geneid | 80816 |
---|---|
ensemblid | ENSG00000141431.14 |
hgncid | 29357 |
symbol | ASXL3 |
name | ASXL transcriptional regulator 3 |
refseq_nuc | NM_030632.3 |
refseq_prot | NP_085135.1 |
ensembl_nuc | ENST00000269197.12 |
ensembl_prot | ENSP00000269197.4 |
mane_status | MANE Select |
chr | chr18 |
start | 33578219 |
end | 33751195 |
strand | + |
ver | v1.2 |
region | chr18:33578219-33751195 |
region5000 | chr18:33573219-33756195 |
regionname0 | ASXL3_chr18_33578219_33751195 |
regionname5000 | ASXL3_chr18_33573219_33756195 |
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 | 0/1 | 2248 | 137 | 50 | 22 | 45 | 2 | 17 | 36 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002 | 1/0 | 2248 | 50 | 12 | 14 | 10 | 4 | 9 | 7 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003 | 0/0 | 2248 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004 | 0/0 | 2248 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0005 | 0/0 | 2248 | 4 | 1 | 1 | 1 | 0 | 1 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0006 | 0/0 | 2248 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0007 | 0/0 | 2248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0008 | 0/0 | 2248 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0009 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0010 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0011 | 0/0 | 2248 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0012 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0013 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0014 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0015 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0016 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 6747 | 124 | 47 | 21 | 37 | 2 | 16 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0002 | 1/0 | 6747 | 42 | 5 | 14 | 9 | 4 | 9 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0003 | 0/0 | 6747 | 8 | 8 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0004 | 0/0 | 6747 | 7 | 6 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0005 | 0/0 | 6747 | 7 | 0 | 0 | 7 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0006 | 0/0 | 6747 | 7 | 7 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0007 | 0/0 | 6747 | 3 | 0 | 1 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0008 | 0/0 | 6747 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0009 | 0/0 | 6747 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0010 | 0/0 | 6747 | 2 | 1 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0011 | 0/0 | 6747 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0012 | 0/0 | 6747 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0013 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0014 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0015 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0016 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0017 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0018 | 0/0 | 6747 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0019 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0020 | 0/0 | 6747 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0021 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0022 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0023 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0024 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0025 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
c0026 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5007 | 33 | 8 | 8 | 12 | 1 | 4 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0002 | 0/1 | 5010 | 20 | 2 | 10 | 2 | 0 | 5 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0003 | 0/0 | 5011 | 18 | 1 | 7 | 1 | 3 | 6 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0004 | 0/0 | 5012 | 16 | 5 | 0 | 8 | 0 | 3 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0005 | 0/0 | 5012 | 12 | 3 | 2 | 5 | 0 | 2 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0006 | 0/0 | 5015 | 8 | 0 | 0 | 5 | 0 | 3 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0007 | 0/0 | 5007 | 6 | 6 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0008 | 0/0 | 5012 | 5 | 5 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0009 | 0/0 | 5019 | 5 | 5 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0010 | 0/0 | 5006 | 5 | 0 | 0 | 5 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0011 | 0/0 | 5013 | 5 | 1 | 2 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0012 | 0/0 | 5010 | 4 | 4 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0013 | 1/0 | 5014 | 4 | 0 | 3 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0014 | 0/0 | 5021 | 3 | 1 | 0 | 2 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0015 | 0/0 | 4998 | 2 | 0 | 2 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0016 | 0/0 | 5000 | 2 | 0 | 0 | 2 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0017 | 0/0 | 5006 | 2 | 1 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0018 | 0/0 | 5009 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0019 | 0/0 | 5007 | 2 | 0 | 0 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0020 | 0/0 | 5015 | 2 | 0 | 1 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0021 | 0/0 | 5018 | 2 | 0 | 0 | 2 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0022 | 0/0 | 5019 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0023 | 0/0 | 5010 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0024 | 0/0 | 5010 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0025 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0026 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0027 | 0/0 | 5021 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0028 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0029 | 0/0 | 5021 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0030 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0031 | 0/0 | 4993 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0032 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0033 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0034 | 0/0 | 5001 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0035 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0036 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0037 | 0/0 | 5001 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0038 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0039 | 0/0 | 5009 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0040 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0041 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0042 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0043 | 0/0 | 5010 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0044 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0045 | 0/0 | 5024 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0046 | 0/0 | 5012 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0047 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0048 | 0/0 | 5006 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0049 | 0/0 | 5008 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0050 | 0/0 | 5010 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0051 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0052 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0053 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0054 | 0/0 | 5012 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0055 | 0/0 | 5008 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0056 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0057 | 0/0 | 5009 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0058 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0059 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0060 | 0/0 | 5014 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0061 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0062 | 0/0 | 5015 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0063 | 0/0 | 5018 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0064 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0065 | 0/0 | 5013 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0066 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0067 | 0/0 | 5018 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0068 | 0/0 | 5016 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0069 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0070 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0071 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0072 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0073 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0074 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0075 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0076 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0077 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0078 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0079 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0080 | 0/0 | 5040 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0081 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
t0082 | 0/0 | 5063 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
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 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
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 | 0/1 | 6747 | 124 | 47 | 21 | 37 | 2 | 16 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0005 | 0/0 | 6747 | 7 | 0 | 0 | 7 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0008 | 0/0 | 6747 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0016 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0017 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0018 | 0/0 | 6747 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0020 | 0/0 | 6747 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002 | 1/0 | 6747 | 42 | 5 | 14 | 9 | 4 | 9 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0006 | 0/0 | 6747 | 7 | 7 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0013 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003 | 0/0 | 6747 | 8 | 8 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004 | 0/0 | 6747 | 7 | 6 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0005c0007 | 0/0 | 6747 | 3 | 0 | 1 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0005c0024 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0006c0010 | 0/0 | 6747 | 2 | 1 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0006c0025 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0007c0009 | 0/0 | 6747 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0008c0011 | 0/0 | 6747 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0009c0023 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0010c0022 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0011c0012 | 0/0 | 6747 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0012c0021 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0013c0015 | 0/0 | 6747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0014c0019 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0015c0014 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0016c0026 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11753 | 28 | 8 | 6 | 10 | 1 | 3 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0002 | 0/1 | 11756 | 17 | 2 | 10 | 1 | 0 | 3 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0004 | 0/0 | 11758 | 8 | 3 | 0 | 3 | 0 | 2 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0006 | 0/0 | 11761 | 8 | 0 | 0 | 5 | 0 | 3 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0007 | 0/0 | 11753 | 5 | 5 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0008 | 0/0 | 11758 | 5 | 5 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0010 | 0/0 | 11752 | 5 | 0 | 0 | 5 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0011 | 0/0 | 11759 | 5 | 1 | 2 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0012 | 0/0 | 11756 | 4 | 4 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0014 | 0/0 | 11767 | 3 | 1 | 0 | 2 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0015 | 0/0 | 11744 | 2 | 0 | 2 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0016 | 0/0 | 11746 | 2 | 0 | 0 | 2 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0017 | 0/0 | 11752 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0019 | 0/0 | 11753 | 2 | 0 | 0 | 1 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0021 | 0/0 | 11764 | 2 | 0 | 0 | 2 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0022 | 0/0 | 11765 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0026 | 0/0 | 11762 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0027 | 0/0 | 11767 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0028 | 0/0 | 11765 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0029 | 0/0 | 11767 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0034 | 0/0 | 11747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0037 | 0/0 | 11747 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0038 | 0/0 | 11752 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0039 | 0/0 | 11755 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0040 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0041 | 0/0 | 11755 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0047 | 0/0 | 11753 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0048 | 0/0 | 11752 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0049 | 0/0 | 11754 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0051 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0053 | 0/0 | 11757 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0054 | 0/0 | 11758 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0057 | 0/0 | 11755 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0060 | 0/0 | 11760 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0064 | 0/0 | 11760 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0065 | 0/0 | 11759 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0068 | 0/0 | 11762 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0070 | 0/0 | 11773 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0071 | 0/0 | 11771 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0075 | 0/0 | 11776 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0001t0080 | 0/0 | 11786 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0005t0004 | 0/0 | 11758 | 5 | 0 | 0 | 5 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0005t0017 | 0/0 | 11752 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0005t0056 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0008t0025 | 0/0 | 11757 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0008t0081 | 0/0 | 11808 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0016t0062 | 0/0 | 11761 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0017t0076 | 0/0 | 11777 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0018t0001 | 0/0 | 11753 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0001c0020t0001 | 0/0 | 11753 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0002 | 0/0 | 11756 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0003 | 0/0 | 11757 | 17 | 1 | 6 | 1 | 3 | 6 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0005 | 0/0 | 11758 | 11 | 2 | 2 | 5 | 0 | 2 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0013 | 1/0 | 11760 | 3 | 0 | 2 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0018 | 0/0 | 11755 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0020 | 0/0 | 11761 | 2 | 0 | 1 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0030 | 0/0 | 11749 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0033 | 0/0 | 11752 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0042 | 0/0 | 11757 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0043 | 0/0 | 11756 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0044 | 0/0 | 11757 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0002t0067 | 0/0 | 11764 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0006t0009 | 0/0 | 11765 | 5 | 5 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0006t0023 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0006t0036 | 0/0 | 11753 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0002c0013t0046 | 0/0 | 11758 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0024 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0031 | 0/0 | 11739 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0059 | 0/0 | 11760 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0066 | 0/0 | 11763 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0069 | 0/0 | 11766 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0073 | 0/0 | 11774 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0074 | 0/0 | 11775 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0003c0003t0079 | 0/0 | 11784 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0005 | 0/0 | 11758 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0013 | 0/0 | 11760 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0032 | 0/0 | 11749 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0045 | 0/0 | 11770 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0063 | 0/0 | 11764 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0072 | 0/0 | 11776 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0004c0004t0078 | 0/0 | 11782 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0005c0007t0001 | 0/0 | 11753 | 2 | 0 | 1 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0005c0007t0004 | 0/0 | 11758 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0005c0024t0007 | 0/0 | 11753 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0006c0010t0055 | 0/0 | 11754 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0006c0010t0061 | 0/0 | 11757 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0006c0025t0077 | 0/0 | 11776 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0007c0009t0004 | 0/0 | 11758 | 2 | 2 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0008c0011t0003 | 0/0 | 11757 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0009c0023t0050 | 0/0 | 11756 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0010c0022t0035 | 0/0 | 11748 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0011c0012t0002 | 0/0 | 11756 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0012c0021t0001 | 0/0 | 11753 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0013c0015t0002 | 0/0 | 11756 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0014c0019t0058 | 0/0 | 11761 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0015c0014t0082 | 0/0 | 11809 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
a0016c0026t0052 | 0/0 | 11758 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | copy fasta | chr18 | 33573219 | 33756195 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0010g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0011g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0014g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0014g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0015g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0015g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0017g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0019g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0019g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0021g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0021g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0022g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0022g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0026g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0027g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0028g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0029g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0034g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0037g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0038g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0039g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0040g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0041g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0047g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0048g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0049g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0051g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0053g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0054g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0057g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0060g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0064g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0065g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0068g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0070g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0071g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0075g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0001t0080g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0005t0056g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0008t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0008t0081g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0016t0062g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0017t0076g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0018t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0001c0020t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0013g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0013g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0013g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0018g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0020g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0030g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0033g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0042g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0043g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0044g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0002t0067g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0023g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0006t0036g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0002c0013t0046g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0024g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0031g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0059g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0066g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0069g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0073g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0074g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0003c0003t0079g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0013g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0032g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0045g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0063g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0072g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0004c0004t0078g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0007t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0007t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0005c0024t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0006c0010t0055g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0006c0010t0061g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0006c0025t0077g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0007c0009t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0007c0009t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0008c0011t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0009c0023t0050g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0010c0022t0035g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0011c0012t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0012c0021t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0013c0015t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0014c0019t0058g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0015c0014t0082g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
a0016c0026t0052g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0002 | t0044 | g0053 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0106 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00323 | hp1 | a0002 | c0002 | t0003 | g0069 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00438 | hp1 | a0001 | c0001 | t0010 | g0085 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00438 | hp2 | a0002 | c0013 | t0046 | g0079 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00558 | hp2 | a0001 | c0005 | t0004 | g0163 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00621 | hp2 | a0001 | c0005 | t0004 | g0166 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00642 | hp1 | a0002 | c0002 | t0013 | g0078 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00673 | hp1 | a0001 | c0001 | t0034 | g0195 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00673 | hp2 | a0002 | c0002 | t0005 | g0147 | EAS | CHS | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00735 | hp2 | a0001 | c0001 | t0048 | g0165 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00741 | hp1 | a0002 | c0002 | t0005 | g0039 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG00741 | hp2 | a0002 | c0002 | t0003 | g0043 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01070 | hp1 | a0001 | c0001 | t0015 | g0189 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01070 | hp2 | a0002 | c0002 | t0043 | g0134 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01071 | hp1 | a0004 | c0004 | t0013 | g0202 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01071 | hp2 | a0001 | c0001 | t0015 | g0187 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01109 | hp1 | a0002 | c0002 | t0003 | g0108 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01109 | hp2 | a0002 | c0002 | t0030 | g0179 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01192 | hp1 | a0002 | c0002 | t0067 | g0169 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01255 | hp2 | a0006 | c0010 | t0055 | g0170 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0113 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01358 | hp2 | a0002 | c0002 | t0003 | g0145 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01361 | hp2 | a0002 | c0002 | t0020 | g0047 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0055 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01433 | hp2 | a0001 | c0001 | t0011 | g0211 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01496 | hp2 | a0008 | c0011 | t0003 | g0219 | AMR | CLM | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01891 | hp1 | a0001 | c0001 | t0070 | g0214 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01891 | hp2 | a0004 | c0004 | t0005 | g0046 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0137 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01975 | hp2 | a0002 | c0002 | t0005 | g0080 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01981 | hp1 | a0002 | c0002 | t0013 | g0064 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0206 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02055 | hp2 | a0002 | c0002 | t0005 | g0168 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02129 | hp1 | a0001 | c0001 | t0014 | g0212 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02129 | hp2 | a0001 | c0001 | t0010 | g0082 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02145 | hp1 | a0001 | c0001 | t0064 | g0188 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02145 | hp2 | a0002 | c0006 | t0009 | g0037 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02257 | hp2 | a0003 | c0003 | t0069 | g0010 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02258 | hp1 | a0003 | c0003 | t0074 | g0173 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02280 | hp1 | a0001 | c0001 | t0022 | g0076 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02300 | hp1 | a0001 | c0018 | t0001 | g0070 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02300 | hp2 | a0005 | c0007 | t0001 | g0107 | AMR | PEL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02523 | hp1 | a0002 | c0002 | t0020 | g0126 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02572 | hp2 | a0001 | c0001 | t0028 | g0036 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0217 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02615 | hp1 | a0004 | c0004 | t0072 | g0177 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0018 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0139 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02622 | hp2 | a0004 | c0004 | t0063 | g0060 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02630 | hp1 | a0003 | c0003 | t0024 | g0021 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02647 | hp1 | a0002 | c0006 | t0009 | g0032 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02647 | hp2 | a0001 | c0001 | t0071 | g0118 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02723 | hp1 | a0002 | c0006 | t0009 | g0033 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02723 | hp2 | a0001 | c0008 | t0025 | g0026 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0146 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02738 | hp2 | a0001 | c0001 | t0011 | g0122 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02818 | hp1 | a0009 | c0023 | t0050 | g0115 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02886 | hp1 | a0007 | c0009 | t0004 | g0160 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0029 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02895 | hp1 | a0001 | c0008 | t0081 | g0220 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02895 | hp2 | a0002 | c0006 | t0009 | g0030 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02896 | hp2 | a0001 | c0001 | t0057 | g0065 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02897 | hp2 | a0002 | c0006 | t0009 | g0031 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02922 | hp2 | a0001 | c0001 | t0022 | g0176 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02965 | hp1 | a0003 | c0003 | t0059 | g0005 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02965 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02970 | hp1 | a0002 | c0006 | t0023 | g0027 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02976 | hp1 | a0004 | c0004 | t0032 | g0059 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03017 | hp1 | a0002 | c0002 | t0005 | g0129 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03017 | hp2 | a0001 | c0001 | t0060 | g0193 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03098 | hp1 | a0001 | c0001 | t0026 | g0035 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03098 | hp2 | a0003 | c0003 | t0031 | g0174 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03130 | hp1 | a0001 | c0001 | t0041 | g0138 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0008 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03195 | hp2 | a0006 | c0025 | t0077 | g0004 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03209 | hp1 | a0001 | c0017 | t0076 | g0175 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03209 | hp2 | a0015 | c0014 | t0082 | g0003 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03225 | hp1 | a0007 | c0009 | t0004 | g0161 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03225 | hp2 | a0002 | c0006 | t0036 | g0100 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0133 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0136 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03453 | hp1 | a0002 | c0002 | t0018 | g0182 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03486 | hp1 | a0001 | c0001 | t0080 | g0006 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03486 | hp2 | a0003 | c0003 | t0066 | g0216 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03490 | hp2 | a0005 | c0007 | t0004 | g0135 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03516 | hp1 | a0004 | c0004 | t0078 | g0215 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | ESN | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03579 | hp1 | a0005 | c0024 | t0007 | g0028 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03579 | hp2 | a0001 | c0001 | t0027 | g0034 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0112 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0144 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0057 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03704 | hp2 | a0001 | c0001 | t0039 | g0180 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03710 | hp1 | a0011 | c0012 | t0002 | g0040 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0119 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04184 | hp1 | a0001 | c0001 | t0019 | g0154 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04184 | hp2 | a0001 | c0001 | t0068 | g0142 | SAS | BEB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04199 | hp1 | a0002 | c0002 | t0005 | g0130 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0218 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG04204 | hp2 | a0001 | c0020 | t0001 | g0155 | SAS | STU | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18906 | hp2 | a0002 | c0002 | t0018 | g0181 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18943 | hp1 | a0013 | c0015 | t0002 | g0114 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18943 | hp2 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18959 | hp1 | a0001 | c0001 | t0010 | g0156 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18970 | hp1 | a0002 | c0002 | t0005 | g0178 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18970 | hp2 | a0001 | c0001 | t0014 | g0199 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18971 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18972 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18975 | hp2 | a0012 | c0021 | t0001 | g0072 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18982 | hp1 | a0001 | c0001 | t0016 | g0192 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18982 | hp2 | a0005 | c0007 | t0001 | g0074 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18989 | hp1 | a0001 | c0001 | t0021 | g0198 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18989 | hp2 | a0001 | c0001 | t0019 | g0084 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18998 | hp1 | a0002 | c0002 | t0033 | g0194 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18998 | hp2 | a0001 | c0005 | t0017 | g0205 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18999 | hp1 | a0001 | c0001 | t0040 | g0088 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA18999 | hp2 | a0001 | c0005 | t0056 | g0063 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19003 | hp2 | a0001 | c0001 | t0053 | g0102 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19010 | hp1 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19010 | hp2 | a0002 | c0002 | t0005 | g0162 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19030 | hp1 | a0003 | c0003 | t0079 | g0007 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19030 | hp2 | a0016 | c0026 | t0052 | g0044 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19043 | hp2 | a0001 | c0001 | t0075 | g0184 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19054 | hp1 | a0001 | c0001 | t0051 | g0097 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19054 | hp2 | a0001 | c0005 | t0004 | g0001 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19057 | hp1 | a0001 | c0005 | t0004 | g0062 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19057 | hp2 | a0001 | c0001 | t0021 | g0213 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19065 | hp1 | a0002 | c0002 | t0042 | g0140 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19065 | hp2 | a0001 | c0005 | t0004 | g0164 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19066 | hp2 | a0001 | c0001 | t0010 | g0158 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19074 | hp1 | a0001 | c0001 | t0016 | g0204 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19074 | hp2 | a0002 | c0002 | t0005 | g0131 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19076 | hp2 | a0001 | c0016 | t0062 | g0200 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19077 | hp1 | a0001 | c0001 | t0037 | g0196 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19077 | hp2 | a0002 | c0002 | t0005 | g0075 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19240 | hp1 | a0004 | c0004 | t0045 | g0058 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20752 | hp1 | a0002 | c0002 | t0003 | g0143 | EUR | TSI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20752 | hp2 | a0001 | c0001 | t0054 | g0054 | EUR | TSI | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0201 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02486 | hp1 | a0001 | c0001 | t0047 | g0190 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02486 | hp2 | a0002 | c0002 | t0005 | g0121 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG02559 | hp2 | a0001 | c0001 | t0065 | g0067 | AFR | ACB | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03471 | hp1 | a0001 | c0001 | t0049 | g0149 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG03471 | hp2 | a0003 | c0003 | t0073 | g0009 | AFR | MSL | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG06807 | hp1 | a0006 | c0010 | t0061 | g0185 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
HG06807 | hp2 | a0010 | c0022 | t0035 | g0117 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0109 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA20300 | hp2 | a0014 | c0019 | t0058 | g0002 | AFR | USA | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA21309 | hp1 | a0001 | c0001 | t0038 | g0183 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0016 | AFR | LWK | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0186 | REF | REF | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0013 | g0105 | REF | REF | ASXL3_chr18_33573219_33756195 | ASXL3 | chr18 | 33573219 | 33756195 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33670709
|
T | C | 1 | a0008 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.514T>C | p.Ser172Pro | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/12 | 927/11760 | 514/6747 | 172/2248 | chr18 | 33670709 | ||
chr18:33738813
|
A | C | 1 | a0016 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1409A>C | p.His470Pro | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 1822/11760 | 1409/6747 | 470/2248 | chr18 | 33738813 | ||
chr18:33739983
|
T | A | 2 | a0009a0010 | 2 | HG02818.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.2579T>A | p.Met860Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2992/11760 | 2579/6747 | 860/2248 | chr18 | 33739983 | ||
chr18:33740135
|
G | A | 1 | a0011 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.2731G>A | p.Val911Met | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 3144/11760 | 2731/6747 | 911/2248 | chr18 | 33740135 | ||
chr18:33740265
|
A | G | 11 | a0001a0003a0004others(8): Show | 163 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(160): Show |
missense_variant | MODERATE | c.2861A>G | p.Asn954Ser | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 3274/11760 | 2861/6747 | 954/2248 | chr18 | 33740265 | ||
chr18:33743777
|
A | C | 1 | a0012 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.3929A>C | p.Glu1310Ala | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4342/11760 | 3929/6747 | 1310/2248 | chr18 | 33743777 | ||
chr18:33743884
|
A | G | 2 | a0006a0007 | 5 | HG01255.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
missense_variant | MODERATE | c.4036A>G | p.Ile1346Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4449/11760 | 4036/6747 | 1346/2248 | chr18 | 33743884 | ||
chr18:33744088
|
G | A | 1 | a0015 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.4240G>A | p.Ala1414Thr | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4653/11760 | 4240/6747 | 1414/2248 | chr18 | 33744088 | ||
chr18:33744092
|
T | G | 1 | a0003 | 8 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
missense_variant | MODERATE | c.4244T>G | p.Met1415Arg | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4657/11760 | 4244/6747 | 1415/2248 | chr18 | 33744092 | ||
chr18:33744113
|
C | A | 1 | a0013 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.4265C>A | p.Thr1422Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4678/11760 | 4265/6747 | 1422/2248 | chr18 | 33744113 | ||
chr18:33744290
|
T | C | 1 | a0010 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.4442T>C | p.Leu1481Pro | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4855/11760 | 4442/6747 | 1481/2248 | chr18 | 33744290 | ||
chr18:33744506
|
C | T | 1 | a0014 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.4658C>T | p.Pro1553Leu | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5071/11760 | 4658/6747 | 1553/2248 | chr18 | 33744506 | ||
chr18:33744970
|
A | G | 9 | a0001a0003a0005others(6): Show | 157 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(154): Show |
missense_variant | MODERATE | c.5122A>G | p.Met1708Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5535/11760 | 5122/6747 | 1708/2248 | chr18 | 33744970 | ||
chr18:33746207
|
C | T | 1 | a0007 | 2 | HG02886.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.6359C>T | p.Ala2120Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 6772/11760 | 6359/6747 | 2120/2248 | chr18 | 33746207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33739399
|
A | G | 1 | a0006c0025 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1995A>G | p.Arg665Arg | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2408/11760 | 1995/6747 | 665/2248 | chr18 | 33739399 | ||
chr18:33739711
|
A | G | 1 | a0003c0003 | 8 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
synonymous_variant | LOW | c.2307A>G | p.Arg769Arg | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2720/11760 | 2307/6747 | 769/2248 | chr18 | 33739711 | ||
chr18:33739915
|
C | T | 4 | a0002c0006a0005c0024a0009c0023others(1): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
synonymous_variant | LOW | c.2511C>T | p.Thr837Thr | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2924/11760 | 2511/6747 | 837/2248 | chr18 | 33739915 | ||
chr18:33739987
|
A | T | 2 | a0009c0023a0010c0022 | 2 | HG02818.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.2583A>T | p.Ile861Ile | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/12 | 2996/11760 | 2583/6747 | 861/2248 | chr18 | 33739987 | ||
chr18:33743313
|
G | A | 1 | a0001c0008 | 2 | HG02723.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.3465G>A | p.Ser1155Ser | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3878/11760 | 3465/6747 | 1155/2248 | chr18 | 33743313 | ||
