geneid | 93594 |
---|---|
ensemblid | ENSG00000156787.17 |
hgncid | 30888 |
symbol | TBC1D31 |
name | TBC1 domain family member 31 |
refseq_nuc | NM_145647.4 |
refseq_prot | NP_663622.2 |
ensembl_nuc | ENST00000287380.6 |
ensembl_prot | ENSP00000287380.1 |
mane_status | MANE Select |
chr | chr8 |
start | 123072707 |
end | 123152153 |
strand | + |
ver | v1.2 |
region | chr8:123072707-123152153 |
region5000 | chr8:123067707-123157153 |
regionname0 | TBC1D31_chr8_123072707_123152153 |
regionname5000 | TBC1D31_chr8_123067707_123157153 |
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 | 1066 | 290 | 72 | 63 | 108 | 10 | 35 | 74 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0002 | 0/0 | 1066 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0003 | 0/0 | 1066 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0004 | 0/0 | 1066 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0005 | 0/0 | 1066 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0006 | 0/0 | 1066 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0007 | 0/0 | 1066 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0008 | 0/0 | 1066 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0009 | 0/0 | 1066 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0010 | 0/0 | 1066 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0011 | 0/0 | 1066 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0012 | 0/0 | 1066 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
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 | 1/0 | 3201 | 100 | 22 | 12 | 44 | 5 | 16 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0002 | 0/1 | 3201 | 68 | 21 | 19 | 21 | 1 | 5 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0003 | 0/0 | 3201 | 61 | 15 | 9 | 28 | 2 | 7 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0004 | 0/0 | 3201 | 31 | 2 | 14 | 10 | 0 | 5 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0005 | 0/0 | 3201 | 13 | 3 | 7 | 0 | 1 | 2 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0006 | 0/0 | 3201 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0007 | 0/0 | 3201 | 5 | 0 | 5 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0008 | 0/0 | 3201 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0009 | 0/0 | 3201 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0010 | 0/0 | 3201 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0011 | 0/0 | 3201 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0012 | 0/0 | 3201 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0013 | 0/0 | 3201 | 2 | 1 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0014 | 0/0 | 3201 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0015 | 0/0 | 3201 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0016 | 0/0 | 3201 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0017 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0018 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0019 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0020 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0021 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0022 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0023 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0024 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0025 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
c0026 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 278 | 322 | 90 | 72 | 112 | 10 | 36 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
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 | 3 | 0 | 3 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
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 | 1/0 | 3201 | 100 | 22 | 12 | 44 | 5 | 16 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0002 | 0/1 | 3201 | 68 | 21 | 19 | 21 | 1 | 5 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0003 | 0/0 | 3201 | 61 | 15 | 9 | 28 | 2 | 7 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0004 | 0/0 | 3201 | 31 | 2 | 14 | 10 | 0 | 5 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0005 | 0/0 | 3201 | 13 | 3 | 7 | 0 | 1 | 2 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0008 | 0/0 | 3201 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0009 | 0/0 | 3201 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0012 | 0/0 | 3201 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0013 | 0/0 | 3201 | 2 | 1 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0019 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0022 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0024 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0002c0006 | 0/0 | 3201 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0002c0025 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0003c0010 | 0/0 | 3201 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0003c0018 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0004c0007 | 0/0 | 3201 | 5 | 0 | 5 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0005c0015 | 0/0 | 3201 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0005c0016 | 0/0 | 3201 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0006c0011 | 0/0 | 3201 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0007c0014 | 0/0 | 3201 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0008c0026 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0009c0023 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0010c0020 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0011c0021 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0012c0017 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3478 | 100 | 22 | 12 | 44 | 5 | 16 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0002t0001 | 0/1 | 3478 | 68 | 21 | 19 | 21 | 1 | 5 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0003t0001 | 0/0 | 3478 | 61 | 15 | 9 | 28 | 2 | 7 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0004t0001 | 0/0 | 3478 | 31 | 2 | 14 | 10 | 0 | 5 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0005t0001 | 0/0 | 3478 | 13 | 3 | 7 | 0 | 1 | 2 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0008t0001 | 0/0 | 3478 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0009t0001 | 0/0 | 3478 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0012t0001 | 0/0 | 3478 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0013t0001 | 0/0 | 3478 | 2 | 1 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0019t0001 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0022t0001 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0001c0024t0001 | 0/0 | 3478 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0002c0006t0001 | 0/0 | 3478 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0002c0025t0001 | 0/0 | 3478 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0003c0010t0001 | 0/0 | 3478 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0003c0018t0001 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0004c0007t0001 | 0/0 | 3478 | 5 | 0 | 5 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0005c0015t0001 | 0/0 | 3478 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0005c0016t0001 | 0/0 | 3478 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0006c0011t0001 | 0/0 | 3478 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0007c0014t0001 | 0/0 | 3478 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0008c0026t0001 | 0/0 | 3478 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0009c0023t0001 | 0/0 | 3478 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0010c0020t0001 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0011c0021t0001 | 0/0 | 3478 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
a0012c0017t0001 | 0/0 | 3478 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | copy fasta | chr8 | 123067707 | 123157153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0005t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0008t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0008t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0009t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0009t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0009t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0009t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0009t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0012t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0012t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0013t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0013t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0019t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0022t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0001c0024t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0006t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0002c0025t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0003c0010t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0003c0010t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0003c0010t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0003c0010t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0003c0018t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0004c0007t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0004c0007t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0004c0007t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0004c0007t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0004c0007t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0005c0015t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0005c0015t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0005c0016t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0005c0016t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0006c0011t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0006c0011t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0006c0011t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0007c0014t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0007c0014t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0008c0026t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0009c0023t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0010c0020t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0011c0021t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
a0012c0017t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0283 | EUR | FIN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0210 | EUR | FIN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0223 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0200 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00735 | hp1 | a0007 | c0014 | t0001 | g0077 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00735 | hp2 | a0001 | c0005 | t0001 | g0309 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0025 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01074 | hp1 | a0004 | c0007 | t0001 | g0026 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01074 | hp2 | a0010 | c0020 | t0001 | g0222 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01081 | hp1 | a0001 | c0004 | t0001 | g0140 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01099 | hp1 | a0001 | c0005 | t0001 | g0040 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0310 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01167 | hp2 | a0001 | c0005 | t0001 | g0004 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0196 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01168 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01169 | hp1 | a0001 | c0005 | t0001 | g0004 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0191 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01192 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01192 | hp2 | a0001 | c0004 | t0001 | g0147 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01243 | hp1 | a0003 | c0018 | t0001 | g0075 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01256 | hp1 | a0001 | c0022 | t0001 | g0112 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0144 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01258 | hp1 | a0001 | c0004 | t0001 | g0143 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01261 | hp1 | a0001 | c0004 | t0001 | g0141 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0214 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01358 | hp2 | a0001 | c0019 | t0001 | g0311 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0281 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01496 | hp2 | a0001 | c0005 | t0001 | g0260 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01515 | hp2 | a0001 | c0013 | t0001 | g0127 | EUR | IBS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0211 | EUR | IBS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0253 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01952 | hp1 | a0004 | c0007 | t0001 | g0022 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01975 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01978 | hp1 | a0004 | c0007 | t0001 | g0028 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01978 | hp2 | a0012 | c0017 | t0001 | g0062 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01981 | hp2 | a0001 | c0004 | t0001 | g0139 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0206 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0212 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02015 | hp2 | a0001 | c0004 | t0001 | g0096 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02056 | hp2 | a0001 | c0004 | t0001 | g0090 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02074 | hp1 | a0001 | c0004 | t0001 | g0166 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0012 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02145 | hp1 | a0002 | c0006 | t0001 | g0061 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02145 | hp2 | a0007 | c0014 | t0001 | g0076 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02148 | hp1 | a0004 | c0007 | t0001 | g0027 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CDX | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | CDX | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02257 | hp1 | a0001 | c0024 | t0001 | g0037 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0251 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0051 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02273 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0303 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02293 | hp1 | a0004 | c0007 | t0001 | g0033 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02300 | hp2 | a0001 | c0004 | t0001 | g0142 | AMR | PEL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02523 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02572 | hp1 | a0002 | c0006 | t0001 | g0269 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0099 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02602 | hp2 | a0011 | c0021 | t0001 | g0108 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02622 | hp1 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02622 | hp2 | a0001 | c0009 | t0001 | g0010 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02630 | hp2 | a0001 | c0005 | t0001 | g0021 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02717 | hp2 | a0009 | c0023 | t0001 | g0066 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02723 | hp2 | a0001 | c0013 | t0001 | g0272 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02809 | hp1 | a0001 | c0009 | t0001 | g0069 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02809 | hp2 | a0002 | c0006 | t0001 | g0316 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0270 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0307 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0036 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02922 | hp2 | a0001 | c0012 | t0001 | g0304 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02965 | hp1 | a0001 | c0009 | t0001 | g0009 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02965 | hp2 | a0001 | c0009 | t0001 | g0070 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02970 | hp1 | a0002 | c0006 | t0001 | g0249 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02976 | hp2 | a0006 | c0011 | t0001 | g0080 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0221 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03041 | hp1 | a0003 | c0010 | t0001 | g0233 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03098 | hp1 | a0002 | c0025 | t0001 | g0267 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03195 | hp1 | a0006 | c0011 | t0001 | g0079 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03195 | hp2 | a0003 | c0010 | t0001 | g0013 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03209 | hp1 | a0003 | c0010 | t0001 | g0301 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03225 | hp2 | a0008 | c0026 | t0001 | g0092 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0268 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03490 | hp1 | a0001 | c0005 | t0001 | g0005 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0100 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03492 | hp2 | a0001 | c0005 | t0001 | g0005 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03516 | hp1 | a0001 | c0009 | t0001 | g0163 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03516 | hp2 | a0001 | c0012 | t0001 | g0305 | AFR | ESN | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0284 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0296 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0300 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0157 | SAS | PJL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03831 | hp2 | a0001 | c0004 | t0001 | g0158 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0041 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0172 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0059 | SAS | BEB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18522 | hp1 | a0003 | c0010 | t0001 | g0248 | AFR | YRI | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | YRI | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | YRI | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18948 | hp1 | a0001 | c0008 | t0001 | g0060 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0145 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18956 | hp1 | a0001 | c0008 | t0001 | g0049 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18961 | hp1 | a0005 | c0015 | t0001 | g0195 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18972 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18978 | hp1 | a0001 | c0008 | t0001 | g0238 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18982 | hp1 | a0005 | c0016 | t0001 | g0189 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18989 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18994 | hp2 | a0005 | c0016 | t0001 | g0018 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18995 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19005 | hp2 | a0001 | c0008 | t0001 | g0042 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19010 | hp1 | a0005 | c0015 | t0001 | g0194 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19010 | hp2 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0298 | AFR | LWK | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19062 | hp1 | a0001 | c0004 | t0001 | g0177 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19088 | hp2 | a0001 | c0004 | t0001 | g0134 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19091 | hp1 | a0001 | c0008 | t0001 | g0045 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ASW | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0306 | AFR | ASW | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0029 | EUR | TSI | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0156 | SAS | GIH | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG01123 | hp2 | a0001 | c0004 | t0001 | g0024 | AMR | CLM | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02109 | hp2 | a0001 | c0004 | t0001 | g0271 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02486 | hp2 | a0006 | c0011 | t0001 | g0078 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | ACB | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | MSL | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG06807 | hp1 | a0002 | c0006 | t0001 | g0064 | AFR | USA | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | USA | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0063 | AFR | USA | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0290 | AFR | USA | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA21309 | hp1 | a0002 | c0006 | t0001 | g0074 | AFR | LWK | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | LWK | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0299 | REF | REF | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0126 | REF | REF | TBC1D31_chr8_123067707_123157153 | TBC1D31 | chr8 | 123067707 | 123157153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123072803
|
G | T | 1 | a0008 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.34G>T | p.Gly12Cys | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/22 | 97/3478 | 34/3201 | 12/1066 | chr8 | 123072803 | ||
chr8:123093616
|
C | T | 1 | a0009 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.545C>T | p.Thr182Ile | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/22 | 608/3478 | 545/3201 | 182/1066 | chr8 | 123093616 | ||
chr8:123097293
|
T | A | 1 | a0012 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.683T>A | p.Ile228Asn | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/22 | 746/3478 | 683/3201 | 228/1066 | chr8 | 123097293 | ||
chr8:123109345
|
A | G | 1 | a0011 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1238A>G | p.Lys413Arg | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 9/22 | 1301/3478 | 1238/3201 | 413/1066 | chr8 | 123109345 | ||
chr8:123109348
|
G | A | 1 | a0006 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.1241G>A | p.Arg414His | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 9/22 | 1304/3478 | 1241/3201 | 414/1066 | chr8 | 123109348 | ||
chr8:123109509
|
A | G | 1 | a0010 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1325A>G | p.Glu442Gly | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/22 | 1388/3478 | 1325/3201 | 442/1066 | chr8 | 123109509 | ||
chr8:123128429
|
A | G | 1 | a0005 | 4 | NA18961.hp1 NA18982.hp1 NA18994.hp2 others(1): Show |
missense_variant | MODERATE | c.2033A>G | p.Asn678Ser | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/22 | 2096/3478 | 2033/3201 | 678/1066 | chr8 | 123128429 | ||
chr8:123129073
|
G | T | 1 | a0006 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.2125G>T | p.Val709Phe | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/22 | 2188/3478 | 2125/3201 | 709/1066 | chr8 | 123129073 | ||
chr8:123129100
|
C | A | 1 | a0003 | 5 | HG01243.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
