135739
|
T | A | 2 | a0010c0018t0011g0021a0010c0018t0011g0039 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.980-1904A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135739 | ||||||
chr16:48135960
|
G | A | 3 | a0016c0017t0002g0109a0016c0017t0002g0111a0022c0025t0001g0110 | 3 | HG01891.hp1 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.980-2125C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48135960 | ||||||
chr16:48136108
|
G | T | 1 | a0002c0002t0001g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.979+2120C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136108 | ||||||
chr16:48136173
|
A | T | 1 | a0006c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.979+2055T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136173 | ||||||
chr16:48136390
|
C | G | 4 | a0008c0008t0009g0005a0008c0008t0010g0014a0008c0008t0010g0015others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1838G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136390 | ||||||
chr16:48136761
|
G | A | 2 | a0010c0018t0011g0021a0010c0018t0011g0039 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.979+1467C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136761 | ||||||
chr16:48136851
|
C | T | 2 | a0018c0012t0007g0012a0023c0022t0012g0028 | 3 | HG02280.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.979+1377G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48136851 | ||||||
chr16:48137021
|
A | G | 39 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(36): Show | 43 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.979+1207T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137021 | ||||||
chr16:48137050
|
C | T | 10 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(7): Show | 11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+1178G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137050 | ||||||
chr16:48137132
|
G | GC | 21 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(18): Show | 23 | HG01496.hp2 HG01891.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.979+1095dupG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137132 | ||||||
chr16:48137581
|
C | T | 2 | a0018c0012t0007g0012a0023c0022t0012g0028 | 3 | HG02280.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.979+647G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137581 | ||||||
chr16:48137802
|
T | C | 11 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(8): Show | 12 | HG01496.hp2 HG02622.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.979+426A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137802 | ||||||
chr16:48137827
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.979+401T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137827 | ||||||
chr16:48137943
|
GT | G | 10 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(7): Show | 11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+284delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 8/30 | chr16 | 48137943 | ||||||
chr16:48138787
|
C | T | 2 | a0004c0007t0003g0104a0004c0007t0003g0105 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.831+376G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138787 | ||||||
chr16:48138805
|
AT | A | 35 | a0004c0007t0003g0104a0004c0007t0003g0105a0004c0013t0003g0108others(32): Show | 39 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.831+357delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138805 | ||||||
chr16:48138973
|
CAAAAACA others(5): Show |
C | 18 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(15): Show | 20 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+178_831+189del others(12): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138973 | ||||||
chr16:48138992
|
AAAAC | A | 4 | a0001c0004t0001g0083a0006c0010t0002g0023a0006c0010t0002g0024others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+167_831+170del others(4): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 7/30 | chr16 | 48138992 | ||||||
chr16:48139444
|
C | T | 2 | a0018c0012t0007g0012a0023c0022t0012g0028 | 3 | HG02280.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.658-108G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139444 | ||||||
chr16:48139470
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0032others(29): Show | 36 | HG00544.hp1 HG00558.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.658-134C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139470 | ||||||
chr16:48139493
|
T | C | 28 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(25): Show | 31 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.658-157A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139493 | ||||||
chr16:48139520
|
T | C | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.658-184A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139520 | ||||||
chr16:48139627
|
C | A | 1 | a0014c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.658-291G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139627 | ||||||
chr16:48139794
|
A | C | 17 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(14): Show | 20 | HG01496.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.658-458T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139794 | ||||||
chr16:48139910
|
CATG | C | 17 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(14): Show | 19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.658-577_658-575del others(3): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139910 | ||||||
chr16:48139918
|
C | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.658-582G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139918 | ||||||
chr16:48139973
|
G | A | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.658-637C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48139973 | ||||||
chr16:48140036
|
T | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+651A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140036 | ||||||
chr16:48140136
|
C | T | 4 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+551G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140136 | ||||||
chr16:48140176
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+511T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140176 | ||||||
chr16:48140243
|
T | TAAGGATT others(8): Show |
16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+443_657+444ins others(15): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140243 | ||||||
chr16:48140421
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+266G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140421 | ||||||
chr16:48140453
|
C | T | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+234G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140453 | ||||||
chr16:48140523
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.657+164C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140523 | ||||||
chr16:48140648
|
G | A | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.657+39C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 6/30 | chr16 | 48140648 | ||||||
chr16:48140938
|
G | C | 1 | a0003c0003t0004g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.424-18C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 5/30 | chr16 | 48140938 | ||||||
chr16:48141368
|
CAG | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-17_276-16delCT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141368 | ||||||
chr16:48141444
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.276-91G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141444 | ||||||
chr16:48141667