chr18:33744087
|
C | T | 1 | a0001c0020 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.4239C>T | p.Val1413Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4652/11760 | 4239/6747 | 1413/2248 | chr18 | 33744087 | ||
chr18:33744597
|
A | G | 1 | a0016c0026 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.4749A>G | p.Ala1583Ala | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5162/11760 | 4749/6747 | 1583/2248 | chr18 | 33744597 | ||
chr18:33744768
|
G | A | 1 | a0002c0013 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.4920G>A | p.Lys1640Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5333/11760 | 4920/6747 | 1640/2248 | chr18 | 33744768 | ||
chr18:33744954
|
A | G | 1 | a0001c0018 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.5106A>G | p.Val1702Val | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 5519/11760 | 5106/6747 | 1702/2248 | chr18 | 33744954 | ||
chr18:33745779
|
T | A | 1 | a0001c0016 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.5931T>A | p.Leu1977Leu | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 6344/11760 | 5931/6747 | 1977/2248 | chr18 | 33745779 | ||
chr18:33745839
|
A | G | 2 | a0001c0008a0001c0017 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.5991A>G | p.Lys1997Lys | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 6404/11760 | 5991/6747 | 1997/2248 | chr18 | 33745839 | ||
chr18:33746451
|
C | T | 1 | a0001c0005 | 7 | HG00558.hp2 HG00621.hp2 NA18998.hp2 others(4): Show |
synonymous_variant | LOW | c.6603C>T | p.Ala2201Ala | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 7016/11760 | 6603/6747 | 2201/2248 | chr18 | 33746451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33578269
|
C | A | 12 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(9): Show | 27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-363C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 363 | chr18 | 33578269 | |||||
chr18:33578458
|
C | CCCG | 7 | a0001c0001t0011a0001c0001t0021a0001c0001t0064others(4): Show | 12 | HG01192.hp1 HG01433.hp2 HG01981.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-135_-133dupGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCG | 7 | a0001c0001t0014a0001c0001t0026a0001c0001t0027others(4): Show | 13 | HG02109.hp1 HG02129.hp1 HG02145.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-138_-133dupGCCGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(2): Show |
2 | a0001c0001t0022a0001c0001t0028 | 3 | HG02280.hp1 HG02572.hp2 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-141_-133dupGCCGCC others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(8): Show |
6 | a0001c0001t0070a0001c0001t0071a0001c0001t0075others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-147_-133dupGCCGCC others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(11): Show |
2 | a0001c0017t0076a0006c0025t0077 | 2 | HG03195.hp2 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-150_-133dupGCCGCC others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(14): Show |
1 | a0004c0004t0078 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153_-133dupGCCGCC others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(17): Show |
1 | a0003c0003t0079 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-156_-133dupGCCGCC others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(23): Show |
1 | a0001c0001t0080 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162_-133dupGCCGCC others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
C | CCCGCCGC others(41): Show |
2 | a0001c0008t0081a0015c0014t0082 | 2 | HG02895.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-133_-132insGCCGCC others(42): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
CCCG | C | 36 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(33): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-135_-133delGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
CCCGCCG | C | 3 | a0001c0001t0038a0001c0001t0039a0002c0002t0018 | 4 | HG03453.hp1 HG03704.hp2 NA18906.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-138_-133delGCCGCC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
CCCGCCGC others(2): Show |
C | 8 | a0001c0001t0016a0001c0001t0017a0001c0001t0034others(5): Show | 9 | HG00673.hp1 HG03130.hp2 HG03225.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-141_-133delGCCGCC others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
CCCGCCGC others(5): Show |
C | 3 | a0001c0001t0015a0002c0002t0030a0004c0004t0032 | 4 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-144_-133delGCCGCC others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578458
|
CCCGCCGC others(14): Show |
C | 1 | a0003c0003t0031 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153_-133delGCCGCC others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 133 | INFO_REALIGN_3_PRIME | chr18 | 33578458 | ||||
chr18:33578472
|
C | A | 1 | a0002c0002t0030 | 1 | HG01109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 160 | chr18 | 33578472 | |||||
chr18:33578473
|
G | C | 1 | a0002c0002t0030 | 1 | HG01109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 159 | chr18 | 33578473 | |||||
chr18:33578497
|
G | A | 2 | a0001c0001t0040a0001c0005t0056 | 2 | NA18999.hp1 NA18999.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 135 | chr18 | 33578497 | |||||
chr18:33578500
|
A | G | 4 | a0001c0001t0029a0001c0001t0040a0001c0005t0056others(1): Show | 4 | HG02886.hp2 HG03209.hp2 NA18999.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-132A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 132 | chr18 | 33578500 | |||||
chr18:33578503
|
G | A | 1 | a0001c0001t0040 | 1 | NA18999.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 129 | chr18 | 33578503 | |||||
chr18:33578504
|
C | A | 1 | a0001c0005t0056 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/12 | 128 | chr18 | 33578504 | |||||
chr18:33746927
|
A | G | 1 | a0002c0002t0067 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 332 | chr18 | 33746927 | |||||
chr18:33746933
|
C | A | 2 | a0001c0001t0041a0001c0001t0070 | 2 | HG01891.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*338C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 338 | chr18 | 33746933 | |||||
chr18:33747246
|
C | G | 2 | a0001c0001t0019a0001c0001t0037 | 3 | HG04184.hp1 NA18989.hp2 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*651C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 651 | chr18 | 33747246 | |||||
chr18:33747332
|
A | C | 41 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(38): Show | 67 | HG00558.hp2 HG00621.hp2 HG01255.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*737A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 737 | chr18 | 33747332 | |||||
chr18:33747347
|
G | T | 1 | a0001c0016t0062 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 752 | chr18 | 33747347 | |||||
chr18:33747413
|
GA | G | 5 | a0002c0006t0009a0002c0006t0023a0003c0003t0066others(2): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*834delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 834 | INFO_REALIGN_3_PRIME | chr18 | 33747413 | ||||
chr18:33747756
|
T | G | 1 | a0003c0003t0066 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1161T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1161 | chr18 | 33747756 | |||||
chr18:33747885
|
G | A | 1 | a0001c0001t0071 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1290 | chr18 | 33747885 | |||||
chr18:33747921
|
C | T | 1 | a0010c0022t0035 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1326 | chr18 | 33747921 | |||||
chr18:33747944
|
C | T | 2 | a0006c0010t0055a0006c0010t0061 | 2 | HG01255.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1349C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1349 | chr18 | 33747944 | |||||
chr18:33748119
|
TG | T | 71 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(68): Show | 160 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1532delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1532 | INFO_REALIGN_3_PRIME | chr18 | 33748119 | ||||
chr18:33748234
|
G | A | 1 | a0001c0001t0047 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1639 | chr18 | 33748234 | |||||
chr18:33748316
|
T | A | 1 | a0002c0002t0042 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1721 | chr18 | 33748316 | |||||
chr18:33748378
|
G | A | 1 | a0016c0026t0052 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1783G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1783 | chr18 | 33748378 | |||||
chr18:33748555
|
C | T | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(27): Show | 93 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1960C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 1960 | chr18 | 33748555 | |||||
chr18:33748600
|
A | G | 2 | a0001c0001t0039a0001c0001t0054 | 2 | HG03704.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2005A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2005 | chr18 | 33748600 | |||||
chr18:33748679
|
C | T | 1 | a0001c0001t0065 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2084 | chr18 | 33748679 | |||||
chr18:33748756
|
T | G | 71 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(68): Show | 160 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2161T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2161 | chr18 | 33748756 | |||||
chr18:33748856
|
C | A | 2 | a0001c0001t0010a0001c0001t0016 | 7 | HG00438.hp1 HG02129.hp2 NA18959.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2261C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2261 | chr18 | 33748856 | |||||
chr18:33748914
|
A | T | 1 | a0002c0013t0046 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2319 | chr18 | 33748914 | |||||
chr18:33749076
|
C | CT | 16 | a0001c0001t0051a0002c0002t0005a0002c0002t0018others(13): Show | 28 | HG00438.hp2 HG00673.hp2 HG00741.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2498dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2499 | INFO_REALIGN_3_PRIME | chr18 | 33749076 | ||||
chr18:33749076
|
CT | C | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(54): Show | 146 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*2498delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2498 | INFO_REALIGN_3_PRIME | chr18 | 33749076 | ||||
chr18:33749076
|
CTT | C | 6 | a0001c0001t0048a0001c0017t0076a0003c0003t0024others(3): Show | 6 | HG00735.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2497_*2498delTT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2497 | INFO_REALIGN_3_PRIME | chr18 | 33749076 | ||||
chr18:33749439
|
AT | A | 10 | a0001c0001t0010a0001c0001t0016a0001c0001t0057others(7): Show | 15 | HG00438.hp1 HG01070.hp2 HG02129.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2857delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2857 | INFO_REALIGN_3_PRIME | chr18 | 33749439 | ||||
chr18:33749551
|
C | G | 1 | a0002c0006t0036 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2956C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 2956 | chr18 | 33749551 | |||||
chr18:33749728
|
A | G | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3133A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3133 | chr18 | 33749728 | |||||
chr18:33749729
|
A | G | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3134A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3134 | chr18 | 33749729 | |||||
chr18:33749733
|
A | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3138A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3138 | chr18 | 33749733 | |||||
chr18:33749746
|
C | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3151C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3151 | chr18 | 33749746 | |||||
chr18:33749748
|
A | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3153A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3153 | chr18 | 33749748 | |||||
chr18:33749750
|
C | A | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3155C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3155 | chr18 | 33749750 | |||||
chr18:33749756
|
A | G | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3161A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3161 | chr18 | 33749756 | |||||
chr18:33749757
|
G | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3162G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3162 | chr18 | 33749757 | |||||
chr18:33749759
|
T | C | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3164T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3164 | chr18 | 33749759 | |||||
chr18:33749761
|
G | C | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3166G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3166 | chr18 | 33749761 | |||||
chr18:33749763
|
G | GTTCACCA others(5): Show |
1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3168_*3169insTTCA others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3169 | chr18 | 33749763 | |||||
chr18:33749764
|
C | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3169 | chr18 | 33749764 | |||||
chr18:33749767
|
G | A | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3172G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3172 | chr18 | 33749767 | |||||
chr18:33749768
|
G | C | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3173 | chr18 | 33749768 | |||||
chr18:33749770
|
T | A | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3175T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3175 | chr18 | 33749770 | |||||
chr18:33749771
|
G | C | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3176G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3176 | chr18 | 33749771 | |||||
chr18:33749772
|
C | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3177C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3177 | chr18 | 33749772 | |||||
chr18:33749776
|
A | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3181A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3181 | chr18 | 33749776 | |||||
chr18:33749777
|
A | C | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3182 | chr18 | 33749777 | |||||
chr18:33749778
|
A | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3183A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3183 | chr18 | 33749778 | |||||
chr18:33749779
|
G | C | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3184G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3184 | chr18 | 33749779 | |||||
chr18:33749781
|
C | T | 1 | a0004c0004t0045 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3186C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3186 | chr18 | 33749781 | |||||
chr18:33749991
|
C | T | 1 | a0001c0001t0065 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3396C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3396 | chr18 | 33749991 | |||||
chr18:33750402
|
C | G | 3 | a0001c0008t0025a0001c0008t0081a0001c0017t0076 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3807C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3807 | chr18 | 33750402 | |||||
chr18:33750511
|
C | T | 1 | a0010c0022t0035 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3916C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3916 | chr18 | 33750511 | |||||
chr18:33750568
|
A | AT | 30 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(27): Show | 56 | HG00558.hp2 HG00621.hp2 HG01884.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3985dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3986 | INFO_REALIGN_3_PRIME | chr18 | 33750568 | ||||
chr18:33750568
|
AT | A | 7 | a0001c0001t0038a0001c0001t0041a0001c0001t0070others(4): Show | 7 | HG01255.hp2 HG01891.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3985delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3985 | INFO_REALIGN_3_PRIME | chr18 | 33750568 | ||||
chr18:33750568
|
ATT | A | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(28): Show | 94 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*3984_*3985delTT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 3984 | INFO_REALIGN_3_PRIME | chr18 | 33750568 | ||||
chr18:33750845
|
C | G | 1 | a0002c0002t0044 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4250C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4250 | chr18 | 33750845 | |||||
chr18:33751033
|
G | GAA | 34 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(31): Show | 60 | HG00558.hp2 HG00621.hp2 HG01884.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4441_*4442dupAA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4443 | INFO_REALIGN_3_PRIME | chr18 | 33751033 | ||||
chr18:33751107
|
A | T | 1 | a0001c0001t0038 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4512A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 12/12 | 4512 | chr18 | 33751107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:33578701
|
C | A | 1 | a0001c0005t0004g0001 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.54+16C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578701 | ||||||
chr18:33578779
|
C | T | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+94C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578779 | ||||||
chr18:33578868
|
G | T | 1 | a0008c0011t0003g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54+183G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578868 | ||||||
chr18:33578882
|
A | T | 2 | a0001c0001t0006g0217a0002c0002t0003g0218 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.54+197A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578882 | ||||||
chr18:33578904
|
G | GCGTCCGG others(3): Show |
2 | a0003c0003t0066g0216a0004c0004t0078g0215 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54+222_54+231dupTC others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33578904 | |||||
chr18:33578989
|
C | T | 1 | a0001c0001t0070g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.54+304C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578989 | ||||||
chr18:33578991
|
C | T | 22 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(19): Show | 22 | HG00673.hp1 HG01071.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+306C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33578991 | ||||||
chr18:33579023
|
G | A | 1 | a0014c0019t0058g0002 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54+338G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579023 | ||||||
chr18:33579075
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.54+390A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579075 | ||||||
chr18:33579122
|
T | C | 8 | a0001c0001t0017g0008a0001c0001t0080g0006a0003c0003t0059g0005others(5): Show | 8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+437T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579122 | ||||||
chr18:33579232
|
A | G | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+547A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579232 | ||||||
chr18:33579835
|
C | G | 4 | a0001c0001t0002g0186a0001c0001t0015g0187a0001c0001t0015g0189others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+1150C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33579835 | ||||||
chr18:33580029
|
C | A | 27 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(24): Show | 27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.54+1344C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580029 | ||||||
chr18:33580364
|
A | G | 1 | a0006c0010t0061g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.54+1679A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580364 | ||||||
chr18:33580437
|
A | G | 19 | a0001c0001t0017g0008a0001c0001t0038g0183a0001c0001t0039g0180others(16): Show | 19 | HG01109.hp2 HG02257.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+1752A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580437 | ||||||
chr18:33580534
|
G | T | 1 | a0002c0002t0005g0178 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.54+1849G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580534 | ||||||
chr18:33580608
|
A | G | 3 | a0001c0001t0022g0176a0001c0001t0070g0214a0004c0004t0072g0177 | 3 | HG01891.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.54+1923A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33580608 | ||||||
chr18:33581031
|
C | T | 69 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(66): Show | 69 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.54+2346C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581031 | ||||||
chr18:33581136
|
A | G | 1 | a0001c0001t0004g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.54+2451A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581136 | ||||||
chr18:33581148
|
T | A | 27 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(24): Show | 27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.54+2463T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581148 | ||||||
chr18:33581209
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG01884.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+2524C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581209 | ||||||
chr18:33581379
|
T | G | 19 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(16): Show | 19 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+2694T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581379 | ||||||
chr18:33581462
|
T | G | 38 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(35): Show | 38 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.54+2777T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581462 | ||||||
chr18:33581472
|
A | AGT | 8 | a0001c0001t0002g0148a0001c0001t0004g0172a0001c0001t0014g0212others(5): Show | 8 | HG00735.hp1 HG02129.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+2815_54+2816dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGT | 2 | a0001c0001t0021g0213a0001c0001t0029g0029 | 2 | HG02886.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.54+2813_54+2816dup others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGT | 16 | a0001c0001t0017g0008a0001c0001t0026g0035a0001c0001t0027g0034others(13): Show | 16 | HG01109.hp2 HG02257.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.54+2811_54+2816dup others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGTG others(1): Show |
2 | a0002c0006t0009g0037a0004c0004t0078g0215 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54+2809_54+2816dup others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0039g0180a0002c0002t0018g0181a0002c0002t0018g0182 | 3 | HG03453.hp1 HG03704.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.54+2807_54+2816dup others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0019g0154a0001c0008t0081g0220a0001c0017t0076g0175others(1): Show | 4 | HG02895.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+2805_54+2816dup others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGTG others(7): Show |
4 | a0001c0001t0001g0157a0001c0001t0010g0156a0001c0001t0010g0158others(1): Show | 4 | HG04204.hp2 NA18959.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+2803_54+2816dup others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGTG others(9): Show |
14 | a0001c0001t0002g0159a0001c0001t0004g0167a0001c0001t0038g0183others(11): Show | 14 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.54+2801_54+2816dup others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
A | AGTGTGTG others(11): Show |
4 | a0001c0001t0006g0171a0002c0002t0005g0168a0002c0002t0067g0169others(1): Show | 4 | HG01192.hp1 HG01255.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+2799_54+2816dup others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581472
|
AGT | A | 3 | a0001c0001t0002g0038a0002c0002t0005g0039a0011c0012t0002g0040 | 3 | HG00741.hp1 HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.54+2815_54+2816del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33581472 | |||||
chr18:33581652
|
C | A | 1 | a0004c0004t0078g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.54+2967C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581652 | ||||||
chr18:33581652
|
C | G | 27 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(24): Show | 27 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.54+2967C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581652 | ||||||
chr18:33581688
|
G | T | 1 | a0002c0002t0005g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.54+3003G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581688 | ||||||
chr18:33581707
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.54+3022C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581707 | ||||||
chr18:33581955
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54+3270G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581955 | ||||||
chr18:33581989
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+3304T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33581989 | ||||||
chr18:33582049
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+3364A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582049 | ||||||
chr18:33582100
|
C | G | 23 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(20): Show | 23 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.54+3415C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582100 | ||||||
chr18:33582145
|
T | C | 19 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(16): Show | 19 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+3460T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582145 | ||||||
chr18:33582206
|
G | T | 1 | a0002c0002t0003g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54+3521G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582206 | ||||||
chr18:33582409
|
T | A | 62 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(59): Show | 62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+3724T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582409 | ||||||
chr18:33582428
|
A | G | 19 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(16): Show | 19 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+3743A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582428 | ||||||
chr18:33582547
|
A | ATTTG | 62 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(59): Show | 62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+3865_54+3866ins others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582547 | |||||
chr18:33582698
|
G | T | 22 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(19): Show | 22 | HG00673.hp1 HG01071.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.54+4013G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582698 | ||||||
chr18:33582706
|
C | CTG | 25 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0056others(22): Show | 25 | HG00280.hp1 HG01361.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.54+4055_54+4056dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | |||||
chr18:33582706
|
C | CTGTG | 8 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0007g0011others(5): Show | 8 | HG00558.hp1 HG00741.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+4053_54+4056dup others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | |||||
chr18:33582706
|
CTG | C | 51 | a0001c0001t0001g0157a0001c0001t0002g0132a0001c0001t0002g0159others(48): Show | 51 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.54+4055_54+4056del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | |||||
chr18:33582706
|
CTGTG | C | 11 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(8): Show | 11 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.54+4053_54+4056del others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582706 | |||||
chr18:33582736
|
G | T | 17 | a0001c0001t0001g0157a0001c0001t0004g0167a0001c0001t0006g0171others(14): Show | 17 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.54+4051G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582736 | ||||||
chr18:33582738
|
G | T | 24 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(21): Show | 24 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.54+4053G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582738 | ||||||
chr18:33582740
|
G | GTGTT | 15 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(12): Show | 15 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.54+4056_54+4057ins others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582740 | |||||
chr18:33582740
|
G | GTT | 13 | a0001c0001t0007g0025a0001c0001t0017g0008a0001c0001t0038g0183others(10): Show | 13 | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+4058_54+4059dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33582740 | |||||
chr18:33582740
|
G | T | 36 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(33): Show | 36 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.54+4055G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33582740 | ||||||
chr18:33583130
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+4445A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583130 | ||||||
chr18:33583252
|
A | G | 17 | a0001c0001t0017g0008a0001c0001t0038g0183a0001c0001t0039g0180others(14): Show | 17 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+4567A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583252 | ||||||
chr18:33583267
|
A | G | 4 | a0001c0008t0025g0026a0001c0017t0076g0175a0002c0006t0023g0027others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+4582A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583267 | ||||||
chr18:33583422
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+4737G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583422 | ||||||
chr18:33583452
|
A | G | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.54+4767A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583452 | ||||||
chr18:33583547
|
G | C | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+4862G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583547 | ||||||
chr18:33583651
|
T | C | 1 | a0002c0002t0005g0162 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.54+4966T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583651 | ||||||
chr18:33583676
|
A | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0128 | 2 | HG01496.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.54+4991A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583676 | ||||||
chr18:33583693
|
G | T | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+5008G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583693 | ||||||
chr18:33583712
|
A | G | 2 | a0001c0001t0016g0204a0001c0005t0017g0205 | 2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.54+5027A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583712 | ||||||
chr18:33583749
|
T | G | 1 | a0002c0002t0003g0069 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54+5064T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33583749 | ||||||
chr18:33584059
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+5374G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584059 | ||||||
chr18:33584094
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+5409C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584094 | ||||||
chr18:33584163
|
C | A | 63 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(60): Show | 63 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.54+5478C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584163 | ||||||
chr18:33584475
|
G | A | 1 | a0004c0004t0005g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+5790G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584475 | ||||||
chr18:33584668
|
A | T | 62 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(59): Show | 62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+5983A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584668 | ||||||
chr18:33584729
|
A | G | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+6044A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584729 | ||||||
chr18:33584880
|
A | ATG | 19 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(16): Show | 19 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.54+6207_54+6208dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33584880 | |||||
chr18:33584880
|
A | G | 17 | a0001c0001t0017g0008a0001c0001t0038g0183a0001c0001t0039g0180others(14): Show | 17 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.54+6195A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33584880 | ||||||
chr18:33585029
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+6344C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585029 | ||||||
chr18:33585130
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54+6445C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585130 | ||||||
chr18:33585346
|
A | G | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+6661A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585346 | ||||||
chr18:33585547
|
A | G | 4 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0006g0125others(1): Show | 4 | HG02523.hp1 NA18943.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+6862A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585547 | ||||||
chr18:33585681
|
T | C | 1 | a0001c0018t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.54+6996T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585681 | ||||||
chr18:33585885
|
C | T | 4 | a0001c0001t0004g0167a0001c0001t0006g0171a0001c0005t0004g0001others(1): Show | 4 | HG00621.hp2 NA18994.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+7200C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585885 | ||||||
chr18:33585988
|
AT | A | 8 | a0001c0001t0017g0008a0001c0001t0080g0006a0003c0003t0059g0005others(5): Show | 8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+7304delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585988 | ||||||
chr18:33585991
|
A | C | 8 | a0001c0001t0017g0008a0001c0001t0080g0006a0003c0003t0059g0005others(5): Show | 8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+7306A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33585991 | ||||||
chr18:33586138
|
G | C | 1 | a0001c0001t0002g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.54+7453G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586138 | ||||||
chr18:33586181
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.54+7496A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586181 | ||||||
chr18:33586192
|
CTGT | C | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG00673.hp1 HG01071.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.54+7512_54+7514del others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33586192 | |||||
chr18:33586404
|
C | CTT | 23 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(20): Show | 23 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.54+7727_54+7728dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33586404 | |||||
chr18:33586404
|
C | CTTT | 44 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(41): Show | 44 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.54+7726_54+7728dup others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33586404 | |||||
chr18:33586545
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54+7860A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586545 | ||||||
chr18:33586621
|
G | T | 1 | a0001c0001t0065g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54+7936G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586621 | ||||||
chr18:33586661
|
G | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.54+7976G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586661 | ||||||
chr18:33586826
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.54+8141A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586826 | ||||||
chr18:33586892
|
T | A | 8 | a0001c0001t0017g0008a0001c0001t0080g0006a0003c0003t0059g0005others(5): Show | 8 | HG02257.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+8207T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33586892 | ||||||
chr18:33587226
|
C | A | 67 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(64): Show | 67 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.54+8541C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587226 | ||||||
chr18:33587283
|
G | A | 1 | a0001c0001t0060g0193 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.54+8598G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587283 | ||||||
chr18:33587319
|
C | T | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+8634C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587319 | ||||||
chr18:33587731
|
C | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54+9046C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33587731 | ||||||
chr18:33588010
|
AGTCT | A | 4 | a0001c0001t0026g0035a0001c0001t0027g0034a0001c0001t0028g0036others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+9330_54+9333del others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588010 | |||||
chr18:33588061
|
A | C | 1 | a0002c0002t0042g0140 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.54+9376A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588061 | ||||||
chr18:33588359
|
G | GT | 6 | a0001c0001t0001g0045a0001c0001t0011g0122a0001c0008t0025g0026others(3): Show | 6 | HG02055.hp1 HG02723.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+9688dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588359 | |||||
chr18:33588359
|
G | GTT | 58 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(55): Show | 58 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.54+9687_54+9688dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588359 | |||||
chr18:33588359
|
G | GTTT | 5 | a0001c0001t0004g0172a0001c0001t0010g0158a0001c0008t0081g0220others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+9686_54+9688dup others(3): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33588359 | |||||
chr18:33588447
|
G | A | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+9762G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588447 | ||||||
chr18:33588449
|
T | A | 2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.54+9764T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588449 | ||||||
chr18:33588551
|
C | T | 3 | a0001c0001t0011g0139a0001c0001t0041g0138a0002c0002t0005g0121 | 3 | HG02486.hp2 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.54+9866C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588551 | ||||||
chr18:33588750
|
A | C | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+10065A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588750 | ||||||
chr18:33588841
|
T | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0150others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+10156T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588841 | ||||||
chr18:33588859
|
C | T | 1 | a0002c0002t0003g0137 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.54+10174C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33588859 | ||||||
chr18:33589018
|
T | C | 62 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(59): Show | 62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+10333T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589018 | ||||||
chr18:33589199
|
A | G | 2 | a0001c0001t0002g0120a0001c0001t0057g0065 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.54+10514A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589199 | ||||||
chr18:33589350
|
C | A | 1 | a0003c0003t0059g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54+10665C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589350 | ||||||
chr18:33589454
|
C | T | 8 | a0001c0001t0039g0180a0002c0002t0018g0181a0002c0002t0018g0182others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+10769C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589454 | ||||||
chr18:33589554
|
A | G | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54+10869A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589554 | ||||||
chr18:33589816
|
A | G | 4 | a0001c0008t0025g0026a0001c0017t0076g0175a0002c0006t0023g0027others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+11131A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589816 | ||||||
chr18:33589987
|
G | A | 1 | a0001c0001t0002g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.54+11302G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33589987 | ||||||
chr18:33590105
|
T | A | 2 | a0001c0001t0001g0071a0012c0021t0001g0072 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.54+11420T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590105 | ||||||
chr18:33590107
|
C | G | 2 | a0001c0001t0001g0071a0012c0021t0001g0072 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.54+11422C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590107 | ||||||
chr18:33590108
|
TATG | T | 2 | a0001c0001t0001g0071a0012c0021t0001g0072 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.54+11424_54+11426d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590108 | ||||||
chr18:33590111
|
G | GT | 7 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0021g0213others(4): Show | 7 | HG02647.hp2 HG03688.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+11445dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(9): Show |
1 | a0003c0003t0059g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.54+11435_54+11436i others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+11433_54+11445d others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0038g0183a0001c0001t0075g0184a0001c0008t0081g0220others(1): Show | 4 | HG02895.hp1 NA19043.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+11432_54+11445d others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(8): Show |
4 | a0001c0001t0012g0015a0002c0002t0018g0181a0002c0006t0009g0030others(1): Show | 4 | HG02895.hp2 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+11431_54+11445d others(17): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(9): Show |
12 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(9): Show | 12 | HG02257.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.54+11430_54+11445d others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(10): Show |
9 | a0001c0001t0027g0034a0001c0001t0039g0180a0001c0001t0080g0006others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.54+11429_54+11445d others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(11): Show |
11 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0006g0171others(8): Show | 11 | HG01884.hp1 HG02572.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+11428_54+11445d others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(12): Show |
15 | a0001c0001t0007g0025a0001c0001t0008g0020a0001c0001t0008g0022others(12): Show | 15 | HG00621.hp2 HG00735.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+11427_54+11445d others(21): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(13): Show |
