geneid | 9113 |
---|---|
ensemblid | ENSG00000131023.13 |
hgncid | 6514 |
symbol | LATS1 |
name | large tumor suppressor kinase 1 |
refseq_nuc | NM_004690.4 |
refseq_prot | NP_004681.1 |
ensembl_nuc | ENST00000543571.6 |
ensembl_prot | ENSP00000437550.1 |
mane_status | MANE Select |
chr | chr6 |
start | 149658153 |
end | 149718101 |
strand | - |
ver | v1.2 |
region | chr6:149658153-149718101 |
region5000 | chr6:149653153-149723101 |
regionname0 | LATS1_chr6_149658153_149718101 |
regionname5000 | LATS1_chr6_149653153_149723101 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1130 | 252 | 77 | 36 | 100 | 12 | 25 | 82 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0002 | 0/0 | 1130 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0003 | 0/0 | 1130 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0004 | 0/0 | 1130 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0005 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0006 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0007 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0008 | 0/0 | 1130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0009 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0010 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0011 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0012 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0013 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
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 | 3393 | 130 | 38 | 17 | 58 | 6 | 10 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0002 | 1/0 | 3393 | 117 | 34 | 19 | 42 | 6 | 15 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0003 | 0/0 | 3393 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0004 | 0/0 | 3393 | 4 | 4 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0005 | 0/0 | 3393 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0006 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0007 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0008 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0009 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0010 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0011 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0012 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0013 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0014 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0015 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
c0016 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3971 | 73 | 11 | 13 | 35 | 6 | 7 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0002 | 1/0 | 3970 | 69 | 8 | 10 | 39 | 4 | 7 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0003 | 0/0 | 3970 | 28 | 18 | 1 | 3 | 1 | 5 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0004 | 0/0 | 3971 | 27 | 0 | 4 | 20 | 0 | 3 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0005 | 0/0 | 3973 | 11 | 11 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0006 | 0/0 | 3971 | 8 | 8 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0007 | 0/0 | 3970 | 8 | 8 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0008 | 0/0 | 3970 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0009 | 0/0 | 3970 | 7 | 0 | 2 | 0 | 1 | 4 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0010 | 0/0 | 3970 | 5 | 1 | 4 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0011 | 0/0 | 3971 | 3 | 1 | 2 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0012 | 0/0 | 3971 | 3 | 3 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0013 | 0/0 | 3971 | 3 | 3 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0014 | 0/0 | 3970 | 2 | 1 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0015 | 0/0 | 3970 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0016 | 0/0 | 3973 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0017 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0018 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0019 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0020 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0021 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0022 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0023 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0024 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0025 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0026 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0027 | 0/0 | 3971 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0028 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0029 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
t0030 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
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 | 2 | 1 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
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 | 3393 | 130 | 38 | 17 | 58 | 6 | 10 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002 | 1/0 | 3393 | 117 | 34 | 19 | 42 | 6 | 15 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0004 | 0/0 | 3393 | 4 | 4 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0010 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0002c0003 | 0/0 | 3393 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0003c0006 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0004c0005 | 0/0 | 3393 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0005c0015 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0006c0014 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0007c0008 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0008c0012 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0009c0011 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0010c0009 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0011c0013 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0012c0007 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0013c0016 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7363 | 72 | 11 | 12 | 35 | 6 | 7 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0004 | 0/0 | 7363 | 26 | 0 | 3 | 20 | 0 | 3 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0005 | 0/0 | 7365 | 11 | 11 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0006 | 0/0 | 7363 | 8 | 8 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0007 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0011 | 0/0 | 7363 | 3 | 1 | 2 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0012 | 0/0 | 7363 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0016 | 0/0 | 7365 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0017 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0026 | 0/0 | 7363 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0028 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0029 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0001t0030 | 0/0 | 7365 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0002 | 1/0 | 7362 | 65 | 6 | 10 | 37 | 4 | 7 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0003 | 0/0 | 7362 | 24 | 17 | 1 | 1 | 1 | 4 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0008 | 0/0 | 7362 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0009 | 0/0 | 7362 | 7 | 0 | 2 | 0 | 1 | 4 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0010 | 0/0 | 7362 | 5 | 1 | 4 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0014 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0015 | 0/0 | 7362 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0018 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0019 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0020 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0022 | 0/0 | 7362 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0024 | 0/0 | 7362 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0002t0025 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0004t0012 | 0/0 | 7363 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0004t0013 | 0/0 | 7363 | 3 | 3 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0001c0010t0023 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0002c0003t0007 | 0/0 | 7362 | 7 | 7 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0003c0006t0002 | 0/0 | 7362 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0004c0005t0003 | 0/0 | 7362 | 2 | 0 | 0 | 2 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0005c0015t0021 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0006c0014t0002 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0007c0008t0002 | 0/0 | 7362 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0008c0012t0003 | 0/0 | 7362 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0009c0011t0003 | 0/0 | 7362 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0010c0009t0027 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0011c0013t0004 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0012c0007t0014 | 0/0 | 7362 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
a0013c0016t0001 | 0/0 | 7363 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | copy fasta | chr6 | 149653153 | 149723101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0011g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0016g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0026g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0028g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0029g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0001t0030g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0010g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0015g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0018g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0022g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0024g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0002t0025g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0004t0013g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0001c0010t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0002c0003t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0003c0006t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0003c0006t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0004c0005t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0004c0005t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0005c0015t0021g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0006c0014t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0007c0008t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0008c0012t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0009c0011t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0010c0009t0027g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0011c0013t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0012c0007t0014g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
a0013c0016t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0060 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00140 | hp1 | a0001 | c0002 | t0009 | g0064 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00642 | hp1 | a0001 | c0002 | t0009 | g0091 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00642 | hp2 | a0013 | c0016 | t0001 | g0203 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00738 | hp1 | a0001 | c0002 | t0010 | g0128 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01074 | hp1 | a0011 | c0013 | t0004 | g0174 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01106 | hp1 | a0001 | c0002 | t0022 | g0104 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01109 | hp1 | a0012 | c0007 | t0014 | g0124 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01109 | hp2 | a0001 | c0002 | t0010 | g0002 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01175 | hp2 | a0010 | c0009 | t0027 | g0236 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01192 | hp1 | a0001 | c0002 | t0010 | g0002 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01433 | hp1 | a0001 | c0001 | t0011 | g0188 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01433 | hp2 | a0001 | c0002 | t0009 | g0102 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0096 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0111 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0097 | EUR | IBS | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01884 | hp1 | a0001 | c0001 | t0030 | g0268 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG01975 | hp2 | a0001 | c0002 | t0010 | g0125 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02004 | hp2 | a0001 | c0002 | t0024 | g0127 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02055 | hp2 | a0001 | c0002 | t0008 | g0029 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0084 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02145 | hp2 | a0001 | c0002 | t0008 | g0027 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0114 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02273 | hp2 | a0001 | c0001 | t0011 | g0230 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02451 | hp2 | a0001 | c0002 | t0010 | g0126 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | KHV | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0115 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0171 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0263 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0121 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0078 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0172 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0079 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02647 | hp2 | a0001 | c0002 | t0019 | g0118 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02683 | hp1 | a0008 | c0012 | t0003 | g0059 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02717 | hp2 | a0001 | c0001 | t0016 | g0261 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0076 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02886 | hp1 | a0002 | c0003 | t0007 | g0145 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02886 | hp2 | a0001 | c0002 | t0008 | g0025 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02895 | hp1 | a0001 | c0004 | t0013 | g0254 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0108 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0109 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02897 | hp1 | a0001 | c0004 | t0013 | g0253 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02922 | hp2 | a0002 | c0003 | t0007 | g0144 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0112 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02970 | hp1 | a0002 | c0003 | t0007 | g0146 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0141 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03195 | hp2 | a0001 | c0004 | t0012 | g0147 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0045 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03209 | hp2 | a0003 | c0006 | t0002 | g0047 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03453 | hp2 | a0003 | c0006 | t0002 | g0061 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0262 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0026 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0119 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03491 | hp1 | a0001 | c0002 | t0009 | g0016 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03492 | hp2 | a0001 | c0002 | t0009 | g0015 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0023 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03516 | hp2 | a0001 | c0001 | t0028 | g0142 | AFR | ESN | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0120 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03579 | hp1 | a0002 | c0003 | t0007 | g0138 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03688 | hp2 | a0001 | c0002 | t0009 | g0098 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | PJL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03831 | hp1 | a0001 | c0002 | t0009 | g0032 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0101 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0106 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0086 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0020 | SAS | STU | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18943 | hp1 | a0001 | c0002 | t0025 | g0129 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18944 | hp2 | a0006 | c0014 | t0002 | g0083 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18949 | hp1 | a0001 | c0002 | t0020 | g0074 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18960 | hp1 | a0001 | c0001 | t0017 | g0005 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18969 | hp2 | a0004 | c0005 | t0003 | g0049 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18995 | hp1 | a0004 | c0005 | t0003 | g0062 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19009 | hp2 | a0001 | c0002 | t0015 | g0092 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19010 | hp1 | a0001 | c0001 | t0029 | g0251 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0122 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19030 | hp2 | a0001 | c0002 | t0018 | g0011 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19043 | hp1 | a0002 | c0003 | t0007 | g0137 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19043 | hp2 | a0001 | c0002 | t0008 | g0028 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19054 | hp1 | a0001 | c0002 | t0015 | g0034 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19055 | hp1 | a0001 | c0001 | t0026 | g0185 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19087 | hp1 | a0007 | c0008 | t0002 | g0030 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19240 | hp1 | a0002 | c0003 | t0007 | g0143 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA19240 | hp2 | a0009 | c0011 | t0003 | g0085 | AFR | YRI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | ASW | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0187 | AFR | ASW | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0105 | EUR | TSI | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02109 | hp2 | a0001 | c0002 | t0008 | g0024 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0041 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0077 | AFR | ACB | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03471 | hp1 | a0001 | c0002 | t0014 | g0007 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG03471 | hp2 | a0001 | c0004 | t0013 | g0252 | AFR | MSL | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG06807 | hp1 | a0002 | c0003 | t0007 | g0136 | AFR | USA | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