missense_variant | MODERATE | c.2152C>A | p.Gln718Lys | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/22 | 2215/3478 | 2152/3201 | 718/1066 | chr8 | 123129100 | ||
chr8:123130257
|
G | A | 1 | a0007 | 2 | HG00735.hp1 HG02145.hp2 |
missense_variant | MODERATE | c.2330G>A | p.Arg777Lys | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/22 | 2393/3478 | 2330/3201 | 777/1066 | chr8 | 123130257 | ||
chr8:123150123
|
C | T | 1 | a0004 | 5 | HG01074.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
missense_variant | MODERATE | c.3062C>T | p.Thr1021Ile | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/22 | 3125/3478 | 3062/3201 | 1021/1066 | chr8 | 123150123 | ||
chr8:123151931
|
G | A | 1 | a0002 | 8 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
missense_variant | MODERATE | c.3193G>A | p.Ala1065Thr | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 22/22 | 3256/3478 | 3193/3201 | 1065/1066 | chr8 | 123151931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123077189
|
C | T | 1 | a0002c0025 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.156C>T | p.Gly52Gly | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/22 | 219/3478 | 156/3201 | 52/1066 | chr8 | 123077189 | ||
chr8:123084250
|
A | G | 1 | a0001c0024 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.429A>G | p.Thr143Thr | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/22 | 492/3478 | 429/3201 | 143/1066 | chr8 | 123084250 | ||
chr8:123105380
|
A | G | 1 | a0001c0022 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1125A>G | p.Val375Val | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/22 | 1188/3478 | 1125/3201 | 375/1066 | chr8 | 123105380 | ||
chr8:123109558
|
A | G | 8 | a0001c0002a0001c0005a0001c0009others(5): Show | 97 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(94): Show |
synonymous_variant | LOW | c.1374A>G | p.Ala458Ala | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/22 | 1437/3478 | 1374/3201 | 458/1066 | chr8 | 123109558 | ||
chr8:123120058
|
C | T | 1 | a0001c0008 | 5 | NA18948.hp1 NA18956.hp1 NA18978.hp1 others(2): Show |
synonymous_variant | LOW | c.1440C>T | p.Thr480Thr | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/22 | 1503/3478 | 1440/3201 | 480/1066 | chr8 | 123120058 | ||
chr8:123126615
|
G | A | 10 | a0001c0003a0001c0004a0001c0008others(7): Show | 121 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
synonymous_variant | LOW | c.1812G>A | p.Leu604Leu | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/22 | 1875/3478 | 1812/3201 | 604/1066 | chr8 | 123126615 | ||
chr8:123126621
|
T | G | 1 | a0001c0012 | 2 | HG02922.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1818T>G | p.Thr606Thr | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/22 | 1881/3478 | 1818/3201 | 606/1066 | chr8 | 123126621 | ||
chr8:123126651
|
G | A | 3 | a0001c0004a0001c0012a0004c0007 | 38 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(35): Show |
synonymous_variant | LOW | c.1848G>A | p.Thr616Thr | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/22 | 1911/3478 | 1848/3201 | 616/1066 | chr8 | 123126651 | ||
chr8:123128394
|
T | C | 2 | a0001c0004a0004c0007 | 36 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(33): Show |
synonymous_variant | LOW | c.1998T>C | p.Phe666Phe | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/22 | 2061/3478 | 1998/3201 | 666/1066 | chr8 | 123128394 | ||
chr8:123128493
|
A | G | 1 | a0006c0011 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.2097A>G | p.Glu699Glu | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/22 | 2160/3478 | 2097/3201 | 699/1066 | chr8 | 123128493 | ||
chr8:123129216
|
G | A | 1 | a0001c0024 | 1 | HG02257.hp1 | splice_region_variant&synonymous_variant | LOW | c.2268G>A | p.Gln756Gln | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/22 | 2331/3478 | 2268/3201 | 756/1066 | chr8 | 123129216 | ||
chr8:123130249
|
T | C | 13 | a0001c0003a0001c0004a0001c0005others(10): Show | 137 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(134): Show |
synonymous_variant | LOW | c.2322T>C | p.Asp774Asp | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/22 | 2385/3478 | 2322/3201 | 774/1066 | chr8 | 123130249 | ||
chr8:123140859
|
G | A | 1 | a0006c0011 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.2598G>A | p.Lys866Lys | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/22 | 2661/3478 | 2598/3201 | 866/1066 | chr8 | 123140859 | ||
chr8:123142406
|
A | C | 1 | a0001c0019 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.2785A>C | p.Arg929Arg | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/22 | 2848/3478 | 2785/3201 | 929/1066 | chr8 | 123142406 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:123073476
|
C | G | 45 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(42): Show | 46 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.77+630C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123073476 | ||||||
chr8:123073527
|
T | C | 1 | a0001c0003t0001g0006 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.77+681T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123073527 | ||||||
chr8:123073620
|
C | T | 1 | a0001c0013t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.77+774C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123073620 | ||||||
chr8:123073677
|
G | GTGATTTT others(4): Show |
1 | a0002c0006t0001g0007 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.77+832_77+833insGA others(9): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123073677 | |||||
chr8:123073680
|
C | T | 22 | a0001c0001t0001g0302a0001c0001t0001g0312a0001c0002t0001g0297others(19): Show | 23 | HG00735.hp2 HG01106.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.77+834C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123073680 | ||||||
chr8:123073709
|
G | C | 1 | a0001c0003t0001g0008 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.77+863G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123073709 | ||||||
chr8:123073722
|
G | C | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.77+876G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123073722 | ||||||
chr8:123074029
|
T | C | 24 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(21): Show | 24 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.77+1183T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074029 | ||||||
chr8:123074079
|
T | C | 1 | a0001c0004t0001g0012 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.77+1233T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074079 | ||||||
chr8:123074192
|
A | G | 5 | a0001c0003t0001g0268a0001c0004t0001g0270a0001c0004t0001g0271others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.77+1346A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074192 | ||||||
chr8:123074277
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.77+1431C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074277 | ||||||
chr8:123074340
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.77+1494C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074340 | ||||||
chr8:123074402
|
T | A | 1 | a0001c0013t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.77+1556T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074402 | ||||||
chr8:123074587
|
A | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0192others(105): Show | 110 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.77+1741A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074587 | ||||||
chr8:123074633
|
G | A | 1 | a0001c0004t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.77+1787G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074633 | ||||||
chr8:123074655
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.77+1809G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074655 | ||||||
chr8:123074949
|
A | G | 1 | a0001c0013t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.77+2103A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123074949 | ||||||
chr8:123075220
|
T | C | 67 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(64): Show | 70 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.78-1891T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123075220 | ||||||
chr8:123075267
|
C | G | 10 | a0001c0002t0001g0180a0001c0002t0001g0273a0001c0002t0001g0274others(7): Show | 11 | HG00735.hp2 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.78-1844C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123075267 | ||||||
chr8:123075286
|
A | G | 1 | a0001c0002t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78-1825A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123075286 | ||||||
chr8:123075296
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(198): Show | 206 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.78-1815G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123075296 | ||||||
chr8:123075693
|
A | G | 1 | a0001c0019t0001g0311 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.78-1418A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123075693 | ||||||
chr8:123075826
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-1285C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123075826 | ||||||
chr8:123076002
|
T | C | 1 | a0001c0002t0001g0282 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.78-1109T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076002 | ||||||
chr8:123076153
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0192 | 2 | NA18960.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.78-958G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076153 | ||||||
chr8:123076267
|
T | C | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-844T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076267 | ||||||
chr8:123076338
|
A | ATG | 10 | a0001c0001t0001g0179a0001c0001t0001g0263a0001c0001t0001g0276others(7): Show | 10 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.78-745_78-744dupGT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076338
|
A | ATGTG | 3 | a0001c0002t0001g0308a0007c0014t0001g0076a0007c0014t0001g0077 | 3 | HG00735.hp1 HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.78-747_78-744dupGT others(2): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076338
|
A | ATGTGTGT others(5): Show |
1 | a0006c0011t0001g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.78-755_78-744dupGT others(10): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076338
|
A | ATGTGTGT others(7): Show |
2 | a0006c0011t0001g0079a0006c0011t0001g0080 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.78-757_78-744dupGT others(12): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076338
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.78-773A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076338 | ||||||
chr8:123076338
|
ATG | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0088others(108): Show | 112 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.78-745_78-744delGT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076338
|
ATGTG | A | 9 | a0001c0001t0001g0302a0001c0002t0001g0011a0001c0002t0001g0180others(6): Show | 9 | HG01167.hp1 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.78-747_78-744delGT others(2): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076338
|
ATGTGTG | A | 57 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(54): Show | 60 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.78-749_78-744delGT others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | 123076338 | |||||
chr8:123076448
|
T | C | 3 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275 | 3 | HG01255.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.78-663T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076448 | ||||||
chr8:123076554
|
T | G | 1 | a0002c0006t0001g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78-557T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076554 | ||||||
chr8:123076683
|
G | A | 1 | a0003c0010t0001g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78-428G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076683 | ||||||
chr8:123076703
|
C | G | 1 | a0001c0004t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.78-408C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076703 | ||||||
chr8:123076766
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.78-345T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076766 | ||||||
chr8:123076791
|
A | G | 205 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(202): Show | 210 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.78-320A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076791 | ||||||
chr8:123076797
|
C | G | 4 | a0001c0004t0001g0270a0001c0004t0001g0271a0002c0006t0001g0269others(1): Show | 4 | HG01243.hp1 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-314C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 1/21 | chr8 | 123076797 | ||||||
chr8:123077286
|
C | A | 65 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(62): Show | 68 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.224+29C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077286 | ||||||
chr8:123077419
|
G | A | 1 | a0001c0002t0001g0014 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.224+162G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077419 | ||||||
chr8:123077419
|
G | GA | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.224+168dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123077419 | |||||
chr8:123077495
|
CT | C | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+248delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123077495 | |||||
chr8:123077505
|
T | C | 1 | a0007c0014t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.224+248T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077505 | ||||||
chr8:123077533
|
A | ATTT | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.224+287_224+289dup others(3): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123077533 | |||||
chr8:123077533
|
AT | A | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+289delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123077533 | |||||
chr8:123077555
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02622.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+298G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077555 | ||||||
chr8:123077624
|
C | A | 1 | a0001c0005t0001g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.224+367C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077624 | ||||||
chr8:123077638
|
C | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(202): Show | 210 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.224+381C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077638 | ||||||
chr8:123077644
|
C | G | 9 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(6): Show | 10 | HG00735.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+387C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077644 | ||||||
chr8:123077782
|
A | G | 205 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(202): Show | 210 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.224+525A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077782 | ||||||
chr8:123077828
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.224+571C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123077828 | ||||||
chr8:123078053
|
C | CA | 10 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.224+807dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123078053 | |||||
chr8:123078097
|
C | G | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.224+840C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123078097 | ||||||
chr8:123078272
|
C | A | 65 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(62): Show | 68 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.224+1015C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123078272 | ||||||
chr8:123078516
|
G | A | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+1259G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123078516 | ||||||
chr8:123078519
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.224+1262A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123078519 | ||||||
chr8:123078688
|
A | G | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.224+1431A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123078688 | ||||||
chr8:123078696
|
A | G | 7 | a0001c0001t0001g0302a0001c0002t0001g0011a0001c0002t0001g0313others(4): Show | 7 | HG01167.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+1439A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123078696 | ||||||
chr8:123078843
|
A | AC | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.224+1593dupC | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123078843 | |||||
chr8:123079026
|
C | G | 1 | a0001c0002t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.224+1769C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079026 | ||||||
chr8:123079293
|
G | A | 2 | a0001c0004t0001g0090a0001c0004t0001g0091 | 2 | HG00673.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.224+2036G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079293 | ||||||
chr8:123079306
|
G | A | 9 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(6): Show | 10 | HG00735.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+2049G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079306 | ||||||
chr8:123079450
|
C | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0085a0001c0002t0001g0086others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+2193C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079450 | ||||||
chr8:123079601
|
C | CAGAA | 72 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(69): Show | 75 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.224+2344_224+2345i others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079601 | ||||||
chr8:123079651
|
G | T | 1 | a0001c0005t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.224+2394G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079651 | ||||||
chr8:123079731
|
G | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(202): Show | 210 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.224+2474G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079731 | ||||||
chr8:123079835
|
C | A | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.224+2578C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079835 | ||||||
chr8:123079835
|
CCATTACC others(21): Show |
C | 55 | a0001c0001t0001g0043a0001c0001t0001g0198a0001c0001t0001g0199others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.224+2597_224+2624d others(30): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123079835 | |||||
chr8:123079855
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.224+2598T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123079855 | ||||||
chr8:123080003
|
A | G | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.225-2699A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080003 | ||||||
chr8:123080156
|
T | C | 2 | a0001c0002t0001g0011a0001c0013t0001g0272 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.225-2546T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080156 | ||||||
chr8:123080180
|
C | T | 1 | a0001c0002t0001g0014 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.225-2522C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080180 | ||||||
chr8:123080181
|
G | A | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-2521G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080181 | ||||||
chr8:123080227
|
G | A | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-2475G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080227 | ||||||
chr8:123080385
|
G | A | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.225-2317G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080385 | ||||||
chr8:123080456
|
CT | C | 5 | a0001c0009t0001g0069a0001c0009t0001g0070a0006c0011t0001g0078others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-2243delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080456 | |||||
chr8:123080505
|
GCTTTTCT others(3): Show |
G | 64 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(61): Show | 67 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.225-2186_225-2177d others(12): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080505 | |||||
chr8:123080526
|
A | C | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-2176A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080526 | ||||||
chr8:123080529
|
C | CT | 9 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG01109.hp2 HG01175.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-2147dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080529 | |||||
chr8:123080529
|
C | T | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-2173C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080529 | ||||||
chr8:123080529
|
CT | C | 25 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(22): Show | 25 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.225-2147delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080529 | |||||
chr8:123080529
|
CTT | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(156): Show | 163 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.225-2148_225-2147d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080529 | |||||
chr8:123080529
|
CTTT | C | 6 | a0001c0002t0001g0182a0001c0002t0001g0197a0001c0003t0001g0196others(3): Show | 6 | HG01168.hp1 HG01975.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-2149_225-2147d others(5): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080529 | |||||
chr8:123080529
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0264others(2): Show | 5 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-2159_225-2147d others(15): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | 123080529 | |||||
chr8:123080531
|
T | C | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-2171T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080531 | ||||||
chr8:123080664
|
G | A | 2 | a0001c0004t0001g0096a0001c0004t0001g0166 | 2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.225-2038G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080664 | ||||||
chr8:123080783
|
C | T | 3 | a0001c0002t0001g0067a0001c0002t0001g0068a0009c0023t0001g0066 | 3 | HG02559.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.225-1919C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080783 | ||||||
chr8:123080798
|
G | C | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-1904G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080798 | ||||||
chr8:123080910
|
G | A | 1 | a0001c0002t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225-1792G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123080910 | ||||||
chr8:123081049
|
A | G | 1 | a0001c0004t0001g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-1653A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081049 | ||||||