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-314C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141667 | ||||||
chr16:48141943
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-590T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141943 | ||||||
chr16:48141944
|
T | A | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-591A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48141944 | ||||||
chr16:48142097
|
C | T | 1 | a0006c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.276-744G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142097 | ||||||
chr16:48142098
|
C | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-745G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142098 | ||||||
chr16:48142182
|
CT | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-830delA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142182 | ||||||
chr16:48142184
|
A | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-831T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142184 | ||||||
chr16:48142277
|
T | C | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.276-924A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142277 | ||||||
chr16:48142319
|
C | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-966G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142319 | ||||||
chr16:48142322
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-969G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142322 | ||||||
chr16:48142328
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-975A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142328 | ||||||
chr16:48142336
|
G | C | 17 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(14): Show | 19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.276-983C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142336 | ||||||
chr16:48142382
|
T | A | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.276-1029A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142382 | ||||||
chr16:48142385
|
A | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-1032T>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142385 | ||||||
chr16:48142585
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.276-1232C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142585 | ||||||
chr16:48142618
|
G | C | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-1265C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142618 | ||||||
chr16:48142732
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+1178G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142732 | ||||||
chr16:48142864
|
A | G | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+1046T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142864 | ||||||
chr16:48142950
|
C | T | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.275+960G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48142950 | ||||||
chr16:48143151
|
G | T | 17 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(14): Show | 19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.275+759C>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143151 | ||||||
chr16:48143160
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+750T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143160 | ||||||
chr16:48143233
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.275+677G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143233 | ||||||
chr16:48143309
|
T | C | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.275+601A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143309 | ||||||
chr16:48143377
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.275+533G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143377 | ||||||
chr16:48143422
|
T | G | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.275+488A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143422 | ||||||
chr16:48143651
|
T | A | 17 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(14): Show | 19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.275+259A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143651 | ||||||
chr16:48143720
|
C | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+190G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143720 | ||||||
chr16:48143787
|
C | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.275+123G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 4/30 | chr16 | 48143787 | ||||||
chr16:48144300
|
A | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-235T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144300 | ||||||
chr16:48144351
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-286A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144351 | ||||||
chr16:48144436
|
C | A | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.120-371G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144436 | ||||||
chr16:48144484
|
C | A | 17 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(14): Show | 19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.120-419G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144484 | ||||||
chr16:48144561
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.120-496G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144561 | ||||||
chr16:48144651
|
T | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-586A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144651 | ||||||
chr16:48144665
|
C | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-600G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144665 | ||||||
chr16:48144868
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-803T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144868 | ||||||
chr16:48144910
|
A | G | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.120-845T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144910 | ||||||
chr16:48144962
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-897C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48144962 | ||||||
chr16:48145033
|
T | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-968A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145033 | ||||||
chr16:48145071
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-1006G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145071 | ||||||
chr16:48145134
|
A | G | 1 | a0014c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.120-1069T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145134 | ||||||
chr16:48145243
|
G | A | 2 | a0017c0011t0006g0115a0017c0011t0006g0117 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.119+1063C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145243 | ||||||
chr16:48145266
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+1040C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145266 | ||||||
chr16:48145380
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+926A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145380 | ||||||
chr16:48145496
|
C | A | 1 | a0002c0002t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.119+810G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145496 | ||||||
chr16:48145663
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+643T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145663 | ||||||
chr16:48145701
|
G | A | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+605C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145701 | ||||||
chr16:48145712
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+594G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145712 | ||||||
chr16:48145749
|