HG06807 | hp2 | a0001 | c0010 | t0023 | g0006 | AFR | USA | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA21309 | hp1 | a0005 | c0015 | t0021 | g0008 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | LWK | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0164 | REF | REF | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0094 | REF | REF | LATS1_chr6_149653153_149723101 | LATS1 | chr6 | 149653153 | 149723101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149676644
|
C | T | 1 | a0003 | 2 | HG03209.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.2687G>A | p.Arg896Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 6/8 | 3080/7362 | 2687/3393 | 896/1130 | chr6 | 149676644 | ||
chr6:149676725
|
C | T | 1 | a0010 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.2606G>A | p.Arg869Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 6/8 | 2999/7362 | 2606/3393 | 869/1130 | chr6 | 149676725 | ||
chr6:149683150
|
C | T | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1939G>A | p.Val647Ile | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 2332/7362 | 1939/3393 | 647/1130 | chr6 | 149683150 | ||
chr6:149683603
|
G | C | 1 | a0008 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1486C>G | p.Gln496Glu | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1879/7362 | 1486/3393 | 496/1130 | chr6 | 149683603 | ||
chr6:149684127
|
C | T | 1 | a0007 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.962G>A | p.Ser321Asn | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1355/7362 | 962/3393 | 321/1130 | chr6 | 149684127 | ||
chr6:149684250
|
T | C | 1 | a0011 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.839A>G | p.Asn280Ser | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1232/7362 | 839/3393 | 280/1130 | chr6 | 149684250 | ||
chr6:149684379
|
G | T | 1 | a0004 | 2 | NA18969.hp2 NA18995.hp1 |
missense_variant | MODERATE | c.710C>A | p.Pro237Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1103/7362 | 710/3393 | 237/1130 | chr6 | 149684379 | ||
chr6:149684479
|
T | C | 1 | a0002 | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
missense_variant | MODERATE | c.610A>G | p.Ser204Gly | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1003/7362 | 610/3393 | 204/1130 | chr6 | 149684479 | ||
chr6:149684569
|
G | A | 1 | a0006 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.520C>T | p.Arg174Cys | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 913/7362 | 520/3393 | 174/1130 | chr6 | 149684569 | ||
chr6:149695107
|
C | T | 1 | a0012 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.463G>A | p.Ala155Thr | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/8 | 856/7362 | 463/3393 | 155/1130 | chr6 | 149695107 | ||
chr6:149701838
|
T | C | 1 | a0005 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.289A>G | p.Ser97Gly | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/8 | 682/7362 | 289/3393 | 97/1130 | chr6 | 149701838 | ||
chr6:149701841
|
G | A | 1 | a0013 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.286C>T | p.Arg96Trp | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/8 | 679/7362 | 286/3393 | 96/1130 | chr6 | 149701841 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149662059
|
C | T | 1 | a0001c0004 | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.3063G>A | p.Gln1021Gln | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3456/7362 | 3063/3393 | 1021/1130 | chr6 | 149662059 | ||
chr6:149662080
|
G | A | 7 | a0001c0001a0001c0004a0002c0003others(4): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
synonymous_variant | LOW | c.3042C>T | p.Asp1014Asp | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3435/7362 | 3042/3393 | 1014/1130 | chr6 | 149662080 | ||
chr6:149683469
|
C | T | 1 | a0001c0010 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1620G>A | p.Val540Val | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 2013/7362 | 1620/3393 | 540/1130 | chr6 | 149683469 | ||
chr6:149683643
|
A | G | 8 | a0001c0001a0001c0004a0002c0003others(5): Show | 146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
synonymous_variant | LOW | c.1446T>C | p.Ser482Ser | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/8 | 1839/7362 | 1446/3393 | 482/1130 | chr6 | 149683643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149658280
|
G | A | 5 | a0001c0001t0001a0001c0001t0011a0001c0001t0026others(2): Show | 78 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3449C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3449 | chr6 | 149658280 | |||||
chr6:149658437
|
T | C | 1 | a0001c0001t0028 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3292A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3292 | chr6 | 149658437 | |||||
chr6:149658547
|
A | T | 19 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(16): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3182T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3182 | chr6 | 149658547 | |||||
chr6:149658700
|
A | T | 1 | a0001c0002t0009 | 7 | HG00140.hp1 HG00642.hp1 HG01433.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3029T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 3029 | chr6 | 149658700 | |||||
chr6:149658764
|
G | A | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(17): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2965C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2965 | chr6 | 149658764 | |||||
chr6:149659093
|
T | C | 1 | a0001c0001t0016 | 2 | HG02717.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2636A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2636 | chr6 | 149659093 | |||||
chr6:149659178
|
C | T | 1 | a0001c0002t0015 | 2 | NA19009.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2551G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2551 | chr6 | 149659178 | |||||
chr6:149659317
|
A | C | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(12): Show | 134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2412T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2412 | chr6 | 149659317 | |||||
chr6:149659442
|
G | C | 4 | a0001c0002t0003a0004c0005t0003a0008c0012t0003others(1): Show | 28 | HG00099.hp1 HG01192.hp2 HG02080.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2287C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2287 | chr6 | 149659442 | |||||
chr6:149659444
|
G | A | 1 | a0001c0002t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2285 | chr6 | 149659444 | |||||
chr6:149659591
|
A | G | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(12): Show | 134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2138T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 2138 | chr6 | 149659591 | |||||
chr6:149660024
|
G | A | 1 | a0001c0001t0006 | 8 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1705C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1705 | chr6 | 149660024 | |||||
chr6:149660024
|
G | T | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1705C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1705 | chr6 | 149660024 | |||||
chr6:149660025
|
T | A | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1704A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1704 | chr6 | 149660025 | |||||
chr6:149660027
|
A | G | 1 | a0001c0001t0026 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1702T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1702 | chr6 | 149660027 | |||||
chr6:149660122
|
T | C | 1 | a0010c0009t0027 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1607A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1607 | chr6 | 149660122 | |||||
chr6:149660233
|
G | A | 1 | a0005c0015t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1496C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1496 | chr6 | 149660233 | |||||
chr6:149660323
|
A | G | 23 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(20): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1406T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1406 | chr6 | 149660323 | |||||
chr6:149660518
|
T | A | 1 | a0001c0010t0023 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1211A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1211 | chr6 | 149660518 | |||||
chr6:149660635
|
C | T | 1 | a0001c0002t0008 | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1094G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 1094 | chr6 | 149660635 | |||||
chr6:149660828
|
A | G | 1 | a0001c0002t0024 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 901 | chr6 | 149660828 | |||||
chr6:149661076
|
A | G | 1 | a0001c0002t0020 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*653T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 653 | chr6 | 149661076 | |||||
chr6:149661108
|
C | T | 1 | a0001c0002t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 621 | chr6 | 149661108 | |||||
chr6:149661115
|
T | TG | 12 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(9): Show | 120 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*613dupC | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 613 | chr6 | 149661115 | |||||
chr6:149661281
|
A | G | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(12): Show | 134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 448 | chr6 | 149661281 | |||||
chr6:149661516
|
C | T | 1 | a0001c0002t0018 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 213 | chr6 | 149661516 | |||||
chr6:149661557
|
G | A | 1 | a0001c0001t0011 | 3 | HG01433.hp1 HG02273.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*172C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 8/8 | 172 | chr6 | 149661557 | |||||
chr6:149702212
|
C | G | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(6): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/8 | 86 | chr6 | 149702212 | |||||
chr6:149717856
|
G | A | 1 | a0001c0001t0029 | 1 | NA19010.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15730 | chr6 | 149717856 | |||||
chr6:149717936
|
G | A | 1 | a0001c0004t0013 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-228C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15810 | chr6 | 149717936 | |||||
chr6:149717955
|
G | A | 2 | a0001c0002t0010a0001c0002t0024 | 6 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-247C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15829 | chr6 | 149717955 | |||||
chr6:149718005
|
G | C | 1 | a0001c0002t0025 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-297C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15879 | chr6 | 149718005 | |||||
chr6:149718012
|
G | A | 19 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(16): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-304C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15886 | chr6 | 149718012 | |||||
chr6:149718068
|
C | T | 1 | a0001c0001t0017 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-360G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15942 | chr6 | 149718068 | |||||
chr6:149718081
|
T | TCGC | 3 | a0001c0001t0005a0001c0001t0016a0001c0001t0030 | 14 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-376_-374dupGCG | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/8 | 15956 | chr6 | 149718081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:149662474
|
A | G | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884-236T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662474 | ||||||
chr6:149662486
|
C | G | 2 | a0001c0001t0004g0003a0001c0001t0004g0211 | 3 | HG02602.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2884-248G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662486 | ||||||
chr6:149662672
|
T | C | 1 | a0001c0002t0024g0127 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2884-434A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662672 | ||||||
chr6:149662687
|
C | T | 1 | a0001c0001t0004g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2884-449G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662687 | ||||||
chr6:149662957
|
C | T | 1 | a0001c0002t0003g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2884-719G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662957 | ||||||
chr6:149662966
|
C | CA | 10 | a0001c0002t0002g0018a0001c0002t0002g0052a0001c0002t0002g0067others(7): Show | 10 | HG01243.hp2 HG02040.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2884-729dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662966 | ||||||
chr6:149662966
|
CA | C | 139 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(136): Show | 141 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.2884-729delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662966 | ||||||
chr6:149662981
|
A | G | 1 | a0001c0002t0003g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2884-743T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662981 | ||||||
chr6:149662982
|
A | G | 132 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(129): Show | 134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2884-744T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662982 | ||||||
chr6:149662983
|
A | G | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2884-745T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149662983 | ||||||
chr6:149663057
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2884-819T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663057 | ||||||
chr6:149663096
|
G | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2884-858C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663096 | ||||||
chr6:149663451
|
G | T | 6 | a0001c0002t0003g0042a0001c0002t0003g0043a0001c0002t0003g0045others(3): Show | 6 | HG03209.hp1 HG03225.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.2884-1213C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663451 | ||||||
chr6:149663634
|
T | C | 2 | a0001c0002t0002g0021a0001c0002t0022g0104 | 2 | HG01106.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2884-1396A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149663634 | ||||||
chr6:149664079
|
T | G | 183 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2884-1841A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664079 | ||||||
chr6:149664161
|
CA | C | 134 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(131): Show | 136 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2884-1924delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664161 | ||||||
chr6:149664265
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2884-2027T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664265 | ||||||
chr6:149664340
|
T | TGAG | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2884-2103_2884-210 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664340 | ||||||
chr6:149664357
|
T | A | 3 | a0001c0004t0013g0252a0001c0004t0013g0253a0001c0004t0013g0254 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2884-2119A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664357 | ||||||
chr6:149664708
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2884-2470C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664708 | ||||||
chr6:149664737
|
A | T | 2 | a0001c0001t0001g0237a0010c0009t0027g0236 | 2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2884-2499T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664737 | ||||||
chr6:149664947
|
T | G | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2884-2709A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149664947 | ||||||
chr6:149665035
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2884-2797G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665035 | ||||||
chr6:149665191
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2884-2953C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665191 | ||||||
chr6:149665371
|
T | C | 1 | a0001c0002t0002g0050 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2884-3133A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665371 | ||||||
chr6:149665490
|
T | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884-3252A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665490 | ||||||
chr6:149665658
|