chr8:123081267
|
T | G | 1 | a0001c0002t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.225-1435T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081267 | ||||||
chr8:123081284
|
G | A | 8 | a0001c0002t0001g0308a0001c0009t0001g0069a0001c0009t0001g0070others(5): Show | 8 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-1418G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081284 | ||||||
chr8:123081391
|
C | CT | 215 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(212): Show | 220 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.225-1311_225-1310i others(3): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081391 | ||||||
chr8:123081452
|
A | G | 3 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0003t0001g0065 | 3 | HG01884.hp2 HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-1250A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081452 | ||||||
chr8:123081478
|
A | G | 71 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0032others(68): Show | 74 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.225-1224A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081478 | ||||||
chr8:123081800
|
A | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(181): Show | 188 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.225-902A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081800 | ||||||
chr8:123081818
|
C | T | 1 | a0001c0003t0001g0225 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.225-884C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081818 | ||||||
chr8:123081870
|
G | A | 6 | a0001c0002t0001g0308a0006c0011t0001g0078a0006c0011t0001g0079others(3): Show | 6 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-832G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081870 | ||||||
chr8:123081884
|
CAT | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(193): Show | 202 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.225-817_225-816del others(2): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081884 | ||||||
chr8:123081944
|
C | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0136a0001c0001t0001g0137others(24): Show | 27 | HG00673.hp1 HG01081.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.225-758C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081944 | ||||||
chr8:123081952
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0032others(87): Show | 95 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.225-750A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123081952 | ||||||
chr8:123082025
|
A | T | 1 | a0001c0002t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-677A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082025 | ||||||
chr8:123082069
|
G | C | 77 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0081others(74): Show | 78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.225-633G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082069 | ||||||
chr8:123082193
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0088others(86): Show | 91 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.225-509G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082193 | ||||||
chr8:123082256
|
T | C | 8 | a0001c0002t0001g0255a0001c0004t0001g0001a0001c0004t0001g0270others(5): Show | 10 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-446T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082256 | ||||||
chr8:123082277
|
C | T | 1 | a0004c0007t0001g0033 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.225-425C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082277 | ||||||
chr8:123082381
|
G | A | 1 | a0001c0008t0001g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.225-321G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082381 | ||||||
chr8:123082600
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.225-102A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082600 | ||||||
chr8:123082607
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225-95T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082607 | ||||||
chr8:123082624
|
G | A | 1 | a0001c0003t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-78G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 2/21 | chr8 | 123082624 | ||||||
chr8:123082907
|
G | C | 21 | a0001c0001t0001g0020a0001c0002t0001g0082a0001c0002t0001g0083others(18): Show | 23 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.340+90G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123082907 | ||||||
chr8:123082908
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01099.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.340+91G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123082908 | ||||||
chr8:123083165
|
G | A | 27 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(24): Show | 29 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.340+348G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083165 | ||||||
chr8:123083254
|
C | T | 4 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271others(1): Show | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+437C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083254 | ||||||
chr8:123083306
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.340+489G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083306 | ||||||
chr8:123083331
|
A | G | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.340+514A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083331 | ||||||
chr8:123083410
|
TTTA | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.340+599_340+601del others(3): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | 123083410 | |||||
chr8:123083579
|
C | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-583C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083579 | ||||||
chr8:123083635
|
C | T | 1 | a0001c0004t0001g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.341-527C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083635 | ||||||
chr8:123083935
|
C | G | 3 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0315 | 3 | HG01167.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.341-227C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083935 | ||||||
chr8:123083950
|
C | T | 1 | a0001c0004t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.341-212C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083950 | ||||||
chr8:123083983
|
A | G | 12 | a0001c0002t0001g0097a0001c0002t0001g0115a0001c0002t0001g0116others(9): Show | 12 | HG00558.hp2 HG02165.hp1 NA18962.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-179A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083983 | ||||||
chr8:123083987
|
T | C | 137 | a0001c0001t0001g0017a0001c0001t0001g0101a0001c0001t0001g0263others(134): Show | 141 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(138): Show |
intron_variant | MODIFIER | c.341-175T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123083987 | ||||||
chr8:123084075
|
C | G | 136 | a0001c0001t0001g0017a0001c0001t0001g0101a0001c0001t0001g0263others(133): Show | 140 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.341-87C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 3/21 | chr8 | 123084075 | ||||||
chr8:123084481
|
A | G | 69 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(66): Show | 69 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.519+141A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123084481 | ||||||
chr8:123084484
|
A | G | 30 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(27): Show | 32 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.519+144A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123084484 | ||||||
chr8:123084774
|
CT | C | 97 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(94): Show | 99 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.519+445delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123084774 | |||||
chr8:123084785
|
T | G | 1 | a0001c0005t0001g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.519+445T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123084785 | ||||||
chr8:123084787
|
G | T | 1 | a0001c0005t0001g0191 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.519+447G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123084787 | ||||||
chr8:123084843
|
G | A | 2 | a0005c0015t0001g0194a0005c0015t0001g0195 | 2 | NA18961.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.519+503G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123084843 | ||||||
chr8:123084868
|
T | TA | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+530dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123084868 | |||||
chr8:123084892
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.519+552C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123084892 | ||||||
chr8:123085034
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.519+694C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085034 | ||||||
chr8:123085379
|
A | G | 36 | a0001c0001t0001g0017a0001c0001t0001g0101a0001c0003t0001g0038others(33): Show | 38 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.519+1039A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085379 | ||||||
chr8:123085433
|
T | TTTTG | 15 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.519+1110_519+1113d others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123085433 | |||||
chr8:123085449
|
G | GTTTT | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+1112_519+1113i others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123085449 | |||||
chr8:123085480
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.519+1140G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085480 | ||||||
chr8:123085561
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0224 | 3 | HG00544.hp1 NA18747.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.519+1221A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085561 | ||||||
chr8:123085655
|
C | T | 1 | a0001c0003t0001g0172 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.519+1315C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085655 | ||||||
chr8:123085656
|
G | A | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.519+1316G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085656 | ||||||
chr8:123085704
|
G | A | 1 | a0001c0002t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.519+1364G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085704 | ||||||
chr8:123085789
|
C | T | 69 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(66): Show | 69 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.519+1449C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085789 | ||||||
chr8:123085820
|
C | A | 2 | a0001c0009t0001g0069a0001c0009t0001g0070 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.519+1480C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085820 | ||||||
chr8:123085840
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.519+1500A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085840 | ||||||
chr8:123085893
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.519+1553C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085893 | ||||||
chr8:123085908
|
A | C | 4 | a0003c0010t0001g0013a0003c0010t0001g0233a0003c0010t0001g0248others(1): Show | 4 | HG03041.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1568A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085908 | ||||||
chr8:123085913
|
G | A | 1 | a0003c0010t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.519+1573G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123085913 | ||||||
chr8:123086111
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+1771T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086111 | ||||||
chr8:123086143
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519+1803A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086143 | ||||||
chr8:123086188
|
A | AC | 70 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(67): Show | 70 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.519+1852dupC | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123086188 | |||||
chr8:123086237
|
C | T | 1 | a0003c0010t0001g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.519+1897C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086237 | ||||||
chr8:123086292
|
A | G | 1 | a0010c0020t0001g0222 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.519+1952A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086292 | ||||||
chr8:123086326
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.519+1986A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086326 | ||||||
chr8:123086383
|
C | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0128a0001c0001t0001g0136others(4): Show | 7 | HG01123.hp1 HG01256.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+2043C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086383 | ||||||
chr8:123086469
|
G | C | 93 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0029others(90): Show | 95 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.519+2129G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086469 | ||||||
chr8:123086514
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2174G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086514 | ||||||
chr8:123086544
|
T | A | 1 | a0001c0003t0001g0268 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.519+2204T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086544 | ||||||
chr8:123086751
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2411G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086751 | ||||||
chr8:123086760
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2420T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086760 | ||||||
chr8:123086906
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2566C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123086906 | ||||||
chr8:123087007
|
A | G | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.519+2667A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087007 | ||||||
chr8:123087008
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2668T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087008 | ||||||
chr8:123087211
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.519+2871G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087211 | ||||||
chr8:123087222
|
T | G | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2882T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087222 | ||||||
chr8:123087228
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+2888T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087228 | ||||||
chr8:123087246
|
T | G | 39 | a0001c0001t0001g0017a0001c0002t0001g0067a0001c0002t0001g0068others(36): Show | 41 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+2906T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087246 | ||||||
chr8:123087505
|
A | G | 98 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(95): Show | 100 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.519+3165A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087505 | ||||||
chr8:123087719
|
G | A | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519+3379G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087719 | ||||||
chr8:123087955
|
G | C | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519+3615G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123087955 | ||||||
chr8:123087985
|
ACAGCCT | A | 98 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(95): Show | 100 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.519+3652_519+3657d others(8): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123087985 | |||||
chr8:123088113
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+3773C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088113 | ||||||
chr8:123088189
|
C | CA | 109 | a0001c0001t0001g0017a0001c0001t0001g0101a0001c0001t0001g0263others(106): Show | 111 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.519+3862dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123088189 | |||||
chr8:123088189
|
C | CAA | 29 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(26): Show | 31 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.519+3861_519+3862d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123088189 | |||||
chr8:123088492
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+4152T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088492 | ||||||
chr8:123088495
|
A | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+4155A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088495 | ||||||
chr8:123088543
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+4203C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088543 | ||||||
chr8:123088551
|
A | T | 4 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271others(1): Show | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+4211A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088551 | ||||||
chr8:123088557
|
T | A | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519+4217T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088557 | ||||||
chr8:123088791
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+4451C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088791 | ||||||
chr8:123088993
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.520-4598A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123088993 | ||||||
chr8:123089086
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.520-4505T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089086 | ||||||
chr8:123089182
|
T | C | 1 | a0008c0026t0001g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.520-4409T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089182 | ||||||
chr8:123089278
|
C | T | 5 | a0002c0006t0001g0007a0002c0006t0001g0061a0002c0006t0001g0064others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-4313C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089278 | ||||||
chr8:123089434
|
T | C | 60 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0029others(57): Show | 60 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.520-4157T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089434 | ||||||
chr8:123089435
|
G | A | 1 | a0001c0003t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520-4156G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089435 | ||||||
chr8:123089521
|
A | T | 1 | a0001c0003t0001g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.520-4070A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089521 | ||||||
chr8:123089528
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520-4063G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089528 | ||||||
chr8:123089640
|
A | G | 138 | a0001c0001t0001g0017a0001c0001t0001g0101a0001c0001t0001g0263others(135): Show | 142 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.520-3951A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089640 | ||||||
chr8:123089686
|
C | T | 1 | a0001c0003t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.520-3905C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123089686 | ||||||
chr8:123090090
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.520-3501G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090090 | ||||||
chr8:123090169
|
A | G | 1 | a0001c0002t0001g0308 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.520-3422A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090169 | ||||||
chr8:123090215
|
A | G | 14 | a0001c0002t0001g0035a0001c0002t0001g0129a0001c0002t0001g0236others(11): Show | 14 | HG00642.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.520-3376A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090215 | ||||||
chr8:123090224
|
G | A | 3 | a0001c0009t0001g0009a0001c0009t0001g0010a0006c0011t0001g0080 | 3 | HG02622.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.520-3367G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090224 | ||||||
chr8:123090334
|
T | C | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(312): Show | 321 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.520-3257T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090334 | ||||||
chr8:123090399
|
A | G | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.520-3192A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090399 | ||||||
chr8:123090450
|
G | A | 2 | a0001c0004t0001g0090a0001c0004t0001g0091 | 2 | HG00673.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.520-3141G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090450 | ||||||
chr8:123090655
|
G | A | 5 | a0001c0003t0001g0038a0001c0003t0001g0063a0001c0003t0001g0303others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-2936G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090655 | ||||||
chr8:123090709
|
G | A | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-2882G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123090709 | ||||||
chr8:123090961
|
T | TAATA | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.520-2616_520-2613d others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123090961 | |||||
chr8:123091155
|
G | T | 13 | a0001c0001t0001g0101a0001c0004t0001g0015a0001c0004t0001g0023others(10): Show | 13 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-2436G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091155 | ||||||
chr8:123091564
|
T | C | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.520-2027T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091564 | ||||||
chr8:123091602
|
A | C | 1 | a0001c0005t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.520-1989A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091602 | ||||||
chr8:123091602
|
A | T | 1 | a0003c0010t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.520-1989A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091602 | ||||||
chr8:123091805
|
G | A | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-1786G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091805 | ||||||
chr8:123091830
|
G | A | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-1761G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091830 | ||||||
chr8:123091844
|
T | A | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.520-1747T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123091844 | ||||||
chr8:123092075
|
C | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | NA18955.hp2 NA18961.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-1516C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123092075 | ||||||
chr8:123092408
|
A | C | 1 | a0001c0013t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.520-1183A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123092408 | ||||||
chr8:123092464
|
G | A | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-1127G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123092464 | ||||||
chr8:123092774
|
T | A | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG01891.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.520-817T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123092774 | ||||||