2 | a0001c0001t0004g0167a0001c0020t0001g0155 | 2 | HG04204.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.54+11445_54+11446i others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(14): Show |
1 | a0006c0010t0055g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.54+11445_54+11446i others(23): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(15): Show |
1 | a0001c0001t0008g0023 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54+11445_54+11446i others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590111
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0008g0024 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.54+11445_54+11446i others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33590111 | |||||
chr18:33590153
|
A | G | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.54+11468A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590153 | ||||||
chr18:33590244
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+11559C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590244 | ||||||
chr18:33590426
|
G | A | 1 | a0016c0026t0052g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.54+11741G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590426 | ||||||
chr18:33590631
|
T | C | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.54+11946T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590631 | ||||||
chr18:33590631
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.54+11946T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590631 | ||||||
chr18:33590753
|
A | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.54+12068A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33590753 | ||||||
chr18:33591116
|
A | T | 1 | a0001c0001t0008g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.54+12431A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591116 | ||||||
chr18:33591240
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.54+12555C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591240 | ||||||
chr18:33591278
|
G | A | 1 | a0001c0001t0071g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54+12593G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591278 | ||||||
chr18:33591314
|
A | G | 1 | a0002c0002t0013g0064 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.54+12629A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591314 | ||||||
chr18:33591396
|
T | C | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.54+12711T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591396 | ||||||
chr18:33591486
|
A | C | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.54+12801A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591486 | ||||||
chr18:33591591
|
G | A | 62 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(59): Show | 62 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.54+12906G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591591 | ||||||
chr18:33591638
|
CT | C | 65 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(62): Show | 65 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.54+12968delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33591638 | |||||
chr18:33591665
|
G | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+12980G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591665 | ||||||
chr18:33591703
|
G | A | 2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.54+13018G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591703 | ||||||
chr18:33591850
|
C | T | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.54+13165C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591850 | ||||||
chr18:33591883
|
C | T | 5 | a0001c0001t0080g0006a0003c0003t0059g0005a0003c0003t0069g0010others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+13198C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591883 | ||||||
chr18:33591924
|
A | G | 9 | a0001c0001t0038g0183a0001c0001t0039g0180a0002c0002t0018g0181others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+13239A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591924 | ||||||
chr18:33591934
|
T | G | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.54+13249T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591934 | ||||||
chr18:33591942
|
T | G | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+13257T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33591942 | ||||||
chr18:33592495
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.54+13810A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592495 | ||||||
chr18:33592532
|
C | T | 1 | a0009c0023t0050g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.54+13847C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592532 | ||||||
chr18:33592533
|
G | A | 1 | a0002c0002t0020g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.54+13848G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592533 | ||||||
chr18:33592578
|
T | G | 67 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(64): Show | 67 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.54+13893T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592578 | ||||||
chr18:33592594
|
T | C | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54+13909T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592594 | ||||||
chr18:33592637
|
G | A | 19 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(16): Show | 19 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.54+13952G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592637 | ||||||
chr18:33592847
|
C | G | 6 | a0001c0001t0004g0172a0001c0008t0025g0026a0001c0017t0076g0175others(3): Show | 6 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+14162C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592847 | ||||||
chr18:33592866
|
A | G | 1 | a0005c0024t0007g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54+14181A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592866 | ||||||
chr18:33592937
|
C | A | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.54+14252C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33592937 | ||||||
chr18:33593223
|
T | C | 79 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0004g0167others(76): Show | 79 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.55-14371T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593223 | ||||||
chr18:33593258
|
C | CT | 60 | a0001c0001t0001g0061a0001c0001t0001g0127a0001c0001t0001g0157others(57): Show | 60 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.55-14313dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33593258 | |||||
chr18:33593258
|
C | CTT | 7 | a0001c0008t0025g0026a0002c0002t0003g0218a0002c0002t0005g0168others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-14314_55-14313d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33593258 | |||||
chr18:33593258
|
CT | C | 5 | a0001c0001t0011g0081a0001c0001t0012g0015a0002c0002t0005g0075others(2): Show | 5 | HG02965.hp1 HG02965.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-14313delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33593258 | |||||
chr18:33593342
|
C | G | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.55-14252C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593342 | ||||||
chr18:33593564
|
G | T | 85 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0001g0157others(82): Show | 85 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.55-14030G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593564 | ||||||
chr18:33593591
|
C | T | 4 | a0001c0001t0038g0183a0001c0001t0039g0180a0007c0009t0004g0160others(1): Show | 4 | HG02886.hp1 HG03225.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-14003C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593591 | ||||||
chr18:33593866
|
C | G | 9 | a0001c0001t0026g0035a0001c0001t0028g0036a0001c0001t0080g0006others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.55-13728C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33593866 | ||||||
chr18:33594211
|
G | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.55-13383G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594211 | ||||||
chr18:33594242
|
G | A | 9 | a0001c0001t0026g0035a0001c0001t0028g0036a0001c0001t0080g0006others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.55-13352G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594242 | ||||||
chr18:33594369
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.55-13225T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594369 | ||||||
chr18:33594408
|
C | G | 30 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(27): Show | 30 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.55-13186C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594408 | ||||||
chr18:33594428
|
C | G | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.55-13166C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594428 | ||||||
chr18:33594578
|
T | C | 1 | a0001c0001t0022g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-13016T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594578 | ||||||
chr18:33594698
|
A | G | 4 | a0001c0001t0026g0035a0001c0001t0028g0036a0001c0001t0038g0183others(1): Show | 4 | HG01109.hp2 HG02572.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-12896A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594698 | ||||||
chr18:33594752
|
A | G | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.55-12842A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594752 | ||||||
chr18:33594801
|
C | A | 1 | a0002c0002t0020g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.55-12793C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594801 | ||||||
chr18:33594842
|
T | C | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.55-12752T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594842 | ||||||
chr18:33594898
|
G | C | 1 | a0002c0006t0023g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.55-12696G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33594898 | ||||||
chr18:33595042
|
C | G | 1 | a0004c0004t0013g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.55-12552C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595042 | ||||||
chr18:33595184
|
C | T | 24 | a0001c0001t0001g0127a0001c0001t0006g0123a0001c0001t0006g0124others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-12410C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595184 | ||||||
chr18:33595221
|
T | C | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55-12373T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595221 | ||||||
chr18:33595518
|
A | C | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.55-12076A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595518 | ||||||
chr18:33595545
|
T | C | 1 | a0001c0001t0010g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.55-12049T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595545 | ||||||
chr18:33595688
|
A | G | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-11906A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33595688 | ||||||
chr18:33596084
|
T | C | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.55-11510T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596084 | ||||||
chr18:33596254
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-11340A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596254 | ||||||
chr18:33596264
|
A | G | 46 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(43): Show | 46 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.55-11330A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596264 | ||||||
chr18:33596271
|
G | T | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-11323G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596271 | ||||||
chr18:33596278
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.55-11316T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596278 | ||||||
chr18:33596486
|
A | G | 1 | a0001c0001t0075g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.55-11108A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596486 | ||||||
chr18:33596538
|
G | A | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-11056G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596538 | ||||||
chr18:33596621
|
A | G | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-10973A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596621 | ||||||
chr18:33596969
|
C | A | 1 | a0001c0001t0019g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.55-10625C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33596969 | ||||||
chr18:33597049
|
G | A | 138 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.55-10545G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597049 | ||||||
chr18:33597094
|
C | T | 2 | a0001c0001t0029g0029a0002c0002t0005g0147 | 2 | HG00673.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.55-10500C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597094 | ||||||
chr18:33597099
|
C | G | 43 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.55-10495C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597099 | ||||||
chr18:33597278
|
A | G | 1 | a0002c0002t0003g0069 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.55-10316A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597278 | ||||||
chr18:33597318
|
G | A | 1 | a0001c0001t0012g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-10276G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597318 | ||||||
chr18:33597409
|
A | C | 74 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(71): Show | 74 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.55-10185A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597409 | ||||||
chr18:33597535
|
A | G | 135 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.55-10059A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597535 | ||||||
chr18:33597623
|
T | C | 219 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.55-9971T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597623 | ||||||
chr18:33597781
|
T | C | 1 | a0001c0001t0002g0207 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.55-9813T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597781 | ||||||
chr18:33597793
|
C | CA | 8 | a0001c0001t0010g0085a0001c0001t0016g0192a0001c0001t0016g0204others(5): Show | 8 | HG00438.hp1 HG00673.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-9788dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33597793 | |||||
chr18:33597793
|
CA | C | 138 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.55-9788delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33597793 | |||||
chr18:33597802
|
A | C | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-9792A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597802 | ||||||
chr18:33597811
|
A | C | 1 | a0002c0002t0003g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.55-9783A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597811 | ||||||
chr18:33597812
|
A | C | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-9782A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597812 | ||||||
chr18:33597815
|
AC | A | 35 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.55-9778delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597815 | ||||||
chr18:33597816
|
C | A | 1 | a0001c0001t0006g0171 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.55-9778C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597816 | ||||||
chr18:33597913
|
C | T | 1 | a0001c0001t0014g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.55-9681C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597913 | ||||||
chr18:33597953
|
A | G | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.55-9641A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33597953 | ||||||
chr18:33598248
|
T | C | 1 | a0001c0001t0060g0193 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.55-9346T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598248 | ||||||
chr18:33598475
|
G | A | 1 | a0001c0001t0011g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.55-9119G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598475 | ||||||
chr18:33598504
|
T | C | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-9090T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598504 | ||||||
chr18:33598846
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.55-8748G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598846 | ||||||
chr18:33598912
|
G | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.55-8682G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598912 | ||||||
chr18:33598971
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55-8623T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33598971 | ||||||
chr18:33599039
|
A | G | 8 | a0001c0001t0004g0172a0001c0001t0038g0183a0001c0008t0025g0026others(5): Show | 8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-8555A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599039 | ||||||
chr18:33599057
|
G | C | 1 | a0004c0004t0013g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.55-8537G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599057 | ||||||
chr18:33599230
|
A | T | 1 | a0002c0002t0005g0075 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.55-8364A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599230 | ||||||
chr18:33599231
|
T | A | 1 | a0002c0002t0005g0075 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.55-8363T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599231 | ||||||
chr18:33599306
|
G | T | 1 | a0001c0001t0037g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.55-8288G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599306 | ||||||
chr18:33599921
|
G | A | 1 | a0002c0002t0003g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.55-7673G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33599921 | ||||||
chr18:33600476
|
C | T | 1 | a0001c0001t0048g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.55-7118C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600476 | ||||||
chr18:33600497
|
G | GT | 43 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.55-7091dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33600497 | |||||
chr18:33600511
|
GAAGTTTT others(12): Show |
G | 13 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(10): Show | 13 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.55-7073_55-7055del others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33600511 | |||||
chr18:33600786
|
G | T | 56 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(53): Show | 56 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.55-6808G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600786 | ||||||
chr18:33600821
|
C | A | 2 | a0002c0006t0009g0030a0002c0006t0009g0031 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.55-6773C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600821 | ||||||
chr18:33600845
|
C | CA | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.55-6748dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33600845 | |||||
chr18:33600955
|
A | G | 1 | a0002c0002t0044g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.55-6639A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33600955 | ||||||
chr18:33601745
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.55-5849G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601745 | ||||||
chr18:33601785
|
G | GTATATAT others(17): Show |
1 | a0005c0024t0007g0028 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.55-5799_55-5798ins others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(19): Show |
1 | a0001c0008t0025g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.55-5799_55-5798ins others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0027g0034a0004c0004t0078g0215 | 2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(30): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(25): Show |
5 | a0001c0001t0004g0066a0001c0001t0054g0054a0002c0002t0003g0043others(2): Show | 5 | HG00741.hp2 HG01433.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(32): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(27): Show |
10 | a0001c0001t0007g0011a0001c0001t0008g0019a0001c0001t0008g0020others(7): Show | 10 | HG01070.hp2 HG01361.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(34): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(29): Show |
10 | a0001c0001t0001g0127a0001c0001t0006g0123a0001c0001t0008g0023others(7): Show | 10 | HG02559.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(36): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(31): Show |
11 | a0001c0001t0001g0056a0001c0001t0006g0124a0001c0001t0007g0012others(8): Show | 11 | HG00642.hp1 HG00673.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(38): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(33): Show |
11 | a0001c0001t0006g0125a0001c0001t0007g0014a0001c0001t0012g0018others(8): Show | 11 | HG00741.hp1 HG01943.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(40): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(35): Show |
8 | a0001c0001t0004g0172a0001c0001t0007g0025a0002c0002t0003g0069others(5): Show | 8 | HG00323.hp1 HG01261.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(42): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTATATAT others(39): Show |
2 | a0001c0001t0006g0217a0002c0002t0003g0136 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.55-5799_55-5798ins others(46): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTGTATAT others(3): Show |
7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(3): Show |
8 | a0001c0001t0039g0180a0002c0002t0018g0181a0002c0002t0018g0182others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(15): Show |
3 | a0002c0002t0005g0080a0002c0002t0005g0178a0002c0013t0046g0079 | 3 | HG00438.hp2 HG01975.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(17): Show |
1 | a0006c0010t0055g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(19): Show |
1 | a0001c0005t0017g0205 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(23): Show |
1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(30): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(25): Show |
2 | a0002c0002t0005g0168a0007c0009t0004g0160 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(32): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(27): Show |
2 | a0001c0017t0076g0175a0015c0014t0082g0003 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(34): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(29): Show |
5 | a0001c0001t0004g0141a0001c0001t0010g0156a0004c0004t0005g0046others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(36): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(31): Show |
6 | a0001c0001t0001g0157a0001c0001t0006g0171a0001c0001t0010g0158others(3): Show | 6 | HG00280.hp2 NA19003.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(38): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(33): Show |
7 | a0001c0001t0048g0165a0001c0005t0004g0062a0001c0005t0004g0166others(4): Show | 7 | HG00621.hp2 HG00735.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(40): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(35): Show |
7 | a0001c0001t0001g0041a0001c0001t0004g0167a0001c0001t0019g0154others(4): Show | 7 | HG00558.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(42): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(37): Show |
2 | a0001c0001t0075g0184a0001c0008t0081g0220 | 2 | HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(44): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(39): Show |
3 | a0001c0005t0056g0063a0002c0002t0005g0121a0014c0019t0058g0002 | 3 | HG02486.hp2 NA18999.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.55-5808_55-5807ins others(46): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601785
|
G | GTTTATAT others(41): Show |
1 | a0001c0001t0002g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55-5808_55-5807ins others(48): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33601785 | |||||
chr18:33601795
|
A | G | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55-5799A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601795 | ||||||
chr18:33601910
|
C | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55-5684C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601910 | ||||||
chr18:33601942
|
C | T | 1 | a0002c0002t0005g0039 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.55-5652C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33601942 | ||||||
chr18:33602059
|
T | C | 67 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(64): Show | 67 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.55-5535T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33602059 | ||||||
chr18:33602187
|
T | C | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-5407T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33602187 | ||||||
chr18:33602803
|
GATCAAAT others(26): Show |
G | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-4788_55-4756del others(33): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33602803 | |||||
chr18:33603396
|
G | A | 1 | a0004c0004t0005g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.55-4198G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603396 | ||||||
chr18:33603435
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.55-4159C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603435 | ||||||
chr18:33603445
|
C | T | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.55-4149C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603445 | ||||||
chr18:33603571
|
A | T | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-4023A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603571 | ||||||
chr18:33603617
|
T | A | 1 | a0001c0001t0006g0217 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55-3977T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603617 | ||||||
chr18:33603619
|
C | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-3975C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603619 | ||||||
chr18:33603715
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.55-3879G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603715 | ||||||
chr18:33603877
|
A | T | 1 | a0001c0001t0004g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.55-3717A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603877 | ||||||
chr18:33603878
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.55-3716A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33603878 | ||||||
chr18:33604421
|
C | T | 6 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-3173C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604421 | ||||||
chr18:33604449
|
G | GA | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-3140dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33604449 | |||||
chr18:33604607
|
C | T | 53 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0004g0066others(50): Show | 53 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.55-2987C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604607 | ||||||
chr18:33604617
|
A | G | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.55-2977A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604617 | ||||||
chr18:33604622
|
G | A | 35 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.55-2972G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604622 | ||||||
chr18:33604646
|
C | CT | 4 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(1): Show | 4 | HG02486.hp1 HG02895.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-2946dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 33604646 | |||||
chr18:33604667
|
G | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55-2927G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33604667 | ||||||
chr18:33605092
|
C | T | 6 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(3): Show | 6 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-2502C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605092 | ||||||
chr18:33605252
|
A | G | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-2342A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605252 | ||||||
chr18:33605411
|
T | C | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.55-2183T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605411 | ||||||
chr18:33605680
|
T | C | 1 | a0002c0002t0003g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.55-1914T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605680 | ||||||
chr18:33605732
|
G | A | 53 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0004g0066others(50): Show | 53 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.55-1862G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605732 | ||||||
chr18:33605888
|
C | G | 1 | a0001c0001t0014g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.55-1706C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605888 | ||||||
chr18:33605920
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55-1674G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33605920 | ||||||
chr18:33606130
|
C | T | 1 | a0005c0007t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.55-1464C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606130 | ||||||
chr18:33606153
|
A | G | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1441A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606153 | ||||||
chr18:33606374
|
G | T | 1 | a0001c0016t0062g0200 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.55-1220G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606374 | ||||||
chr18:33606636
|
T | C | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-958T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606636 | ||||||
chr18:33606772
|
C | G | 1 | a0001c0001t0002g0132 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.55-822C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606772 | ||||||
chr18:33606777
|
A | G | 5 | a0001c0001t0016g0192a0001c0001t0016g0204a0001c0001t0034g0195others(2): Show | 5 | HG00673.hp1 NA18982.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-817A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33606777 | ||||||
chr18:33607021
|
C | G | 138 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.55-573C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33607021 | ||||||
chr18:33607145
|
C | G | 3 | a0003c0003t0059g0005a0003c0003t0073g0009a0003c0003t0079g0007 | 3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.55-449C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 1/11 | chr18 | 33607145 | ||||||
chr18:33607742
|
G | A | 66 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(63): Show | 66 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.137+66G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607742 | ||||||
chr18:33607822
|
G | A | 1 | a0001c0001t0012g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+146G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607822 | ||||||
chr18:33607946
|
C | A | 38 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0004g0066others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.137+270C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607946 | ||||||
chr18:33607970
|
T | G | 3 | a0001c0001t0017g0008a0003c0003t0031g0174a0003c0003t0074g0173 | 3 | HG02258.hp1 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.137+294T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33607970 | ||||||
chr18:33608121
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137+445G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608121 | ||||||
chr18:33608176
|
G | A | 31 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(28): Show | 31 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.137+500G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608176 | ||||||
chr18:33608929
|
G | A | 1 | a0001c0001t0004g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.137+1253G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608929 | ||||||
chr18:33608932
|
C | G | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137+1256C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33608932 | ||||||
chr18:33608973
|
CT | C | 67 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(64): Show | 67 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.137+1308delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33608973 | |||||
chr18:33609211
|
A | T | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+1535A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609211 | ||||||
chr18:33609293
|
A | G | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+1617A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609293 | ||||||
chr18:33609377
|
G | C | 7 | a0002c0002t0018g0181a0002c0002t0018g0182a0002c0006t0009g0030others(4): Show | 7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+1701G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609377 | ||||||
chr18:33609459
|
C | T | 1 | a0002c0002t0018g0182 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.137+1783C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609459 | ||||||
chr18:33609514
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.137+1838T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609514 | ||||||
chr18:33609592
|
A | G | 35 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+1916A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609592 | ||||||
chr18:33609884
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.137+2208T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609884 | ||||||
chr18:33609903
|
T | C | 2 | a0001c0017t0076g0175a0015c0014t0082g0003 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.137+2227T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33609903 | ||||||
chr18:33610059
|
G | T | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.137+2383G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610059 | ||||||
chr18:33610527
|
A | G | 1 | a0002c0002t0042g0140 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.137+2851A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610527 | ||||||
chr18:33610529
|
C | T | 2 | a0001c0001t0002g0120a0001c0001t0057g0065 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.137+2853C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610529 | ||||||
chr18:33610545
|
A | G | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137+2869A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610545 | ||||||
chr18:33610580
|
C | T | 3 | a0001c0001t0075g0184a0001c0008t0081g0220a0014c0019t0058g0002 | 3 | HG02895.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137+2904C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610580 | ||||||
chr18:33610668
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.137+2992C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610668 | ||||||
chr18:33610691
|
T | G | 1 | a0002c0002t0013g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.137+3015T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610691 | ||||||
chr18:33610716
|
C | T | 30 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(27): Show | 30 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.137+3040C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610716 | ||||||
chr18:33610746
|
C | T | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+3070C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33610746 | ||||||
chr18:33610801
|
GATATTTA | G | 35 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+3129_137+3135d others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33610801 | |||||
chr18:33611215
|
G | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137+3539G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611215 | ||||||
chr18:33611305
|
T | C | 1 | a0005c0007t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.137+3629T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611305 | ||||||
chr18:33611347
|
T | C | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+3671T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611347 | ||||||
chr18:33611532
|
T | C | 1 | a0001c0001t0002g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.137+3856T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611532 | ||||||
chr18:33611583
|
T | C | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+3907T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611583 | ||||||
chr18:33611842
|
G | A | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+4166G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611842 | ||||||
chr18:33611916
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.137+4240C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33611916 | ||||||
chr18:33611959
|
T | TA | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137+4284dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33611959 | |||||
chr18:33612106
|
G | A | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+4430G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612106 | ||||||
chr18:33612106
|
G | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.137+4430G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612106 | ||||||
chr18:33612184
|
C | CAT | 33 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0002g0207others(30): Show | 33 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.137+4522_137+4523d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33612184 | |||||
chr18:33612184
|
C | CATAT | 2 | a0001c0001t0039g0180a0002c0006t0009g0037 | 2 | HG02145.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.137+4520_137+4523d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33612184 | |||||
chr18:33612184
|
C | CATATAT | 35 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+4518_137+4523d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33612184 | |||||
chr18:33612565
|
A | G | 55 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0004g0066others(52): Show | 55 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.137+4889A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612565 | ||||||
chr18:33612668
|
G | A | 1 | a0002c0002t0005g0178 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.137+4992G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612668 | ||||||
chr18:33612835
|
C | A | 1 | a0004c0004t0078g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.137+5159C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612835 | ||||||
chr18:33612863
|
T | C | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+5187T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33612863 | ||||||
chr18:33613335
|
C | G | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+5659C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613335 | ||||||
chr18:33613525
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0049others(4): Show | 7 | HG00558.hp1 HG02148.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+5849T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613525 | ||||||
chr18:33613585
|
T | A | 3 | a0003c0003t0059g0005a0003c0003t0073g0009a0003c0003t0079g0007 | 3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.137+5909T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613585 | ||||||
chr18:33613614
|
A | G | 1 | a0001c0001t0011g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.137+5938A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613614 | ||||||
chr18:33613678
|
G | A | 1 | a0005c0007t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.137+6002G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613678 | ||||||
chr18:33613800
|
A | G | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.137+6124A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33613800 | ||||||
chr18:33614066
|
A | G | 1 | a0001c0001t0012g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.137+6390A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614066 | ||||||
chr18:33614163
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0004g0103a0001c0001t0053g0102 | 3 | NA18971.hp2 NA19003.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.137+6487A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614163 | ||||||
chr18:33614284
|
C | T | 1 | a0001c0001t0029g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.137+6608C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614284 | ||||||
chr18:33614435
|
C | T | 1 | a0007c0009t0004g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137+6759C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614435 | ||||||
chr18:33614556
|
T | C | 1 | a0001c0001t0040g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.137+6880T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614556 | ||||||
chr18:33614588
|
A | G | 1 | a0002c0002t0003g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.137+6912A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614588 | ||||||
chr18:33614672
|
T | A | 2 | a0002c0002t0003g0143a0002c0002t0003g0144 | 2 | HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.137+6996T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614672 | ||||||
chr18:33614821
|
CT | C | 6 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(3): Show | 6 | HG01943.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+7157delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33614821 | |||||
chr18:33614980
|
G | A | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137+7304G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33614980 | ||||||
chr18:33615179
|
A | G | 1 | a0003c0003t0059g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.137+7503A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615179 | ||||||
chr18:33615238
|
T | C | 1 | a0001c0005t0004g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.137+7562T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615238 | ||||||
chr18:33615460
|
G | A | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+7784G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615460 | ||||||
chr18:33615841
|
A | G | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+8165A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615841 | ||||||
chr18:33615845
|
C | T | 1 | a0008c0011t0003g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.137+8169C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33615845 | ||||||
chr18:33616039
|
A | G | 7 | a0002c0002t0018g0181a0002c0002t0018g0182a0002c0006t0009g0030others(4): Show | 7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+8363A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616039 | ||||||
chr18:33616128
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.137+8452A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616128 | ||||||
chr18:33616177
|
T | C | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+8501T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616177 | ||||||
chr18:33616366
|
C | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0191others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+8690C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616366 | ||||||
chr18:33616398
|