T | A | 4 | a0001c0004t0012g0147a0001c0004t0013g0252a0001c0004t0013g0253others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2884-3420A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149665658 | ||||||
chr6:149666014
|
C | G | 1 | a0001c0001t0004g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3776G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666014 | ||||||
chr6:149666015
|
G | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884-3777C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666015 | ||||||
chr6:149666015
|
G | C | 1 | a0001c0001t0004g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3777C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666015 | ||||||
chr6:149666016
|
C | T | 1 | a0001c0001t0004g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3778G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666016 | ||||||
chr6:149666018
|
T | C | 1 | a0001c0001t0004g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-3780A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666018 | ||||||
chr6:149666139
|
C | CA | 56 | a0001c0001t0001g0132a0001c0001t0001g0168a0001c0001t0001g0225others(53): Show | 57 | HG00099.hp1 HG01106.hp2 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.2884-3902dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | ||||||
chr6:149666139
|
C | CAA | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0134others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2884-3903_2884-390 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | ||||||
chr6:149666139
|
C | CAAA | 27 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0163others(24): Show | 28 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.2884-3904_2884-390 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | ||||||
chr6:149666139
|
C | CAAAA | 5 | a0001c0001t0006g0004a0001c0001t0006g0243a0001c0001t0006g0245others(2): Show | 6 | HG02109.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2884-3905_2884-390 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666139 | ||||||
chr6:149666223
|
A | G | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2884-3985T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666223 | ||||||
chr6:149666272
|
A | C | 1 | a0001c0002t0003g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2884-4034T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666272 | ||||||
chr6:149666359
|
TGTAATCC others(2): Show |
T | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2884-4130_2884-412 others(13): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666359 | ||||||
chr6:149666388
|
C | T | 2 | a0001c0001t0007g0141a0001c0001t0028g0142 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2884-4150G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666388 | ||||||
chr6:149666433
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2884-4195G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666433 | ||||||
chr6:149666434
|
G | A | 13 | a0001c0001t0001g0213a0001c0001t0005g0255a0001c0001t0005g0257others(10): Show | 13 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2884-4196C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666434 | ||||||
chr6:149666461
|
CA | C | 4 | a0001c0001t0005g0255a0001c0001t0005g0264a0001c0001t0005g0265others(1): Show | 4 | HG02055.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2884-4224delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666461 | ||||||
chr6:149666803
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2884-4565C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666803 | ||||||
chr6:149666811
|
G | A | 1 | a0001c0002t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2884-4573C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666811 | ||||||
chr6:149666892
|
A | T | 2 | a0001c0004t0013g0253a0001c0004t0013g0254 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2884-4654T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666892 | ||||||
chr6:149666900
|
A | T | 2 | a0001c0004t0013g0253a0001c0004t0013g0254 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2884-4662T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666900 | ||||||
chr6:149666940
|
T | C | 13 | a0001c0002t0002g0052a0001c0002t0002g0053a0001c0002t0002g0057others(10): Show | 13 | HG01358.hp1 HG02040.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.2884-4702A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666940 | ||||||
chr6:149666943
|
C | CA | 11 | a0001c0001t0001g0163a0001c0001t0001g0233a0001c0001t0004g0205others(8): Show | 11 | HG01496.hp2 HG02257.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.2884-4706dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666943 | ||||||
chr6:149666943
|
CA | C | 6 | a0001c0001t0001g0226a0001c0001t0007g0141a0001c0001t0028g0142others(3): Show | 6 | HG01069.hp1 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2884-4706delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666943 | ||||||
chr6:149666974
|
G | A | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2884-4736C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149666974 | ||||||
chr6:149667200
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2884-4962G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667200 | ||||||
chr6:149667438
|
C | CA | 26 | a0001c0001t0004g0205a0001c0002t0002g0018a0001c0002t0002g0019others(23): Show | 26 | HG00099.hp1 HG01106.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.2884-5201dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | ||||||
chr6:149667438
|
CA | C | 24 | a0001c0001t0004g0178a0001c0001t0004g0179a0001c0001t0004g0208others(21): Show | 25 | HG00140.hp1 HG01515.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.2884-5201delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | ||||||
chr6:149667438
|
CAA | C | 56 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0168others(53): Show | 57 | HG00423.hp1 HG00423.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.2884-5202_2884-520 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | ||||||
chr6:149667438
|
CAAA | C | 60 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2884-5203_2884-520 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | ||||||
chr6:149667438
|
CAAAA | C | 9 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0192others(6): Show | 9 | HG00741.hp2 HG01975.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2884-5204_2884-520 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667438 | ||||||
chr6:149667526
|
C | A | 1 | a0001c0001t0004g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-5288G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667526 | ||||||
chr6:149667527
|
A | C | 1 | a0001c0001t0004g0205 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2884-5289T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667527 | ||||||
chr6:149667567
|
A | G | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2884-5329T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667567 | ||||||
chr6:149667660
|
C | T | 1 | a0001c0002t0003g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2884-5422G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667660 | ||||||
chr6:149667702
|
C | A | 1 | a0001c0002t0003g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2884-5464G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667702 | ||||||
chr6:149667929
|
T | C | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2884-5691A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667929 | ||||||
chr6:149667952
|
G | C | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2884-5714C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667952 | ||||||
chr6:149667964
|
C | T | 10 | a0001c0002t0002g0021a0001c0002t0002g0033a0001c0002t0002g0087others(7): Show | 10 | HG01106.hp1 HG01169.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.2884-5726G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149667964 | ||||||
chr6:149668107
|
C | T | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2884-5869G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668107 | ||||||
chr6:149668117
|
ACATGTTG others(6149): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2883+1987_2884-588 others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668117 | ||||||
chr6:149668443
|
A | AT | 134 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.2884-6206dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668443 | ||||||
chr6:149668443
|
A | ATT | 7 | a0001c0001t0001g0235a0001c0001t0006g0004a0001c0001t0006g0242others(4): Show | 8 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2884-6207_2884-620 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668443 | ||||||
chr6:149668496
|
T | C | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2884-6258A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668496 | ||||||
chr6:149668608
|
AT | A | 140 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(137): Show | 142 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2884-6371delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668608 | ||||||
chr6:149668635
|
T | C | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2884-6397A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668635 | ||||||
chr6:149668666
|
A | C | 2 | a0001c0002t0002g0063a0001c0002t0018g0011 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2884-6428T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668666 | ||||||
chr6:149668870
|
A | G | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2884-6632T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149668870 | ||||||
chr6:149669173
|
A | G | 145 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2884-6935T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669173 | ||||||
chr6:149669224
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2884-6986G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669224 | ||||||
chr6:149669372
|
A | G | 1 | a0001c0001t0007g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2883+6888T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669372 | ||||||
chr6:149669447
|
A | G | 145 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2883+6813T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669447 | ||||||
chr6:149669482
|
C | G | 1 | a0013c0016t0001g0203 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2883+6778G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669482 | ||||||
chr6:149669601
|
T | C | 1 | a0001c0001t0004g0208 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2883+6659A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669601 | ||||||
chr6:149669715
|
C | T | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2883+6545G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669715 | ||||||
chr6:149669744
|
G | A | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2883+6516C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669744 | ||||||
chr6:149669820
|
T | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2883+6440A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149669820 | ||||||
chr6:149670008
|
C | T | 2 | a0001c0001t0012g0171a0001c0001t0012g0172 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2883+6252G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670008 | ||||||
chr6:149670171
|
C | CA | 10 | a0001c0002t0002g0009a0001c0002t0002g0036a0001c0002t0002g0039others(7): Show | 10 | HG01175.hp1 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.2883+6088dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670171 | ||||||
chr6:149670171
|
CA | C | 8 | a0001c0002t0002g0090a0001c0002t0002g0116a0001c0002t0002g0123others(5): Show | 8 | HG00140.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2883+6088delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670171 | ||||||
chr6:149670182
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2883+6066_2883+607 others(16): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670182 | ||||||
chr6:149670188
|
AAAAAAGA others(4): Show |
A | 28 | a0001c0002t0002g0048a0001c0002t0003g0001a0001c0002t0003g0020others(25): Show | 29 | HG01192.hp2 HG02258.hp2 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.2883+6061_2883+607 others(15): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670188 | ||||||
chr6:149670188
|
AAAAAAGA others(9): Show |
A | 1 | a0001c0002t0002g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2883+6056_2883+607 others(20): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670188 | ||||||
chr6:149670189
|
AAAAAG | A | 120 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(117): Show | 122 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2883+6066_2883+607 others(9): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670189 | ||||||
chr6:149670189
|
AAAAAGAA others(3): Show |
A | 4 | a0001c0001t0004g0151a0001c0002t0003g0060a0001c0002t0003g0106others(1): Show | 4 | HG00099.hp1 HG01169.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2883+6061_2883+607 others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670189 | ||||||
chr6:149670190
|
AAAAG | A | 12 | a0001c0001t0001g0184a0001c0001t0001g0191a0001c0001t0001g0197others(9): Show | 12 | HG00738.hp2 HG03471.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.2883+6066_2883+606 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670190 | ||||||
chr6:149670267
|
A | G | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2883+5993T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670267 | ||||||
chr6:149670284
|
T | G | 6 | a0001c0001t0012g0171a0001c0001t0012g0172a0001c0004t0012g0147others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2883+5976A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670284 | ||||||
chr6:149670380
|
G | T | 105 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(102): Show | 106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2883+5880C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670380 | ||||||
chr6:149670625
|
T | C | 182 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2883+5635A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670625 | ||||||
chr6:149670685
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2883+5575G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670685 | ||||||
chr6:149670880
|
G | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+5380C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149670880 | ||||||
chr6:149671122
|
TTTTG | T | 141 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(138): Show | 143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2883+5134_2883+513 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671122 | ||||||
chr6:149671172
|
A | G | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2883+5088T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671172 | ||||||
chr6:149671182
|
G | A | 1 | a0001c0004t0013g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2883+5078C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671182 | ||||||
chr6:149671240
|
C | T | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2883+5020G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671240 | ||||||
chr6:149671294
|
T | C | 3 | a0001c0002t0002g0048a0003c0006t0002g0047a0003c0006t0002g0061 | 3 | HG03209.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2883+4966A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671294 | ||||||
chr6:149671397
|
G | A | 1 | a0001c0002t0003g0060 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2883+4863C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671397 | ||||||
chr6:149671424
|
G | A | 1 | a0001c0002t0003g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2883+4836C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671424 | ||||||
chr6:149671508
|
T | G | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2883+4752A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671508 | ||||||
chr6:149671572
|
C | G | 145 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2883+4688G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671572 | ||||||
chr6:149671588
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2883+4672A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671588 | ||||||
chr6:149671673
|
T | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+4587A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671673 | ||||||
chr6:149671974
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0232 | 2 | HG03491.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2883+4286G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671974 | ||||||
chr6:149671999
|
C | T | 130 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(127): Show | 132 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.2883+4261G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149671999 | ||||||
chr6:149672171
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2883+4089G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672171 | ||||||
chr6:149672458
|
C | T | 2 | a0001c0001t0007g0141a0001c0001t0028g0142 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2883+3802G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672458 | ||||||
chr6:149672717
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2883+3543C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672717 | ||||||
chr6:149672905
|
T | C | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2883+3355A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149672905 | ||||||