chr8:123092808
|
A | AT | 6 | a0001c0001t0001g0073a0001c0001t0001g0111a0001c0001t0001g0244others(3): Show | 6 | HG01981.hp1 HG03453.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-762dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(1): Show |
9 | a0001c0002t0001g0068a0001c0002t0001g0180a0001c0002t0001g0308others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-769_520-762dup others(8): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(2): Show |
7 | a0001c0001t0001g0017a0001c0002t0001g0067a0001c0002t0001g0115others(4): Show | 7 | HG01255.hp1 HG01257.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-770_520-762dup others(9): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(3): Show |
33 | a0001c0002t0001g0035a0001c0002t0001g0097a0001c0002t0001g0116others(30): Show | 35 | HG00323.hp1 HG00558.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.520-771_520-762dup others(10): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(4): Show |
31 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0279others(28): Show | 31 | HG00642.hp1 HG01069.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.520-772_520-762dup others(11): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(5): Show |
16 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0002t0001g0039others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-773_520-762dup others(12): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.520-774_520-762dup others(13): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
A | ATTTTTTT others(7): Show |
3 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0315 | 3 | HG01167.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.520-775_520-762dup others(14): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123092808
|
AT | A | 15 | a0001c0001t0001g0102a0001c0001t0001g0237a0001c0001t0001g0264others(12): Show | 15 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-762delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123092808 | |||||
chr8:123093014
|
G | A | 31 | a0001c0001t0001g0017a0001c0002t0001g0067a0001c0002t0001g0068others(28): Show | 33 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.520-577G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093014 | ||||||
chr8:123093017
|
G | A | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.520-574G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093017 | ||||||
chr8:123093059
|
G | A | 15 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-532G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093059 | ||||||
chr8:123093192
|
G | A | 2 | a0001c0002t0001g0067a0001c0002t0001g0068 | 2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.520-399G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093192 | ||||||
chr8:123093201
|
G | A | 1 | a0001c0003t0001g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.520-390G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093201 | ||||||
chr8:123093337
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.520-254A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093337 | ||||||
chr8:123093402
|
G | GTT | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-180_520-179dup others(2): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr8 | 123093402 | |||||
chr8:123093579
|
A | G | 1 | a0001c0002t0001g0315 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.520-12A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 4/21 | chr8 | 123093579 | ||||||
chr8:123093793
|
T | TA | 31 | a0001c0001t0001g0017a0001c0002t0001g0067a0001c0002t0001g0068others(28): Show | 33 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.671+57dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123093793 | |||||
chr8:123093841
|
A | G | 1 | a0001c0002t0001g0299 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.671+99A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123093841 | ||||||
chr8:123094158
|
G | A | 1 | a0001c0004t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.671+416G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094158 | ||||||
chr8:123094166
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02040.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.671+424G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094166 | ||||||
chr8:123094223
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.671+481C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094223 | ||||||
chr8:123094305
|
G | A | 5 | a0001c0002t0001g0180a0001c0004t0001g0001a0001c0004t0001g0270others(2): Show | 7 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.671+563G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094305 | ||||||
chr8:123094309
|
G | T | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.671+567G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094309 | ||||||
chr8:123094501
|
A | G | 29 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(26): Show | 31 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.671+759A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094501 | ||||||
chr8:123094507
|
C | CTTTA | 37 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0171others(34): Show | 39 | HG00735.hp1 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.671+809_671+812dup others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123094507 | |||||
chr8:123094507
|
CTTTA | C | 21 | a0001c0001t0001g0020a0001c0002t0001g0159a0001c0002t0001g0160others(18): Show | 21 | HG01106.hp2 HG01167.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.671+809_671+812del others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123094507 | |||||
chr8:123094507
|
CTTTATTT others(1): Show |
C | 72 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0029others(69): Show | 74 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.671+805_671+812del others(8): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123094507 | |||||
chr8:123094507
|
CTTTATTT others(5): Show |
C | 6 | a0002c0006t0001g0007a0002c0006t0001g0061a0002c0006t0001g0064others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.671+801_671+812del others(12): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123094507 | |||||
chr8:123094507
|
CTTTATTT others(9): Show |
C | 1 | a0001c0001t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.671+797_671+812del others(16): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123094507 | |||||
chr8:123094523
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0088others(29): Show | 33 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.671+781A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094523 | ||||||
chr8:123094561
|
C | T | 1 | a0001c0003t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.671+819C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094561 | ||||||
chr8:123094569
|
C | G | 1 | a0001c0013t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671+827C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094569 | ||||||
chr8:123094589
|
G | C | 12 | a0001c0004t0001g0015a0001c0004t0001g0023a0001c0004t0001g0024others(9): Show | 12 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.671+847G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094589 | ||||||
chr8:123094728
|
C | T | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.671+986C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094728 | ||||||
chr8:123094729
|
G | A | 3 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0315 | 3 | HG01167.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.671+987G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094729 | ||||||
chr8:123094777
|
G | T | 26 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(23): Show | 28 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.671+1035G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094777 | ||||||
chr8:123094784
|
G | A | 1 | a0001c0003t0001g0055 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.671+1042G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094784 | ||||||
chr8:123094821
|
G | A | 1 | a0001c0004t0001g0296 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.671+1079G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123094821 | ||||||
chr8:123095003
|
G | A | 29 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(26): Show | 31 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.671+1261G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095003 | ||||||
chr8:123095066
|
A | G | 29 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(26): Show | 31 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.671+1324A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095066 | ||||||
chr8:123095123
|
C | T | 96 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(93): Show | 98 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.671+1381C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095123 | ||||||
chr8:123095142
|
C | A | 67 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(64): Show | 67 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.671+1400C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095142 | ||||||
chr8:123095158
|
T | A | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.671+1416T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095158 | ||||||
chr8:123095286
|
C | T | 62 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0029others(59): Show | 62 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.671+1544C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095286 | ||||||
chr8:123095430
|
G | A | 4 | a0001c0002t0001g0285a0006c0011t0001g0078a0006c0011t0001g0079others(1): Show | 4 | HG02486.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+1688G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095430 | ||||||
chr8:123095537
|
G | A | 6 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-1745G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095537 | ||||||
chr8:123095889
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.672-1393G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123095889 | ||||||
chr8:123095948
|
TA | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-1331delA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr8 | 123095948 | |||||
chr8:123096159
|
A | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-1123A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096159 | ||||||
chr8:123096297
|
C | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-985C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096297 | ||||||
chr8:123096318
|
A | T | 4 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271others(1): Show | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-964A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096318 | ||||||
chr8:123096378
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0136a0001c0022t0001g0112 | 3 | HG01256.hp1 HG02148.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.672-904C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096378 | ||||||
chr8:123096383
|
T | C | 2 | a0001c0003t0001g0031a0010c0020t0001g0222 | 2 | HG01074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.672-899T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096383 | ||||||
chr8:123096385
|
C | G | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-897C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096385 | ||||||
chr8:123096457
|
T | C | 124 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0101others(121): Show | 126 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.672-825T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096457 | ||||||
chr8:123096653
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.672-629A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096653 | ||||||
chr8:123096770
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.672-512G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096770 | ||||||
chr8:123096793
|
A | G | 71 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.672-489A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096793 | ||||||
chr8:123096960
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-322G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123096960 | ||||||
chr8:123097027
|
G | A | 1 | a0001c0002t0001g0308 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.672-255G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123097027 | ||||||
chr8:123097084
|
C | T | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-198C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123097084 | ||||||
chr8:123097099
|
T | G | 93 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(90): Show | 95 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.672-183T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123097099 | ||||||
chr8:123097221
|
C | T | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.672-61C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 5/21 | chr8 | 123097221 | ||||||
chr8:123097543
|
C | T | 4 | a0001c0003t0001g0006a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02165.hp2 NA18949.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+102C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123097543 | ||||||
chr8:123097562
|
A | G | 1 | a0001c0005t0001g0260 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.831+121A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123097562 | ||||||
chr8:123097709
|
A | G | 22 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(19): Show | 24 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.831+268A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123097709 | ||||||
chr8:123097798
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.831+357G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123097798 | ||||||
chr8:123097921
|
G | A | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.831+480G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123097921 | ||||||
chr8:123098052
|
G | C | 93 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(90): Show | 95 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.831+611G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123098052 | ||||||
chr8:123098101
|
A | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831+660A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123098101 | ||||||
chr8:123098337
|
T | C | 1 | a0001c0002t0001g0308 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.831+896T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123098337 | ||||||
chr8:123098911
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+1470C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123098911 | ||||||
chr8:123098970
|
A | G | 1 | a0001c0005t0001g0036 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.831+1529A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123098970 | ||||||
chr8:123099132
|
G | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG02895.hp1 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.832-1675G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123099132 | ||||||
chr8:123099188
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG02922.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.832-1619C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123099188 | ||||||
chr8:123099206
|
G | T | 93 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(90): Show | 95 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.832-1601G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123099206 | ||||||
chr8:123099255
|
G | A | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.832-1552G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123099255 | ||||||
chr8:123099280
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.832-1527C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123099280 | ||||||
chr8:123099831
|
A | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.832-976A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123099831 | ||||||
chr8:123100163
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-644G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123100163 | ||||||
chr8:123100195
|
A | G | 13 | a0001c0003t0001g0046a0001c0003t0001g0047a0001c0003t0001g0048others(10): Show | 13 | HG02273.hp1 NA18948.hp1 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-612A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123100195 | ||||||
chr8:123100198
|
G | A | 1 | a0001c0008t0001g0238 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.832-609G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123100198 | ||||||
chr8:123100505
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.832-302G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123100505 | ||||||
chr8:123100562
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832-245G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 6/21 | chr8 | 123100562 | ||||||
chr8:123101085
|
C | G | 5 | a0001c0003t0001g0008a0001c0003t0001g0200a0001c0003t0001g0201others(2): Show | 5 | HG00438.hp2 NA18972.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+78C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101085 | ||||||
chr8:123101146
|
T | C | 114 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0162others(111): Show | 114 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1032+139T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101146 | ||||||
chr8:123101224
|
G | A | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1032+217G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101224 | ||||||
chr8:123101260
|
C | T | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1032+253C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101260 | ||||||
chr8:123101450
|
C | T | 79 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(76): Show | 79 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1032+443C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101450 | ||||||
chr8:123101511
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1032+504T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101511 | ||||||
chr8:123101559
|
C | T | 93 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(90): Show | 95 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1032+552C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101559 | ||||||
chr8:123101560
|
G | A | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1032+553G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101560 | ||||||
chr8:123101606
|
G | T | 6 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271others(3): Show | 8 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1032+599G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101606 | ||||||
chr8:123101710
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1032+703G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101710 | ||||||
chr8:123101733
|
A | T | 79 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0192others(76): Show | 79 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1032+726A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101733 | ||||||
chr8:123101737
|
G | A | 219 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0192others(216): Show | 223 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.1032+730G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101737 | ||||||
chr8:123101907
|
G | A | 101 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(98): Show | 103 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.1032+900G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123101907 | ||||||
chr8:123102005
|
C | G | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1032+998C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102005 | ||||||
chr8:123102093
|
G | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(163): Show | 169 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1032+1086G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102093 | ||||||
chr8:123102108
|
ACTTCT | A | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1032+1109_1032+111 others(9): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 123102108 | |||||
chr8:123102161
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1032+1154G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102161 | ||||||
chr8:123102171
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1032+1164C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102171 | ||||||
chr8:123102220
|
C | G | 1 | a0001c0003t0001g0054 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1032+1213C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102220 | ||||||
chr8:123102227
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1032+1220A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102227 | ||||||
chr8:123102257
|
G | A | 8 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+1250G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102257 | ||||||
chr8:123102320
|
T | C | 221 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0162others(218): Show | 225 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(222): Show |
intron_variant | MODIFIER | c.1032+1313T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102320 | ||||||
chr8:123102343
|
A | AGTGGCAT others(5): Show |
70 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(67): Show | 70 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1032+1341_1032+134 others(16): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 123102343 | |||||
chr8:123102349
|
G | A | 92 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1032+1342G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102349 | ||||||
chr8:123102349
|
G | GTTTGCCG others(5): Show |
1 | a0001c0002t0001g0197 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1032+1348_1032+134 others(16): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 123102349 | |||||
chr8:123102358
|
C | CT | 92 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1032+1358dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 123102358 | |||||
chr8:123102456
|
G | T | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1032+1449G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102456 | ||||||
chr8:123102906
|
A | G | 80 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0192others(77): Show | 80 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1032+1899A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123102906 | ||||||
chr8:123103170
|
G | A | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1033-2118G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103170 | ||||||
chr8:123103189
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0150others(5): Show | 9 | HG00280.hp2 HG00738.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1033-2099A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103189 | ||||||
chr8:123103210
|
CAT | C | 5 | a0001c0003t0001g0038a0001c0003t0001g0063a0001c0003t0001g0303others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1033-2077_1033-207 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103210 | ||||||