C | CTG | 54 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0002g0120others(51): Show | 54 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.137+8752_137+8753d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
C | CTGTG | 3 | a0001c0001t0029g0029a0002c0002t0003g0057a0002c0002t0003g0144 | 3 | HG02886.hp2 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.137+8750_137+8753d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
CTG | C | 47 | a0001c0001t0001g0045a0001c0001t0001g0083a0001c0001t0001g0101others(44): Show | 47 | HG00280.hp1 HG00438.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.137+8752_137+8753d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
CTGTG | C | 4 | a0001c0001t0006g0090a0001c0008t0025g0026a0005c0024t0007g0028others(1): Show | 4 | HG02723.hp2 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+8750_137+8753d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
CTGTGTG | C | 34 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(31): Show | 34 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.137+8748_137+8753d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
CTGTGTGT others(1): Show |
C | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137+8746_137+8753d others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0014g0199 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.137+8742_137+8753d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616398
|
CTGTGTGT others(7): Show |
C | 29 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(26): Show | 29 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.137+8740_137+8753d others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33616398 | |||||
chr18:33616665
|
T | A | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+8989T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616665 | ||||||
chr18:33616701
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.137+9025A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33616701 | ||||||
chr18:33617030
|
T | C | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.137+9354T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617030 | ||||||
chr18:33617274
|
T | C | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.137+9598T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617274 | ||||||
chr18:33617297
|
G | A | 4 | a0001c0001t0016g0192a0001c0001t0016g0204a0001c0001t0037g0196others(1): Show | 4 | NA18982.hp1 NA18998.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+9621G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617297 | ||||||
chr18:33617367
|
C | T | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.137+9691C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617367 | ||||||
chr18:33617368
|
G | A | 29 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(26): Show | 29 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.137+9692G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617368 | ||||||
chr18:33617390
|
CTGAGGCA others(6): Show |
C | 1 | a0002c0002t0005g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+9716_137+9728d others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33617390 | |||||
chr18:33617924
|
T | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.137+10248T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617924 | ||||||
chr18:33617954
|
C | T | 1 | a0001c0001t0011g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.137+10278C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33617954 | ||||||
chr18:33618085
|
T | C | 1 | a0006c0010t0061g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.137+10409T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618085 | ||||||
chr18:33618325
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.137+10649A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618325 | ||||||
chr18:33618655
|
G | T | 2 | a0001c0001t0004g0172a0002c0002t0030g0179 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+10979G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618655 | ||||||
chr18:33618769
|
TTGA | T | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+11096_137+1109 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33618769 | |||||
chr18:33618831
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.137+11155A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33618831 | ||||||
chr18:33619159
|
C | G | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+11483C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619159 | ||||||
chr18:33619446
|
GA | G | 41 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(38): Show | 41 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.137+11785delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33619446 | |||||
chr18:33619446
|
GAA | G | 90 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(87): Show | 90 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.137+11784_137+1178 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33619446 | |||||
chr18:33619446
|
GAAA | G | 6 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+11783_137+1178 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33619446 | |||||
chr18:33619455
|
A | T | 8 | a0001c0001t0004g0172a0001c0001t0038g0183a0001c0008t0025g0026others(5): Show | 8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+11779A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619455 | ||||||
chr18:33619499
|
C | T | 9 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(6): Show | 9 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+11823C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619499 | ||||||
chr18:33619560
|
T | C | 14 | a0001c0001t0001g0157a0001c0001t0004g0167a0001c0001t0006g0171others(11): Show | 14 | HG00558.hp2 HG00621.hp2 HG04184.hp1 others(11): Show |
intron_variant | MODIFIER | c.137+11884T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619560 | ||||||
chr18:33619741
|
T | C | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+12065T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619741 | ||||||
chr18:33619809
|
C | T | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+12133C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619809 | ||||||
chr18:33619867
|
C | G | 32 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(29): Show | 32 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.137+12191C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33619867 | ||||||
chr18:33620431
|
C | T | 1 | a0001c0001t0006g0171 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.137+12755C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620431 | ||||||
chr18:33620491
|
G | A | 1 | a0001c0001t0007g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137+12815G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620491 | ||||||
chr18:33620713
|
A | C | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+13037A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620713 | ||||||
chr18:33620836
|
C | G | 32 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(29): Show | 32 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(29): Show |
intron_variant | MODIFIER | c.137+13160C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620836 | ||||||
chr18:33620943
|
A | G | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+13267A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33620943 | ||||||
chr18:33621364
|
G | A | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+13688G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621364 | ||||||
chr18:33621378
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137+13702G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621378 | ||||||
chr18:33621443
|
C | A | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.137+13767C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621443 | ||||||
chr18:33621462
|
A | G | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+13786A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621462 | ||||||
chr18:33621541
|
T | C | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+13865T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33621541 | ||||||
chr18:33622142
|
G | A | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+14466G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622142 | ||||||
chr18:33622189
|
T | A | 5 | a0001c0001t0004g0141a0004c0004t0005g0046a0004c0004t0032g0059others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+14513T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622189 | ||||||
chr18:33622229
|
G | A | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.137+14553G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622229 | ||||||
chr18:33622246
|
C | T | 1 | a0002c0002t0003g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.137+14570C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622246 | ||||||
chr18:33622308
|
GT | G | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.137+14633delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622308 | ||||||
chr18:33622353
|
G | A | 34 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(31): Show | 34 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.137+14677G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622353 | ||||||
chr18:33622397
|
T | G | 67 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(64): Show | 67 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.137+14721T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622397 | ||||||
chr18:33622413
|
T | C | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.137+14737T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622413 | ||||||
chr18:33622587
|
G | A | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+14911G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622587 | ||||||
chr18:33622803
|
A | T | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137+15127A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33622803 | ||||||
chr18:33623014
|
T | A | 1 | a0014c0019t0058g0002 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137+15338T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623014 | ||||||
chr18:33623083
|
C | G | 6 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(3): Show | 6 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+15407C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623083 | ||||||
chr18:33623091
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0051g0097a0002c0002t0005g0075 | 3 | HG00621.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.137+15415A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623091 | ||||||
chr18:33623259
|
A | G | 1 | a0009c0023t0050g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.137+15583A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623259 | ||||||
chr18:33623336
|
C | T | 35 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(32): Show | 35 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.137+15660C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623336 | ||||||
chr18:33623659
|
C | T | 55 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0004g0066others(52): Show | 55 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.137+15983C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623659 | ||||||
chr18:33623795
|
T | C | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.137+16119T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623795 | ||||||
chr18:33623830
|
A | C | 1 | a0002c0006t0036g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.137+16154A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623830 | ||||||
chr18:33623855
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0096 | 2 | HG00323.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.137+16179A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623855 | ||||||
chr18:33623965
|
T | C | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+16289T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33623965 | ||||||
chr18:33624009
|
C | A | 1 | a0001c0001t0016g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.137+16333C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624009 | ||||||
chr18:33624237
|
A | G | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+16561A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624237 | ||||||
chr18:33624264
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.137+16588G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624264 | ||||||
chr18:33624264
|
G | C | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+16588G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624264 | ||||||
chr18:33624766
|
T | G | 1 | a0004c0004t0072g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.137+17090T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624766 | ||||||
chr18:33624974
|
C | T | 2 | a0001c0001t0014g0201a0006c0025t0077g0004 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.137+17298C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33624974 | ||||||
chr18:33625059
|
A | G | 2 | a0001c0001t0004g0172a0002c0002t0030g0179 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+17383A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625059 | ||||||
chr18:33625152
|
A | C | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+17476A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625152 | ||||||
chr18:33625225
|
C | G | 30 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(27): Show | 30 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.137+17549C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625225 | ||||||
chr18:33625245
|
G | A | 24 | a0001c0001t0001g0127a0001c0001t0006g0123a0001c0001t0006g0124others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.137+17569G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625245 | ||||||
chr18:33625324
|
A | T | 1 | a0008c0011t0003g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.137+17648A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625324 | ||||||
chr18:33625730
|
G | A | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+18054G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625730 | ||||||
chr18:33625988
|
T | G | 17 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(14): Show | 17 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.137+18312T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33625988 | ||||||
chr18:33626030
|
A | G | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.137+18354A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626030 | ||||||
chr18:33626202
|
T | C | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.137+18526T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626202 | ||||||
chr18:33626360
|
T | A | 218 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.138-18534T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626360 | ||||||
chr18:33626385
|
A | G | 105 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.138-18509A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626385 | ||||||
chr18:33626416
|
C | A | 137 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.138-18478C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626416 | ||||||
chr18:33626657
|
A | T | 138 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(135): Show | 138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.138-18237A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33626657 | ||||||
chr18:33628037
|
C | A | 1 | a0001c0001t0019g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.138-16857C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628037 | ||||||
chr18:33628489
|
G | A | 68 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0002g0207others(65): Show | 68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-16405G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628489 | ||||||
chr18:33628532
|
A | T | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-16362A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628532 | ||||||
chr18:33628568
|
A | T | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-16326A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628568 | ||||||
chr18:33628688
|
G | A | 1 | a0002c0002t0003g0137 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.138-16206G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628688 | ||||||
chr18:33628696
|
T | A | 68 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0002g0207others(65): Show | 68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-16198T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628696 | ||||||
chr18:33628754
|
TC | T | 68 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0002g0207others(65): Show | 68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-16139delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628754 | ||||||
chr18:33628831
|
T | G | 1 | a0001c0005t0004g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.138-16063T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628831 | ||||||
chr18:33628982
|
G | T | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.138-15912G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33628982 | ||||||
chr18:33629491
|
T | C | 1 | a0002c0002t0005g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.138-15403T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33629491 | ||||||
chr18:33629814
|
C | T | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.138-15080C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33629814 | ||||||
chr18:33630020
|
C | T | 5 | a0001c0001t0004g0066a0001c0001t0027g0034a0001c0001t0029g0029others(2): Show | 5 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-14874C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630020 | ||||||
chr18:33630066
|
G | T | 6 | a0001c0001t0004g0172a0001c0001t0038g0183a0001c0008t0025g0026others(3): Show | 6 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-14828G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630066 | ||||||
chr18:33630112
|
G | C | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-14782G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630112 | ||||||
chr18:33630168
|
G | A | 128 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0127others(125): Show | 128 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.138-14726G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630168 | ||||||
chr18:33630246
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.138-14648C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630246 | ||||||
chr18:33630274
|
G | C | 1 | a0006c0010t0055g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138-14620G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630274 | ||||||
chr18:33630386
|
C | CT | 39 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0157others(36): Show | 39 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.138-14498dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33630386 | |||||
chr18:33630408
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.138-14486A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630408 | ||||||
chr18:33630509
|
G | T | 4 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(1): Show | 4 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-14385G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630509 | ||||||
chr18:33630609
|
T | G | 1 | a0002c0002t0003g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.138-14285T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630609 | ||||||
chr18:33630645
|
C | A | 1 | a0002c0002t0003g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138-14249C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33630645 | ||||||
chr18:33631050
|
A | C | 1 | a0001c0001t0029g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.138-13844A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631050 | ||||||
chr18:33631122
|
ACATT | A | 5 | a0001c0001t0004g0066a0001c0001t0027g0034a0001c0001t0029g0029others(2): Show | 5 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-13771_138-1376 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631122 | ||||||
chr18:33631241
|
A | G | 2 | a0001c0001t0065g0067a0001c0001t0075g0184 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.138-13653A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631241 | ||||||
chr18:33631295
|
A | C | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.138-13599A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631295 | ||||||
chr18:33631373
|
A | G | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.138-13521A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631373 | ||||||
chr18:33631555
|
T | C | 1 | a0001c0001t0070g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.138-13339T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631555 | ||||||
chr18:33631656
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138-13238T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631656 | ||||||
chr18:33631846
|
T | A | 1 | a0001c0001t0007g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.138-13048T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631846 | ||||||
chr18:33631863
|
A | G | 1 | a0001c0001t0006g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.138-13031A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33631863 | ||||||
chr18:33632002
|
A | G | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.138-12892A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632002 | ||||||
chr18:33632245
|
G | A | 68 | a0001c0001t0001g0056a0001c0001t0001g0127a0001c0001t0002g0207others(65): Show | 68 | HG00323.hp1 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.138-12649G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632245 | ||||||
chr18:33632248
|
T | A | 7 | a0001c0001t0026g0035a0001c0001t0028g0036a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-12646T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632248 | ||||||
chr18:33632644
|
A | G | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.138-12250A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632644 | ||||||
chr18:33632801
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.138-12093C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632801 | ||||||
chr18:33632881
|
T | C | 1 | a0001c0001t0006g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138-12013T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33632881 | ||||||
chr18:33633166
|
A | G | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-11728A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633166 | ||||||
chr18:33633374
|
A | G | 1 | a0004c0004t0078g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.138-11520A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633374 | ||||||
chr18:33633562
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.138-11332C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633562 | ||||||
chr18:33633575
|
G | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-11319G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633575 | ||||||
chr18:33633579
|
C | T | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-11315C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633579 | ||||||
chr18:33633667
|
C | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138-11227C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633667 | ||||||
chr18:33633737
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.138-11157C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633737 | ||||||
chr18:33633843
|
CA | C | 77 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0061others(74): Show | 77 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.138-11029delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633843 | |||||
chr18:33633843
|
CAA | C | 27 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0002g0186others(24): Show | 27 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.138-11030_138-1102 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633843 | |||||
chr18:33633843
|
CAAA | C | 43 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0004g0167others(40): Show | 43 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.138-11031_138-1102 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633843 | |||||
chr18:33633875
|
CAATT | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG00558.hp1 HG02148.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-11015_138-1101 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33633875 | |||||
chr18:33633893
|
G | A | 1 | a0001c0001t0029g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.138-11001G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633893 | ||||||
chr18:33633999
|
T | C | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-10895T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33633999 | ||||||
chr18:33634161
|
G | T | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-10733G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634161 | ||||||
chr18:33634285
|
A | G | 2 | a0001c0001t0002g0120a0001c0001t0057g0065 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.138-10609A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634285 | ||||||
chr18:33634667
|
A | G | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-10227A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634667 | ||||||
chr18:33634810
|
C | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-10084C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634810 | ||||||
chr18:33634872
|
G | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138-10022G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634872 | ||||||
chr18:33634929
|
T | C | 1 | a0001c0001t0065g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.138-9965T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634929 | ||||||
chr18:33634964
|
A | T | 45 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.138-9930A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634964 | ||||||
chr18:33634986
|
G | C | 147 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(144): Show | 147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.138-9908G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33634986 | ||||||
chr18:33635031
|
A | T | 1 | a0001c0001t0064g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138-9863A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635031 | ||||||
chr18:33635311
|
T | C | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138-9583T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635311 | ||||||
chr18:33635354
|
T | C | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-9540T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635354 | ||||||
chr18:33635516
|
A | C | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.138-9378A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635516 | ||||||
chr18:33635730
|
T | A | 4 | a0001c0001t0006g0197a0001c0001t0014g0199a0001c0001t0021g0198others(1): Show | 4 | NA18948.hp2 NA18970.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-9164T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635730 | ||||||
chr18:33635848
|
A | G | 8 | a0001c0001t0004g0172a0001c0001t0038g0183a0001c0008t0025g0026others(5): Show | 8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-9046A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33635848 | ||||||
chr18:33636115
|
G | A | 103 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.138-8779G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636115 | ||||||
chr18:33636281
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138-8613C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636281 | ||||||
chr18:33636305
|
T | TCAA | 6 | a0001c0001t0039g0180a0001c0008t0025g0026a0002c0002t0013g0064others(3): Show | 6 | HG01981.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-8562_138-8560d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636305 | |||||
chr18:33636305
|
T | TCAACAA | 2 | a0001c0001t0038g0183a0003c0003t0066g0216 | 2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138-8565_138-8560d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636305 | |||||
chr18:33636305
|
TCAACAAC others(5): Show |
T | 20 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(17): Show | 20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.138-8571_138-8560d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636305 | |||||
chr18:33636329
|
ACAACAG | A | 34 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(31): Show | 34 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.138-8559_138-8554d others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636329 | |||||
chr18:33636331
|
AACAGCAA others(11): Show |
A | 11 | a0001c0001t0001g0045a0001c0001t0001g0095a0001c0001t0004g0052others(8): Show | 11 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-8559_138-8542d others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636331 | |||||
chr18:33636332
|
ACAG | A | 3 | a0002c0002t0005g0168a0004c0004t0005g0046a0006c0010t0055g0170 | 3 | HG01255.hp2 HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.138-8559_138-8557d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636332 | |||||
chr18:33636334
|
AGCAACAA others(8): Show |
A | 71 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0073others(68): Show | 71 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.138-8559_138-8545d others(17): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636334 | ||||||
chr18:33636335
|
G | A | 21 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0083others(18): Show | 21 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.138-8559G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636335 | ||||||
chr18:33636337
|
A | C | 7 | a0001c0001t0004g0172a0001c0001t0038g0183a0001c0008t0025g0026others(4): Show | 7 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-8557A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636337 | ||||||
chr18:33636337
|
AACAACAA others(5): Show |
A | 19 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0083others(16): Show | 19 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.138-8529_138-8518d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636337 | |||||
chr18:33636340
|
AACAACAG others(2): Show |
A | 2 | a0001c0001t0001g0092a0006c0025t0077g0004 | 2 | HG02602.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.138-8547_138-8539d others(11): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33636340 | |||||
chr18:33636349
|
C | A | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-8545C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636349 | ||||||
chr18:33636412
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.138-8482G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636412 | ||||||
chr18:33636568
|
G | A | 147 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(144): Show | 147 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.138-8326G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636568 | ||||||
chr18:33636626
|
A | G | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-8268A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636626 | ||||||
chr18:33636792
|
T | C | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-8102T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636792 | ||||||
chr18:33636805
|
T | A | 9 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0027g0034others(6): Show | 9 | HG00673.hp2 HG02258.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-8089T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636805 | ||||||
chr18:33636806
|
A | T | 2 | a0002c0002t0002g0112a0002c0002t0030g0179 | 2 | HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.138-8088A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33636806 | ||||||
chr18:33637104
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138-7790C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637104 | ||||||
chr18:33637230
|
A | G | 154 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.138-7664A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637230 | ||||||
chr18:33637251
|
A | G | 1 | a0001c0001t0004g0167 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.138-7643A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637251 | ||||||
chr18:33637422
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.138-7472A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637422 | ||||||
chr18:33637460
|
A | G | 2 | a0002c0002t0003g0136a0002c0002t0043g0134 | 2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.138-7434A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637460 | ||||||
chr18:33637625
|
T | G | 2 | a0001c0001t0054g0054a0002c0002t0003g0043 | 2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.138-7269T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637625 | ||||||
chr18:33637981
|
G | A | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(3): Show | 6 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-6913G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33637981 | ||||||
chr18:33638005
|
A | C | 88 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.138-6889A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638005 | ||||||
chr18:33638011
|
C | T | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.138-6883C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638011 | ||||||
chr18:33638056
|
T | C | 4 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(1): Show | 4 | HG00280.hp2 HG01109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-6838T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638056 | ||||||
chr18:33638112
|
G | A | 44 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(41): Show | 44 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.138-6782G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638112 | ||||||
chr18:33638133
|
G | GTA | 58 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(55): Show | 58 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.138-6748_138-6747d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33638133 | |||||
chr18:33638146
|
T | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138-6748T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638146 | ||||||
chr18:33638159
|
TAGTG | T | 4 | a0001c0008t0025g0026a0002c0006t0023g0027a0004c0004t0078g0215others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-6734_138-6731d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638159 | ||||||
chr18:33638181
|
T | A | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-6713T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638181 | ||||||
chr18:33638205
|
G | GAT | 4 | a0001c0001t0010g0082a0001c0001t0010g0085a0002c0002t0005g0131others(1): Show | 4 | HG00438.hp1 HG02129.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-6678_138-6677d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33638205 | |||||
chr18:33638310
|
G | A | 5 | a0001c0001t0016g0192a0001c0001t0016g0204a0001c0001t0034g0195others(2): Show | 5 | HG00673.hp1 NA18982.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-6584G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638310 | ||||||
chr18:33638397
|
G | A | 1 | a0001c0001t0028g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.138-6497G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638397 | ||||||
chr18:33638815
|
A | T | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.138-6079A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638815 | ||||||
chr18:33638937
|
C | T | 5 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(2): Show | 5 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-5957C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33638937 | ||||||
chr18:33639130
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.138-5764G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639130 | ||||||
chr18:33639270
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.138-5624C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639270 | ||||||
chr18:33639271
|
A | G | 151 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.138-5623A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639271 | ||||||
chr18:33639380
|
G | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-5514G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639380 | ||||||
chr18:33639555
|
A | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138-5339A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639555 | ||||||
chr18:33639815
|
T | A | 45 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.138-5079T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639815 | ||||||
chr18:33639838
|
T | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-5056T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639838 | ||||||
chr18:33639908
|
A | C | 148 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.138-4986A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33639908 | ||||||
chr18:33640285
|
C | T | 6 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0027g0034others(3): Show | 6 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-4609C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640285 | ||||||
chr18:33640286
|
A | G | 4 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(1): Show | 4 | HG02486.hp1 HG02895.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-4608A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640286 | ||||||
chr18:33640333
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.138-4561C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640333 | ||||||
chr18:33640542
|
T | C | 1 | a0001c0001t0004g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.138-4352T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640542 | ||||||
chr18:33640789
|
A | G | 1 | a0002c0002t0005g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.138-4105A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640789 | ||||||
chr18:33640852
|
T | TCA | 149 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.138-4042_138-4041i others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33640852 | ||||||
chr18:33641331
|
C | T | 2 | a0001c0001t0075g0184a0014c0019t0058g0002 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.138-3563C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641331 | ||||||
chr18:33641332
|
G | A | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-3562G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641332 | ||||||
chr18:33641406
|
AAAC | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-3485_138-3483d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33641406 | |||||
chr18:33641726
|
G | T | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138-3168G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641726 | ||||||
chr18:33641871
|
T | C | 1 | a0002c0002t0005g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138-3023T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641871 | ||||||
chr18:33641995
|
C | G | 2 | a0001c0001t0001g0157a0002c0002t0005g0162 | 2 | NA19003.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.138-2899C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33641995 | ||||||
chr18:33642118
|
A | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138-2776A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642118 | ||||||
chr18:33642551
|
A | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138-2343A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642551 | ||||||
chr18:33642682
|
A | T | 1 | a0001c0001t0010g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.138-2212A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642682 | ||||||
chr18:33642880
|
G | A | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.138-2014G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642880 | ||||||
chr18:33642953
|
G | T | 1 | a0001c0001t0001g0061 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.138-1941G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33642953 | ||||||
chr18:33643100
|
C | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-1794C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643100 | ||||||
chr18:33643159
|
C | A | 1 | a0001c0001t0016g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.138-1735C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643159 | ||||||
chr18:33643576
|
A | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138-1318A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643576 | ||||||
chr18:33643632
|
G | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-1262G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643632 | ||||||
chr18:33643745
|
T | A | 2 | a0002c0002t0003g0136a0002c0002t0043g0134 | 2 | HG01070.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.138-1149T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643745 | ||||||
chr18:33643760
|
T | C | 149 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.138-1134T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643760 | ||||||
chr18:33643812
|
A | G | 83 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.138-1082A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33643812 | ||||||
chr18:33644203
|
A | G | 2 | a0001c0001t0006g0217a0002c0002t0003g0218 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.138-691A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644203 | ||||||
chr18:33644311
|
A | G | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-583A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644311 | ||||||
chr18:33644366
|
G | A | 1 | a0001c0001t0004g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.138-528G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644366 | ||||||
chr18:33644478
|
G | GT | 8 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0006g0123others(5): Show | 8 | HG01358.hp1 HG02145.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-403dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 33644478 | |||||
chr18:33644482
|
T | C | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138-412T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644482 | ||||||
chr18:33644558
|
G | T | 3 | a0002c0002t0003g0108a0002c0002t0003g0109a0005c0007t0001g0107 | 3 | HG01109.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.138-336G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644558 | ||||||
chr18:33644559
|
T | A | 3 | a0002c0002t0003g0108a0002c0002t0003g0109a0005c0007t0001g0107 | 3 | HG01109.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.138-335T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644559 | ||||||
chr18:33644560
|
A | C | 3 | a0002c0002t0003g0108a0002c0002t0003g0109a0005c0007t0001g0107 | 3 | HG01109.hp1 HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.138-334A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644560 | ||||||
chr18:33644705
|
G | A | 1 | a0001c0001t0034g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.138-189G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644705 | ||||||