C | T | 1 | a0007c0006t0001g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.119+557G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48145749 | ||||||
chr16:48146072
|
T | C | 17 | a0004c0013t0003g0108a0004c0013t0003g0114a0007c0006t0001g0011others(14): Show | 19 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.119+234A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146072 | ||||||
chr16:48146072
|
T | TC | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+233dupG | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146072 | ||||||
chr16:48146171
|
C | T | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.119+135G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146171 | ||||||
chr16:48146199
|
C | T | 6 | a0001c0001t0001g0049a0002c0002t0001g0046a0002c0002t0001g0047others(3): Show | 6 | HG00544.hp2 HG00735.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+107G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146199 | ||||||
chr16:48146209
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+97C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146209 | ||||||
chr16:48146287
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+19A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146287 | ||||||
chr16:48146288
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.119+18C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 3/30 | chr16 | 48146288 | ||||||
chr16:48146480
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.-50-6C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146480 | ||||||
chr16:48146941
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-50-467G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146941 | ||||||
chr16:48146942
|
G | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-468C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146942 | ||||||
chr16:48146949
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-475C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146949 | ||||||
chr16:48146970
|
C | T | 1 | a0006c0029t0018g0029 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-50-496G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146970 | ||||||
chr16:48146975
|
A | G | 2 | a0006c0010t0002g0023a0006c0010t0002g0024 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-50-501T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48146975 | ||||||
chr16:48147028
|
T | G | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-554A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147028 | ||||||
chr16:48147069
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-595C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147069 | ||||||
chr16:48147082
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-608T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147082 | ||||||
chr16:48147090
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-616A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147090 | ||||||
chr16:48147382
|
G | A | 17 | a0001c0001t0001g0087a0006c0010t0002g0023a0006c0010t0002g0024others(14): Show | 19 | HG01496.hp2 HG02109.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50-908C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147382 | ||||||
chr16:48147439
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-965C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147439 | ||||||
chr16:48147446
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-972G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147446 | ||||||
chr16:48147448
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-50-974A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147448 | ||||||
chr16:48147708
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1234G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147708 | ||||||
chr16:48147812
|
G | A | 1 | a0018c0012t0007g0012 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-50-1338C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147812 | ||||||
chr16:48147843
|
G | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1369C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147843 | ||||||
chr16:48147956
|
G | GGTT | 43 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(40): Show | 48 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.-50-1485_-50-1483d others(5): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48147956 | ||||||
chr16:48148134
|
G | C | 1 | a0003c0003t0001g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-50-1660C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148134 | ||||||
chr16:48148165
|
A | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1691T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148165 | ||||||
chr16:48148227
|
C | T | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1753G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148227 | ||||||
chr16:48148237
|
CA | C | 23 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(20): Show | 26 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-50-1764delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148237 | ||||||
chr16:48148237
|
CAA | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-1765_-50-1764d others(4): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148237 | ||||||
chr16:48148348
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-50-1874G>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148348 | ||||||
chr16:48148524
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2050A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148524 | ||||||
chr16:48148536
|
T | C | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2062A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148536 | ||||||
chr16:48148596
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2122T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148596 | ||||||
chr16:48148602
|
G | A | 33 | a0004c0013t0003g0108a0004c0013t0003g0114a0006c0010t0002g0023others(30): Show | 37 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-50-2128C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148602 | ||||||
chr16:48148911
|
T | A | 37 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(34): Show | 41 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.-50-2437A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148911 | ||||||
chr16:48148945
|
C | T | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-2471G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148945 | ||||||
chr16:48148964
|
A | G | 1 | a0003c0003t0004g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-50-2490T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148964 | ||||||
chr16:48148966
|
C | T | 1 | a0002c0002t0001g0044 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50-2492G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148966 | ||||||
chr16:48148967
|
G | A | 27 | a0004c0013t0003g0108a0004c0013t0003g0114a0006c0010t0002g0023others(24): Show | 30 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-50-2493C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148967 | ||||||
chr16:48148970
|
A | G | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2496T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48148970 | ||||||
chr16:48149014
|
T | A | 16 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(13): Show | 18 | HG01496.hp2 HG02109.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50-2540A>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149014 | ||||||
chr16:48149040
|
T | C | 1 | a0002c0002t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-50-2566A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149040 | ||||||