chr8:123103293
|
A | G | 4 | a0003c0010t0001g0013a0003c0010t0001g0233a0003c0010t0001g0248others(1): Show | 4 | HG03041.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1033-1995A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103293 | ||||||
chr8:123103338
|
A | T | 2 | a0001c0024t0001g0037a0002c0025t0001g0267 | 2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1033-1950A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103338 | ||||||
chr8:123103357
|
T | C | 65 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0029others(62): Show | 65 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.1033-1931T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103357 | ||||||
chr8:123103420
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1033-1868C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103420 | ||||||
chr8:123103429
|
C | CT | 96 | a0001c0001t0001g0168a0001c0002t0001g0011a0001c0002t0001g0014others(93): Show | 98 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1033-1848dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | 123103429 | |||||
chr8:123103515
|
C | T | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1033-1773C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103515 | ||||||
chr8:123103516
|
G | A | 3 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0315 | 3 | HG01167.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1033-1772G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103516 | ||||||
chr8:123103537
|
C | T | 3 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275 | 3 | HG01255.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1033-1751C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103537 | ||||||
chr8:123103622
|
C | A | 1 | a0001c0022t0001g0112 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1033-1666C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103622 | ||||||
chr8:123103640
|
C | G | 1 | a0009c0023t0001g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1033-1648C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103640 | ||||||
chr8:123103730
|
C | T | 1 | a0001c0013t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1033-1558C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103730 | ||||||
chr8:123103880
|
A | C | 117 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0162others(114): Show | 117 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1033-1408A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123103880 | ||||||
chr8:123104060
|
A | G | 22 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(19): Show | 24 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1033-1228A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104060 | ||||||
chr8:123104158
|
C | T | 2 | a0001c0024t0001g0037a0002c0025t0001g0267 | 2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1033-1130C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104158 | ||||||
chr8:123104185
|
A | C | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1033-1103A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104185 | ||||||
chr8:123104233
|
T | A | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-1055T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104233 | ||||||
chr8:123104277
|
T | C | 1 | a0001c0004t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1033-1011T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104277 | ||||||
chr8:123104297
|
A | G | 222 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0162others(219): Show | 226 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.1033-991A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104297 | ||||||
chr8:123104350
|
G | A | 95 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(92): Show | 97 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1033-938G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104350 | ||||||
chr8:123104420
|
A | T | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-868A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104420 | ||||||
chr8:123104435
|
A | C | 4 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271others(1): Show | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1033-853A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104435 | ||||||
chr8:123104583
|
T | C | 72 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(69): Show | 72 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1033-705T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123104583 | ||||||
chr8:123105068
|
A | C | 1 | a0001c0003t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1033-220A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123105068 | ||||||
chr8:123105092
|
A | G | 70 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(67): Show | 70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1033-196A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123105092 | ||||||
chr8:123105109
|
T | C | 1 | a0009c0023t0001g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1033-179T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123105109 | ||||||
chr8:123105167
|
C | G | 1 | a0001c0004t0001g0015 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1033-121C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123105167 | ||||||
chr8:123105262
|
A | G | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1033-26A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 7/21 | chr8 | 123105262 | ||||||
chr8:123105691
|
C | T | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209+227C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123105691 | ||||||
chr8:123105826
|
A | G | 33 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0004t0001g0012others(30): Show | 33 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1209+362A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123105826 | ||||||
chr8:123106004
|
A | G | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1209+540A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106004 | ||||||
chr8:123106268
|
G | C | 1 | a0001c0004t0001g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1209+804G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106268 | ||||||
chr8:123106349
|
T | C | 1 | a0001c0002t0001g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1209+885T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106349 | ||||||
chr8:123106586
|
C | G | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1209+1122C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106586 | ||||||
chr8:123106588
|
G | A | 103 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(100): Show | 105 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.1209+1124G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106588 | ||||||
chr8:123106596
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1209+1132T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106596 | ||||||
chr8:123106609
|
C | T | 1 | a0001c0002t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1209+1145C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106609 | ||||||
chr8:123106670
|
T | C | 1 | a0001c0002t0001g0183 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1209+1206T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106670 | ||||||
chr8:123106839
|
A | T | 4 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0184others(1): Show | 4 | NA18955.hp2 NA18961.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209+1375A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106839 | ||||||
chr8:123106873
|
T | C | 3 | a0001c0002t0001g0185a0001c0002t0001g0186a0001c0002t0001g0187 | 3 | HG01891.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1209+1409T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123106873 | ||||||
chr8:123107103
|
G | A | 30 | a0001c0002t0001g0035a0001c0002t0001g0097a0001c0002t0001g0115others(27): Show | 30 | HG00558.hp2 HG00642.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1209+1639G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107103 | ||||||
chr8:123107136
|
T | A | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1209+1672T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107136 | ||||||
chr8:123107418
|
C | T | 5 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-1899C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107418 | ||||||
chr8:123107609
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1210-1708A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107609 | ||||||
chr8:123107649
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1210-1668G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107649 | ||||||
chr8:123107837
|
A | G | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1210-1480A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107837 | ||||||
chr8:123107837
|
A | T | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG01891.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1210-1480A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107837 | ||||||
chr8:123107857
|
G | A | 59 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0029others(56): Show | 59 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1210-1460G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107857 | ||||||
chr8:123107928
|
C | T | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1210-1389C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123107928 | ||||||
chr8:123108049
|
T | C | 220 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0171others(217): Show | 224 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.1210-1268T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108049 | ||||||
chr8:123108129
|
C | G | 218 | a0001c0001t0001g0043a0001c0001t0001g0171a0001c0001t0001g0192others(215): Show | 222 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.1210-1188C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108129 | ||||||
chr8:123108215
|
C | T | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-1102C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108215 | ||||||
chr8:123108307
|
G | A | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-1010G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108307 | ||||||
chr8:123108511
|
G | C | 2 | a0001c0002t0001g0185a0001c0002t0001g0187 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1210-806G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108511 | ||||||
chr8:123108521
|
C | G | 1 | a0001c0013t0001g0127 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1210-796C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108521 | ||||||
chr8:123108522
|
G | T | 95 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(92): Show | 97 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1210-795G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108522 | ||||||
chr8:123108746
|
A | T | 95 | a0001c0002t0001g0011a0001c0002t0001g0014a0001c0002t0001g0019others(92): Show | 97 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1210-571A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108746 | ||||||
chr8:123108927
|
A | T | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1210-390A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108927 | ||||||
chr8:123108936
|
A | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG01175.hp1 HG01358.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-381A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123108936 | ||||||
chr8:123109211
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1210-106T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123109211 | ||||||
chr8:123109313
|
G | A | 1 | a0001c0009t0001g0163 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.1210-4G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 8/21 | chr8 | 123109313 | ||||||
chr8:123109794
|
G | T | 2 | a0001c0024t0001g0037a0002c0025t0001g0267 | 2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1436+174G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123109794 | ||||||
chr8:123110196
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1436+576G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110196 | ||||||
chr8:123110274
|
A | C | 111 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0171others(108): Show | 111 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1436+654A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110274 | ||||||
chr8:123110305
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1436+685T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110305 | ||||||
chr8:123110424
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0150others(5): Show | 9 | HG00280.hp2 HG00738.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1436+804T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110424 | ||||||
chr8:123110485
|
T | C | 60 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(57): Show | 60 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1436+865T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110485 | ||||||
chr8:123110554
|
T | G | 14 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(11): Show | 16 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1436+934T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110554 | ||||||
chr8:123110730
|
A | AAGT | 96 | a0001c0001t0001g0250a0001c0002t0001g0011a0001c0002t0001g0014others(93): Show | 98 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1436+1112_1436+111 others(7): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123110730 | |||||
chr8:123110770
|
T | C | 22 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0082others(19): Show | 24 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1436+1150T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110770 | ||||||
chr8:123110960
|
G | T | 1 | a0001c0002t0001g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1436+1340G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123110960 | ||||||
chr8:123111016
|
T | A | 14 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1436+1396T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123111016 | ||||||
chr8:123111091
|
GT | G | 30 | a0001c0002t0001g0035a0001c0002t0001g0097a0001c0002t0001g0115others(27): Show | 30 | HG00558.hp2 HG00642.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1436+1481delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123111091 | |||||
chr8:123111345
|
T | C | 5 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(2): Show | 5 | HG02109.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436+1725T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123111345 | ||||||
chr8:123111408
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1436+1788T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123111408 | ||||||
chr8:123111431
|
A | G | 4 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271others(1): Show | 6 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1436+1811A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123111431 | ||||||
chr8:123111663
|
T | C | 1 | a0005c0015t0001g0194 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1436+2043T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123111663 | ||||||
chr8:123111967
|
C | G | 1 | a0001c0002t0001g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1436+2347C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123111967 | ||||||
chr8:123112091
|
A | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1436+2471A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123112091 | ||||||
chr8:123112528
|
C | T | 1 | a0001c0003t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1436+2908C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123112528 | ||||||
chr8:123112571
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1436+2951T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123112571 | ||||||
chr8:123112713
|
C | T | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1436+3093C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123112713 | ||||||
chr8:123112803
|
C | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1436+3183C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123112803 | ||||||
chr8:123112849
|
A | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1436+3229A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123112849 | ||||||
chr8:123113239
|
C | G | 220 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0171others(217): Show | 224 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.1436+3619C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113239 | ||||||
chr8:123113241
|
G | A | 1 | a0001c0003t0001g0216 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1436+3621G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113241 | ||||||
chr8:123113459
|
A | G | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1436+3839A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113459 | ||||||
chr8:123113661
|
A | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0162others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.1436+4041A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113661 | ||||||
chr8:123113746
|
AT | A | 91 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(88): Show | 93 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1436+4134delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123113746 | |||||
chr8:123113827
|
A | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1436+4207A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113827 | ||||||
chr8:123113849
|
G | T | 5 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161others(2): Show | 5 | NA18964.hp2 NA18974.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436+4229G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113849 | ||||||
chr8:123113870
|
A | G | 5 | a0001c0003t0001g0038a0001c0003t0001g0063a0001c0003t0001g0303others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1436+4250A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113870 | ||||||
chr8:123113986
|
T | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0003t0001g0006others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1436+4366T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123113986 | ||||||
chr8:123114250
|
T | C | 104 | a0001c0001t0001g0250a0001c0001t0001g0263a0001c0001t0001g0276others(101): Show | 106 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.1436+4630T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114250 | ||||||
chr8:123114259
|
A | G | 12 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1436+4639A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114259 | ||||||
chr8:123114272
|
T | G | 103 | a0001c0001t0001g0250a0001c0001t0001g0263a0001c0001t0001g0276others(100): Show | 105 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.1436+4652T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114272 | ||||||
chr8:123114317
|
T | G | 4 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(1): Show | 4 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1436+4697T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114317 | ||||||
chr8:123114317
|
T | TTTGTTG | 88 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(85): Show | 90 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1436+4713_1436+471 others(10): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123114317 | |||||
chr8:123114428
|
G | C | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1436+4808G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114428 | ||||||
chr8:123114774
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1436+5154T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114774 | ||||||
chr8:123114898
|
C | G | 1 | a0009c0023t0001g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1437-5157C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114898 | ||||||
chr8:123114936
|
G | C | 1 | a0001c0002t0001g0308 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1437-5119G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123114936 | ||||||
chr8:123115065
|
A | G | 5 | a0001c0002t0001g0011a0001c0009t0001g0069a0001c0009t0001g0070others(2): Show | 5 | HG02809.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1437-4990A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115065 | ||||||
chr8:123115111
|
A | G | 1 | a0001c0002t0001g0197 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1437-4944A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115111 | ||||||
chr8:123115195
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1437-4860G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115195 | ||||||
chr8:123115243
|
C | G | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1437-4812C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115243 | ||||||
chr8:123115253
|
C | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-4802C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115253 | ||||||
chr8:123115307
|
G | T | 32 | a0001c0004t0001g0012a0001c0004t0001g0015a0001c0004t0001g0023others(29): Show | 32 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1437-4748G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115307 | ||||||
chr8:123115355
|
G | A | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-4700G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115355 | ||||||
chr8:123115476
|
C | A | 11 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1437-4579C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115476 | ||||||
chr8:123115518
|
TACC | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00280.hp1 HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1437-4534_1437-453 others(7): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123115518 | |||||
chr8:123115528
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1437-4527G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115528 | ||||||
chr8:123115689
|
A | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-4366A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115689 | ||||||
chr8:123115764
|
G | A | 1 | a0001c0004t0001g0156 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1437-4291G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115764 | ||||||
chr8:123115780
|
G | A | 2 | a0001c0003t0001g0065a0002c0006t0001g0316 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1437-4275G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115780 | ||||||
chr8:123115862
|
A | G | 32 | a0001c0002t0001g0035a0001c0002t0001g0097a0001c0002t0001g0115others(29): Show | 32 | HG00558.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1437-4193A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115862 | ||||||
chr8:123115893
|
A | G | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1437-4162A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115893 | ||||||
chr8:123115968
|
T | G | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1437-4087T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115968 | ||||||
chr8:123115970
|
T | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-4085T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123115970 | ||||||
chr8:123116050
|
G | T | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-4005G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116050 | ||||||
chr8:123116217
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1437-3838G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116217 | ||||||
chr8:123116268
|
C | T | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-3787C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116268 | ||||||
chr8:123116333
|
A | G | 92 | a0001c0001t0001g0250a0001c0002t0001g0014a0001c0002t0001g0019others(89): Show | 94 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1437-3722A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116333 | ||||||
chr8:123116408
|
C | A | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(312): Show | 321 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.1437-3647C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116408 | ||||||
chr8:123116595
|
G | T | 206 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(203): Show | 210 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.1437-3460G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116595 | ||||||
chr8:123116598
|
A | C | 180 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(177): Show | 180 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.1437-3457A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116598 | ||||||
chr8:123116659
|
G | T | 1 | a0001c0002t0001g0030 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1437-3396G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116659 | ||||||
chr8:123116715
|
A | C | 1 | a0001c0001t0001g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1437-3340A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116715 | ||||||
chr8:123116890
|
T | C | 204 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0192others(201): Show | 206 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1437-3165T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116890 | ||||||
chr8:123116955
|
T | C | 204 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0192others(201): Show | 206 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1437-3100T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116955 | ||||||
chr8:123116966
|
G | A | 218 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(215): Show | 222 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.1437-3089G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116966 | ||||||
chr8:123116972
|
A | C | 1 | a0001c0013t0001g0127 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1437-3083A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123116972 | ||||||
chr8:123117042
|
C | T | 11 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1437-3013C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117042 | ||||||
chr8:123117085
|
C | T | 203 | a0001c0001t0001g0043a0001c0001t0001g0162a0001c0001t0001g0192others(200): Show | 205 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.1437-2970C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117085 | ||||||
chr8:123117193
|
T | TA | 9 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0040others(6): Show | 11 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1437-2860dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117193 | |||||
chr8:123117247
|
A | G | 202 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(199): Show | 204 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1437-2808A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117247 | ||||||
chr8:123117289
|
G | A | 2 | a0001c0004t0001g0090a0001c0004t0001g0091 | 2 | HG00673.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1437-2766G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117289 | ||||||
chr8:123117534
|
G | C | 202 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(199): Show | 204 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1437-2521G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117534 | ||||||
chr8:123117623
|
C | T | 6 | a0001c0002t0001g0011a0001c0009t0001g0069a0001c0009t0001g0070others(3): Show | 6 | HG02257.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1437-2432C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117623 | ||||||
chr8:123117625
|
C | T | 3 | a0001c0001t0001g0017a0001c0003t0001g0016a0001c0003t0001g0084 | 3 | HG02258.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1437-2430C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117625 | ||||||
chr8:123117645
|
C | T | 202 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(199): Show | 204 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1437-2410C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117645 | ||||||
chr8:123117689
|
G | C | 202 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0001t0001g0250others(199): Show | 204 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1437-2366G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117689 | ||||||
chr8:123117739
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437-2316C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123117739 | ||||||
chr8:123117752
|
C | CA | 33 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0071others(30): Show | 34 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1437-2275dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117752 | |||||
chr8:123117752
|
C | CAA | 6 | a0001c0001t0001g0020a0001c0001t0001g0181a0001c0001t0001g0227others(3): Show | 6 | HG00544.hp2 HG01106.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1437-2276_1437-227 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117752 | |||||
chr8:123117752
|
CAAAAAA | C | 10 | a0001c0002t0001g0039a0001c0002t0001g0182a0001c0002t0001g0187others(7): Show | 10 | HG01981.hp2 HG02027.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1437-2280_1437-227 others(10): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117752 | |||||
chr8:123117752
|
CAAAAAAA | C | 187 | a0001c0001t0001g0043a0001c0001t0001g0132a0001c0001t0001g0192others(184): Show | 189 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.1437-2281_1437-227 others(11): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117752 | |||||
chr8:123117752
|
CAAAAAAA others(1): Show |
C | 12 | a0001c0002t0001g0011a0001c0002t0001g0308a0001c0003t0001g0006others(9): Show | 12 | HG01243.hp2 HG02165.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1437-2282_1437-227 others(12): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117752 | |||||
chr8:123117752
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0176 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1437-2286_1437-227 others(16): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr8 | 123117752 | |||||
chr8:123118048
|
T | C | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1437-2007T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118048 | ||||||
chr8:123118155
|
A | G | 1 | a0001c0004t0001g0139 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1437-1900A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118155 | ||||||
chr8:123118233
|
T | G | 1 | a0001c0001t0001g0113 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1437-1822T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118233 | ||||||
chr8:123118248
|
T | C | 1 | a0001c0002t0001g0308 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1437-1807T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118248 | ||||||
chr8:123118265
|
T | TC | 213 | a0001c0001t0001g0043a0001c0001t0001g0171a0001c0001t0001g0192others(210): Show | 217 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.1437-1790_1437-178 others(5): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118265 | ||||||
chr8:123118319
|
C | T | 68 | a0001c0001t0001g0043a0001c0001t0001g0192a0001c0003t0001g0006others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1437-1736C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118319 | ||||||
chr8:123118337
|
C | T | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1437-1718C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118337 | ||||||
chr8:123118415
|
A | G | 1 | a0002c0006t0001g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1437-1640A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118415 | ||||||
chr8:123118487
|
C | A | 5 | a0001c0004t0001g0139a0001c0004t0001g0140a0001c0004t0001g0141others(2): Show | 5 | HG01081.hp1 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1437-1568C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118487 | ||||||
chr8:123118608
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1437-1447G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118608 | ||||||
chr8:123118727
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1437-1328T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118727 | ||||||
chr8:123118784
|
G | A | 1 | a0001c0002t0001g0273 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1437-1271G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118784 | ||||||
chr8:123118822
|
T | G | 114 | a0001c0001t0001g0081a0001c0001t0001g0171a0001c0003t0001g0006others(111): Show | 116 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1437-1233T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118822 | ||||||
chr8:123118868
|
C | T | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1437-1187C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118868 | ||||||
chr8:123118922
|
C | T | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1437-1133C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118922 | ||||||
chr8:123118985
|
C | T | 15 | a0001c0002t0001g0273a0001c0002t0001g0274a0001c0002t0001g0275others(12): Show | 17 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1437-1070C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123118985 | ||||||
chr8:123119003
|
T | C | 6 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG01891.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1437-1052T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119003 | ||||||
chr8:123119097
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1437-958G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119097 | ||||||
chr8:123119482
|
G | A | 2 | a0001c0003t0001g0251a0001c0003t0001g0252 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1437-573G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119482 | ||||||
chr8:123119513
|
C | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0237 | 2 | NA18964.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1437-542C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119513 | ||||||
chr8:123119554
|
G | A | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1437-501G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119554 | ||||||
chr8:123119700
|
A | G | 156 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0171others(153): Show | 160 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1437-355A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119700 | ||||||
chr8:123119926
|
G | A | 73 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(70): Show | 73 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1437-129G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 10/21 | chr8 | 123119926 | ||||||
chr8:123120212
|
T | C | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1570+24T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120212 | ||||||
chr8:123120268
|
T | C | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0009c0023t0001g0066 | 3 | HG01099.hp2 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1570+80T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120268 | ||||||
chr8:123120302
|
C | T | 2 | a0001c0003t0001g0065a0002c0006t0001g0316 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1570+114C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120302 | ||||||
chr8:123120370
|
T | C | 1 | a0001c0003t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1570+182T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120370 | ||||||
chr8:123120387
|
G | A | 3 | a0001c0002t0001g0308a0007c0014t0001g0076a0007c0014t0001g0077 | 3 | HG00735.hp1 HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1570+199G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120387 | ||||||
chr8:123120443
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+255A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120443 | ||||||
chr8:123120488
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1570+300G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120488 | ||||||
chr8:123120616
|
G | A | 2 | a0001c0002t0001g0115a0001c0002t0001g0117 | 2 | HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1570+428G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120616 | ||||||
chr8:123120729
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+541A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120729 | ||||||
chr8:123120737
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+549A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120737 | ||||||
chr8:123120753
|
A | G | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1570+565A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120753 | ||||||
chr8:123120949
|
C | T | 155 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0171others(152): Show | 159 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1570+761C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123120949 | ||||||
chr8:123120963
|
C | CT | 14 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0002t0001g0097others(11): Show | 16 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1570+791dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123120963 | |||||
chr8:123120963
|
C | CTT | 32 | a0001c0001t0001g0171a0001c0004t0001g0012a0001c0004t0001g0015others(29): Show | 32 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1570+790_1570+791d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123120963 | |||||
chr8:123121079
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+891A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121079 | ||||||
chr8:123121119
|
C | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1570+931C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121119 | ||||||
chr8:123121133
|
G | T | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+945G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121133 | ||||||
chr8:123121199
|
C | CCGCCCAC others(91): Show |
4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1058_1570+105 others(102): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123121199 | |||||
chr8:123121200
|
C | T | 24 | a0001c0001t0001g0081a0001c0001t0001g0095a0001c0001t0001g0098others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1570+1012C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121200 | ||||||
chr8:123121247
|
T | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1059T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121247 | ||||||
chr8:123121256
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1068A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121256 | ||||||
chr8:123121278
|
C | T | 52 | a0001c0001t0001g0171a0001c0003t0001g0169a0001c0004t0001g0001others(49): Show | 56 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1570+1090C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121278 | ||||||
chr8:123121323
|
C | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1135C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121323 | ||||||
chr8:123121331
|
T | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1143T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121331 | ||||||
chr8:123121384
|
G | A | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1196G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121384 | ||||||
chr8:123121484
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1570+1296G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121484 | ||||||
chr8:123121486
|
G | C | 1 | a0008c0026t0001g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1570+1298G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121486 | ||||||
chr8:123121532
|
G | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1344G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121532 | ||||||
chr8:123121534
|
G | A | 1 | a0001c0002t0001g0197 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1570+1346G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121534 | ||||||
chr8:123121614
|
C | G | 66 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(63): Show | 66 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1570+1426C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121614 | ||||||
chr8:123121710
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1522A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121710 | ||||||
chr8:123121739
|
G | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+1551G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121739 | ||||||
chr8:123121817
|
G | A | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1570+1629G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123121817 | ||||||
chr8:123122081
|
A | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1570+1893A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122081 | ||||||
chr8:123122154
|
T | C | 1 | a0001c0002t0001g0308 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1570+1966T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122154 | ||||||
chr8:123122164
|
G | A | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1570+1976G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122164 | ||||||
chr8:123122523
|
G | A | 52 | a0001c0001t0001g0171a0001c0003t0001g0169a0001c0004t0001g0001others(49): Show | 56 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1570+2335G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122523 | ||||||
chr8:123122628
|
T | C | 2 | a0001c0002t0001g0185a0001c0002t0001g0187 | 2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1570+2440T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122628 | ||||||
chr8:123122747
|
G | A | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1570+2559G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122747 | ||||||
chr8:123122814
|
C | T | 56 | a0001c0001t0001g0171a0001c0003t0001g0146a0001c0003t0001g0169others(53): Show | 60 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1570+2626C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122814 | ||||||
chr8:123122845
|
C | T | 5 | a0004c0007t0001g0022a0004c0007t0001g0026a0004c0007t0001g0027others(2): Show | 5 | HG01074.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1570+2657C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122845 | ||||||
chr8:123122854
|
A | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1570+2666A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122854 | ||||||
chr8:123122928
|
A | G | 52 | a0001c0001t0001g0171a0001c0003t0001g0169a0001c0004t0001g0001others(49): Show | 56 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1570+2740A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123122928 | ||||||
chr8:123123037
|
C | T | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1570+2849C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123123037 | ||||||
chr8:123123545
|
C | CA | 78 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(75): Show | 78 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1571-2508dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123123545 | |||||
chr8:123123602
|
C | T | 51 | a0001c0003t0001g0169a0001c0004t0001g0001a0001c0004t0001g0012others(48): Show | 55 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1571-2454C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123123602 | ||||||
chr8:123123610
|
G | A | 34 | a0001c0004t0001g0001a0001c0004t0001g0012a0001c0004t0001g0015others(31): Show | 36 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1571-2446G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123123610 | ||||||
chr8:123123804
|
T | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-2252T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123123804 | ||||||
chr8:123123938
|
G | A | 1 | a0001c0002t0001g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1571-2118G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123123938 | ||||||
chr8:123124067
|
GA | G | 18 | a0001c0001t0001g0124a0001c0001t0001g0263a0001c0001t0001g0276others(15): Show | 18 | HG01243.hp1 HG01515.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1571-1973delA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124067 | |||||
chr8:123124081
|
A | AAG | 13 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(10): Show | 15 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1571-1974_1571-197 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124081 | |||||
chr8:123124269
|
G | A | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-1787G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124269 | ||||||
chr8:123124351
|
C | T | 1 | a0001c0022t0001g0112 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1571-1705C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124351 | ||||||
chr8:123124376
|
G | T | 4 | a0001c0003t0001g0169a0006c0011t0001g0078a0006c0011t0001g0079others(1): Show | 4 | HG02486.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-1680G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124376 | ||||||
chr8:123124407
|
A | AC | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-1646dupC | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124407 | |||||
chr8:123124677
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1571-1379C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124677 | ||||||
chr8:123124773
|
C | A | 1 | a0001c0001t0001g0259 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1571-1283C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124773 | ||||||
chr8:123124773
|
C | CA | 8 | a0001c0001t0001g0176a0001c0003t0001g0046a0001c0003t0001g0217others(5): Show | 8 | HG00735.hp1 HG02145.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1571-1269dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124773 | |||||
chr8:123124773
|
C | CAA | 13 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(10): Show | 15 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1571-1270_1571-126 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124773 | |||||
chr8:123124773
|
C | CAAA | 38 | a0001c0001t0001g0171a0001c0003t0001g0169a0001c0004t0001g0001others(35): Show | 40 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1571-1271_1571-126 others(7): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124773 | |||||
chr8:123124773
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1571-1283C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124773 | ||||||
chr8:123124862
|