chr6:149673096
|
C | CT | 15 | a0001c0002t0002g0048a0001c0002t0002g0052a0001c0002t0002g0053others(12): Show | 15 | HG01358.hp1 HG02040.hp2 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.2883+3163dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | ||||||
chr6:149673096
|
CT | C | 7 | a0001c0002t0002g0013a0001c0002t0002g0051a0001c0002t0002g0107others(4): Show | 7 | HG01069.hp2 HG01109.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2883+3163delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | ||||||
chr6:149673096
|
CTT | C | 8 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(5): Show | 9 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2883+3162_2883+316 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | ||||||
chr6:149673096
|
CTTT | C | 128 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(125): Show | 129 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2883+3161_2883+316 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673096 | ||||||
chr6:149673678
|
C | CT | 5 | a0001c0002t0002g0039a0001c0002t0002g0081a0001c0002t0009g0015others(2): Show | 5 | HG00140.hp1 HG01358.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2883+2581dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673678 | ||||||
chr6:149673678
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2883+2582G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673678 | ||||||
chr6:149673704
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2883+2556G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673704 | ||||||
chr6:149673831
|
T | C | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2883+2429A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673831 | ||||||
chr6:149673970
|
C | T | 3 | a0001c0002t0003g0086a0004c0005t0003g0049a0004c0005t0003g0062 | 3 | HG04115.hp1 NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2883+2290G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149673970 | ||||||
chr6:149674221
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0232a0001c0001t0012g0171others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2883+2039G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674221 | ||||||
chr6:149674402
|
A | C | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+1858T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674402 | ||||||
chr6:149674414
|
C | T | 1 | a0001c0001t0004g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2883+1846G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674414 | ||||||
chr6:149674433
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2883+1827A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674433 | ||||||
chr6:149674482
|
C | G | 1 | a0001c0001t0007g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2883+1778G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674482 | ||||||
chr6:149674639
|
G | A | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2883+1621C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674639 | ||||||
chr6:149674660
|
C | G | 1 | a0001c0001t0004g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2883+1600G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674660 | ||||||
chr6:149674695
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2883+1565A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674695 | ||||||
chr6:149674770
|
C | CA | 13 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0001t0005g0258others(10): Show | 13 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2883+1489dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149674770 | ||||||
chr6:149675046
|
G | A | 1 | a0001c0001t0004g0151 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2883+1214C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675046 | ||||||
chr6:149675109
|
C | G | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2883+1151G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675109 | ||||||
chr6:149675111
|
G | A | 1 | a0009c0011t0003g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2883+1149C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675111 | ||||||
chr6:149675215
|
C | CA | 15 | a0001c0002t0002g0039a0001c0002t0008g0023a0001c0002t0008g0024others(12): Show | 15 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2883+1044dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675215 | ||||||
chr6:149675215
|
CA | C | 133 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(130): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.2883+1044delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675215 | ||||||
chr6:149675387
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2883+873C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675387 | ||||||
chr6:149675588
|
G | A | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2883+672C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675588 | ||||||
chr6:149675693
|
A | T | 1 | a0001c0002t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2883+567T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675693 | ||||||
chr6:149675705
|
T | C | 183 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2883+555A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675705 | ||||||
chr6:149675847
|
G | A | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2883+413C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675847 | ||||||
chr6:149675853
|
G | A | 3 | a0001c0001t0011g0187a0001c0001t0011g0188a0001c0001t0011g0230 | 3 | HG01433.hp1 HG02273.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2883+407C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675853 | ||||||
chr6:149675858
|
A | G | 1 | a0001c0002t0003g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2883+402T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675858 | ||||||
chr6:149675878
|
T | C | 1 | a0001c0002t0003g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2883+382A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149675878 | ||||||
chr6:149676001
|
C | A | 7 | a0001c0002t0008g0023a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2883+259G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149676001 | ||||||
chr6:149676109
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2883+151G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149676109 | ||||||
chr6:149676207
|
C | A | 36 | a0001c0002t0002g0048a0001c0002t0003g0001a0001c0002t0003g0020others(33): Show | 37 | HG00099.hp1 HG01192.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.2883+53G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 7/7 | chr6 | 149676207 | ||||||
chr6:149676521
|
T | C | 183 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2776+34A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 6/7 | chr6 | 149676521 | ||||||
chr6:149676818
|
G | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2594-81C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149676818 | ||||||
chr6:149676908
|
T | C | 1 | a0009c0011t0003g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2594-171A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149676908 | ||||||
chr6:149677034
|
C | A | 1 | a0001c0001t0004g0139 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2594-297G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677034 | ||||||
chr6:149677039
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2594-302A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677039 | ||||||
chr6:149677147
|
A | AAAAC | 183 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2594-414_2594-411d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677147 | ||||||
chr6:149677261
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2594-524C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677261 | ||||||
chr6:149677368
|
C | A | 1 | a0008c0012t0003g0059 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2594-631G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677368 | ||||||
chr6:149677372
|
A | G | 267 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2594-635T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677372 | ||||||
chr6:149677378
|
G | C | 1 | a0008c0012t0003g0059 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2594-641C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677378 | ||||||
chr6:149677438
|
T | C | 186 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2594-701A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677438 | ||||||
chr6:149677456
|
T | TAGAAATG others(333): Show |
1 | a0001c0002t0008g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2594-720_2594-719i others(342): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677456 | ||||||
chr6:149677587
|
A | G | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2594-850T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677587 | ||||||
chr6:149677969
|
G | A | 1 | a0001c0001t0004g0139 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2594-1232C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677969 | ||||||
chr6:149677977
|
G | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2594-1240C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677977 | ||||||
chr6:149677993
|
C | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2594-1256G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149677993 | ||||||
chr6:149678018
|
CA | C | 141 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(138): Show | 143 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2594-1282delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678018 | ||||||
chr6:149678031
|
A | C | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2594-1294T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678031 | ||||||
chr6:149678046
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2594-1309C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678046 | ||||||
chr6:149678086
|
A | G | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2594-1349T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678086 | ||||||
chr6:149678094
|
G | A | 1 | a0001c0001t0004g0139 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2594-1357C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678094 | ||||||
chr6:149678162
|
T | TA | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2594-1426_2594-142 others(5): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | ||||||
chr6:149678162
|
TCC | T | 24 | a0001c0001t0028g0142a0001c0002t0002g0048a0001c0002t0003g0001others(21): Show | 25 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.2594-1427_2594-142 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | ||||||
chr6:149678162
|
TCCA | T | 4 | a0001c0001t0006g0140a0001c0002t0003g0120a0001c0010t0023g0006others(1): Show | 4 | HG02717.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2594-1428_2594-142 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | ||||||
chr6:149678162
|
TCCAAAAA others(4): Show |
T | 1 | a0001c0002t0002g0035 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2594-1436_2594-142 others(15): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | ||||||
chr6:149678162
|
TCCAAAAA others(8): Show |
T | 6 | a0001c0002t0002g0031a0001c0002t0002g0050a0001c0002t0002g0068others(3): Show | 6 | NA18955.hp2 NA18984.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.2594-1440_2594-142 others(19): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678162 | ||||||
chr6:149678163
|
C | A | 174 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0153others(171): Show | 177 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.2594-1426G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678163 | ||||||
chr6:149678164
|
C | A | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2594-1427G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | ||||||
chr6:149678164
|
C | CAA | 73 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0001g0154others(70): Show | 74 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.2594-1429_2594-142 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | ||||||
chr6:149678164
|
C | CAAA | 19 | a0001c0001t0001g0150a0001c0001t0001g0162a0001c0001t0001g0169others(16): Show | 19 | HG00423.hp2 HG02027.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.2594-1430_2594-142 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | ||||||
chr6:149678164
|
CA | C | 23 | a0001c0001t0007g0141a0001c0001t0030g0268a0001c0002t0002g0063others(20): Show | 23 | HG01515.hp1 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2594-1428delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678164 | ||||||
chr6:149678166
|
A | C | 24 | a0001c0001t0028g0142a0001c0002t0002g0048a0001c0002t0003g0001others(21): Show | 25 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.2594-1429T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678166 | ||||||
chr6:149678167
|
A | C | 4 | a0001c0001t0006g0140a0001c0002t0003g0120a0001c0010t0023g0006others(1): Show | 4 | HG02717.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2594-1430T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678167 | ||||||
chr6:149678173
|
A | C | 2 | a0004c0005t0003g0049a0004c0005t0003g0062 | 2 | NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2594-1436T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678173 | ||||||
chr6:149678175
|
A | C | 1 | a0001c0002t0002g0035 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2594-1438T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678175 | ||||||
chr6:149678179
|
A | C | 6 | a0001c0002t0002g0031a0001c0002t0002g0050a0001c0002t0002g0068others(3): Show | 6 | NA18955.hp2 NA18984.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.2594-1442T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678179 | ||||||
chr6:149678292
|
C | A | 1 | a0009c0011t0003g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2594-1555G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678292 | ||||||
chr6:149678345
|
A | AAAAC | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2593+1526_2593+152 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678345 | ||||||
chr6:149678426
|
G | C | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2593+1449C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678426 | ||||||
chr6:149678467
|
A | G | 2 | a0001c0001t0007g0141a0001c0001t0028g0142 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2593+1408T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678467 | ||||||
chr6:149678615
|
C | T | 1 | a0001c0001t0005g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2593+1260G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678615 | ||||||
chr6:149678624
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2593+1251A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678624 | ||||||
chr6:149678651
|
A | G | 14 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(11): Show | 14 | HG00423.hp2 HG01975.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.2593+1224T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678651 | ||||||
chr6:149678652
|
T | C | 3 | a0001c0002t0002g0048a0003c0006t0002g0047a0003c0006t0002g0061 | 3 | HG03209.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2593+1223A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678652 | ||||||
chr6:149678831
|
G | A | 5 | a0001c0002t0010g0002a0001c0002t0010g0125a0001c0002t0010g0126others(2): Show | 6 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2593+1044C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149678831 | ||||||
chr6:149679181
|
T | C | 1 | a0001c0001t0004g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2593+694A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679181 | ||||||
chr6:149679506
|
G | C | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2593+369C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679506 | ||||||
chr6:149679531
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2593+344C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679531 | ||||||
chr6:149679549
|
C | CA | 21 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0189others(18): Show | 21 | HG01109.hp1 HG01516.hp2 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.2593+325dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679549 | ||||||
chr6:149679549
|
CA | C | 17 | a0001c0001t0001g0135a0001c0001t0001g0192a0001c0001t0006g0004others(14): Show | 18 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2593+325delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679549 | ||||||
chr6:149679555
|
A | C | 2 | a0003c0006t0002g0047a0003c0006t0002g0061 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2593+320T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 5/7 | chr6 | 149679555 | ||||||
chr6:149680602
|
C | A | 8 | a0001c0002t0002g0057a0001c0002t0002g0058a0001c0002t0002g0070others(5): Show | 8 | NA18947.hp1 NA18952.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.2011-145G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680602 | ||||||
chr6:149680638
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2011-181C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680638 | ||||||
chr6:149680743
|
G | GA | 112 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(109): Show | 113 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2011-287dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680743 | ||||||
chr6:149680743
|