chr18:33644796
|
T | A | 1 | a0001c0001t0011g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138-98T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 2/11 | chr18 | 33644796 | ||||||
chr18:33645066
|
G | T | 84 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.246+64G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645066 | ||||||
chr18:33645182
|
A | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.246+180A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645182 | ||||||
chr18:33645402
|
T | G | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.246+400T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645402 | ||||||
chr18:33645499
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0065g0067a0016c0026t0052g0044 | 3 | HG02055.hp1 HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.246+497G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33645499 | ||||||
chr18:33645754
|
G | GT | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.247-482dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 33645754 | |||||
chr18:33646036
|
A | G | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.247-209A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646036 | ||||||
chr18:33646050
|
A | T | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.247-195A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646050 | ||||||
chr18:33646094
|
T | C | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.247-151T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646094 | ||||||
chr18:33646175
|
C | T | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.247-70C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 3/11 | chr18 | 33646175 | ||||||
chr18:33646473
|
C | T | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.355+120C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646473 | ||||||
chr18:33646474
|
G | A | 1 | a0001c0001t0022g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355+121G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646474 | ||||||
chr18:33646610
|
C | T | 196 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(193): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.355+257C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646610 | ||||||
chr18:33646635
|
G | A | 2 | a0001c0001t0002g0038a0002c0002t0003g0137 | 2 | HG01943.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.355+282G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646635 | ||||||
chr18:33646880
|
C | CG | 59 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0001g0087others(56): Show | 59 | HG00280.hp2 HG00438.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.355+539dupG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33646880 | |||||
chr18:33646880
|
C | CGG | 26 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0127others(23): Show | 26 | HG00642.hp1 HG00673.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.355+538_355+539dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33646880 | |||||
chr18:33646880
|
CG | C | 20 | a0001c0001t0002g0110a0001c0001t0002g0132a0001c0001t0002g0186others(17): Show | 20 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.355+539delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33646880 | |||||
chr18:33646881
|
G | C | 8 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0006g0125others(5): Show | 8 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+528G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646881 | ||||||
chr18:33646891
|
G | A | 8 | a0001c0001t0001g0056a0001c0001t0054g0054a0002c0002t0003g0043others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+538G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646891 | ||||||
chr18:33646892
|
G | GA | 15 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0006g0171others(12): Show | 15 | HG00558.hp2 HG00735.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.355+539_355+540ins others(1): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646892 | ||||||
chr18:33646946
|
A | C | 1 | a0008c0011t0003g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.355+593A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646946 | ||||||
chr18:33646950
|
A | G | 1 | a0002c0002t0005g0039 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.355+597A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33646950 | ||||||
chr18:33647098
|
GTC | G | 5 | a0004c0004t0005g0046a0004c0004t0032g0059a0004c0004t0045g0058others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+749_355+750del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33647098 | |||||
chr18:33647247
|
G | T | 82 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.355+894G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647247 | ||||||
chr18:33647261
|
C | A | 1 | a0001c0001t0006g0197 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.355+908C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647261 | ||||||
chr18:33647287
|
C | G | 1 | a0002c0002t0020g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.355+934C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647287 | ||||||
chr18:33647309
|
C | T | 1 | a0001c0001t0080g0006 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.355+956C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647309 | ||||||
chr18:33647310
|
G | A | 1 | a0001c0001t0011g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.355+957G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647310 | ||||||
chr18:33647655
|
C | T | 4 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(1): Show | 4 | HG00280.hp2 HG01109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1302C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647655 | ||||||
chr18:33647698
|
T | C | 1 | a0001c0001t0026g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.355+1345T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647698 | ||||||
chr18:33647731
|
C | A | 1 | a0001c0001t0071g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.355+1378C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647731 | ||||||
chr18:33647797
|
T | C | 1 | a0001c0005t0056g0063 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.355+1444T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647797 | ||||||
chr18:33647803
|
T | C | 143 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.355+1450T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647803 | ||||||
chr18:33647850
|
A | G | 1 | a0001c0001t0070g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355+1497A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647850 | ||||||
chr18:33647892
|
G | C | 1 | a0001c0001t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.355+1539G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33647892 | ||||||
chr18:33648205
|
G | A | 2 | a0001c0001t0075g0184a0014c0019t0058g0002 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355+1852G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648205 | ||||||
chr18:33648326
|
A | T | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.355+1973A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648326 | ||||||
chr18:33648392
|
G | A | 1 | a0006c0010t0061g0185 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.355+2039G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648392 | ||||||
chr18:33648692
|
TAGAAA | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG01884.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+2346_355+2350d others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33648692 | |||||
chr18:33648753
|
A | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.355+2400A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33648753 | ||||||
chr18:33649683
|
G | A | 103 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.355+3330G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649683 | ||||||
chr18:33649691
|
A | T | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+3338A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649691 | ||||||
chr18:33649854
|
A | G | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.355+3501A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649854 | ||||||
chr18:33649888
|
C | A | 44 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(41): Show | 44 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.355+3535C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33649888 | ||||||
chr18:33650020
|
G | A | 148 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.355+3667G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650020 | ||||||
chr18:33650077
|
A | C | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.355+3724A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650077 | ||||||
chr18:33650170
|
A | C | 4 | a0001c0008t0025g0026a0002c0006t0023g0027a0004c0004t0078g0215others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3817A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650170 | ||||||
chr18:33650265
|
G | A | 45 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+3912G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650265 | ||||||
chr18:33650412
|
G | C | 1 | a0002c0002t0044g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.355+4059G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650412 | ||||||
chr18:33650442
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.355+4089C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650442 | ||||||
chr18:33650511
|
T | C | 6 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0027g0034others(3): Show | 6 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+4158T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650511 | ||||||
chr18:33650540
|
A | C | 2 | a0001c0001t0075g0184a0014c0019t0058g0002 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.355+4187A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650540 | ||||||
chr18:33650667
|
T | C | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.355+4314T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650667 | ||||||
chr18:33650698
|
C | T | 2 | a0001c0001t0004g0172a0002c0002t0030g0179 | 2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.355+4345C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33650698 | ||||||
chr18:33651052
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.355+4699C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33651052 | ||||||
chr18:33651916
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.355+5563A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33651916 | ||||||
chr18:33652094
|
C | T | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.355+5741C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652094 | ||||||
chr18:33652516
|
G | C | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.355+6163G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652516 | ||||||
chr18:33652585
|
T | C | 103 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.355+6232T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652585 | ||||||
chr18:33652603
|
C | CAAAAAAA others(3): Show |
76 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(73): Show | 76 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.355+6254_355+6263d others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652603
|
C | CAAAAAAA others(4): Show |
22 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0127others(19): Show | 22 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.355+6253_355+6263d others(13): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652603
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0007g0025a0002c0013t0046g0079a0003c0003t0069g0010others(1): Show | 4 | HG00438.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+6252_355+6263d others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652603
|
C | CAAAAAAA others(9): Show |
26 | a0001c0001t0001g0157a0001c0001t0002g0159a0001c0001t0006g0171others(23): Show | 26 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.355+6263_355+6264i others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652603
|
C | CAAAAAAA others(10): Show |
8 | a0001c0001t0001g0041a0001c0001t0004g0141a0001c0001t0004g0167others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+6263_355+6264i others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652603
|
C | CAAAAAAA others(11): Show |
1 | a0001c0005t0017g0205 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.355+6263_355+6264i others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652603
|
C | CAAAAAAA others(13): Show |
1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355+6263_355+6264i others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33652603 | |||||
chr18:33652997
|
G | A | 2 | a0002c0002t0003g0055a0002c0002t0003g0057 | 2 | HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.355+6644G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33652997 | ||||||
chr18:33653251
|
G | A | 25 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(22): Show | 25 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.355+6898G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653251 | ||||||
chr18:33653427
|
T | C | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+7074T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653427 | ||||||
chr18:33653441
|
C | G | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.355+7088C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653441 | ||||||
chr18:33653607
|
C | T | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.355+7254C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653607 | ||||||
chr18:33653615
|
C | A | 1 | a0012c0021t0001g0072 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.355+7262C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653615 | ||||||
chr18:33653708
|
A | G | 1 | a0001c0001t0006g0217 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.355+7355A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33653708 | ||||||
chr18:33653863
|
C | CT | 45 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+7520dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33653863 | |||||
chr18:33654044
|
A | G | 1 | a0001c0001t0071g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.356-7572A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654044 | ||||||
chr18:33654373
|
A | G | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.356-7243A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654373 | ||||||
chr18:33654488
|
G | T | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-7128G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654488 | ||||||
chr18:33654530
|
T | C | 3 | a0003c0003t0059g0005a0003c0003t0073g0009a0003c0003t0079g0007 | 3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.356-7086T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654530 | ||||||
chr18:33654535
|
A | G | 1 | a0001c0001t0022g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.356-7081A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654535 | ||||||
chr18:33654596
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.356-7020T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654596 | ||||||
chr18:33654656
|
C | G | 5 | a0004c0004t0005g0046a0004c0004t0032g0059a0004c0004t0045g0058others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-6960C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654656 | ||||||
chr18:33654656
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-6960C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33654656 | ||||||
chr18:33654703
|
GC | G | 84 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.356-6911delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 33654703 | |||||
chr18:33655081
|
G | A | 1 | a0004c0004t0013g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.356-6535G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655081 | ||||||
chr18:33655295
|
A | G | 1 | a0001c0001t0071g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.356-6321A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655295 | ||||||
chr18:33655314
|
A | G | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.356-6302A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655314 | ||||||
chr18:33655334
|
A | G | 1 | a0001c0001t0012g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.356-6282A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655334 | ||||||
chr18:33655390
|
G | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.356-6226G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655390 | ||||||
chr18:33655572
|
T | C | 45 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.356-6044T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655572 | ||||||
chr18:33655588
|
G | A | 219 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.356-6028G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655588 | ||||||
chr18:33655631
|
A | G | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.356-5985A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655631 | ||||||
chr18:33655963
|
A | T | 1 | a0001c0001t0014g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.356-5653A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33655963 | ||||||
chr18:33656116
|
G | A | 2 | a0001c0001t0022g0076a0001c0001t0039g0180 | 2 | HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.356-5500G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656116 | ||||||
chr18:33656183
|
C | T | 103 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.356-5433C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656183 | ||||||
chr18:33656281
|
G | C | 1 | a0002c0002t0005g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.356-5335G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656281 | ||||||
chr18:33656481
|
C | T | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.356-5135C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656481 | ||||||
chr18:33656643
|
A | G | 1 | a0002c0002t0005g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.356-4973A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33656643 | ||||||
chr18:33657016
|
G | C | 104 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(101): Show | 104 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.356-4600G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657016 | ||||||
chr18:33657394
|
C | T | 13 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(10): Show | 13 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.356-4222C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657394 | ||||||
chr18:33657502
|
A | G | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.356-4114A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657502 | ||||||
chr18:33657710
|
G | C | 1 | a0002c0006t0009g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.356-3906G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657710 | ||||||
chr18:33657729
|
A | AAC | 3 | a0001c0001t0001g0089a0001c0001t0001g0116a0001c0001t0002g0128 | 3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3887_356-3886i others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657729 | ||||||
chr18:33657730
|
G | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0116a0001c0001t0002g0128 | 3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3886G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657730 | ||||||
chr18:33657731
|
A | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0116a0001c0001t0002g0128 | 3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3885A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657731 | ||||||
chr18:33657732
|
G | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0116a0001c0001t0002g0128 | 3 | HG01261.hp1 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.356-3884G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657732 | ||||||
chr18:33657955
|
A | G | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.356-3661A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33657955 | ||||||
chr18:33658054
|
G | A | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.356-3562G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33658054 | ||||||
chr18:33659219
|
A | G | 148 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.356-2397A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659219 | ||||||
chr18:33659380
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.356-2236C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659380 | ||||||
chr18:33659411
|
A | G | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.356-2205A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659411 | ||||||
chr18:33659730
|
A | G | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-1886A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659730 | ||||||
chr18:33659786
|
T | G | 2 | a0007c0009t0004g0160a0007c0009t0004g0161 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.356-1830T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33659786 | ||||||
chr18:33660189
|
A | G | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.356-1427A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660189 | ||||||
chr18:33660299
|
C | A | 1 | a0001c0001t0070g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.356-1317C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660299 | ||||||
chr18:33660419
|
C | T | 1 | a0001c0001t0060g0193 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.356-1197C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660419 | ||||||
chr18:33660899
|
C | T | 1 | a0002c0006t0036g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356-717C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660899 | ||||||
chr18:33660994
|
T | C | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.356-622T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33660994 | ||||||
chr18:33661131
|
T | G | 3 | a0001c0001t0001g0098a0001c0001t0051g0097a0002c0002t0005g0075 | 3 | HG00621.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.356-485T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661131 | ||||||
chr18:33661241
|
T | G | 4 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-375T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661241 | ||||||
chr18:33661246
|
T | G | 1 | a0001c0001t0048g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.356-370T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661246 | ||||||
chr18:33661366
|
C | G | 1 | a0001c0001t0034g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.356-250C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661366 | ||||||
chr18:33661389
|
A | G | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.356-227A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661389 | ||||||
chr18:33661435
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.356-181C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661435 | ||||||
chr18:33661460
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.356-156C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661460 | ||||||
chr18:33661533
|
C | G | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.356-83C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 4/11 | chr18 | 33661533 | ||||||
chr18:33661804
|
G | C | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+67G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661804 | ||||||
chr18:33661868
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.477+131A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661868 | ||||||
chr18:33661888
|
A | G | 6 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0027g0034others(3): Show | 6 | HG00673.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+151A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661888 | ||||||
chr18:33661897
|
T | TA | 16 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(13): Show | 16 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.477+169dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33661897 | |||||
chr18:33661897
|
T | TAA | 82 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.477+168_477+169dup others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33661897 | |||||
chr18:33661934
|
A | G | 1 | a0001c0001t0007g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.477+197A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661934 | ||||||
chr18:33661991
|
C | T | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.477+254C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33661991 | ||||||
chr18:33662245
|
G | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.477+508G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662245 | ||||||
chr18:33662429
|
T | C | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.477+692T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662429 | ||||||
chr18:33662635
|
C | T | 1 | a0001c0001t0011g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.477+898C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662635 | ||||||
chr18:33662661
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477+924C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662661 | ||||||
chr18:33662947
|
T | C | 84 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.477+1210T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662947 | ||||||
chr18:33662959
|
T | C | 2 | a0001c0001t0038g0183a0003c0003t0066g0216 | 2 | HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.477+1222T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33662959 | ||||||
chr18:33663560
|
A | G | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477+1823A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663560 | ||||||
chr18:33663562
|
CTTTGT | C | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.477+1829_477+1833d others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33663562 | |||||
chr18:33663693
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.477+1956A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663693 | ||||||
chr18:33663716
|
T | C | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.477+1979T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663716 | ||||||
chr18:33663934
|
C | CAT | 47 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(44): Show | 47 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.477+2208_477+2209d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33663934 | |||||
chr18:33663964
|
C | G | 84 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.477+2227C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33663964 | ||||||
chr18:33664247
|
G | A | 1 | a0002c0002t0003g0069 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.477+2510G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664247 | ||||||
chr18:33664318
|
A | G | 15 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.477+2581A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664318 | ||||||
chr18:33664468
|
A | G | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.477+2731A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664468 | ||||||
chr18:33664470
|
A | C | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.477+2733A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664470 | ||||||
chr18:33664573
|
T | A | 1 | a0001c0001t0011g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.477+2836T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664573 | ||||||
chr18:33664689
|
G | A | 1 | a0004c0004t0005g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.477+2952G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664689 | ||||||
chr18:33664823
|
G | A | 1 | a0003c0003t0069g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.477+3086G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664823 | ||||||
chr18:33664889
|
C | T | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.477+3152C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664889 | ||||||
chr18:33664893
|
A | G | 1 | a0002c0002t0005g0039 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.477+3156A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664893 | ||||||
chr18:33664982
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0002g0128 | 2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.477+3245G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33664982 | ||||||
chr18:33665200
|
A | G | 1 | a0002c0002t0044g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.477+3463A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665200 | ||||||
chr18:33665374
|
T | A | 2 | a0002c0006t0009g0030a0002c0006t0009g0031 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.477+3637T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665374 | ||||||
chr18:33665501
|
C | T | 1 | a0008c0011t0003g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.477+3764C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665501 | ||||||
chr18:33665655
|
G | A | 4 | a0001c0001t0006g0197a0001c0001t0014g0199a0001c0001t0021g0198others(1): Show | 4 | NA18948.hp2 NA18970.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+3918G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665655 | ||||||
chr18:33665739
|
T | G | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.477+4002T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665739 | ||||||
chr18:33665839
|
T | C | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.477+4102T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665839 | ||||||
chr18:33665907
|
A | G | 189 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.477+4170A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665907 | ||||||
chr18:33665954
|
G | C | 1 | a0002c0002t0003g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.477+4217G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33665954 | ||||||
chr18:33666022
|
A | G | 4 | a0001c0001t0006g0197a0001c0001t0014g0199a0001c0001t0021g0198others(1): Show | 4 | NA18948.hp2 NA18970.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+4285A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666022 | ||||||
chr18:33666040
|
A | G | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.477+4303A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666040 | ||||||
chr18:33666055
|
G | A | 1 | a0001c0020t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.477+4318G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666055 | ||||||
chr18:33666083
|
A | G | 2 | a0001c0001t0004g0066a0001c0001t0027g0034 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.477+4346A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666083 | ||||||
chr18:33666280
|
A | G | 1 | a0002c0002t0003g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.478-4393A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666280 | ||||||
chr18:33666331
|
C | G | 2 | a0001c0001t0006g0217a0002c0002t0003g0218 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.478-4342C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666331 | ||||||
chr18:33666630
|
G | A | 151 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.478-4043G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666630 | ||||||
chr18:33666956
|
A | G | 9 | a0002c0002t0018g0181a0002c0002t0018g0182a0002c0006t0009g0030others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.478-3717A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33666956 | ||||||
chr18:33667035
|
T | C | 1 | a0001c0001t0049g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.478-3638T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667035 | ||||||
chr18:33667097
|
C | T | 29 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(26): Show | 29 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.478-3576C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667097 | ||||||
chr18:33667323
|
C | T | 1 | a0001c0001t0075g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.478-3350C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667323 | ||||||
chr18:33667565
|
G | A | 1 | a0003c0003t0073g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.478-3108G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667565 | ||||||
chr18:33667618
|
C | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-3055C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667618 | ||||||
chr18:33667717
|
C | G | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.478-2956C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667717 | ||||||
chr18:33667942
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.478-2731A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33667942 | ||||||
chr18:33668124
|
C | T | 3 | a0003c0003t0059g0005a0003c0003t0073g0009a0003c0003t0079g0007 | 3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.478-2549C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668124 | ||||||
chr18:33668359
|
T | C | 184 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(181): Show | 184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.478-2314T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668359 | ||||||
chr18:33668427
|
C | CAA | 8 | a0001c0001t0004g0172a0001c0008t0025g0026a0002c0002t0030g0179others(5): Show | 8 | HG01109.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2231_478-2230d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668427 | |||||
chr18:33668427
|
CA | C | 88 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.478-2230delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668427 | |||||
chr18:33668427
|
CAA | C | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-2231_478-2230d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668427 | |||||
chr18:33668458
|
T | A | 18 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(15): Show | 18 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.478-2215T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668458 | ||||||
chr18:33668664
|
A | G | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.478-2009A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668664 | ||||||
chr18:33668770
|
C | T | 5 | a0001c0008t0025g0026a0002c0006t0023g0027a0004c0004t0078g0215others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1903C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668770 | ||||||
chr18:33668895
|
A | AAC | 97 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.478-1765_478-1764d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668895 | |||||
chr18:33668907
|
C | CAT | 6 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1765_478-1764i others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33668907 | |||||
chr18:33668961
|
G | A | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.478-1712G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33668961 | ||||||
chr18:33669033
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0004g0052 | 2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.478-1640G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669033 | ||||||
chr18:33669040
|
A | G | 2 | a0006c0010t0055g0170a0006c0010t0061g0185 | 2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.478-1633A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669040 | ||||||
chr18:33669095
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0004g0052 | 2 | NA18972.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.478-1578A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669095 | ||||||
chr18:33669180
|
G | T | 1 | a0001c0001t0019g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.478-1493G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669180 | ||||||
chr18:33669447
|
C | G | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478-1226C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669447 | ||||||
chr18:33669564
|
A | G | 4 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1109A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669564 | ||||||
chr18:33669617
|
C | CA | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.478-1055dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 33669617 | |||||
chr18:33669922
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.478-751T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669922 | ||||||
chr18:33669949
|
C | A | 1 | a0002c0002t0005g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.478-724C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669949 | ||||||
chr18:33669960
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.478-713T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669960 | ||||||
chr18:33669981
|
C | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-692C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669981 | ||||||
chr18:33669984
|
C | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-689C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33669984 | ||||||
chr18:33670011
|
C | A | 1 | a0001c0001t0004g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.478-662C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 5/11 | chr18 | 33670011 | ||||||
chr18:33670964
|
C | T | 25 | a0001c0001t0004g0172a0001c0001t0007g0011a0001c0001t0007g0012others(22): Show | 25 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.595+174C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33670964 | ||||||
chr18:33671053
|
C | T | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.595+263C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671053 | ||||||
chr18:33671124
|
G | A | 82 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.595+334G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671124 | ||||||
chr18:33671138
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0026g0035a0001c0001t0028g0036others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+348A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671138 | ||||||
chr18:33671257
|
G | T | 193 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(190): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.595+467G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671257 | ||||||
chr18:33671312
|
G | A | 98 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(95): Show | 98 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.596-435G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671312 | ||||||
chr18:33671456
|
C | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.596-291C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671456 | ||||||
chr18:33671519
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.596-228C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671519 | ||||||
chr18:33671663
|
C | T | 1 | a0009c0023t0050g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.596-84C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671663 | ||||||
chr18:33671674
|
C | T | 2 | a0001c0001t0047g0190a0001c0008t0081g0220 | 2 | HG02486.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.596-73C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 6/11 | chr18 | 33671674 | ||||||
chr18:33672165
|
G | A | 129 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.715+299G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672165 | ||||||
chr18:33672392
|
G | A | 1 | a0001c0001t0039g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.715+526G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672392 | ||||||
chr18:33672505
|
A | G | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.715+639A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672505 | ||||||
chr18:33672637
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.715+771G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672637 | ||||||
chr18:33672641
|
C | T | 134 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.715+775C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672641 | ||||||
chr18:33672682
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG01884.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+816G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672682 | ||||||
chr18:33672848
|
C | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+982C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33672848 | ||||||
chr18:33673108
|
A | G | 128 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.715+1242A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673108 | ||||||
chr18:33673188
|
A | G | 219 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.715+1322A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673188 | ||||||
chr18:33673373
|
AT | A | 69 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(66): Show | 69 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.715+1525delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33673373 | |||||
chr18:33673373
|
ATT | A | 81 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(78): Show | 81 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.715+1524_715+1525d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33673373 | |||||
chr18:33673405
|
G | T | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.715+1539G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673405 | ||||||
chr18:33673441
|
C | T | 30 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(27): Show | 30 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.715+1575C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673441 | ||||||
chr18:33673498
|
T | G | 4 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(1): Show | 4 | HG00280.hp2 HG01109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+1632T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673498 | ||||||
chr18:33673621
|
C | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.715+1755C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673621 | ||||||
chr18:33673674
|
G | A | 32 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(29): Show | 32 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.715+1808G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673674 | ||||||
chr18:33673831
|
G | A | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.715+1965G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33673831 | ||||||
chr18:33674049
|
G | A | 138 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.715+2183G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674049 | ||||||
chr18:33674399
|
T | C | 1 | a0001c0001t0012g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715+2533T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674399 | ||||||
chr18:33674399
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.715+2533T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674399 | ||||||
chr18:33674601
|
T | C | 1 | a0001c0001t0075g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.715+2735T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674601 | ||||||
chr18:33674687
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0191others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+2821C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674687 | ||||||
chr18:33674722
|
C | G | 1 | a0001c0001t0010g0156 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.715+2856C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674722 | ||||||