G | A | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1571-1194G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124862 | ||||||
chr8:123124893
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1571-1163C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124893 | ||||||
chr8:123124894
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1571-1162G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124894 | ||||||
chr8:123124938
|
C | CA | 58 | a0001c0001t0001g0124a0001c0001t0001g0136a0001c0001t0001g0170others(55): Show | 60 | HG00323.hp1 HG00438.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1571-1100dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124938 | |||||
chr8:123124938
|
C | CAA | 7 | a0001c0003t0001g0169a0001c0004t0001g0001a0001c0004t0001g0099others(4): Show | 9 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1571-1101_1571-110 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124938 | |||||
chr8:123124938
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0009c0023t0001g0066 | 3 | HG01099.hp2 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1571-1118C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123124938 | ||||||
chr8:123124938
|
CA | C | 12 | a0001c0001t0001g0081a0001c0001t0001g0154a0001c0001t0001g0263others(9): Show | 12 | HG01891.hp2 HG01993.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1571-1100delA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | 123124938 | |||||
chr8:123125046
|
A | G | 56 | a0001c0001t0001g0171a0001c0003t0001g0146a0001c0003t0001g0169others(53): Show | 60 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1571-1010A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125046 | ||||||
chr8:123125118
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1571-938G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125118 | ||||||
chr8:123125199
|
A | T | 1 | a0001c0003t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1571-857A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125199 | ||||||
chr8:123125240
|
A | T | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1571-816A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125240 | ||||||
chr8:123125466
|
G | A | 1 | a0001c0002t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1571-590G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125466 | ||||||
chr8:123125744
|
G | A | 34 | a0001c0004t0001g0001a0001c0004t0001g0012a0001c0004t0001g0015others(31): Show | 36 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1571-312G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125744 | ||||||
chr8:123125744
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1571-312G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125744 | ||||||
chr8:123125750
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1571-306C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125750 | ||||||
chr8:123125768
|
G | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1571-288G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125768 | ||||||
chr8:123125950
|
A | G | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571-106A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 11/21 | chr8 | 123125950 | ||||||
chr8:123126696
|
C | T | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1884+9C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123126696 | ||||||
chr8:123126773
|
G | A | 1 | a0001c0022t0001g0112 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1884+86G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123126773 | ||||||
chr8:123126828
|
G | A | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1884+141G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123126828 | ||||||
chr8:123126845
|
G | A | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1884+158G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123126845 | ||||||
chr8:123126888
|
C | T | 3 | a0001c0001t0001g0279a0001c0005t0001g0298a0001c0013t0001g0272 | 3 | HG02723.hp2 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1884+201C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123126888 | ||||||
chr8:123127207
|
A | G | 2 | a0002c0006t0001g0061a0002c0006t0001g0249 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1884+520A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127207 | ||||||
chr8:123127261
|
A | AT | 73 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0114others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1884+600dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATT | 103 | a0001c0001t0001g0250a0001c0002t0001g0011a0001c0002t0001g0034others(100): Show | 105 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1884+599_1884+600d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATTT | 38 | a0001c0001t0001g0171a0001c0003t0001g0053a0001c0003t0001g0059others(35): Show | 40 | HG00423.hp2 HG00438.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1884+598_1884+600d others(5): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATTTT | 8 | a0001c0004t0001g0270a0001c0008t0001g0238a0002c0006t0001g0007others(5): Show | 8 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1884+597_1884+600d others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATTTTTTT others(9): Show |
1 | a0001c0009t0001g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1884+585_1884+600d others(18): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATTTTTTT others(10): Show |
1 | a0001c0009t0001g0069 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1884+584_1884+600d others(19): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATTTTTTT others(14): Show |
1 | a0001c0009t0001g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1884+580_1884+600d others(23): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | ATTTTTTT others(15): Show |
1 | a0001c0003t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1884+579_1884+600d others(24): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | 123127261 | |||||
chr8:123127261
|
A | T | 1 | a0001c0004t0001g0145 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1884+574A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127261 | ||||||
chr8:123127468
|
T | C | 5 | a0001c0003t0001g0038a0001c0003t0001g0063a0001c0003t0001g0303others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1884+781T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127468 | ||||||
chr8:123127497
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1885-784C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127497 | ||||||
chr8:123127568
|
C | T | 9 | a0001c0002t0001g0011a0001c0002t0001g0067a0001c0002t0001g0068others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1885-713C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127568 | ||||||
chr8:123127569
|
G | A | 113 | a0001c0001t0001g0171a0001c0003t0001g0006a0001c0003t0001g0008others(110): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1885-712G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127569 | ||||||
chr8:123127667
|
T | G | 2 | a0001c0003t0001g0065a0002c0006t0001g0316 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1885-614T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127667 | ||||||
chr8:123127760
|
C | G | 4 | a0001c0003t0001g0057a0001c0003t0001g0058a0001c0003t0001g0059others(1): Show | 4 | HG01496.hp1 HG02683.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885-521C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127760 | ||||||
chr8:123127836
|
C | T | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1885-445C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127836 | ||||||
chr8:123127958
|
G | T | 113 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(110): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1885-323G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123127958 | ||||||
chr8:123128048
|
A | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1885-233A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123128048 | ||||||
chr8:123128153
|
T | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-128T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123128153 | ||||||
chr8:123128173
|
AT | A | 68 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1885-107delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123128173 | ||||||
chr8:123128205
|
T | A | 3 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271 | 5 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1885-76T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123128205 | ||||||
chr8:123128226
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1885-55C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 13/21 | chr8 | 123128226 | ||||||
chr8:123128561
|
T | C | 1 | a0001c0003t0001g0044 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2117+48T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128561 | ||||||
chr8:123128565
|
C | CATA | 119 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0263others(116): Show | 121 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2117+54_2117+56dup others(3): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 123128565 | |||||
chr8:123128567
|
T | TAAA | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2117+56_2117+57ins others(3): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 123128567 | |||||
chr8:123128605
|
G | A | 2 | a0001c0002t0001g0082a0001c0002t0001g0087 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2117+92G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128605 | ||||||
chr8:123128614
|
C | T | 3 | a0001c0002t0001g0185a0001c0002t0001g0186a0001c0002t0001g0187 | 3 | HG01891.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2117+101C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128614 | ||||||
chr8:123128699
|
A | AC | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2117+190dupC | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 123128699 | |||||
chr8:123128747
|
G | A | 6 | a0001c0003t0001g0146a0001c0009t0001g0009a0001c0009t0001g0010others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2117+234G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128747 | ||||||
chr8:123128747
|
GC | G | 3 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271 | 5 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2117+238delC | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 123128747 | |||||
chr8:123128844
|
C | A | 3 | a0001c0002t0001g0185a0001c0002t0001g0186a0001c0002t0001g0187 | 3 | HG01891.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2118-222C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128844 | ||||||
chr8:123128875
|
CA | C | 11 | a0001c0002t0001g0292a0002c0006t0001g0007a0002c0006t0001g0061others(8): Show | 11 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2118-178delA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | 123128875 | |||||
chr8:123128971
|
A | G | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0308others(3): Show | 6 | HG00735.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2118-95A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128971 | ||||||
chr8:123128993
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2118-73C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 14/21 | chr8 | 123128993 | ||||||
chr8:123129302
|
A | T | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2270+84A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129302 | ||||||
chr8:123129467
|
C | A | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2270+249C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129467 | ||||||
chr8:123129554
|
T | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2270+336T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129554 | ||||||
chr8:123129565
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2270+347T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129565 | ||||||
chr8:123129584
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2270+366C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129584 | ||||||
chr8:123129803
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2271-395A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129803 | ||||||
chr8:123129934
|
C | T | 7 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(4): Show | 7 | HG02486.hp2 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2271-264C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123129934 | ||||||
chr8:123130073
|
A | G | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2271-125A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123130073 | ||||||
chr8:123130156
|
G | T | 14 | a0001c0002t0001g0035a0001c0002t0001g0129a0001c0002t0001g0236others(11): Show | 14 | HG00642.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2271-42G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 15/21 | chr8 | 123130156 | ||||||
chr8:123130517
|
A | G | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2406+184A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123130517 | ||||||
chr8:123130714
|
C | T | 3 | a0001c0003t0001g0056a0001c0003t0001g0223a0001c0003t0001g0225 | 3 | HG00423.hp2 NA18998.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2406+381C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123130714 | ||||||
chr8:123130770
|
C | T | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2406+437C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123130770 | ||||||
chr8:123130847
|
C | T | 2 | a0001c0004t0001g0099a0001c0004t0001g0100 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2406+514C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123130847 | ||||||
chr8:123131162
|
G | A | 7 | a0001c0003t0001g0044a0001c0003t0001g0120a0001c0003t0001g0148others(4): Show | 7 | HG00609.hp2 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2406+829G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131162 | ||||||
chr8:123131235
|
G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0020others(32): Show | 36 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.2406+902G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131235 | ||||||
chr8:123131237
|
G | A | 1 | a0001c0002t0001g0029 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2406+904G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131237 | ||||||
chr8:123131241
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0009c0023t0001g0066 | 3 | HG01099.hp2 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2406+908G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131241 | ||||||
chr8:123131262
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2406+929G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131262 | ||||||
chr8:123131363
|
C | CA | 50 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0095others(47): Show | 50 | HG00735.hp1 HG01099.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.2406+1053dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 123131363 | |||||
chr8:123131363
|
C | CAAA | 7 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0036others(4): Show | 9 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2406+1051_2406+105 others(7): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 123131363 | |||||
chr8:123131363
|
CA | C | 94 | a0001c0001t0001g0247a0001c0003t0001g0008a0001c0003t0001g0016others(91): Show | 96 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2406+1053delA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 123131363 | |||||
chr8:123131763
|
CT | C | 113 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(110): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2406+1431delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131763 | ||||||
chr8:123131766
|
T | G | 113 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(110): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2406+1433T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131766 | ||||||
chr8:123131772
|
G | A | 113 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(110): Show | 115 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2406+1439G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131772 | ||||||
chr8:123131993
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2406+1660A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123131993 | ||||||
chr8:123132049
|
C | T | 1 | a0001c0008t0001g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2406+1716C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132049 | ||||||
chr8:123132050
|
T | C | 1 | a0001c0008t0001g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2406+1717T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132050 | ||||||
chr8:123132060
|
G | T | 1 | a0001c0008t0001g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2406+1727G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132060 | ||||||
chr8:123132061
|
T | TAATCCAT others(3): Show |
1 | a0001c0008t0001g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2406+1728_2406+172 others(14): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132061 | ||||||
chr8:123132062
|
C | A | 1 | a0001c0008t0001g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2406+1729C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132062 | ||||||
chr8:123132160
|
T | G | 1 | a0001c0003t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2406+1827T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132160 | ||||||
chr8:123132295
|
C | T | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-1819C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132295 | ||||||
chr8:123132314
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2407-1800T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132314 | ||||||
chr8:123132403
|
C | CT | 102 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0106others(99): Show | 104 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2407-1683dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 123132403 | |||||
chr8:123132403
|
C | CTT | 34 | a0001c0001t0001g0107a0001c0001t0001g0295a0001c0003t0001g0008others(31): Show | 34 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.2407-1684_2407-168 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 123132403 | |||||
chr8:123132403
|
CT | C | 8 | a0001c0001t0001g0089a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 8 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2407-1683delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | 123132403 | |||||
chr8:123132477
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2407-1637G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132477 | ||||||
chr8:123132483
|
G | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2407-1631G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132483 | ||||||
chr8:123132805
|
T | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-1309T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132805 | ||||||
chr8:123132816
|
C | T | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2407-1298C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132816 | ||||||
chr8:123132844
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2407-1270T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123132844 | ||||||
chr8:123133016
|
G | C | 133 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(130): Show | 137 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.2407-1098G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133016 | ||||||
chr8:123133229
|
C | T | 68 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0016others(65): Show | 68 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2407-885C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133229 | ||||||
chr8:123133386
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0308others(3): Show | 6 | HG00735.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2407-728G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133386 | ||||||
chr8:123133479
|
C | T | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-635C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133479 | ||||||
chr8:123133536
|
T | C | 1 | a0001c0003t0001g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2407-578T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133536 | ||||||
chr8:123133900
|
T | C | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2407-214T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133900 | ||||||
chr8:123133923
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2407-191A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 16/21 | chr8 | 123133923 | ||||||
chr8:123134440
|
T | C | 1 | a0001c0003t0001g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2499+234T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123134440 | ||||||
chr8:123134538
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2499+332A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123134538 | ||||||
chr8:123134605
|
C | T | 1 | a0001c0002t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2499+399C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123134605 | ||||||
chr8:123134661
|
G | C | 1 | a0001c0004t0001g0270 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2499+455G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123134661 | ||||||
chr8:123134881
|
A | ACTTT | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2499+684_2499+687d others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123134881 | |||||
chr8:123135045
|
G | T | 1 | a0001c0002t0001g0019 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2499+839G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123135045 | ||||||
chr8:123135056
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2499+850A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123135056 | ||||||
chr8:123135170
|
G | A | 1 | a0006c0011t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2499+964G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123135170 | ||||||
chr8:123135339
|
A | C | 8 | a0001c0001t0001g0250a0001c0002t0001g0185a0001c0002t0001g0186others(5): Show | 8 | HG01167.hp1 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2499+1133A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123135339 | ||||||
chr8:123135471
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2499+1265C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123135471 | ||||||
chr8:123135526
|
G | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2499+1320G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123135526 | ||||||
chr8:123136161
|
G | T | 3 | a0002c0006t0001g0007a0002c0006t0001g0064a0002c0006t0001g0269 | 3 | HG02572.hp1 HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2499+1955G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136161 | ||||||
chr8:123136169
|
A | T | 2 | a0001c0003t0001g0251a0001c0003t0001g0252 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2499+1963A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136169 | ||||||
chr8:123136288
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2499+2082T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136288 | ||||||
chr8:123136289
|