G | GAA | 24 | a0001c0001t0001g0161a0001c0001t0001g0225a0001c0001t0006g0004others(21): Show | 25 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.2011-288_2011-287d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680743 | ||||||
chr6:149680743
|
G | GGA | 12 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0001t0005g0258others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2011-287_2011-286i others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680743 | ||||||
chr6:149680786
|
G | A | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2011-329C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680786 | ||||||
chr6:149680975
|
T | C | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2011-518A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680975 | ||||||
chr6:149680990
|
T | A | 1 | a0001c0001t0026g0185 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2011-533A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149680990 | ||||||
chr6:149681766
|
T | C | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2011-1309A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149681766 | ||||||
chr6:149681942
|
G | A | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2010+1137C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149681942 | ||||||
chr6:149681975
|
G | A | 2 | a0001c0001t0007g0141a0001c0001t0028g0142 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2010+1104C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149681975 | ||||||
chr6:149682036
|
C | T | 1 | a0001c0002t0002g0052 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2010+1043G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682036 | ||||||
chr6:149682044
|
G | A | 3 | a0001c0002t0002g0021a0001c0002t0002g0105a0001c0002t0022g0104 | 3 | HG01106.hp1 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2010+1035C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682044 | ||||||
chr6:149682067
|
G | C | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+1012C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682067 | ||||||
chr6:149682090
|
GAC | G | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2010+987_2010+988d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682090 | ||||||
chr6:149682110
|
C | CA | 124 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(121): Show | 125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2010+968dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682110 | ||||||
chr6:149682120
|
A | AT | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+958_2010+959i others(3): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682120 | ||||||
chr6:149682184
|
G | A | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2010+895C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682184 | ||||||
chr6:149682379
|
G | C | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2010+700C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682379 | ||||||
chr6:149682415
|
C | CT | 6 | a0001c0001t0004g0240a0001c0001t0005g0259a0001c0002t0002g0100others(3): Show | 6 | HG02257.hp1 HG02698.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2010+663dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682415 | ||||||
chr6:149682419
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0216 | 2 | HG02523.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2010+660A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682419 | ||||||
chr6:149682472
|
C | T | 26 | a0001c0002t0003g0001a0001c0002t0003g0020a0001c0002t0003g0040others(23): Show | 27 | HG00099.hp1 HG01192.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.2010+607G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682472 | ||||||
chr6:149682693
|
C | A | 1 | a0001c0001t0026g0185 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2010+386G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682693 | ||||||
chr6:149682696
|
G | A | 7 | a0001c0002t0008g0023a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+383C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682696 | ||||||
chr6:149682706
|
G | A | 1 | a0001c0001t0011g0188 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2010+373C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682706 | ||||||
chr6:149682759
|
T | C | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2010+320A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682759 | ||||||
chr6:149682790
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2010+289G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682790 | ||||||
chr6:149682891
|
A | C | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2010+188T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 4/7 | chr6 | 149682891 | ||||||
chr6:149684603
|
A | G | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-11T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149684603 | ||||||
chr6:149684888
|
A | G | 5 | a0001c0001t0005g0258a0001c0001t0005g0259a0001c0001t0005g0260others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-296T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149684888 | ||||||
chr6:149684938
|
A | G | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.497-346T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149684938 | ||||||
chr6:149685131
|
G | A | 1 | a0001c0002t0002g0036 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.497-539C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685131 | ||||||
chr6:149685192
|
C | T | 4 | a0001c0004t0012g0147a0001c0004t0013g0252a0001c0004t0013g0253others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-600G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685192 | ||||||
chr6:149685244
|
A | T | 4 | a0001c0001t0005g0256a0001c0002t0024g0127a0001c0004t0013g0253others(1): Show | 4 | HG02004.hp2 HG02258.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-652T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685244 | ||||||
chr6:149685246
|
T | A | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-654A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685246 | ||||||
chr6:149685543
|
G | A | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-951C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685543 | ||||||
chr6:149685803
|
CA | C | 140 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(137): Show | 142 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.497-1212delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149685803 | ||||||
chr6:149686020
|
C | A | 2 | a0001c0001t0004g0210a0001c0001t0029g0251 | 2 | NA18961.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.497-1428G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686020 | ||||||
chr6:149686274
|
AAT | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-1684_497-1683d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686274 | ||||||
chr6:149686463
|
G | C | 1 | a0001c0002t0003g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497-1871C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686463 | ||||||
chr6:149686478
|
G | A | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1886C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686478 | ||||||
chr6:149686479
|
C | T | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1887G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686479 | ||||||
chr6:149686520
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.497-1928A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686520 | ||||||
chr6:149686926
|
T | C | 1 | a0001c0002t0008g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.497-2334A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686926 | ||||||
chr6:149686941
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.497-2349A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149686941 | ||||||
chr6:149687095
|
A | AT | 138 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(135): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.497-2504dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687095 | ||||||
chr6:149687102
|
T | A | 1 | a0001c0001t0028g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.497-2510A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687102 | ||||||
chr6:149687145
|
C | T | 1 | a0001c0002t0002g0065 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.497-2553G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687145 | ||||||
chr6:149687167
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.497-2575G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687167 | ||||||
chr6:149687758
|
G | A | 4 | a0002c0003t0007g0143a0002c0003t0007g0144a0002c0003t0007g0145others(1): Show | 4 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-3166C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687758 | ||||||
chr6:149687873
|
C | CT | 24 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(21): Show | 24 | HG01175.hp1 HG02055.hp1 HG02273.hp1 others(21): Show |
intron_variant | MODIFIER | c.497-3282dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687873 | ||||||
chr6:149687905
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.497-3313C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687905 | ||||||
chr6:149687975
|
C | T | 6 | a0001c0001t0012g0171a0001c0001t0012g0172a0001c0004t0012g0147others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-3383G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149687975 | ||||||
chr6:149688122
|
G | C | 131 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(128): Show | 133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.497-3530C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688122 | ||||||
chr6:149688390
|
C | A | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-3798G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688390 | ||||||
chr6:149688410
|
A | G | 1 | a0001c0002t0009g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.497-3818T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688410 | ||||||
chr6:149688459
|
C | T | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.497-3867G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688459 | ||||||
chr6:149688465
|
C | A | 1 | a0006c0014t0002g0083 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.497-3873G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688465 | ||||||
chr6:149688507
|
A | G | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.497-3915T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688507 | ||||||
chr6:149688551
|
G | A | 11 | a0001c0001t0006g0140a0001c0001t0007g0141a0001c0001t0028g0142others(8): Show | 11 | HG01884.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-3959C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688551 | ||||||
chr6:149688603
|
C | T | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-4011G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688603 | ||||||
chr6:149688609
|
G | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.497-4017C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688609 | ||||||
chr6:149688609
|
G | C | 11 | a0001c0001t0006g0140a0001c0001t0007g0141a0001c0001t0028g0142others(8): Show | 11 | HG01884.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-4017C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688609 | ||||||
chr6:149688650
|
C | T | 1 | a0001c0001t0005g0267 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-4058G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688650 | ||||||
chr6:149688893
|
C | T | 1 | a0001c0001t0005g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.497-4301G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149688893 | ||||||
chr6:149689054
|
G | C | 1 | a0001c0001t0007g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497-4462C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689054 | ||||||
chr6:149689358
|
C | A | 1 | a0001c0001t0028g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.497-4766G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689358 | ||||||
chr6:149689418
|
C | CA | 118 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(115): Show | 119 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-4827dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689418 | ||||||
chr6:149689418
|
C | CAA | 10 | a0001c0001t0001g0167a0001c0001t0001g0214a0001c0001t0001g0229others(7): Show | 11 | HG00738.hp2 HG00741.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-4828_497-4827d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689418 | ||||||
chr6:149689533
|
C | T | 12 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0001t0005g0258others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.497-4941G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689533 | ||||||
chr6:149689596
|
C | T | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-5004G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689596 | ||||||
chr6:149689653
|
C | T | 1 | a0001c0001t0026g0185 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.497-5061G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689653 | ||||||
chr6:149689781
|
T | A | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-5189A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689781 | ||||||
chr6:149689971
|
T | TA | 41 | a0001c0001t0004g0148a0001c0002t0002g0009a0001c0002t0002g0017others(38): Show | 42 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.496+5102dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689971 | ||||||
chr6:149689985
|
T | A | 1 | a0001c0002t0003g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+5089A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149689985 | ||||||
chr6:149690150
|
C | T | 182 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.496+4924G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690150 | ||||||
chr6:149690186
|
T | C | 9 | a0001c0001t0005g0255a0001c0001t0005g0258a0001c0001t0005g0259others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+4888A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690186 | ||||||
chr6:149690213
|
C | CT | 5 | a0001c0002t0002g0046a0001c0002t0003g0084a0001c0002t0003g0106others(2): Show | 5 | HG01109.hp1 HG02080.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+4860dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690213 | ||||||
chr6:149690213
|
CT | C | 133 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(130): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.496+4860delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690213 | ||||||
chr6:149690266
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.496+4808A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690266 | ||||||
chr6:149690449
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.496+4625C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690449 | ||||||
chr6:149690506
|
C | A | 1 | a0001c0002t0003g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+4568G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690506 | ||||||
chr6:149690551
|
C | CT | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4522dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690551 | ||||||
chr6:149690581
|
C | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+4493G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690581 | ||||||
chr6:149690605
|
G | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+4469C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149690605 | ||||||
chr6:149691226
|
T | C | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.496+3848A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691226 | ||||||
chr6:149691286
|
C | T | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+3788G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691286 | ||||||
chr6:149691668
|
A | G | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+3406T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691668 | ||||||
chr6:149691770
|
C | T | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.496+3304G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691770 | ||||||
chr6:149691832
|
T | C | 5 | a0001c0002t0003g0001a0001c0002t0003g0041a0001c0002t0003g0120others(2): Show | 6 | HG01192.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+3242A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691832 | ||||||
chr6:149691880
|
A | G | 1 | a0001c0002t0002g0035 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.496+3194T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691880 | ||||||
chr6:149691923
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+3151G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149691923 | ||||||
chr6:149692155
|
C | T | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.496+2919G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692155 | ||||||
chr6:149692163
|
T | G | 6 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0194others(3): Show | 6 | HG00099.hp2 HG00738.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+2911A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692163 | ||||||
chr6:149692208
|
G | C | 1 | a0001c0001t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.496+2866C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692208 | ||||||
chr6:149692442
|
T | C | 2 | a0001c0001t0012g0171a0001c0001t0012g0172 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496+2632A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692442 | ||||||
chr6:149692677
|