chr16:48149146
|
T | C | 2 | a0001c0001t0001g0096a0002c0002t0001g0097 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-50-2672A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149146 | ||||||
chr16:48149244
|
CA | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0043a0005c0005t0001g0042others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-2771delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149244 | ||||||
chr16:48149244
|
CAA | C | 13 | a0004c0013t0003g0108a0004c0013t0003g0114a0013c0014t0001g0106others(10): Show | 15 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-50-2772_-50-2771d others(4): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149244 | ||||||
chr16:48149244
|
CAAA | C | 6 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-2773_-50-2771d others(5): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149244 | ||||||
chr16:48149263
|
AG | A | 14 | a0006c0010t0002g0023a0006c0010t0002g0024a0006c0010t0002g0027others(11): Show | 16 | HG01496.hp2 HG02622.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50-2790delC | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149263 | ||||||
chr16:48149388
|
T | C | 11 | a0004c0013t0003g0108a0004c0013t0003g0114a0013c0014t0001g0106others(8): Show | 12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50-2914A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149388 | ||||||
chr16:48149649
|
A | ACAGATGT others(8): Show |
20 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(17): Show | 21 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-50-3176_-50-3175i others(17): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149649 | ||||||
chr16:48149837
|
A | G | 4 | a0006c0029t0018g0029a0017c0011t0006g0115a0017c0011t0006g0117others(1): Show | 4 | HG02280.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-3363T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48149837 | ||||||
chr16:48150024
|
A | G | 7 | a0002c0002t0001g0040a0004c0007t0003g0101a0004c0007t0003g0102others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-3550T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150024 | ||||||
chr16:48150204
|
C | T | 1 | a0001c0004t0001g0098 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-51+3412G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150204 | ||||||
chr16:48150405
|
C | G | 10 | a0002c0002t0001g0013a0008c0008t0009g0005a0008c0008t0010g0014others(7): Show | 12 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+3211G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150405 | ||||||
chr16:48150459
|
T | C | 1 | a0004c0013t0003g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-51+3157A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150459 | ||||||
chr16:48150816
|
G | A | 2 | a0017c0011t0006g0115a0017c0011t0006g0117 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-51+2800C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48150816 | ||||||
chr16:48151257
|
C | T | 11 | a0001c0001t0001g0113a0002c0002t0001g0038a0004c0013t0003g0108others(8): Show | 11 | HG01074.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51+2359G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48151257 | ||||||
chr16:48151412
|
T | G | 5 | a0009c0009t0001g0003a0009c0009t0001g0017a0009c0009t0001g0019others(2): Show | 6 | HG02109.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+2204A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48151412 | ||||||
chr16:48151891
|
A | G | 1 | a0014c0016t0005g0004 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-51+1725T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48151891 | ||||||
chr16:48152049
|
G | A | 2 | a0001c0004t0001g0098a0001c0004t0001g0099 | 2 | HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-51+1567C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152049 | ||||||
chr16:48152284
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51+1332T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152284 | ||||||
chr16:48152462
|
A | C | 42 | a0001c0001t0001g0036a0001c0001t0001g0113a0002c0002t0001g0002others(39): Show | 47 | HG01074.hp1 HG01496.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.-51+1154T>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152462 | ||||||
chr16:48152943
|
C | T | 1 | a0001c0004t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-51+673G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48152943 | ||||||
chr16:48153065
|
T | C | 12 | a0002c0002t0001g0002a0002c0002t0001g0022a0006c0010t0002g0023others(9): Show | 15 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51+551A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153065 | ||||||
chr16:48153129
|
T | C | 7 | a0004c0007t0003g0101a0004c0007t0003g0102a0004c0007t0003g0103others(4): Show | 8 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51+487A>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153129 | ||||||
chr16:48153384
|
A | AT | 28 | a0002c0002t0001g0002a0002c0002t0001g0013a0002c0002t0001g0022others(25): Show | 33 | HG01496.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-51+231dupA | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153384 | ||||||
chr16:48153448
|
A | G | 1 | a0006c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-51+168T>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 2/30 | chr16 | 48153448 | ||||||
chr16:48153950
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-319-66C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48153950 | ||||||
chr16:48154440
|
C | T | 21 | a0002c0002t0001g0002a0002c0002t0001g0013a0002c0002t0001g0022others(18): Show | 25 | HG01496.hp2 HG01884.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-319-556G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48154440 | ||||||
chr16:48154939
|
C | G | 1 | a0002c0002t0001g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-320+902G>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48154939 | ||||||
chr16:48155019
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-320+822G>A | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155019 | ||||||
chr16:48155193
|
G | C | 1 | a0003c0003t0004g0100 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-320+648C>G | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155193 | ||||||
chr16:48155376
|
TA | T | 40 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0113others(37): Show | 45 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.-320+464delT | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155376 | ||||||
chr16:48155436
|
T | G | 2 | a0006c0029t0018g0029a0023c0022t0012g0028 | 2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-320+405A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155436 | ||||||
chr16:48155452
|
T | G | 19 | a0001c0001t0001g0113a0001c0004t0017g0118a0004c0007t0003g0101others(16): Show | 20 | HG01123.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-320+389A>C | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155452 | ||||||
chr16:48155727
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CCACA | C | 21 | a0002c0002t0001g0002a0002c0002t0001g0013a0002c0002t0001g0022others(18): Show | 25 | HG01496.hp2 HG01884.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-320+110_-320+113d others(6): Show |
ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155727 | ||||||
chr16:48155754
|
G | A | 1 | a0006c0030t0001g0119 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-320+87C>T | ABCC12 | ENSG00000140798.17 | transcript | ENST00000311303.8 | protein_coding | 1/30 | chr16 | 48155754 |