chr18:33674747
|
T | A | 83 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.715+2881T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674747 | ||||||
chr18:33674869
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.715+3003C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674869 | ||||||
chr18:33674898
|
G | A | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.715+3032G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674898 | ||||||
chr18:33674908
|
G | A | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.715+3042G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33674908 | ||||||
chr18:33675082
|
C | A | 134 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.715+3216C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675082 | ||||||
chr18:33675406
|
G | GTT | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.715+3545_715+3546d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33675406 | |||||
chr18:33675569
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.715+3703C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675569 | ||||||
chr18:33675692
|
T | G | 134 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.715+3826T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675692 | ||||||
chr18:33675865
|
T | C | 14 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.715+3999T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675865 | ||||||
chr18:33675865
|
T | G | 32 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(29): Show | 32 | HG00673.hp2 HG01071.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.715+3999T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675865 | ||||||
chr18:33675907
|
T | C | 32 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(29): Show | 32 | HG00673.hp2 HG01071.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.715+4041T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675907 | ||||||
chr18:33675928
|
A | G | 1 | a0001c0018t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.715+4062A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675928 | ||||||
chr18:33675954
|
A | G | 86 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.715+4088A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675954 | ||||||
chr18:33675999
|
C | T | 1 | a0005c0007t0004g0135 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.715+4133C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33675999 | ||||||
chr18:33676020
|
C | G | 3 | a0001c0001t0001g0116a0001c0001t0002g0128a0001c0018t0001g0070 | 3 | HG01928.hp2 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.715+4154C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676020 | ||||||
chr18:33676065
|
C | A | 4 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0008t0081g0220others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+4199C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676065 | ||||||
chr18:33676148
|
C | T | 8 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.715+4282C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676148 | ||||||
chr18:33676209
|
C | T | 2 | a0001c0001t0010g0156a0001c0001t0010g0158 | 2 | NA18959.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.715+4343C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676209 | ||||||
chr18:33676222
|
C | CA | 16 | a0001c0001t0004g0172a0001c0001t0006g0124a0001c0001t0007g0011others(13): Show | 16 | HG00280.hp2 HG01109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.715+4381dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(3): Show |
1 | a0002c0006t0023g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.715+4372_715+4381d others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(6): Show |
3 | a0003c0003t0074g0173a0004c0004t0078g0215a0016c0026t0052g0044 | 3 | HG02258.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.715+4369_715+4381d others(15): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(7): Show |
1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.715+4368_715+4381d others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0038g0183a0003c0003t0031g0174 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.715+4367_715+4381d others(17): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0116a0001c0001t0011g0081a0001c0001t0019g0084others(1): Show | 4 | HG01975.hp1 NA18959.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+4366_715+4381d others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(10): Show |
10 | a0001c0001t0001g0104a0001c0001t0001g0191a0001c0001t0015g0187others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.715+4365_715+4381d others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(11): Show |
40 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(37): Show | 40 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.715+4364_715+4381d others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(12): Show |
15 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0089others(12): Show | 15 | HG00438.hp1 HG00642.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.715+4363_715+4381d others(21): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.715+4362_715+4381d others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(14): Show |
2 | a0002c0002t0044g0053a0013c0015t0002g0114 | 2 | HG00280.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.715+4361_715+4381d others(23): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0096a0001c0001t0002g0128a0001c0001t0002g0186others(2): Show | 5 | HG00323.hp2 HG01928.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+4360_715+4381d others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0098 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.715+4359_715+4381d others(25): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.715+4358_715+4381d others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676222
|
CA | C | 20 | a0001c0001t0001g0157a0001c0001t0002g0207a0001c0001t0002g0208others(17): Show | 20 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.715+4381delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33676222 | |||||
chr18:33676300
|
T | C | 1 | a0004c0004t0072g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.715+4434T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676300 | ||||||
chr18:33676403
|
C | G | 83 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.715+4537C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676403 | ||||||
chr18:33676430
|
C | T | 8 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.715+4564C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676430 | ||||||
chr18:33676431
|
T | C | 6 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.715+4565T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676431 | ||||||
chr18:33676738
|
G | A | 133 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(130): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.715+4872G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676738 | ||||||
chr18:33676989
|
G | C | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.715+5123G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33676989 | ||||||
chr18:33677261
|
A | G | 5 | a0001c0008t0025g0026a0002c0006t0023g0027a0004c0004t0078g0215others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+5395A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677261 | ||||||
chr18:33677635
|
G | A | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.715+5769G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677635 | ||||||
chr18:33677769
|
C | A | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-5636C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677769 | ||||||
chr18:33677851
|
T | C | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.716-5554T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677851 | ||||||
chr18:33677894
|
T | G | 1 | a0001c0001t0006g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.716-5511T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33677894 | ||||||
chr18:33678009
|
C | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.716-5396C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678009 | ||||||
chr18:33678077
|
A | ATTAT | 2 | a0001c0001t0001g0087a0001c0020t0001g0155 | 2 | HG02148.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.716-5297_716-5294d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | |||||
chr18:33678077
|
ATTAT | A | 88 | a0001c0001t0001g0041a0001c0001t0001g0096a0001c0001t0001g0157others(85): Show | 88 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.716-5297_716-5294d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | |||||
chr18:33678077
|
ATTATTTA others(1): Show |
A | 6 | a0001c0001t0022g0076a0003c0003t0059g0005a0003c0003t0069g0010others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-5301_716-5294d others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | |||||
chr18:33678077
|
ATTATTTA others(9): Show |
A | 13 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(10): Show | 13 | HG00673.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.716-5309_716-5294d others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33678077 | |||||
chr18:33678235
|
T | A | 133 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(130): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.716-5170T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678235 | ||||||
chr18:33678351
|
A | C | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.716-5054A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678351 | ||||||
chr18:33678653
|
C | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.716-4752C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678653 | ||||||
chr18:33678807
|
G | A | 1 | a0001c0001t0006g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.716-4598G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33678807 | ||||||
chr18:33679058
|
CAT | C | 31 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(28): Show | 31 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.716-4346_716-4345d others(4): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679058 | ||||||
chr18:33679191
|
A | T | 128 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.716-4214A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679191 | ||||||
chr18:33679209
|
C | A | 78 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0001g0157others(75): Show | 78 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.716-4196C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679209 | ||||||
chr18:33679211
|
A | C | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.716-4194A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679211 | ||||||
chr18:33679582
|
A | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.716-3823A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679582 | ||||||
chr18:33679584
|
A | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.716-3821A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679584 | ||||||
chr18:33679615
|
A | G | 87 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.716-3790A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679615 | ||||||
chr18:33679670
|
G | T | 1 | a0002c0002t0003g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.716-3735G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679670 | ||||||
chr18:33679673
|
C | T | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.716-3732C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679673 | ||||||
chr18:33679717
|
C | G | 1 | a0002c0002t0005g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.716-3688C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679717 | ||||||
chr18:33679773
|
A | G | 1 | a0001c0001t0048g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.716-3632A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679773 | ||||||
chr18:33679787
|
A | C | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.716-3618A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679787 | ||||||
chr18:33679832
|
C | T | 1 | a0002c0002t0003g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.716-3573C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33679832 | ||||||
chr18:33680370
|
G | A | 1 | a0001c0001t0012g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.716-3035G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680370 | ||||||
chr18:33680523
|
T | C | 83 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.716-2882T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680523 | ||||||
chr18:33680530
|
A | G | 88 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.716-2875A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680530 | ||||||
chr18:33680544
|
G | A | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.716-2861G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33680544 | ||||||
chr18:33681386
|
A | G | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.716-2019A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681386 | ||||||
chr18:33681503
|
G | T | 3 | a0001c0001t0001g0116a0001c0001t0002g0128a0001c0018t0001g0070 | 3 | HG01928.hp2 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.716-1902G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681503 | ||||||
chr18:33681549
|
C | G | 1 | a0001c0001t0006g0217 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.716-1856C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681549 | ||||||
chr18:33681553
|
G | C | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-1852G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681553 | ||||||
chr18:33681665
|
G | T | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.716-1740G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681665 | ||||||
chr18:33681775
|
TA | T | 5 | a0001c0008t0025g0026a0002c0006t0023g0027a0004c0004t0078g0215others(2): Show | 5 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.716-1626delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33681775 | |||||
chr18:33681776
|
A | T | 132 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(129): Show | 132 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.716-1629A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681776 | ||||||
chr18:33681827
|
A | G | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.716-1578A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681827 | ||||||
chr18:33681942
|
T | A | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-1463T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33681942 | ||||||
chr18:33682032
|
T | A | 6 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-1373T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682032 | ||||||
chr18:33682042
|
A | T | 1 | a0001c0001t0051g0097 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.716-1363A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682042 | ||||||
chr18:33682113
|
G | A | 1 | a0001c0001t0040g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.716-1292G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682113 | ||||||
chr18:33682175
|
G | A | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.716-1230G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682175 | ||||||
chr18:33682588
|
A | G | 181 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(178): Show | 181 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.716-817A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682588 | ||||||
chr18:33682621
|
C | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.716-784C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682621 | ||||||
chr18:33682626
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.716-779C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682626 | ||||||
chr18:33682702
|
A | ACACTGGT others(6): Show |
1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-700_716-699ins others(13): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33682702 | |||||
chr18:33682711
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-694T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682711 | ||||||
chr18:33682713
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-692A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682713 | ||||||
chr18:33682714
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-691T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682714 | ||||||
chr18:33682717
|
A | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-688A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682717 | ||||||
chr18:33682718
|
A | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-687A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682718 | ||||||
chr18:33682719
|
A | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-686A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682719 | ||||||
chr18:33682720
|
A | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-685A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682720 | ||||||
chr18:33682722
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-683A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682722 | ||||||
chr18:33682724
|
T | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-681T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682724 | ||||||
chr18:33682726
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-679T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682726 | ||||||
chr18:33682728
|
T | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-677T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682728 | ||||||
chr18:33682729
|
G | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-676G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682729 | ||||||
chr18:33682730
|
T | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-675T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682730 | ||||||
chr18:33682734
|
T | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-671T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682734 | ||||||
chr18:33682736
|
C | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-669C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682736 | ||||||
chr18:33682737
|
A | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-668A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682737 | ||||||
chr18:33682740
|
T | TACTTAAG others(3): Show |
1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-665_716-664ins others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682740 | ||||||
chr18:33682751
|
C | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-654C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682751 | ||||||
chr18:33682752
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-653A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682752 | ||||||
chr18:33682755
|
T | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-650T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682755 | ||||||
chr18:33682763
|
A | T | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-642A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682763 | ||||||
chr18:33682764
|
C | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-641C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682764 | ||||||
chr18:33682764
|
C | T | 5 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(2): Show | 5 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.716-641C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682764 | ||||||
chr18:33682766
|
G | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-639G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682766 | ||||||
chr18:33682770
|
T | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-635T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682770 | ||||||
chr18:33682773
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-632A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682773 | ||||||
chr18:33682775
|
C | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-630C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682775 | ||||||
chr18:33682776
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-629T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682776 | ||||||
chr18:33682784
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-621T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682784 | ||||||
chr18:33682786
|
A | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-619A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682786 | ||||||
chr18:33682788
|
G | T | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-617G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682788 | ||||||
chr18:33682790
|
A | T | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-615A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682790 | ||||||
chr18:33682792
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-613T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682792 | ||||||
chr18:33682793
|
C | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-612C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682793 | ||||||
chr18:33682795
|
T | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-610T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682795 | ||||||
chr18:33682798
|
T | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-607T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682798 | ||||||
chr18:33682807
|
C | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-598C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682807 | ||||||
chr18:33682808
|
T | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-597T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682808 | ||||||
chr18:33682813
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-592A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682813 | ||||||
chr18:33682817
|
GATGGGAT others(3): Show |
G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-586_716-577del others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 33682817 | |||||
chr18:33682830
|
G | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-575G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682830 | ||||||
chr18:33682844
|
G | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-561G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682844 | ||||||
chr18:33682845
|
C | T | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-560C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682845 | ||||||
chr18:33682847
|
G | C | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-558G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682847 | ||||||
chr18:33682852
|
T | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-553T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682852 | ||||||
chr18:33682870
|
A | G | 135 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.716-535A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682870 | ||||||
chr18:33682872
|
G | A | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-533G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682872 | ||||||
chr18:33682885
|
T | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.716-520T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33682885 | ||||||
chr18:33683043
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.716-362G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33683043 | ||||||
chr18:33683059
|
T | C | 84 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.716-346T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33683059 | ||||||
chr18:33683356
|
G | A | 180 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.716-49G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 7/11 | chr18 | 33683356 | ||||||
chr18:33683639
|
A | G | 38 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.879+71A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683639 | ||||||
chr18:33683837
|
A | G | 135 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+269A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683837 | ||||||
chr18:33683919
|
G | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.879+351G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683919 | ||||||
chr18:33683953
|
A | G | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+385A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683953 | ||||||
chr18:33683982
|
T | C | 2 | a0006c0010t0055g0170a0006c0010t0061g0185 | 2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+414T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33683982 | ||||||
chr18:33684028
|
C | G | 45 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(42): Show | 45 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(42): Show |
intron_variant | MODIFIER | c.879+460C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684028 | ||||||
chr18:33684152
|
A | G | 1 | a0001c0001t0004g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.879+584A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684152 | ||||||
chr18:33684748
|
C | A | 135 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+1180C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684748 | ||||||
chr18:33684790
|
C | T | 2 | a0001c0005t0004g0062a0001c0005t0056g0063 | 2 | NA18999.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.879+1222C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684790 | ||||||
chr18:33684831
|
A | T | 1 | a0001c0001t0011g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.879+1263A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684831 | ||||||
chr18:33684936
|
G | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1368G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33684936 | ||||||
chr18:33685123
|
C | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+1555C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685123 | ||||||
chr18:33685447
|
G | T | 135 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+1879G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685447 | ||||||
chr18:33685464
|
G | A | 1 | a0001c0001t0019g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.879+1896G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685464 | ||||||
chr18:33685465
|
A | T | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.879+1897A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685465 | ||||||
chr18:33685505
|
G | T | 30 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(27): Show | 30 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.879+1937G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685505 | ||||||
chr18:33685633
|
G | T | 13 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+2065G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685633 | ||||||
chr18:33685881
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.879+2313C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685881 | ||||||
chr18:33685915
|
C | T | 1 | a0001c0001t0071g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.879+2347C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685915 | ||||||
chr18:33685916
|
G | A | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+2348G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685916 | ||||||
chr18:33685955
|
G | A | 1 | a0001c0001t0041g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.879+2387G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685955 | ||||||
chr18:33685985
|
G | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.879+2417G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33685985 | ||||||
chr18:33686176
|
T | C | 2 | a0001c0001t0011g0139a0001c0001t0012g0018 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.879+2608T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686176 | ||||||
chr18:33686331
|
C | G | 31 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(28): Show | 31 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+2763C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686331 | ||||||
chr18:33686383
|
A | G | 1 | a0002c0002t0013g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.879+2815A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686383 | ||||||
chr18:33686422
|
T | C | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+2854T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686422 | ||||||
chr18:33686445
|
A | G | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.879+2877A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686445 | ||||||
chr18:33686484
|
A | C | 135 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+2916A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686484 | ||||||
chr18:33686506
|
G | A | 1 | a0001c0001t0012g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879+2938G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686506 | ||||||
chr18:33686613
|
T | G | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.879+3045T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686613 | ||||||
chr18:33686777
|
A | G | 136 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.879+3209A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33686777 | ||||||
chr18:33687129
|
G | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+3561G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687129 | ||||||
chr18:33687373
|
A | G | 136 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.879+3805A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687373 | ||||||
chr18:33687387
|
G | C | 1 | a0001c0001t0011g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.879+3819G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687387 | ||||||
chr18:33687447
|
A | G | 162 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.879+3879A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687447 | ||||||
chr18:33687485
|
T | C | 136 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.879+3917T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687485 | ||||||
chr18:33687747
|
T | C | 180 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.879+4179T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687747 | ||||||
chr18:33687852
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+4284A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33687852 | ||||||
chr18:33688101
|
C | G | 1 | a0001c0001t0040g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.879+4533C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688101 | ||||||
chr18:33688260
|
G | A | 36 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.879+4692G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688260 | ||||||
chr18:33688349
|
C | T | 1 | a0001c0001t0021g0213 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.879+4781C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688349 | ||||||
chr18:33688671
|
G | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+5103G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688671 | ||||||
chr18:33688746
|
A | T | 8 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.879+5178A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688746 | ||||||
chr18:33688915
|
A | G | 3 | a0003c0003t0059g0005a0003c0003t0073g0009a0003c0003t0079g0007 | 3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.879+5347A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688915 | ||||||
chr18:33688971
|
A | G | 32 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(29): Show | 32 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+5403A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33688971 | ||||||
chr18:33689003
|
C | CT | 135 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.879+5445dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33689003 | |||||
chr18:33689123
|
A | G | 1 | a0003c0003t0031g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+5555A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689123 | ||||||
chr18:33689194
|
A | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0099others(1): Show | 4 | HG01261.hp1 HG01358.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+5626A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689194 | ||||||
chr18:33689253
|
C | T | 45 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(42): Show | 45 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(42): Show |
intron_variant | MODIFIER | c.879+5685C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689253 | ||||||
chr18:33689315
|
C | T | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+5747C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689315 | ||||||
chr18:33689333
|
C | T | 13 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+5765C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689333 | ||||||
chr18:33689339
|
T | C | 185 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(182): Show | 185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.879+5771T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689339 | ||||||
chr18:33689640
|
A | G | 136 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.879+6072A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689640 | ||||||
chr18:33689728
|
G | A | 19 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(16): Show | 19 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.879+6160G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689728 | ||||||
chr18:33689975
|
A | G | 1 | a0002c0006t0023g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.879+6407A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33689975 | ||||||
chr18:33690384
|
C | T | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+6816C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690384 | ||||||
chr18:33690388
|
T | C | 4 | a0002c0002t0018g0181a0002c0002t0018g0182a0009c0023t0050g0115others(1): Show | 4 | HG02818.hp1 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+6820T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690388 | ||||||
chr18:33690454
|
C | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+6886C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690454 | ||||||
chr18:33690491
|
A | G | 1 | a0001c0020t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.879+6923A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690491 | ||||||
chr18:33690589
|
C | A | 41 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.879+7021C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690589 | ||||||
chr18:33690615
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.879+7047A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690615 | ||||||
chr18:33690632
|
C | T | 1 | a0003c0003t0073g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.879+7064C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690632 | ||||||
chr18:33690715
|
A | G | 32 | a0001c0001t0001g0071a0001c0001t0002g0207a0001c0001t0002g0208others(29): Show | 32 | HG00673.hp2 HG01071.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+7147A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690715 | ||||||
chr18:33690777
|
T | C | 187 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(184): Show | 187 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.879+7209T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690777 | ||||||
chr18:33690848
|
T | C | 37 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0002g0159others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.879+7280T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690848 | ||||||
chr18:33690855
|
C | T | 141 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.879+7287C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690855 | ||||||
chr18:33690937
|
C | G | 13 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+7369C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690937 | ||||||
chr18:33690954
|
G | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+7386G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33690954 | ||||||
chr18:33691041
|
C | T | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.879+7473C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691041 | ||||||
chr18:33691249
|
C | G | 2 | a0004c0004t0078g0215a0016c0026t0052g0044 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.879+7681C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691249 | ||||||
chr18:33691490
|
A | C | 3 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0017t0076g0175 | 3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+7922A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691490 | ||||||
chr18:33691509
|
A | G | 5 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+7941A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691509 | ||||||
chr18:33691655
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+8087A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691655 | ||||||
chr18:33691703
|
A | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+8135A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691703 | ||||||
chr18:33691711
|
A | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+8143A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691711 | ||||||
chr18:33691819
|
A | G | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.879+8251A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691819 | ||||||
chr18:33691906
|
A | T | 1 | a0001c0001t0022g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.879+8338A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33691906 | ||||||
chr18:33692051
|
C | T | 1 | a0002c0002t0018g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+8483C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692051 | ||||||
chr18:33692174
|
G | A | 1 | a0001c0001t0011g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.879+8606G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692174 | ||||||
chr18:33692274
|
C | T | 97 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.879+8706C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692274 | ||||||
chr18:33692438
|
A | C | 2 | a0002c0002t0013g0064a0002c0002t0020g0047 | 2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.879+8870A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692438 | ||||||
chr18:33692439
|
T | G | 149 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.879+8871T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692439 | ||||||
chr18:33692500
|
C | T | 1 | a0001c0001t0075g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.879+8932C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692500 | ||||||
chr18:33692711
|
A | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+9143A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33692711 | ||||||
chr18:33693249
|
G | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+9681G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693249 | ||||||
chr18:33693300
|
A | T | 1 | a0001c0001t0019g0084 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.879+9732A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693300 | ||||||
chr18:33693418
|
G | A | 122 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(119): Show | 122 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.879+9850G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693418 | ||||||
chr18:33693507
|
G | A | 190 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(187): Show | 190 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.879+9939G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693507 | ||||||
chr18:33693536
|
A | T | 122 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(119): Show | 122 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.879+9968A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693536 | ||||||
chr18:33693596
|
G | A | 5 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+10028G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693596 | ||||||
chr18:33693683
|
T | G | 1 | a0001c0001t0060g0193 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.879+10115T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693683 | ||||||
chr18:33693891
|
G | A | 14 | a0001c0001t0001g0056a0001c0001t0007g0011a0001c0001t0007g0012others(11): Show | 14 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+10323G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693891 | ||||||
chr18:33693943
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0002g0159 | 2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.879+10375A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33693943 | ||||||
chr18:33694042
|
G | T | 6 | a0001c0001t0006g0197a0001c0001t0014g0199a0001c0001t0014g0212others(3): Show | 6 | HG02129.hp1 NA18948.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+10474G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33694042 | ||||||
chr18:33694341
|
G | A | 189 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.879+10773G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33694341 | ||||||
chr18:33694400
|
A | G | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+10832A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33694400 | ||||||
chr18:33695030
|
C | T | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.879+11462C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695030 | ||||||
chr18:33695037
|
A | G | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+11469A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695037 | ||||||
chr18:33695053
|
C | T | 1 | a0002c0006t0009g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.879+11485C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695053 | ||||||
chr18:33695541
|
T | C | 100 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(97): Show | 100 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.879+11973T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695541 | ||||||
chr18:33695654
|
A | T | 1 | a0001c0005t0004g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.879+12086A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33695654 | ||||||
chr18:33696109
|
G | A | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.879+12541G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696109 | ||||||
chr18:33696214
|
TA | T | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+12653delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33696214 | |||||
chr18:33696283
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+12715G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696283 | ||||||
chr18:33696287
|
T | C | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+12719T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696287 | ||||||
chr18:33696556
|
G | T | 2 | a0006c0010t0055g0170a0006c0010t0061g0185 | 2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+12988G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696556 | ||||||
chr18:33696605
|
A | G | 138 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+13037A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696605 | ||||||
chr18:33696611
|
C | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.879+13043C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696611 | ||||||
chr18:33696719
|
T | TA | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+13152dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33696719 | |||||
chr18:33696844
|
A | G | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+13276A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696844 | ||||||
chr18:33696862
|
G | T | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+13294G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696862 | ||||||
chr18:33696920
|
A | T | 116 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.879+13352A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696920 | ||||||
chr18:33696981
|
T | C | 138 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+13413T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33696981 | ||||||
chr18:33697003
|
T | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+13435T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697003 | ||||||
chr18:33697040
|
T | C | 114 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(111): Show | 114 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.879+13472T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697040 | ||||||
chr18:33697165
|
C | T | 15 | a0001c0001t0054g0054a0002c0002t0003g0106a0002c0002t0003g0108others(12): Show | 15 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.879+13597C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697165 | ||||||
chr18:33697215
|
A | G | 5 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+13647A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697215 | ||||||
chr18:33697530
|
C | T | 1 | a0001c0001t0060g0193 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.879+13962C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697530 | ||||||
chr18:33697567
|
G | C | 219 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.879+13999G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697567 | ||||||
chr18:33697627
|
A | G | 27 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0051g0097others(24): Show | 27 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.879+14059A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697627 | ||||||
chr18:33697688
|
A | G | 1 | a0001c0001t0011g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.879+14120A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697688 | ||||||
chr18:33697752
|
C | T | 139 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(136): Show | 139 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.879+14184C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697752 | ||||||
chr18:33697754
|
A | G | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+14186A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697754 | ||||||
chr18:33697829
|
C | G | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+14261C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33697829 | ||||||
chr18:33697839
|
C | CA | 139 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(136): Show | 139 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.879+14278dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33697839 | |||||
chr18:33698273
|
C | T | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+14705C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698273 | ||||||
chr18:33698447
|
G | C | 2 | a0006c0010t0055g0170a0006c0010t0061g0185 | 2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+14879G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698447 | ||||||
chr18:33698576
|
T | C | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+15008T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698576 | ||||||
chr18:33698650
|
G | C | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.879+15082G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698650 | ||||||
chr18:33698751
|
A | G | 2 | a0001c0001t0004g0066a0001c0001t0004g0141 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.879+15183A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698751 | ||||||
chr18:33698859
|
C | T | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+15291C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698859 | ||||||
chr18:33698960
|
A | G | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+15392A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33698960 | ||||||
chr18:33699070
|
G | A | 1 | a0001c0001t0027g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.879+15502G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699070 | ||||||
chr18:33699082
|
A | G | 1 | a0002c0002t0003g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879+15514A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699082 | ||||||
chr18:33699470
|
T | C | 139 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(136): Show | 139 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.879+15902T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699470 | ||||||
chr18:33699510
|
T | C | 1 | a0001c0001t0016g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.879+15942T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699510 | ||||||
chr18:33699541
|
G | A | 1 | a0001c0001t0012g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879+15973G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699541 | ||||||
chr18:33699548
|
T | G | 125 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(122): Show | 125 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.879+15980T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699548 | ||||||
chr18:33699691
|
G | A | 20 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(17): Show | 20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+16123G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699691 | ||||||
chr18:33699707
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.879+16139C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699707 | ||||||
chr18:33699907
|
C | T | 9 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG00558.hp1 HG01496.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+16339C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699907 | ||||||
chr18:33699921
|
G | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+16353G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699921 | ||||||
chr18:33699939
|
T | G | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+16371T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33699939 | ||||||
chr18:33700158
|
A | G | 140 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(137): Show | 140 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.879+16590A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700158 | ||||||
chr18:33700241
|
A | ATAGGAAT others(1): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02602.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.879+16674_879+1668 others(12): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33700241 | |||||
chr18:33700265
|
C | T | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+16697C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700265 | ||||||
chr18:33700286
|
G | T | 20 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(17): Show | 20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+16718G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700286 | ||||||
chr18:33700291
|
G | A | 1 | a0007c0009t0004g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+16723G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700291 | ||||||
chr18:33700450
|
CA | C | 26 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(23): Show | 26 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.879+16883delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700450 | ||||||
chr18:33700544
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+16976G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700544 | ||||||
chr18:33700616
|
G | C | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+17048G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33700616 | ||||||
chr18:33701059
|
T | A | 1 | a0001c0001t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.879+17491T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701059 | ||||||
chr18:33701168
|
A | T | 3 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0017t0076g0175 | 3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+17600A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701168 | ||||||
chr18:33701193
|
A | C | 27 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0051g0097others(24): Show | 27 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.879+17625A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701193 | ||||||
chr18:33701275
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.879+17707G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701275 | ||||||
chr18:33701607
|
T | G | 6 | a0001c0001t0004g0172a0001c0001t0047g0190a0001c0001t0075g0184others(3): Show | 6 | HG02486.hp1 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+18039T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701607 | ||||||
chr18:33701756
|
T | C | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+18188T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701756 | ||||||
chr18:33701792
|
A | T | 2 | a0001c0001t0001g0098a0001c0001t0037g0196 | 2 | HG00621.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.879+18224A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701792 | ||||||
chr18:33701916
|
T | G | 1 | a0001c0001t0075g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.879+18348T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33701916 | ||||||
chr18:33702127
|
A | G | 1 | a0002c0002t0005g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+18559A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702127 | ||||||
chr18:33702205
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.879+18637G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702205 | ||||||
chr18:33702217
|
A | C | 2 | a0001c0001t0047g0190a0001c0001t0075g0184 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+18649A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702217 | ||||||
chr18:33702356
|
C | A | 15 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(12): Show | 15 | HG02145.hp2 HG02257.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+18788C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702356 | ||||||
chr18:33702366
|
T | C | 1 | a0001c0016t0062g0200 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.879+18798T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702366 | ||||||
chr18:33702418
|
G | C | 140 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(137): Show | 140 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.879+18850G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702418 | ||||||
chr18:33702423
|
T | C | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+18855T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702423 | ||||||
chr18:33702499
|
A | G | 3 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022 | 3 | HG01884.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.879+18931A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702499 | ||||||
chr18:33702904
|
A | G | 1 | a0001c0001t0051g0097 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.879+19336A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702904 | ||||||
chr18:33702969
|
G | C | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+19401G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33702969 | ||||||
chr18:33703011
|
G | C | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+19443G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703011 | ||||||
chr18:33703239
|
T | G | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+19671T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703239 | ||||||
chr18:33703323
|
G | A | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.879+19755G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703323 | ||||||
chr18:33703360
|
G | A | 20 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(17): Show | 20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+19792G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703360 | ||||||
chr18:33703440
|
G | C | 1 | a0001c0001t0006g0171 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.879+19872G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703440 | ||||||
chr18:33703464
|
G | A | 138 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+19896G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703464 | ||||||
chr18:33703478
|
C | A | 1 | a0001c0005t0017g0205 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.879+19910C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703478 | ||||||
chr18:33703494
|
G | A | 2 | a0004c0004t0078g0215a0016c0026t0052g0044 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.879+19926G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703494 | ||||||
chr18:33703564
|
G | A | 1 | a0008c0011t0003g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.879+19996G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703564 | ||||||
chr18:33703835
|
T | C | 1 | a0002c0002t0003g0143 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.879+20267T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703835 | ||||||
chr18:33703911
|
C | T | 1 | a0001c0001t0075g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.879+20343C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33703911 | ||||||
chr18:33704044
|
A | G | 20 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(17): Show | 20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+20476A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704044 | ||||||
chr18:33704134
|
G | A | 6 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+20566G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704134 | ||||||
chr18:33704287
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879+20719T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704287 | ||||||
chr18:33704367
|
G | A | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+20799G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704367 | ||||||
chr18:33704403
|
G | T | 138 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+20835G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704403 | ||||||
chr18:33704488
|
C | T | 203 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(200): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.879+20920C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704488 | ||||||
chr18:33704604
|
A | T | 20 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(17): Show | 20 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+21036A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704604 | ||||||
chr18:33704642
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+21074A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704642 | ||||||
chr18:33704650
|
C | G | 2 | a0001c0001t0010g0111a0013c0015t0002g0114 | 2 | NA18943.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.879+21082C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704650 | ||||||
chr18:33704801
|
C | T | 3 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0017t0076g0175 | 3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+21233C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704801 | ||||||
chr18:33704916
|
G | T | 1 | a0001c0001t0014g0212 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.879+21348G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704916 | ||||||
chr18:33704943
|
T | C | 1 | a0002c0006t0009g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.879+21375T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33704943 | ||||||
chr18:33705053
|
A | G | 1 | a0004c0004t0013g0202 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.879+21485A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705053 | ||||||
chr18:33705093
|
G | A | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+21525G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705093 | ||||||
chr18:33705200
|
A | AT | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+21633dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33705200 | |||||
chr18:33705305
|
A | C | 166 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(163): Show | 166 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.879+21737A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705305 | ||||||
chr18:33705339
|
C | T | 1 | a0001c0001t0070g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.879+21771C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705339 | ||||||
chr18:33705364
|
G | T | 2 | a0001c0001t0014g0212a0001c0001t0016g0204 | 2 | HG02129.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.879+21796G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705364 | ||||||
chr18:33705573
|
C | A | 1 | a0002c0002t0003g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.879+22005C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705573 | ||||||
chr18:33705581
|
A | G | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+22013A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705581 | ||||||
chr18:33705607
|
T | C | 1 | a0001c0008t0081g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.879+22039T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705607 | ||||||
chr18:33705611
|
C | A | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+22043C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705611 | ||||||
chr18:33705773
|
T | A | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22205T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705773 | ||||||
chr18:33705774
|
A | T | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22206A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705774 | ||||||
chr18:33705900
|
G | A | 1 | a0001c0001t0011g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.879+22332G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705900 | ||||||
chr18:33705946
|
T | C | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22378T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705946 | ||||||
chr18:33705947
|
C | A | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22379C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705947 | ||||||
chr18:33705948
|
A | C | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22380A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33705948 | ||||||
chr18:33706001
|
A | G | 1 | a0003c0003t0031g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+22433A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706001 | ||||||
chr18:33706107
|
CT | C | 171 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(168): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.879+22551delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33706107 | |||||
chr18:33706107
|
CTT | C | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.879+22550_879+2255 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33706107 | |||||
chr18:33706165
|
C | T | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+22597C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706165 | ||||||
chr18:33706207
|
A | T | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+22639A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706207 | ||||||
chr18:33706238
|
A | G | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+22670A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706238 | ||||||
chr18:33706348
|
A | AT | 3 | a0001c0001t0047g0190a0001c0001t0075g0184a0001c0017t0076g0175 | 3 | HG02486.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.879+22786dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33706348 | |||||
chr18:33706365
|
A | C | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+22797A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706365 | ||||||
chr18:33706407
|
A | C | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+22839A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706407 | ||||||
chr18:33706516
|
G | A | 138 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+22948G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706516 | ||||||
chr18:33706592
|
A | G | 54 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0002g0159others(51): Show | 54 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.879+23024A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706592 | ||||||
chr18:33706651
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.879+23083C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706651 | ||||||
chr18:33706763
|
T | C | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+23195T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706763 | ||||||
chr18:33706896
|
C | G | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.879+23328C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706896 | ||||||
chr18:33706944
|
G | A | 2 | a0006c0010t0055g0170a0006c0010t0061g0185 | 2 | HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+23376G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33706944 | ||||||
chr18:33707111
|
G | A | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+23543G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707111 | ||||||
chr18:33707129
|
T | A | 1 | a0002c0002t0005g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+23561T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707129 | ||||||
chr18:33707149
|
G | T | 1 | a0002c0002t0003g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.879+23581G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707149 | ||||||
chr18:33707374
|
T | G | 1 | a0001c0005t0004g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.879+23806T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707374 | ||||||
chr18:33707428
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.879+23860C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707428 | ||||||
chr18:33707527
|
AT | A | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.879+23966delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33707527 | |||||
chr18:33707813
|
A | T | 6 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-24155A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33707813 | ||||||
chr18:33708008
|
T | C | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-23960T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708008 | ||||||
chr18:33708041
|
T | C | 26 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-23927T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708041 | ||||||
chr18:33708483
|
A | G | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-23485A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708483 | ||||||
chr18:33708500
|
T | C | 191 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(188): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.880-23468T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708500 | ||||||
chr18:33708500
|
T | G | 1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.880-23468T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708500 | ||||||
chr18:33708599
|
A | G | 192 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.880-23369A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708599 | ||||||
chr18:33708603
|
T | C | 140 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(137): Show | 140 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.880-23365T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708603 | ||||||
chr18:33708650
|
C | G | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-23318C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708650 | ||||||
chr18:33708940
|
C | T | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-23028C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708940 | ||||||
chr18:33708996
|
A | G | 1 | a0001c0001t0027g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880-22972A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33708996 | ||||||
chr18:33709109
|
A | C | 26 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-22859A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709109 | ||||||
chr18:33709182
|
T | G | 1 | a0001c0001t0011g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.880-22786T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709182 | ||||||
chr18:33709224
|
C | T | 1 | a0006c0025t0077g0004 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.880-22744C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709224 | ||||||
chr18:33709301
|
C | CA | 26 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(23): Show | 26 | HG01071.hp1 HG01433.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-22654dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33709301 | |||||
chr18:33709301
|
CA | C | 12 | a0001c0001t0001g0045a0001c0001t0001g0071a0001c0001t0004g0066others(9): Show | 12 | HG01192.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.880-22654delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33709301 | |||||
chr18:33709381
|
A | T | 26 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-22587A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709381 | ||||||
chr18:33709419
|
T | C | 2 | a0001c0001t0004g0172a0003c0003t0066g0216 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.880-22549T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709419 | ||||||
chr18:33709567
|
TC | T | 2 | a0004c0004t0078g0215a0016c0026t0052g0044 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.880-22400delC | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709567 | ||||||
chr18:33709627
|
G | C | 1 | a0001c0001t0004g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.880-22341G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709627 | ||||||
chr18:33709640
|
G | T | 41 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.880-22328G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709640 | ||||||
chr18:33709716
|
A | G | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-22252A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709716 | ||||||
chr18:33709844
|
T | A | 1 | a0002c0002t0003g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.880-22124T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709844 | ||||||
chr18:33709877
|
C | T | 89 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.880-22091C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709877 | ||||||
chr18:33709889
|
T | C | 1 | a0001c0001t0010g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.880-22079T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709889 | ||||||
chr18:33709919
|
A | T | 36 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.880-22049A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709919 | ||||||
chr18:33709978
|
G | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-21990G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33709978 | ||||||
chr18:33710096
|
C | A | 194 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.880-21872C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710096 | ||||||
chr18:33710311
|
T | C | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-21657T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710311 | ||||||
chr18:33710369
|
C | G | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-21599C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710369 | ||||||
chr18:33710460
|
T | G | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-21508T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710460 | ||||||
chr18:33710495
|
A | G | 1 | a0001c0001t0021g0198 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.880-21473A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710495 | ||||||
chr18:33710626
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880-21342A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710626 | ||||||
chr18:33710791
|
A | T | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-21177A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710791 | ||||||
chr18:33710823
|
A | G | 2 | a0001c0001t0010g0156a0001c0001t0010g0158 | 2 | NA18959.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.880-21145A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710823 | ||||||
chr18:33710997
|
T | C | 1 | a0002c0002t0003g0077 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.880-20971T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33710997 | ||||||
chr18:33711088
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-20880T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711088 | ||||||
chr18:33711348
|
A | C | 27 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0051g0097others(24): Show | 27 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.880-20620A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711348 | ||||||
chr18:33711765
|
G | T | 3 | a0002c0002t0005g0129a0002c0002t0005g0130a0002c0002t0013g0078 | 3 | HG00642.hp1 HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.880-20203G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711765 | ||||||
chr18:33711765
|
GCTGTATT others(3): Show |
G | 1 | a0001c0001t0040g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.880-20202_880-2019 others(14): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711765 | ||||||
chr18:33711832
|
C | G | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-20136C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711832 | ||||||
chr18:33711847
|
T | A | 7 | a0001c0001t0001g0071a0001c0001t0004g0103a0001c0001t0004g0146others(4): Show | 7 | HG02735.hp2 HG02886.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-20121T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33711847 | ||||||
chr18:33712200
|
C | G | 10 | a0001c0008t0025g0026a0002c0006t0009g0030a0002c0006t0009g0031others(7): Show | 10 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-19768C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712200 | ||||||
chr18:33712424
|
A | G | 2 | a0001c0001t0004g0172a0003c0003t0066g0216 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.880-19544A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712424 | ||||||
chr18:33712484
|
T | C | 194 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.880-19484T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712484 | ||||||
chr18:33712679
|
GA | G | 5 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-19286delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33712679 | |||||
chr18:33712757
|
G | A | 3 | a0001c0001t0004g0066a0001c0001t0004g0141a0001c0001t0027g0034 | 3 | HG02109.hp2 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.880-19211G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712757 | ||||||
chr18:33712823
|
A | G | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-19145A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712823 | ||||||
chr18:33712935
|
C | T | 1 | a0003c0003t0069g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-19033C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712935 | ||||||
chr18:33712990
|
C | T | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-18978C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33712990 | ||||||
chr18:33713012
|
A | G | 2 | a0002c0002t0018g0181a0002c0002t0018g0182 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.880-18956A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713012 | ||||||
chr18:33713228
|
GGTTTTTT others(12): Show |
G | 5 | a0001c0001t0001g0056a0001c0001t0001g0073a0001c0001t0007g0025others(2): Show | 5 | HG02572.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-18730_880-1871 others(23): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713228 | |||||
chr18:33713229
|
G | GTTTT | 6 | a0001c0001t0001g0083a0001c0001t0006g0090a0001c0001t0011g0206others(3): Show | 6 | HG01358.hp1 HG01981.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-18734_880-1873 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713229
|
G | GTTTTT | 5 | a0001c0001t0001g0127a0001c0001t0021g0213a0001c0001t0070g0214others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-18735_880-1873 others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713229
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0026g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-18731_880-1873 others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713229
|
GTTTTTTT others(13): Show |
G | 3 | a0001c0017t0076g0175a0009c0023t0050g0115a0010c0022t0035g0117 | 3 | HG02818.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(24): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713229
|
GTTTTTTT others(14): Show |
G | 4 | a0001c0001t0002g0068a0001c0001t0047g0190a0001c0001t0075g0184others(1): Show | 4 | HG01496.hp1 HG02486.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-18730_880-1871 others(25): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713229
|
GTTTTTTT others(15): Show |
G | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-18730_880-1870 others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713229
|
GTTTTTTT others(16): Show |
G | 1 | a0001c0001t0002g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.880-18730_880-1870 others(27): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713229 | |||||
chr18:33713230
|
TTTTTTTT others(11): Show |
T | 2 | a0001c0001t0007g0012a0001c0001t0007g0013 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(22): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713230 | |||||
chr18:33713231
|
TTTTTTTG others(10): Show |
T | 2 | a0001c0001t0007g0011a0001c0001t0007g0014 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(21): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713231 | |||||
chr18:33713232
|
TTTTTTGT others(9): Show |
T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-18730_880-1871 others(20): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713232 | |||||
chr18:33713233
|
TTTTTG | T | 9 | a0001c0001t0001g0151a0001c0001t0002g0086a0001c0001t0008g0019others(6): Show | 9 | HG00438.hp1 HG01109.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-18720_880-1871 others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713233 | |||||
chr18:33713233
|
TTTTTGTT others(8): Show |
T | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-18730_880-1871 others(19): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713233 | |||||
chr18:33713234
|
TTTTG | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0002g0091others(6): Show | 9 | HG00280.hp1 HG00642.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713234 | |||||
chr18:33713234
|
TTTTGTTT others(7): Show |
T | 2 | a0001c0001t0022g0176a0001c0001t0060g0193 | 2 | HG02922.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.880-18730_880-1871 others(18): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713234 | |||||
chr18:33713236
|
TTG | T | 23 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(20): Show | 23 | HG00323.hp2 HG01255.hp1 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713236 | |||||
chr18:33713236
|
TTGTTTTG | T | 7 | a0001c0001t0001g0104a0001c0001t0002g0038a0001c0001t0002g0051others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(11): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713236 | |||||
chr18:33713236
|
TTGTTTTG others(5): Show |
T | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.880-18730_880-1871 others(16): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713236 | |||||
chr18:33713237
|
TG | T | 25 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0099others(22): Show | 25 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.880-18730delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713237 | ||||||
chr18:33713237
|
TGTTTTG | T | 9 | a0001c0001t0002g0050a0001c0001t0002g0132a0001c0001t0002g0186others(6): Show | 9 | HG01361.hp1 HG02129.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-18730_880-1872 others(10): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713237 | ||||||
chr18:33713238
|
G | T | 64 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.880-18730G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713238 | ||||||
chr18:33713243
|
G | T | 103 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.880-18725G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713243 | ||||||
chr18:33713248
|
G | GT | 7 | a0001c0001t0048g0165a0001c0008t0025g0026a0002c0002t0003g0055others(4): Show | 7 | HG00735.hp2 HG00741.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-18694dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713248 | |||||
chr18:33713248
|
G | T | 124 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.880-18720G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713248 | ||||||
chr18:33713249
|
T | TTTTG | 8 | a0001c0001t0004g0141a0001c0001t0006g0124a0002c0002t0005g0168others(5): Show | 8 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-18716_880-1871 others(8): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713249 | |||||
chr18:33713250
|
T | TTTG | 29 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0004g0066others(26): Show | 29 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.880-18716_880-1871 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713250 | |||||
chr18:33713253
|
T | G | 5 | a0002c0002t0018g0182a0003c0003t0059g0005a0003c0003t0079g0007others(2): Show | 5 | HG02965.hp1 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-18715T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713253 | ||||||
chr18:33713254
|
T | G | 2 | a0003c0003t0069g0010a0006c0025t0077g0004 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.880-18714T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713254 | ||||||
chr18:33713259
|
T | G | 1 | a0003c0003t0069g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-18709T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713259 | ||||||
chr18:33713265
|
T | G | 6 | a0004c0004t0005g0046a0004c0004t0032g0059a0004c0004t0045g0058others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-18703T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713265 | ||||||
chr18:33713273
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.880-18695T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713273 | ||||||
chr18:33713299
|
G | GGC | 21 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-18668_880-1866 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713299 | |||||
chr18:33713312
|
T | C | 1 | a0002c0002t0003g0137 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.880-18656T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713312 | ||||||
chr18:33713341
|
A | ACCCCCCC | 12 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0006g0090others(9): Show | 12 | HG01071.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-18624_880-1861 others(11): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713341 | |||||
chr18:33713344
|
C | CCG | 121 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.880-18623_880-1862 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713344 | |||||
chr18:33713348
|
C | CCT | 24 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(21): Show | 24 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-18619_880-1861 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33713348 | |||||
chr18:33713348
|
C | T | 1 | a0002c0002t0005g0162 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.880-18620C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713348 | ||||||
chr18:33713360
|
T | C | 194 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.880-18608T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713360 | ||||||
chr18:33713535
|
G | A | 110 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(107): Show | 110 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.880-18433G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713535 | ||||||
chr18:33713595
|
A | G | 1 | a0001c0001t0029g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.880-18373A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713595 | ||||||
chr18:33713685
|
C | T | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-18283C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713685 | ||||||
chr18:33713828
|
C | T | 142 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(139): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.880-18140C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713828 | ||||||
chr18:33713943
|
A | G | 1 | a0001c0001t0034g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.880-18025A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33713943 | ||||||
chr18:33714017
|
G | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(110): Show | 113 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.880-17951G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714017 | ||||||
chr18:33714246
|
G | A | 3 | a0001c0008t0025g0026a0002c0006t0023g0027a0005c0024t0007g0028 | 3 | HG02723.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.880-17722G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714246 | ||||||
chr18:33714297
|
G | A | 196 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(193): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.880-17671G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714297 | ||||||
chr18:33714662
|
C | T | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-17306C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714662 | ||||||
chr18:33714711
|
T | C | 26 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-17257T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714711 | ||||||
chr18:33714816
|
T | G | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-17152T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714816 | ||||||
chr18:33714970
|
T | G | 1 | a0001c0001t0014g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.880-16998T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33714970 | ||||||
chr18:33715036
|
T | C | 194 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(191): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.880-16932T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715036 | ||||||
chr18:33715080
|
A | G | 1 | a0002c0002t0005g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.880-16888A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715080 | ||||||
chr18:33715304
|
G | A | 141 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(138): Show | 141 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.880-16664G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715304 | ||||||
chr18:33715350
|
A | G | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.880-16618A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715350 | ||||||
chr18:33715649
|
A | G | 3 | a0003c0003t0059g0005a0003c0003t0073g0009a0003c0003t0079g0007 | 3 | HG02965.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.880-16319A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33715649 | ||||||