C | CT | 12 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+2396dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692677 | ||||||
chr6:149692677
|
CT | C | 5 | a0001c0001t0004g0151a0001c0001t0026g0185a0001c0002t0002g0014others(2): Show | 5 | HG01169.hp1 HG01975.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+2396delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692677 | ||||||
chr6:149692705
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0165 | 2 | HG00741.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.496+2369C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692705 | ||||||
chr6:149692821
|
C | T | 131 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(128): Show | 133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.496+2253G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692821 | ||||||
chr6:149692824
|
G | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+2250C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149692824 | ||||||
chr6:149693003
|
G | A | 2 | a0001c0001t0006g0140a0001c0002t0002g0105 | 2 | HG02717.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.496+2071C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693003 | ||||||
chr6:149693022
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+2052G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693022 | ||||||
chr6:149693254
|
G | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+1820C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693254 | ||||||
chr6:149693334
|
A | G | 182 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.496+1740T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693334 | ||||||
chr6:149693339
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.496+1735G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693339 | ||||||
chr6:149693567
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0007g0141a0001c0002t0014g0007 | 3 | HG02976.hp2 HG03471.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.496+1507C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693567 | ||||||
chr6:149693591
|
C | T | 4 | a0001c0002t0002g0088a0001c0002t0002g0089a0001c0002t0015g0034others(1): Show | 4 | NA18945.hp2 NA19009.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+1483G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693591 | ||||||
chr6:149693611
|
A | AAAAC | 6 | a0001c0002t0002g0018a0001c0002t0002g0119a0001c0002t0003g0020others(3): Show | 6 | HG03490.hp2 HG04115.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+1459_496+1462d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | ||||||
chr6:149693611
|
AAAAC | A | 10 | a0001c0001t0007g0141a0001c0001t0028g0142a0001c0002t0002g0009others(7): Show | 10 | HG00642.hp1 HG01109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+1459_496+1462d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | ||||||
chr6:149693611
|
AAAACAAA others(1): Show |
A | 133 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(130): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.496+1455_496+1462d others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | ||||||
chr6:149693611
|
AAAACAAA others(5): Show |
A | 1 | a0001c0001t0004g0234 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.496+1451_496+1462d others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693611 | ||||||
chr6:149693743
|
C | T | 1 | a0001c0002t0002g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.496+1331G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693743 | ||||||
chr6:149693835
|
A | G | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.496+1239T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693835 | ||||||
chr6:149693894
|
A | T | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.496+1180T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693894 | ||||||
chr6:149693903
|
A | T | 1 | a0001c0001t0007g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.496+1171T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693903 | ||||||
chr6:149693947
|
C | T | 6 | a0001c0002t0003g0001a0001c0002t0003g0040a0001c0002t0003g0041others(3): Show | 7 | HG01192.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+1127G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149693947 | ||||||
chr6:149694051
|
C | T | 2 | a0001c0001t0006g0140a0001c0001t0030g0268 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.496+1023G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694051 | ||||||
chr6:149694122
|
G | A | 182 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.496+952C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694122 | ||||||
chr6:149694162
|
G | A | 1 | a0002c0003t0007g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+912C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694162 | ||||||
chr6:149694304
|
T | C | 1 | a0001c0002t0002g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+770A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694304 | ||||||
chr6:149694601
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496+473G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694601 | ||||||
chr6:149694765
|
T | C | 2 | a0001c0001t0016g0261a0001c0001t0016g0262 | 2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.496+309A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 3/7 | chr6 | 149694765 | ||||||
chr6:149695345
|
T | A | 2 | a0001c0001t0007g0141a0001c0001t0028g0142 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.349-124A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695345 | ||||||
chr6:149695366
|
A | T | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349-145T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695366 | ||||||
chr6:149695392
|
T | G | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-171A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695392 | ||||||
chr6:149695393
|
C | T | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-172G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695393 | ||||||
chr6:149695440
|
G | A | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.349-219C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695440 | ||||||
chr6:149695491
|
T | C | 1 | a0006c0014t0002g0083 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.349-270A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695491 | ||||||
chr6:149695554
|
G | A | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.349-333C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695554 | ||||||
chr6:149695676
|
G | GA | 17 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(14): Show | 17 | HG00140.hp2 HG00741.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.349-456dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695676 | ||||||
chr6:149695676
|
GA | G | 139 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.349-456delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695676 | ||||||
chr6:149695781
|
C | T | 1 | a0001c0001t0017g0005 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.349-560G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695781 | ||||||
chr6:149695804
|
A | C | 2 | a0001c0001t0007g0141a0001c0001t0028g0142 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.349-583T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695804 | ||||||
chr6:149695812
|
T | C | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.349-591A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695812 | ||||||
chr6:149695949
|
A | G | 1 | a0001c0001t0005g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-728T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695949 | ||||||
chr6:149695958
|
G | A | 1 | a0001c0004t0012g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349-737C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695958 | ||||||
chr6:149695967
|
C | T | 37 | a0001c0002t0002g0048a0001c0002t0003g0001a0001c0002t0003g0020others(34): Show | 38 | HG00099.hp1 HG01192.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.349-746G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695967 | ||||||
chr6:149695968
|
G | A | 1 | a0001c0002t0002g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.349-747C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149695968 | ||||||
chr6:149696152
|
C | T | 2 | a0001c0002t0002g0096a0001c0002t0002g0097 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.349-931G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696152 | ||||||
chr6:149696167
|
A | T | 12 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(9): Show | 13 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-946T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696167 | ||||||
chr6:149696203
|
A | C | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.349-982T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696203 | ||||||
chr6:149696280
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.349-1059A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696280 | ||||||
chr6:149696335
|
G | A | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.349-1114C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696335 | ||||||
chr6:149696414
|
T | C | 30 | a0001c0002t0002g0048a0001c0002t0003g0001a0001c0002t0003g0020others(27): Show | 31 | HG00099.hp1 HG01192.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.349-1193A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696414 | ||||||
chr6:149696554
|
C | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-1333G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696554 | ||||||
chr6:149696555
|
G | A | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349-1334C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696555 | ||||||
chr6:149696559
|
T | TA | 98 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(95): Show | 100 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(97): Show |
intron_variant | MODIFIER | c.349-1339dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | ||||||
chr6:149696559
|
T | TAA | 41 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(38): Show | 41 | HG00642.hp2 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.349-1340_349-1339d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | ||||||
chr6:149696559
|
T | TAAA | 6 | a0001c0001t0001g0162a0001c0001t0001g0219a0001c0001t0001g0220others(3): Show | 6 | HG00423.hp2 HG00438.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-1341_349-1339d others(5): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | ||||||
chr6:149696559
|
TA | T | 8 | a0001c0001t0004g0156a0001c0002t0002g0012a0001c0002t0002g0031others(5): Show | 8 | HG00099.hp1 HG00423.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-1339delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696559 | ||||||
chr6:149696560
|
A | T | 7 | a0001c0002t0008g0023a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-1339T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696560 | ||||||
chr6:149696642
|
C | T | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.349-1421G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696642 | ||||||
chr6:149696840
|
T | C | 1 | a0001c0002t0002g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.349-1619A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696840 | ||||||
chr6:149696911
|
T | C | 1 | a0001c0002t0002g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.349-1690A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696911 | ||||||
chr6:149696964
|
C | A | 1 | a0009c0011t0003g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.349-1743G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696964 | ||||||
chr6:149696988
|
C | T | 6 | a0001c0001t0012g0171a0001c0001t0012g0172a0001c0004t0012g0147others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-1767G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149696988 | ||||||
chr6:149697352
|
G | T | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-2131C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697352 | ||||||
chr6:149697452
|
T | A | 1 | a0001c0002t0002g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.349-2231A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697452 | ||||||
chr6:149697477
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.349-2256C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697477 | ||||||
chr6:149697489
|
G | A | 1 | a0001c0002t0008g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349-2268C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697489 | ||||||
chr6:149697507
|
A | G | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349-2286T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697507 | ||||||
chr6:149697952
|
T | C | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-2731A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697952 | ||||||
chr6:149697960
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.349-2739C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149697960 | ||||||
chr6:149698036
|
G | A | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349-2815C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698036 | ||||||
chr6:149698239
|
CTT | C | 144 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.349-3020_349-3019d others(4): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698239 | ||||||
chr6:149698254
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-3033A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698254 | ||||||
chr6:149698552
|
C | CT | 5 | a0001c0001t0001g0235a0001c0001t0004g0206a0001c0002t0002g0087others(2): Show | 5 | HG01361.hp1 HG02135.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+3226dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698552 | ||||||
chr6:149698589
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+3190G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698589 | ||||||
chr6:149698637
|
G | A | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348+3142C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698637 | ||||||
chr6:149698770
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+3009G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698770 | ||||||
chr6:149698841
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.348+2938C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698841 | ||||||
chr6:149698972
|
A | G | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348+2807T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149698972 | ||||||
chr6:149699020
|
G | T | 1 | a0001c0002t0002g0044 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.348+2759C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699020 | ||||||
chr6:149699058
|
CA | C | 145 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(142): Show | 147 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.348+2720delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699058 | ||||||
chr6:149699199
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+2580G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699199 | ||||||
chr6:149699277
|
A | G | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.348+2502T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699277 | ||||||
chr6:149699308
|
GTCTGGGA others(13): Show |
G | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.348+2451_348+2470d others(22): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699308 | ||||||
chr6:149699365
|
C | A | 1 | a0001c0002t0003g0084 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.348+2414G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699365 | ||||||
chr6:149699365
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.348+2414G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699365 | ||||||
chr6:149699380
|
G | A | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.348+2399C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699380 | ||||||
chr6:149699417
|
G | T | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.348+2362C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699417 | ||||||
chr6:149699453
|
A | C | 1 | a0001c0002t0002g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.348+2326T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699453 | ||||||
chr6:149699482
|
A | T | 8 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(5): Show | 9 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+2297T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699482 | ||||||
chr6:149699483
|
A | T | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+2296T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699483 | ||||||
chr6:149699567
|
T | C | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+2212A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699567 | ||||||
chr6:149699730
|
G | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+2049C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699730 | ||||||
chr6:149699936
|
T | A | 2 | a0001c0001t0012g0171a0001c0001t0012g0172 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.348+1843A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149699936 | ||||||
chr6:149700161
|
C | T | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.348+1618G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700161 | ||||||
chr6:149700168
|
T | C | 1 | a0001c0002t0020g0074 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.348+1611A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700168 | ||||||
chr6:149700285
|
C | T | 6 | a0001c0001t0001g0191a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 6 | HG02523.hp1 NA18967.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+1494G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700285 | ||||||
chr6:149700355
|
C | A | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+1424G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700355 | ||||||
chr6:149700363
|
C | T | 2 | a0001c0002t0003g0020a0008c0012t0003g0059 | 2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.348+1416G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700363 | ||||||
chr6:149700451
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.348+1328A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700451 | ||||||
chr6:149700602
|
G | A | 7 | a0001c0002t0008g0023a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+1177C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700602 | ||||||
chr6:149700602
|
G | C | 1 | a0001c0002t0003g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.348+1177C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700602 | ||||||
chr6:149700733
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.348+1046A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700733 | ||||||
chr6:149700741
|
AT | A | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.348+1037delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700741 | ||||||
chr6:149700852
|
C | T | 9 | a0001c0001t0005g0255a0001c0001t0005g0258a0001c0001t0005g0259others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+927G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700852 | ||||||
chr6:149700885
|
G | A | 9 | a0001c0001t0007g0141a0001c0001t0028g0142a0002c0003t0007g0136others(6): Show | 9 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+894C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149700885 | ||||||
chr6:149701086
|
C | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+693G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701086 | ||||||
chr6:149701097
|
A | G | 11 | a0001c0001t0006g0140a0001c0001t0007g0141a0001c0001t0028g0142others(8): Show | 11 | HG01884.hp1 HG02717.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+682T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701097 | ||||||
chr6:149701291
|
C | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+488G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701291 | ||||||
chr6:149701451
|
C | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.348+328G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701451 | ||||||
chr6:149701752
|
C | T | 3 | a0001c0004t0013g0252a0001c0004t0013g0253a0001c0004t0013g0254 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.348+27G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 2/7 | chr6 | 149701752 | ||||||
chr6:149702291
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-140-25T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702291 | ||||||
chr6:149702367
|
T | G | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-101A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702367 | ||||||
chr6:149702397
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0004g0250 | 2 | HG01243.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-140-131G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702397 | ||||||
chr6:149702480
|
A | AT | 3 | a0001c0004t0012g0147a0001c0004t0013g0253a0001c0004t0013g0254 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-140-215dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702480 | ||||||
chr6:149702483
|
TA | T | 9 | a0001c0001t0001g0184a0001c0001t0001g0190a0001c0001t0001g0199others(6): Show | 9 | HG00099.hp2 HG01069.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140-218delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702483 | ||||||
chr6:149702497
|
AAGTT | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-235_-140-232d others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702497 | ||||||
chr6:149702517
|
C | T | 131 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(128): Show | 133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-140-251G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702517 | ||||||
chr6:149702577
|
T | G | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-140-311A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702577 | ||||||
chr6:149702732
|
T | C | 184 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(181): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-140-466A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702732 | ||||||
chr6:149702799
|
A | G | 1 | a0001c0002t0002g0063 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-140-533T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702799 | ||||||
chr6:149702964
|
T | C | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-140-698A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702964 | ||||||
chr6:149702975
|
T | C | 1 | a0002c0003t0007g0143 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-140-709A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149702975 | ||||||
chr6:149703130
|
C | A | 1 | a0001c0002t0003g0084 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-140-864G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703130 | ||||||
chr6:149703149
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-140-883A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703149 | ||||||
chr6:149703358
|
T | C | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-1092A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703358 | ||||||
chr6:149703730
|
T | C | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-1464A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703730 | ||||||
chr6:149703986
|
C | T | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-140-1720G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149703986 | ||||||
chr6:149704096
|
C | A | 1 | a0001c0002t0002g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-140-1830G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704096 | ||||||
chr6:149704097
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-140-1831C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704097 | ||||||
chr6:149704158
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-140-1892G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704158 | ||||||
chr6:149704159
|
G | A | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-1893C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704159 | ||||||
chr6:149704229
|
C | G | 29 | a0001c0002t0002g0048a0001c0002t0003g0001a0001c0002t0003g0020others(26): Show | 30 | HG00099.hp1 HG01192.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-140-1963G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704229 | ||||||
chr6:149704231
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-140-1965C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704231 | ||||||
chr6:149704483
|
T | G | 2 | a0001c0001t0030g0268a0013c0016t0001g0203 | 2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-140-2217A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704483 | ||||||
chr6:149704493
|
G | GT | 103 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(100): Show | 104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-140-2228dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704493 | ||||||
chr6:149704493
|
G | T | 4 | a0001c0001t0001g0215a0001c0001t0004g0151a0001c0001t0004g0248others(1): Show | 4 | HG01169.hp1 HG03831.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-2227C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704493 | ||||||
chr6:149704510
|
A | G | 2 | a0004c0005t0003g0049a0004c0005t0003g0062 | 2 | NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-140-2244T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704510 | ||||||
chr6:149704824
|
T | G | 1 | a0001c0002t0002g0035 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-140-2558A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704824 | ||||||
chr6:149704860
|
A | T | 29 | a0001c0002t0002g0048a0001c0002t0003g0001a0001c0002t0003g0020others(26): Show | 30 | HG00099.hp1 HG01192.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-140-2594T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704860 | ||||||
chr6:149704880
|
TTAATTA | T | 2 | a0001c0002t0002g0017a0001c0002t0002g0019 | 2 | HG01106.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-140-2620_-140-261 others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704880 | ||||||
chr6:149704883
|
A | C | 3 | a0001c0001t0001g0130a0001c0002t0014g0007a0001c0010t0023g0006 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2617T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704883 | ||||||
chr6:149704884
|
T | A | 3 | a0001c0001t0001g0130a0001c0002t0014g0007a0001c0010t0023g0006 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2618A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704884 | ||||||
chr6:149704884
|
TTA | T | 4 | a0001c0002t0009g0015a0001c0002t0009g0016a0001c0004t0013g0253others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-140-2620_-140-261 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704884 | ||||||
chr6:149704885
|
T | C | 3 | a0001c0001t0001g0130a0001c0002t0014g0007a0001c0010t0023g0006 | 3 | HG02280.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2619A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704885 | ||||||
chr6:149704885
|
TATACACA others(7): Show |
T | 1 | a0001c0004t0012g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-140-2633_-140-262 others(18): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704885 | ||||||
chr6:149704887
|
T | C | 4 | a0001c0001t0001g0130a0001c0002t0014g0007a0001c0004t0013g0252others(1): Show | 4 | HG02280.hp2 HG03471.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-2621A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TAC | 14 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0212others(11): Show | 14 | HG01074.hp2 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-140-2623_-140-262 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TACAC | 12 | a0001c0001t0001g0184a0001c0001t0001g0214a0001c0001t0001g0239others(9): Show | 12 | HG00438.hp1 HG00741.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-140-2625_-140-262 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TACACAC | 34 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(31): Show | 34 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.-140-2627_-140-262 others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TACACACA others(1): Show |
26 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152others(23): Show | 26 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-140-2629_-140-262 others(12): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0166a0001c0001t0001g0204a0001c0001t0005g0256others(1): Show | 4 | HG01361.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-2631_-140-262 others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TACACACA others(5): Show |
11 | a0001c0001t0001g0167a0001c0001t0001g0223a0001c0001t0001g0227others(8): Show | 11 | HG00738.hp2 HG01358.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-140-2633_-140-262 others(16): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
T | TACACACA others(9): Show |
1 | a0001c0001t0005g0264 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-140-2637_-140-262 others(20): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
TAC | T | 89 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0004g0139others(86): Show | 90 | HG00423.hp1 HG00642.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.-140-2623_-140-262 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
TACAC | T | 9 | a0001c0001t0004g0148a0001c0002t0002g0036a0001c0002t0002g0063others(6): Show | 9 | HG00140.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140-2625_-140-262 others(8): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704887
|
TACACAC | T | 36 | a0001c0001t0004g0205a0001c0001t0004g0241a0001c0001t0006g0140others(33): Show | 37 | HG00099.hp1 HG01109.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-140-2627_-140-262 others(10): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704887 | ||||||
chr6:149704889
|
C | T | 2 | a0001c0002t0002g0017a0001c0002t0002g0019 | 2 | HG01106.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-140-2623G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704889 | ||||||
chr6:149704933
|
G | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-2667C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704933 | ||||||
chr6:149704954
|
G | A | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-2688C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149704954 | ||||||
chr6:149705060
|
T | C | 106 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-140-2794A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705060 | ||||||
chr6:149705201
|
C | T | 2 | a0001c0001t0004g0224a0011c0013t0004g0174 | 2 | HG01074.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-140-2935G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705201 | ||||||
chr6:149705292
|
T | C | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-140-3026A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705292 | ||||||
chr6:149705343
|
C | G | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-140-3077G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705343 | ||||||
chr6:149705598
|
G | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-3332C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705598 | ||||||
chr6:149705739
|
T | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-3473A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149705739 | ||||||
chr6:149706059
|
T | C | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-140-3793A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706059 | ||||||
chr6:149706064
|
T | C | 1 | a0001c0002t0003g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-140-3798A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706064 | ||||||
chr6:149706068
|
A | G | 4 | a0001c0004t0012g0147a0001c0004t0013g0252a0001c0004t0013g0253others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140-3802T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706068 | ||||||
chr6:149706075
|
C | T | 1 | a0001c0002t0003g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-140-3809G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706075 | ||||||
chr6:149706124
|
G | A | 1 | a0001c0001t0004g0234 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-140-3858C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706124 | ||||||
chr6:149706144
|
T | C | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-3878A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706144 | ||||||
chr6:149706164
|
C | A | 1 | a0001c0001t0004g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-140-3898G>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706164 | ||||||
chr6:149706183
|
C | CA | 6 | a0001c0002t0002g0014a0001c0002t0002g0096a0001c0002t0002g0097others(3): Show | 6 | HG01175.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-140-3918dupT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
C | CAA | 6 | a0001c0002t0002g0009a0001c0002t0002g0100a0001c0002t0002g0101others(3): Show | 6 | HG01433.hp2 HG02698.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-140-3919_-140-391 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0002g0103 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-140-3930_-140-391 others(17): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CA | C | 23 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0080others(20): Show | 24 | HG01106.hp2 HG01192.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.-140-3918delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAA | C | 31 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0063others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-140-3919_-140-391 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAA | C | 18 | a0001c0002t0002g0031a0001c0002t0002g0044a0001c0002t0002g0048others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.-140-3920_-140-391 others(7): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(2): Show |
C | 12 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0225others(9): Show | 12 | HG02004.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140-3926_-140-391 others(13): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(3): Show |
C | 47 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0150others(44): Show | 48 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-140-3927_-140-391 others(14): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(4): Show |
C | 70 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(67): Show | 71 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-140-3928_-140-391 others(15): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(5): Show |
C | 13 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0001t0005g0258others(10): Show | 13 | HG02615.hp1 HG02895.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.-140-3929_-140-391 others(16): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0004t0013g0253 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-140-3930_-140-391 others(17): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(14): Show |