chr18:33716227
|
G | A | 1 | a0002c0002t0005g0039 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.880-15741G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716227 | ||||||
chr18:33716271
|
G | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-15697G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716271 | ||||||
chr18:33716482
|
G | A | 1 | a0009c0023t0050g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.880-15486G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716482 | ||||||
chr18:33716518
|
G | A | 1 | a0002c0002t0003g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.880-15450G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716518 | ||||||
chr18:33716650
|
G | A | 5 | a0003c0003t0059g0005a0003c0003t0069g0010a0003c0003t0073g0009others(2): Show | 5 | HG02257.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-15318G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716650 | ||||||
chr18:33716894
|
G | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-15074G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716894 | ||||||
chr18:33716897
|
T | TA | 175 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0048others(172): Show | 175 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.880-15056dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33716897 | |||||
chr18:33716897
|
T | TAA | 16 | a0001c0001t0001g0045a0001c0008t0025g0026a0002c0006t0009g0030others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.880-15057_880-1505 others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33716897 | |||||
chr18:33716950
|
T | A | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-15018T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33716950 | ||||||
chr18:33717041
|
A | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.880-14927A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717041 | ||||||
chr18:33717090
|
G | A | 1 | a0001c0001t0007g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880-14878G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717090 | ||||||
chr18:33717117
|
T | C | 1 | a0001c0001t0006g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.880-14851T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717117 | ||||||
chr18:33717520
|
C | T | 25 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(22): Show | 25 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.880-14448C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717520 | ||||||
chr18:33717806
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.880-14162A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717806 | ||||||
chr18:33717856
|
C | T | 11 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(8): Show | 11 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-14112C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717856 | ||||||
chr18:33717882
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0026g0035a0001c0001t0028g0036others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-14086C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717882 | ||||||
chr18:33717900
|
T | C | 26 | a0001c0001t0001g0041a0001c0001t0002g0159a0001c0001t0054g0054others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-14068T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33717900 | ||||||
chr18:33718131
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0002g0128a0001c0018t0001g0070 | 3 | HG01928.hp2 HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.880-13837G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718131 | ||||||
chr18:33718150
|
T | TAAGTTCC others(835): Show |
1 | a0001c0001t0011g0081 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.880-13802_880-1380 others(846): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33718150 | |||||
chr18:33718345
|
G | A | 2 | a0007c0009t0004g0160a0007c0009t0004g0161 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.880-13623G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718345 | ||||||
chr18:33718367
|
T | C | 23 | a0001c0001t0001g0095a0001c0001t0002g0207a0001c0001t0002g0208others(20): Show | 23 | HG01071.hp1 HG01109.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-13601T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718367 | ||||||
chr18:33718537
|
C | T | 4 | a0001c0001t0010g0082a0001c0001t0010g0085a0001c0001t0016g0192others(1): Show | 4 | HG00438.hp1 HG02129.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-13431C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718537 | ||||||
chr18:33718566
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-13402A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718566 | ||||||
chr18:33718581
|
A | G | 2 | a0002c0002t0018g0181a0002c0002t0018g0182 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.880-13387A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718581 | ||||||
chr18:33718594
|
C | T | 4 | a0001c0001t0002g0186a0001c0001t0015g0187a0001c0001t0015g0189others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-13374C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718594 | ||||||
chr18:33718959
|
A | G | 94 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(91): Show | 94 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.880-13009A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33718959 | ||||||
chr18:33719213
|
A | C | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-12755A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719213 | ||||||
chr18:33719338
|
T | C | 13 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(10): Show | 13 | HG02109.hp2 HG02735.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-12630T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719338 | ||||||
chr18:33719409
|
T | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.880-12559T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719409 | ||||||
chr18:33719629
|
A | G | 1 | a0001c0018t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.880-12339A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719629 | ||||||
chr18:33719884
|
T | C | 1 | a0010c0022t0035g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.880-12084T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719884 | ||||||
chr18:33719964
|
A | G | 19 | a0001c0001t0001g0071a0001c0001t0004g0066a0001c0001t0004g0103others(16): Show | 19 | HG01884.hp1 HG02109.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.880-12004A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33719964 | ||||||
chr18:33720289
|
AG | A | 13 | a0001c0001t0001g0056a0001c0001t0007g0011a0001c0001t0007g0012others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.880-11678delG | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720289 | ||||||
chr18:33720381
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.880-11587A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720381 | ||||||
chr18:33720391
|
A | G | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.880-11577A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720391 | ||||||
chr18:33720595
|
G | A | 167 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(164): Show | 167 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.880-11373G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33720595 | ||||||
chr18:33720981
|
CT | C | 18 | a0001c0001t0002g0159a0002c0002t0005g0075a0002c0002t0005g0080others(15): Show | 18 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.880-10984delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33720981 | |||||
chr18:33721029
|
A | G | 1 | a0001c0001t0006g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.880-10939A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721029 | ||||||
chr18:33721231
|
A | G | 18 | a0001c0001t0002g0159a0002c0002t0005g0075a0002c0002t0005g0080others(15): Show | 18 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.880-10737A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721231 | ||||||
chr18:33721259
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0096a0001c0001t0002g0148 | 3 | HG00323.hp2 HG00735.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.880-10709G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721259 | ||||||
chr18:33721404
|
G | T | 5 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-10564G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721404 | ||||||
chr18:33721409
|
T | C | 31 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-10559T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721409 | ||||||
chr18:33721410
|
A | C | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-10558A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721410 | ||||||
chr18:33721631
|
A | G | 6 | a0003c0003t0024g0021a0003c0003t0059g0005a0003c0003t0066g0216others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-10337A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721631 | ||||||
chr18:33721739
|
G | C | 3 | a0001c0017t0076g0175a0003c0003t0031g0174a0003c0003t0074g0173 | 3 | HG02258.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880-10229G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721739 | ||||||
chr18:33721940
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02602.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.880-10028A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33721940 | ||||||
chr18:33722086
|
G | A | 9 | a0001c0001t0004g0172a0001c0001t0041g0138a0001c0001t0070g0214others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-9882G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722086 | ||||||
chr18:33722153
|
G | A | 31 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-9815G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722153 | ||||||
chr18:33722489
|
C | T | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-9479C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722489 | ||||||
chr18:33722574
|
G | A | 9 | a0001c0001t0038g0183a0002c0002t0003g0106a0002c0002t0003g0108others(6): Show | 9 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-9394G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722574 | ||||||
chr18:33722726
|
A | G | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.880-9242A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33722726 | ||||||
chr18:33723019
|
C | T | 1 | a0016c0026t0052g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.880-8949C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723019 | ||||||
chr18:33723369
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.880-8599G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723369 | ||||||
chr18:33723542
|
G | A | 2 | a0002c0002t0005g0080a0002c0013t0046g0079 | 2 | HG00438.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.880-8426G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723542 | ||||||
chr18:33723593
|
C | G | 102 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(99): Show | 102 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.880-8375C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723593 | ||||||
chr18:33723679
|
A | G | 173 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(170): Show | 173 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.880-8289A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723679 | ||||||
chr18:33723905
|
C | T | 1 | a0002c0002t0005g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.880-8063C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33723905 | ||||||
chr18:33724073
|
G | A | 1 | a0001c0001t0026g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-7895G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724073 | ||||||
chr18:33724198
|
T | A | 3 | a0001c0017t0076g0175a0003c0003t0031g0174a0003c0003t0074g0173 | 3 | HG02258.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880-7770T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724198 | ||||||
chr18:33724242
|
A | C | 31 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-7726A>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724242 | ||||||
chr18:33724354
|
G | T | 153 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(150): Show | 153 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.880-7614G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724354 | ||||||
chr18:33724457
|
C | G | 153 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(150): Show | 153 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.880-7511C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724457 | ||||||
chr18:33724574
|
G | C | 5 | a0001c0005t0004g0001a0001c0005t0004g0062a0001c0005t0004g0166others(2): Show | 5 | HG00621.hp2 NA18998.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-7394G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724574 | ||||||
chr18:33724589
|
G | A | 8 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-7379G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724589 | ||||||
chr18:33724949
|
C | T | 3 | a0001c0001t0012g0017a0001c0001t0022g0176a0001c0001t0071g0118 | 3 | HG02559.hp1 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.880-7019C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33724949 | ||||||
chr18:33725010
|
C | T | 82 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.880-6958C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725010 | ||||||
chr18:33725330
|
A | G | 1 | a0015c0014t0082g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880-6638A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725330 | ||||||
chr18:33725490
|
A | G | 19 | a0001c0001t0038g0183a0001c0017t0076g0175a0002c0002t0003g0106others(16): Show | 19 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-6478A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725490 | ||||||
chr18:33725615
|
T | C | 5 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-6353T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725615 | ||||||
chr18:33725617
|
T | C | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-6351T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725617 | ||||||
chr18:33725643
|
C | A | 1 | a0002c0002t0003g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.880-6325C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725643 | ||||||
chr18:33725848
|
C | T | 3 | a0001c0001t0006g0197a0001c0001t0014g0199a0001c0001t0021g0198 | 3 | NA18948.hp2 NA18970.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.880-6120C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33725848 | ||||||
chr18:33726416
|
C | G | 2 | a0001c0001t0015g0187a0001c0001t0015g0189 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.880-5552C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33726416 | ||||||
chr18:33726781
|
C | T | 31 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-5187C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33726781 | ||||||
chr18:33726869
|
C | T | 1 | a0002c0002t0030g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.880-5099C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33726869 | ||||||
chr18:33727083
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.880-4885C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727083 | ||||||
chr18:33727446
|
A | G | 2 | a0003c0003t0031g0174a0003c0003t0074g0173 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.880-4522A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727446 | ||||||
chr18:33727456
|
G | T | 154 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(151): Show | 154 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.880-4512G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727456 | ||||||
chr18:33727591
|
C | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-4377C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727591 | ||||||
chr18:33727804
|
G | A | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-4164G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33727804 | ||||||
chr18:33728028
|
C | G | 1 | a0002c0002t0005g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.880-3940C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728028 | ||||||
chr18:33728325
|
T | A | 1 | a0001c0017t0076g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-3643T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728325 | ||||||
chr18:33728558
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.880-3410C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728558 | ||||||
chr18:33728768
|
C | T | 1 | a0001c0001t0014g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.880-3200C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728768 | ||||||
chr18:33728816
|
T | C | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0006g0125 | 3 | NA18943.hp2 NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.880-3152T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33728816 | ||||||
chr18:33729070
|
T | C | 1 | a0002c0006t0023g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.880-2898T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729070 | ||||||
chr18:33729115
|
G | GAAAC | 16 | a0001c0001t0038g0183a0002c0002t0003g0106a0002c0002t0003g0108others(13): Show | 16 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.880-2851_880-2848d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33729115 | |||||
chr18:33729169
|
G | C | 103 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(100): Show | 103 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.880-2799G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729169 | ||||||
chr18:33729351
|
G | A | 1 | a0013c0015t0002g0114 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.880-2617G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729351 | ||||||
chr18:33729573
|
G | A | 1 | a0001c0001t0007g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880-2395G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729573 | ||||||
chr18:33729719
|
CTCA | C | 3 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0006g0125 | 3 | NA18943.hp2 NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.880-2243_880-2241d others(5): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33729719 | |||||
chr18:33729726
|
T | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-2242T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729726 | ||||||
chr18:33729758
|
T | C | 1 | a0001c0001t0006g0217 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.880-2210T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729758 | ||||||
chr18:33729819
|
C | T | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-2149C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33729819 | ||||||
chr18:33730002
|
C | T | 1 | a0001c0001t0014g0199 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.880-1966C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730002 | ||||||
chr18:33730025
|
C | G | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1943C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730025 | ||||||
chr18:33730216
|
C | T | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.880-1752C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730216 | ||||||
chr18:33730298
|
C | G | 32 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(29): Show | 32 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-1670C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730298 | ||||||
chr18:33730317
|
G | A | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-1651G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730317 | ||||||
chr18:33730452
|
C | T | 155 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(152): Show | 155 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.880-1516C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730452 | ||||||
chr18:33730556
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.880-1412A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730556 | ||||||
chr18:33730602
|
G | A | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1366G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730602 | ||||||
chr18:33730611
|
T | TGGCATGG others(17): Show |
1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-1356_880-1333d others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33730611 | |||||
chr18:33730797
|
T | G | 102 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(99): Show | 102 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.880-1171T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730797 | ||||||
chr18:33730976
|
C | T | 1 | a0001c0001t0006g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.880-992C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33730976 | ||||||
chr18:33731020
|
T | TCTTTGCT others(23): Show |
1 | a0001c0001t0004g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.880-944_880-915dup others(30): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33731020 | |||||
chr18:33731123
|
G | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.880-845G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731123 | ||||||
chr18:33731197
|
G | C | 102 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(99): Show | 102 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.880-771G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731197 | ||||||
chr18:33731210
|
C | CA | 87 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(84): Show | 87 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.880-752dupA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 33731210 | |||||
chr18:33731234
|
CTA | C | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-733_880-732del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731234 | ||||||
chr18:33731352
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.880-616T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731352 | ||||||
chr18:33731414
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.880-554C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731414 | ||||||
chr18:33731416
|
G | A | 1 | a0016c0026t0052g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.880-552G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731416 | ||||||
chr18:33731498
|
C | T | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-470C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731498 | ||||||
chr18:33731556
|
G | A | 9 | a0001c0008t0025g0026a0001c0008t0081g0220a0002c0006t0009g0030others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-412G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731556 | ||||||
chr18:33731639
|
A | T | 17 | a0001c0001t0001g0056a0001c0001t0004g0172a0001c0001t0007g0011others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.880-329A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731639 | ||||||
chr18:33731660
|
C | T | 1 | a0003c0003t0059g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.880-308C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731660 | ||||||
chr18:33731952
|
C | T | 1 | a0001c0005t0004g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.880-16C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 8/11 | chr18 | 33731952 | ||||||
chr18:33732105
|
A | G | 1 | a0001c0001t0054g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.976+41A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732105 | ||||||
chr18:33732142
|
T | C | 194 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(191): Show | 194 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.976+78T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732142 | ||||||
chr18:33732184
|
A | G | 156 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(153): Show | 156 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.976+120A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732184 | ||||||
chr18:33732435
|
C | T | 8 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.976+371C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732435 | ||||||
chr18:33732439
|
T | C | 6 | a0003c0003t0024g0021a0003c0003t0059g0005a0003c0003t0066g0216others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.976+375T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732439 | ||||||
chr18:33732489
|
T | C | 31 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(28): Show | 31 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.976+425T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732489 | ||||||
chr18:33732774
|
G | T | 169 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(166): Show | 169 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.976+710G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732774 | ||||||
chr18:33732821
|
A | G | 10 | a0001c0001t0001g0104a0001c0001t0002g0038a0001c0001t0002g0050others(7): Show | 10 | HG00642.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.976+757A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732821 | ||||||
chr18:33732860
|
CA | C | 62 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0004g0066others(59): Show | 62 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.976+815delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33732860 | |||||
chr18:33732860
|
CAA | C | 108 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(105): Show | 108 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.976+814_976+815del others(2): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33732860 | |||||
chr18:33732882
|
A | G | 17 | a0001c0001t0004g0052a0001c0001t0004g0153a0001c0001t0004g0167others(14): Show | 17 | HG02109.hp1 HG02129.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.976+818A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33732882 | ||||||
chr18:33733160
|
G | T | 153 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(150): Show | 153 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.976+1096G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733160 | ||||||
chr18:33733338
|
T | C | 1 | a0001c0001t0014g0199 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.977-972T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733338 | ||||||
chr18:33733382
|
T | C | 47 | a0001c0001t0051g0097a0001c0001t0075g0184a0001c0017t0076g0175others(44): Show | 47 | HG00323.hp1 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.977-928T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733382 | ||||||
chr18:33733430
|
A | G | 5 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(2): Show | 5 | HG01433.hp2 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-880A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733430 | ||||||
chr18:33733747
|
CA | C | 5 | a0001c0008t0025g0026a0001c0008t0081g0220a0001c0017t0076g0175others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-559delA | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33733747 | |||||
chr18:33733751
|
A | G | 5 | a0001c0008t0025g0026a0001c0008t0081g0220a0001c0017t0076g0175others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-559A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733751 | ||||||
chr18:33733753
|
A | G | 5 | a0001c0008t0025g0026a0001c0008t0081g0220a0001c0017t0076g0175others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-557A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733753 | ||||||
chr18:33733791
|
T | C | 1 | a0011c0012t0002g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.977-519T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733791 | ||||||
chr18:33733802
|
T | G | 24 | a0001c0001t0051g0097a0002c0002t0005g0075a0002c0002t0005g0080others(21): Show | 24 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.977-508T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733802 | ||||||
chr18:33733856
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.977-454G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733856 | ||||||
chr18:33733863
|
C | T | 1 | a0001c0001t0065g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.977-447C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733863 | ||||||
chr18:33733869
|
C | T | 1 | a0003c0003t0031g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.977-441C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733869 | ||||||
chr18:33733901
|
A | G | 1 | a0002c0002t0067g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.977-409A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733901 | ||||||
chr18:33733915
|
T | G | 1 | a0001c0001t0047g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.977-395T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733915 | ||||||
chr18:33733935
|
G | A | 2 | a0001c0001t0075g0184a0014c0019t0058g0002 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.977-375G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33733935 | ||||||
chr18:33734000
|
C | T | 27 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(24): Show | 27 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.977-310C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734000 | ||||||
chr18:33734001
|
G | T | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(147): Show | 150 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.977-309G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734001 | ||||||
chr18:33734039
|
C | G | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.977-271C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734039 | ||||||
chr18:33734044
|
T | TGCTTTAG others(19): Show |
147 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(144): Show | 147 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.977-202_977-177dup others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33734044 | |||||
chr18:33734044
|
T | TGCTTTAG others(45): Show |
26 | a0001c0001t0001g0056a0001c0001t0002g0091a0001c0001t0004g0172others(23): Show | 26 | HG00642.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.977-228_977-177dup others(52): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33734044 | |||||
chr18:33734044
|
TGCTTTAG others(19): Show |
T | 10 | a0001c0001t0038g0183a0001c0005t0004g0163a0002c0002t0003g0106others(7): Show | 10 | HG00280.hp2 HG00558.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.977-202_977-177del others(26): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 33734044 | |||||
chr18:33734194
|
T | C | 5 | a0001c0008t0025g0026a0001c0008t0081g0220a0001c0017t0076g0175others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-116T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734194 | ||||||
chr18:33734232
|
A | G | 151 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(148): Show | 151 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.977-78A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 9/11 | chr18 | 33734232 | ||||||
chr18:33734425
|
A | T | 13 | a0001c0001t0004g0153a0001c0001t0006g0090a0001c0001t0006g0197others(10): Show | 13 | HG02109.hp1 HG02129.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1082+10A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734425 | ||||||
chr18:33734471
|
C | T | 13 | a0001c0001t0004g0153a0001c0001t0006g0090a0001c0001t0006g0197others(10): Show | 13 | HG02109.hp1 HG02129.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1082+56C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734471 | ||||||
chr18:33734757
|
T | C | 86 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(83): Show | 86 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1082+342T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734757 | ||||||
chr18:33734959
|
G | T | 1 | a0002c0006t0036g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1082+544G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33734959 | ||||||
chr18:33735005
|
A | G | 1 | a0002c0006t0036g0100 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1082+590A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735005 | ||||||
chr18:33735376
|
A | G | 21 | a0001c0001t0038g0183a0001c0008t0025g0026a0001c0008t0081g0220others(18): Show | 21 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082+961A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735376 | ||||||
chr18:33735488
|
A | T | 1 | a0003c0003t0069g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1082+1073A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735488 | ||||||
chr18:33735709
|
A | G | 2 | a0001c0001t0022g0076a0001c0001t0080g0006 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1082+1294A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735709 | ||||||
chr18:33735772
|
AT | A | 27 | a0001c0001t0004g0066a0001c0001t0004g0103a0001c0001t0004g0141others(24): Show | 27 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1082+1363delT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33735772 | |||||
chr18:33735822
|
C | T | 8 | a0002c0002t0003g0106a0002c0002t0003g0108a0002c0002t0003g0109others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082+1407C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735822 | ||||||
chr18:33735914
|
G | C | 118 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(115): Show | 118 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1082+1499G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33735914 | ||||||
chr18:33736003
|
TATTTC | T | 156 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(153): Show | 156 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1082+1593_1082+159 others(9): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33736003 | |||||
chr18:33736006
|
T | C | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1082+1591T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736006 | ||||||
chr18:33736116
|
C | A | 13 | a0001c0001t0038g0183a0001c0008t0025g0026a0001c0008t0081g0220others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1082+1701C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736116 | ||||||
chr18:33736205
|
C | T | 107 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(104): Show | 107 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1082+1790C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736205 | ||||||
chr18:33736260
|
G | C | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1082+1845G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736260 | ||||||
chr18:33736328
|
C | A | 6 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082+1913C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736328 | ||||||
chr18:33736345
|
C | CT | 6 | a0003c0003t0024g0021a0003c0003t0059g0005a0003c0003t0066g0216others(3): Show | 6 | HG02257.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082+1938dupT | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33736345 | |||||
chr18:33736345
|
C | CTTT | 19 | a0001c0001t0004g0066a0001c0001t0004g0141a0001c0001t0004g0146others(16): Show | 19 | HG00558.hp2 HG00621.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1082+1936_1082+193 others(7): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 33736345 | |||||
chr18:33736445
|
C | T | 1 | a0002c0006t0009g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1082+2030C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736445 | ||||||
chr18:33736744
|
T | C | 87 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(84): Show | 87 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1083-1743T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736744 | ||||||
chr18:33736782
|
G | A | 5 | a0001c0001t0008g0019a0001c0001t0008g0020a0001c0001t0008g0022others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1083-1705G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736782 | ||||||
chr18:33736933
|
T | C | 2 | a0009c0023t0050g0115a0010c0022t0035g0117 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1083-1554T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33736933 | ||||||
chr18:33737178
|
C | A | 1 | a0001c0001t0017g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1083-1309C>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737178 | ||||||
chr18:33737520
|
G | A | 3 | a0002c0006t0036g0100a0009c0023t0050g0115a0010c0022t0035g0117 | 3 | HG02818.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1083-967G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737520 | ||||||
chr18:33737624
|
A | G | 4 | a0001c0001t0038g0183a0002c0006t0036g0100a0009c0023t0050g0115others(1): Show | 4 | HG02818.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083-863A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737624 | ||||||
chr18:33737791
|
A | G | 172 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(169): Show | 172 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.1083-696A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737791 | ||||||
chr18:33737854
|
C | G | 11 | a0001c0001t0038g0183a0002c0006t0009g0030a0002c0006t0009g0031others(8): Show | 11 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1083-633C>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737854 | ||||||
chr18:33737953
|
T | G | 1 | a0001c0001t0026g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1083-534T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737953 | ||||||
chr18:33737972
|
G | A | 2 | a0001c0001t0041g0138a0001c0001t0070g0214 | 2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1083-515G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33737972 | ||||||
chr18:33738039
|
G | A | 1 | a0002c0002t0003g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1083-448G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738039 | ||||||
chr18:33738122
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1083-365G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738122 | ||||||
chr18:33738218
|
T | C | 7 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(4): Show | 7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083-269T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738218 | ||||||
chr18:33738237
|
C | T | 3 | a0001c0008t0025g0026a0001c0008t0081g0220a0001c0017t0076g0175 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1083-250C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738237 | ||||||
chr18:33738290
|
C | T | 7 | a0002c0006t0009g0030a0002c0006t0009g0031a0002c0006t0009g0032others(4): Show | 7 | HG02145.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1083-197C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738290 | ||||||
chr18:33738292
|
G | C | 160 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(157): Show | 160 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083-195G>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738292 | ||||||
chr18:33738334
|
A | T | 1 | a0001c0001t0048g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1083-153A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738334 | ||||||
chr18:33738372
|
T | C | 154 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(151): Show | 154 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1083-115T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738372 | ||||||
chr18:33738412
|
A | G | 153 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(150): Show | 153 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.1083-75A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 10/11 | chr18 | 33738412 | ||||||
chr18:33740574
|
T | C | 1 | a0001c0001t0012g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3039+131T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33740574 | ||||||
chr18:33740716
|
G | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3039+273G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33740716 | ||||||
chr18:33740752
|
A | G | 102 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(99): Show | 102 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.3039+309A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33740752 | ||||||
chr18:33740850
|
GCTCT | G | 7 | a0003c0003t0024g0021a0003c0003t0031g0174a0003c0003t0059g0005others(4): Show | 7 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3039+410_3039+413d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 33740850 | |||||
chr18:33741325
|
A | T | 165 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(162): Show | 165 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.3039+882A>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741325 | ||||||
chr18:33741687
|
A | G | 1 | a0001c0001t0038g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3040-1201A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741687 | ||||||
chr18:33741731
|
A | G | 1 | a0001c0001t0068g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3040-1157A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741731 | ||||||
chr18:33741853
|
G | T | 2 | a0001c0001t0011g0139a0001c0001t0012g0018 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3040-1035G>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33741853 | ||||||
chr18:33742030
|
C | T | 16 | a0002c0002t0005g0075a0002c0002t0005g0080a0002c0002t0005g0121others(13): Show | 16 | HG00438.hp2 HG00673.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3040-858C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742030 | ||||||
chr18:33742085
|
G | A | 2 | a0002c0002t0005g0080a0002c0013t0046g0079 | 2 | HG00438.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.3040-803G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742085 | ||||||
chr18:33742241
|
G | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3040-647G>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742241 | ||||||
chr18:33742314
|
A | G | 166 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(163): Show | 166 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.3040-574A>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742314 | ||||||
chr18:33742397
|
A | AAAGT | 3 | a0001c0008t0025g0026a0001c0008t0081g0220a0001c0017t0076g0175 | 3 | HG02723.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3040-490_3040-487d others(6): Show |
ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 33742397 | |||||
chr18:33742444
|
C | T | 2 | a0001c0005t0004g0062a0001c0005t0056g0063 | 2 | NA18999.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3040-444C>T | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742444 | ||||||
chr18:33742576
|
T | C | 166 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0045others(163): Show | 166 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.3040-312T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742576 | ||||||
chr18:33742666
|
T | A | 1 | a0003c0003t0066g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3040-222T>A | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742666 | ||||||
chr18:33742688
|
T | C | 1 | a0007c0009t0004g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3040-200T>C | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742688 | ||||||
chr18:33742843
|
T | G | 2 | a0002c0002t0005g0080a0002c0013t0046g0079 | 2 | HG00438.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.3040-45T>G | ASXL3 | ENSG00000141431.14 | transcript | ENST00000269197.12 | protein_coding | 11/11 | chr18 | 33742843 |