C | 2 | a0001c0002t0003g0042a0001c0002t0003g0043 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-140-3938_-140-391 others(25): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706183
|
CAAAAAAA others(15): Show |
C | 1 | a0001c0002t0002g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-140-3939_-140-391 others(26): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706183 | ||||||
chr6:149706196
|
A | G | 1 | a0001c0001t0004g0240 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-140-3930T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706196 | ||||||
chr6:149706336
|
G | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-4070C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706336 | ||||||
chr6:149706349
|
C | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-4083G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149706349 | ||||||
chr6:149707011
|
C | CT | 124 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(121): Show | 125 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-140-4746dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707011 | ||||||
chr6:149707011
|
C | CTT | 12 | a0001c0001t0004g0248a0001c0001t0005g0257a0001c0001t0030g0268others(9): Show | 13 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140-4747_-140-474 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707011 | ||||||
chr6:149707011
|
CT | C | 5 | a0001c0002t0002g0021a0001c0002t0002g0105a0001c0002t0002g0123others(2): Show | 5 | HG01106.hp1 HG01169.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140-4746delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707011 | ||||||
chr6:149707158
|
G | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-4892C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707158 | ||||||
chr6:149707283
|
G | A | 1 | a0001c0001t0028g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-140-5017C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707283 | ||||||
chr6:149707383
|
G | A | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-140-5117C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707383 | ||||||
chr6:149707441
|
G | A | 1 | a0001c0002t0003g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-140-5175C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707441 | ||||||
chr6:149707534
|
T | C | 7 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(4): Show | 7 | HG02027.hp2 HG02132.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-5268A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707534 | ||||||
chr6:149707787
|
G | A | 1 | a0001c0002t0003g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-140-5521C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707787 | ||||||
chr6:149707880
|
A | C | 1 | a0001c0001t0004g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-140-5614T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149707880 | ||||||
chr6:149708151
|
C | G | 2 | a0001c0001t0012g0171a0001c0001t0012g0172 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-140-5885G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708151 | ||||||
chr6:149708172
|
G | T | 12 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0001t0005g0258others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140-5906C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708172 | ||||||
chr6:149708414
|
CA | C | 149 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(146): Show | 151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-140-6149delT | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708414 | ||||||
chr6:149708616
|
A | T | 1 | a0001c0002t0002g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-140-6350T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708616 | ||||||
chr6:149708775
|
A | T | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-140-6509T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708775 | ||||||
chr6:149708870
|
C | T | 7 | a0001c0002t0008g0023a0001c0002t0008g0024a0001c0002t0008g0025others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140-6604G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708870 | ||||||
chr6:149708922
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-140-6656T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149708922 | ||||||
chr6:149709055
|
T | C | 3 | a0001c0004t0013g0252a0001c0004t0013g0253a0001c0004t0013g0254 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-140-6789A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709055 | ||||||
chr6:149709180
|
G | A | 1 | a0001c0001t0005g0267 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-140-6914C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709180 | ||||||
chr6:149709212
|
C | T | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-140-6946G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709212 | ||||||
chr6:149709251
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-140-6985T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709251 | ||||||
chr6:149709463
|
C | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140-7197G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709463 | ||||||
chr6:149709493
|
G | A | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-140-7227C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709493 | ||||||
chr6:149709668
|
C | CT | 99 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(96): Show | 100 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-140-7403dupA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | ||||||
chr6:149709668
|
C | CTT | 25 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152others(22): Show | 25 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.-140-7404_-140-740 others(6): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | ||||||
chr6:149709668
|
CT | C | 15 | a0001c0002t0002g0107a0001c0002t0002g0110a0001c0002t0002g0111others(12): Show | 15 | HG01516.hp1 HG02132.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140-7403delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | ||||||
chr6:149709668
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0019g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-140-7415_-140-740 others(17): Show |
LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709668 | ||||||
chr6:149709678
|
T | C | 7 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140-7412A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709678 | ||||||
chr6:149709937
|
G | A | 1 | a0001c0002t0002g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-140-7671C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149709937 | ||||||
chr6:149710043
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-140-7777G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710043 | ||||||
chr6:149710254
|
T | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+7595A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710254 | ||||||
chr6:149710593
|
C | T | 4 | a0001c0004t0012g0147a0001c0004t0013g0252a0001c0004t0013g0253others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-141+7256G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710593 | ||||||
chr6:149710647
|
T | C | 1 | a0001c0002t0003g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-141+7202A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710647 | ||||||
chr6:149710710
|
G | A | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0010c0009t0027g0236 | 3 | HG01074.hp2 HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-141+7139C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710710 | ||||||
chr6:149710906
|
T | G | 12 | a0001c0001t0005g0255a0001c0001t0005g0257a0001c0001t0005g0258others(9): Show | 12 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-141+6943A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149710906 | ||||||
chr6:149711033
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-141+6816C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711033 | ||||||
chr6:149711111
|
T | C | 143 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(140): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-141+6738A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711111 | ||||||
chr6:149711115
|
C | T | 1 | a0001c0001t0004g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-141+6734G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711115 | ||||||
chr6:149711178
|
T | C | 2 | a0001c0001t0004g0240a0001c0001t0004g0241 | 2 | NA18977.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-141+6671A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711178 | ||||||
chr6:149711253
|
A | T | 11 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(8): Show | 12 | HG01169.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-141+6596T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711253 | ||||||
chr6:149711254
|
AT | A | 8 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0019others(5): Show | 9 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-141+6594delA | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711254 | ||||||
chr6:149711294
|
C | T | 1 | a0001c0002t0003g0020 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-141+6555G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711294 | ||||||
chr6:149711715
|
G | T | 3 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0019 | 3 | HG01106.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-141+6134C>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711715 | ||||||
chr6:149711843
|
G | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+6006C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711843 | ||||||
chr6:149711888
|
G | A | 1 | a0001c0001t0006g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-141+5961C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711888 | ||||||
chr6:149711896
|
T | C | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(143): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-141+5953A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149711896 | ||||||
chr6:149712153
|
A | C | 2 | a0001c0002t0009g0015a0001c0002t0009g0016 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-141+5696T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712153 | ||||||
chr6:149712221
|
T | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+5628A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712221 | ||||||
chr6:149712355
|
C | T | 131 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(128): Show | 133 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-141+5494G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712355 | ||||||
chr6:149712484
|
A | G | 3 | a0001c0002t0002g0012a0001c0002t0002g0013a0001c0002t0002g0014 | 3 | NA18951.hp1 NA19060.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-141+5365T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712484 | ||||||
chr6:149712647
|
G | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+5202C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712647 | ||||||
chr6:149712922
|
G | A | 1 | a0001c0001t0030g0268 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-141+4927C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149712922 | ||||||
chr6:149713003
|
T | A | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+4846A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713003 | ||||||
chr6:149713267
|
C | T | 1 | a0001c0004t0012g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-141+4582G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713267 | ||||||
chr6:149713363
|
C | T | 1 | a0001c0002t0018g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-141+4486G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713363 | ||||||
chr6:149713364
|
G | A | 1 | a0001c0002t0014g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-141+4485C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713364 | ||||||
chr6:149713406
|
T | C | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-141+4443A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713406 | ||||||
chr6:149713455
|
C | T | 1 | a0001c0001t0005g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-141+4394G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713455 | ||||||
chr6:149713496
|
A | G | 3 | a0001c0001t0004g0139a0001c0001t0004g0248a0001c0001t0004g0249 | 3 | NA18990.hp1 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-141+4353T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713496 | ||||||
chr6:149713572
|
A | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+4277T>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713572 | ||||||
chr6:149713574
|
G | A | 6 | a0001c0001t0006g0004a0001c0001t0006g0242a0001c0001t0006g0243others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-141+4275C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713574 | ||||||
chr6:149713752
|
C | T | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+4097G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713752 | ||||||
chr6:149713919
|
C | T | 132 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(129): Show | 134 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-141+3930G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713919 | ||||||
chr6:149713954
|
G | A | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-141+3895C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149713954 | ||||||
chr6:149714174
|
G | A | 2 | a0001c0002t0014g0007a0001c0010t0023g0006 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-141+3675C>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714174 | ||||||
chr6:149714623
|
A | C | 1 | a0005c0015t0021g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-141+3226T>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714623 | ||||||
chr6:149714640
|
T | G | 144 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(141): Show | 146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-141+3209A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714640 | ||||||
chr6:149714836
|
T | C | 4 | a0001c0002t0003g0001a0001c0002t0003g0120a0001c0002t0003g0121others(1): Show | 5 | HG01192.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-141+3013A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149714836 | ||||||
chr6:149715046
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-141+2803A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715046 | ||||||
chr6:149715109
|
C | T | 4 | a0001c0004t0012g0147a0001c0004t0013g0252a0001c0004t0013g0253others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-141+2740G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715109 | ||||||
chr6:149715279
|
G | C | 3 | a0001c0001t0004g0139a0001c0001t0004g0248a0001c0001t0004g0249 | 3 | NA18990.hp1 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-141+2570C>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715279 | ||||||
chr6:149715309
|
T | C | 1 | a0001c0001t0004g0250 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-141+2540A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715309 | ||||||
chr6:149715895
|
T | C | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-141+1954A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149715895 | ||||||
chr6:149716268
|
T | C | 133 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(130): Show | 135 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-141+1581A>G | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716268 | ||||||
chr6:149716299
|
A | G | 1 | a0001c0001t0006g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-141+1550T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716299 | ||||||
chr6:149716436
|
A | G | 147 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(144): Show | 149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.-141+1413T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716436 | ||||||
chr6:149716438
|
C | T | 1 | a0001c0002t0002g0010 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-141+1411G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716438 | ||||||
chr6:149716807
|
A | G | 147 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(144): Show | 149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.-141+1042T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716807 | ||||||
chr6:149716971
|
T | A | 1 | a0001c0002t0002g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-141+878A>T | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149716971 | ||||||
chr6:149717070
|
T | G | 1 | a0012c0007t0014g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-141+779A>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717070 | ||||||
chr6:149717096
|
A | G | 1 | a0001c0010t0023g0006 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-141+753T>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717096 | ||||||
chr6:149717234
|
C | T | 1 | a0001c0001t0004g0139 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-141+615G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717234 | ||||||
chr6:149717667
|
C | T | 3 | a0002c0003t0007g0136a0002c0003t0007g0137a0002c0003t0007g0138 | 3 | HG03579.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-141+182G>A | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717667 | ||||||
chr6:149717707
|
C | G | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-141+142G>C | LATS1 | ENSG00000131023.13 | transcript | ENST00000543571.6 | protein_coding | 1/7 | chr6 | 149717707 |