G | A | 1 | a0001c0009t0001g0009 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2499+2083G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136289 | ||||||
chr8:123136299
|
CTGTCTT | C | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2499+2097_2499+210 others(10): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123136299 | |||||
chr8:123136836
|
TAAAC | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2499+2635_2499+263 others(8): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123136836 | |||||
chr8:123136923
|
C | T | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2499+2717C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136923 | ||||||
chr8:123136968
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2499+2762C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136968 | ||||||
chr8:123136998
|
T | C | 3 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271 | 5 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2499+2792T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123136998 | ||||||
chr8:123137002
|
T | C | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2499+2796T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137002 | ||||||
chr8:123137090
|
C | T | 7 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(4): Show | 7 | HG02486.hp2 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2499+2884C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137090 | ||||||
chr8:123137214
|
T | A | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2499+3008T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137214 | ||||||
chr8:123137266
|
G | C | 155 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0171others(152): Show | 159 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2499+3060G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137266 | ||||||
chr8:123137540
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2500-3221T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137540 | ||||||
chr8:123137561
|
G | A | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2500-3200G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137561 | ||||||
chr8:123137569
|
G | A | 2 | a0001c0005t0001g0021a0001c0005t0001g0036 | 2 | HG02630.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2500-3192G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137569 | ||||||
chr8:123137571
|
A | G | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2500-3190A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137571 | ||||||
chr8:123137682
|
A | G | 134 | a0001c0001t0001g0171a0001c0003t0001g0006a0001c0003t0001g0008others(131): Show | 138 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.2500-3079A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137682 | ||||||
chr8:123137704
|
C | T | 154 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0263others(151): Show | 158 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2500-3057C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123137704 | ||||||
chr8:123138004
|
T | C | 1 | a0001c0002t0001g0226 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2500-2757T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138004 | ||||||
chr8:123138171
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2500-2590T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138171 | ||||||
chr8:123138173
|
G | T | 154 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0263others(151): Show | 158 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.2500-2588G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138173 | ||||||
chr8:123138390
|
A | G | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2500-2371A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138390 | ||||||
chr8:123138391
|
T | TA | 139 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0308others(136): Show | 143 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2500-2368dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123138391 | |||||
chr8:123138437
|
C | T | 1 | a0001c0005t0001g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2500-2324C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138437 | ||||||
chr8:123138441
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2500-2320C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138441 | ||||||
chr8:123138639
|
G | A | 5 | a0001c0003t0001g0006a0001c0003t0001g0209a0001c0003t0001g0216others(2): Show | 5 | HG02165.hp2 NA18949.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.2500-2122G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138639 | ||||||
chr8:123138713
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0150others(5): Show | 9 | HG00280.hp2 HG00738.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2500-2048A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138713 | ||||||
chr8:123138750
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0137others(160): Show | 168 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.2500-2011G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138750 | ||||||
chr8:123138787
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2500-1974A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138787 | ||||||
chr8:123138930
|
C | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2500-1831C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138930 | ||||||
chr8:123138998
|
G | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2500-1763G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123138998 | ||||||
chr8:123139000
|
G | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2500-1761G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139000 | ||||||
chr8:123139086
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2500-1675G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139086 | ||||||
chr8:123139118
|
G | GT | 140 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0107others(137): Show | 145 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.2500-1629dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123139118 | |||||
chr8:123139382
|
G | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0308others(3): Show | 6 | HG00735.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2500-1379G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139382 | ||||||
chr8:123139410
|
C | T | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2500-1351C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139410 | ||||||
chr8:123139573
|
A | C | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2500-1188A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139573 | ||||||
chr8:123139577
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(120): Show | 126 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.2500-1184A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139577 | ||||||
chr8:123139589
|
C | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2500-1172C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139589 | ||||||
chr8:123139694
|
T | TTACACAT others(12): Show |
3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2500-1060_2500-105 others(23): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123139694 | |||||
chr8:123139785
|
A | T | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2500-976A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123139785 | ||||||
chr8:123140005
|
T | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0137others(161): Show | 169 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.2500-756T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140005 | ||||||
chr8:123140010
|
G | A | 1 | a0001c0004t0001g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2500-751G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140010 | ||||||
chr8:123140074
|
T | C | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2500-687T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140074 | ||||||
chr8:123140229
|
G | A | 34 | a0001c0004t0001g0001a0001c0004t0001g0012a0001c0004t0001g0015others(31): Show | 36 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.2500-532G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140229 | ||||||
chr8:123140286
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2500-475C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140286 | ||||||
chr8:123140413
|
A | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2500-348A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140413 | ||||||
chr8:123140630
|
G | A | 1 | a0002c0006t0001g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2500-131G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140630 | ||||||
chr8:123140683
|
T | C | 1 | a0001c0002t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2500-78T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140683 | ||||||
chr8:123140730
|
A | C | 11 | a0001c0005t0001g0004a0001c0005t0001g0005a0001c0005t0001g0021others(8): Show | 13 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2500-31A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | chr8 | 123140730 | ||||||
chr8:123140734
|
A | AT | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0308others(3): Show | 6 | HG00735.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2500-18dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | 123140734 | |||||
chr8:123140924
|
A | G | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2640+23A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123140924 | ||||||
chr8:123140981
|
T | C | 4 | a0005c0015t0001g0194a0005c0015t0001g0195a0005c0016t0001g0018others(1): Show | 4 | NA18961.hp1 NA18982.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2640+80T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123140981 | ||||||
chr8:123141123
|
G | GAAATACA others(14): Show |
3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2640+236_2640+237i others(23): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141123 | |||||
chr8:123141245
|
C | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2640+344C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141245 | ||||||
chr8:123141277
|
T | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(123): Show | 129 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2640+376T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141277 | ||||||
chr8:123141317
|
T | G | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2640+416T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141317 | ||||||
chr8:123141439
|
G | GATACTGT others(12): Show |
3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2640+540_2640+541i others(21): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141439 | |||||
chr8:123141449
|
A | AATTTCCT others(29): Show |
7 | a0001c0003t0001g0044a0001c0003t0001g0120a0001c0003t0001g0148others(4): Show | 7 | HG00609.hp2 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2640+554_2640+555i others(38): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141449 | |||||
chr8:123141449
|
A | AATTTCCT others(29): Show |
81 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(78): Show | 82 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.2640+554_2640+555i others(38): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141449 | |||||
chr8:123141521
|
A | G | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2640+620A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141521 | ||||||
chr8:123141523
|
A | G | 17 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0256others(14): Show | 19 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2640+622A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141523 | ||||||
chr8:123141551
|
T | C | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2640+650T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141551 | ||||||
chr8:123141586
|
A | G | 2 | a0001c0002t0001g0256a0001c0002t0001g0257 | 2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2641-676A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141586 | ||||||
chr8:123141710
|
C | T | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2641-552C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141710 | ||||||
chr8:123141789
|
A | G | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2641-473A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141789 | ||||||
chr8:123141811
|
CCTTGGCT others(14): Show |
C | 17 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0256others(14): Show | 19 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2641-446_2641-426d others(23): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141811 | |||||
chr8:123141819
|
G | A | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2641-443G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141819 | ||||||
chr8:123141844
|
C | CT | 99 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0071others(96): Show | 100 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2641-387dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
C | CTT | 24 | a0001c0001t0001g0020a0001c0001t0001g0110a0001c0001t0001g0111others(21): Show | 24 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2641-388_2641-387d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
C | CTTT | 6 | a0001c0001t0001g0259a0001c0002t0001g0068a0001c0002t0001g0255others(3): Show | 6 | HG00609.hp2 HG01109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2641-389_2641-387d others(5): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
C | CTTTT | 7 | a0001c0002t0001g0011a0001c0002t0001g0067a0001c0002t0001g0082others(4): Show | 7 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2641-390_2641-387d others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CT | C | 6 | a0001c0001t0001g0098a0001c0001t0001g0312a0001c0002t0001g0274others(3): Show | 6 | HG01257.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2641-387delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CTT | C | 9 | a0001c0002t0001g0282a0001c0009t0001g0009a0001c0009t0001g0010others(6): Show | 9 | HG01257.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2641-388_2641-387d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CTTT | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0003t0001g0065others(3): Show | 6 | HG00735.hp2 HG01099.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.2641-389_2641-387d others(5): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CTTTT | C | 13 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0002t0001g0308others(10): Show | 15 | HG00323.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2641-390_2641-387d others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CTTTTTTT | C | 11 | a0001c0001t0001g0109a0001c0002t0001g0035a0001c0002t0001g0236others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.2641-393_2641-387d others(9): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2641-398_2641-387d others(14): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141844
|
CTTTTTTT others(13): Show |
C | 5 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161others(2): Show | 5 | NA18964.hp2 NA18974.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.2641-406_2641-387d others(22): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | 123141844 | |||||
chr8:123141924
|
A | T | 3 | a0001c0003t0001g0016a0001c0003t0001g0084a0001c0003t0001g0169 | 3 | HG03130.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2641-338A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141924 | ||||||
chr8:123141944
|
T | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(85): Show | 89 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2641-318T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123141944 | ||||||
chr8:123142009
|
C | T | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2641-253C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123142009 | ||||||
chr8:123142010
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0266 | 2 | NA18747.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.2641-252G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123142010 | ||||||
chr8:123142035
|
C | A | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2641-227C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123142035 | ||||||
chr8:123142035
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0137others(128): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2641-227C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123142035 | ||||||
chr8:123142087
|
T | C | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2641-175T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123142087 | ||||||
chr8:123142113
|
A | C | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2641-149A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 18/21 | chr8 | 123142113 | ||||||
chr8:123142457
|
G | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(85): Show | 89 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
splice_donor_variant&intron_variant | HIGH | c.2835+1G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123142457 | ||||||
chr8:123142458
|
T | TA | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2835+8dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr8 | 123142458 | |||||
chr8:123142497
|
A | AT | 51 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0263others(48): Show | 53 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.2835+57dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr8 | 123142497 | |||||
chr8:123142497
|
A | ATT | 36 | a0001c0001t0001g0171a0001c0003t0001g0065a0001c0004t0001g0001others(33): Show | 38 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.2835+56_2835+57dup others(2): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr8 | 123142497 | |||||
chr8:123142514
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2835+58A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123142514 | ||||||
chr8:123142515
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2835+59A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123142515 | ||||||
chr8:123142516
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0137others(151): Show | 159 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.2835+60A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123142516 | ||||||
chr8:123142884
|
A | G | 5 | a0001c0004t0001g0139a0001c0004t0001g0140a0001c0004t0001g0141others(2): Show | 5 | HG01081.hp1 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2835+428A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123142884 | ||||||
chr8:123143149
|
G | A | 1 | a0001c0003t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2835+693G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123143149 | ||||||
chr8:123143433
|
G | A | 17 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0256others(14): Show | 19 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2835+977G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123143433 | ||||||
chr8:123143646
|
A | G | 43 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0263others(40): Show | 45 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.2836-1071A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123143646 | ||||||
chr8:123143976
|
C | T | 1 | a0006c0011t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2836-741C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123143976 | ||||||
chr8:123144058
|
AT | A | 10 | a0001c0002t0001g0011a0001c0002t0001g0067a0001c0002t0001g0068others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2836-655delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr8 | 123144058 | |||||
chr8:123144160
|
T | A | 1 | a0001c0003t0001g0120 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2836-557T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123144160 | ||||||
chr8:123144213
|
T | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(85): Show | 89 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2836-504T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123144213 | ||||||
chr8:123144338
|
T | C | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2836-379T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123144338 | ||||||
chr8:123144430
|
G | A | 3 | a0001c0004t0001g0001a0001c0004t0001g0270a0001c0004t0001g0271 | 5 | HG01168.hp2 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2836-287G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123144430 | ||||||
chr8:123144530
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(74): Show | 78 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2836-187G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 19/21 | chr8 | 123144530 | ||||||
chr8:123144926
|
A | AT | 7 | a0001c0001t0001g0107a0001c0002t0001g0308a0001c0004t0001g0135others(4): Show | 7 | HG01243.hp2 HG02074.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.2974+86dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123144926 | |||||
chr8:123144926
|
A | ATTT | 7 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(4): Show | 7 | HG01891.hp2 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2974+84_2974+86dup others(3): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123144926 | |||||
chr8:123144948
|
G | A | 1 | a0001c0002t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2974+93G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123144948 | ||||||
chr8:123145025
|
G | A | 10 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0227others(7): Show | 10 | HG02109.hp1 HG02280.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2974+170G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145025 | ||||||
chr8:123145315
|
A | C | 2 | a0001c0009t0001g0009a0001c0009t0001g0010 | 2 | HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2974+460A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145315 | ||||||
chr8:123145367
|
A | C | 17 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0256others(14): Show | 19 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2974+512A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145367 | ||||||
chr8:123145383
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(123): Show | 129 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2974+528G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145383 | ||||||
chr8:123145386
|
C | T | 1 | a0009c0023t0001g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2974+531C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145386 | ||||||
chr8:123145692
|
T | TA | 84 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(81): Show | 85 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2974+852dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123145692 | |||||
chr8:123145692
|
T | TAA | 13 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0146others(10): Show | 13 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.2974+851_2974+852d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123145692 | |||||
chr8:123145692
|
T | TAAA | 35 | a0001c0001t0001g0171a0001c0004t0001g0001a0001c0004t0001g0012others(32): Show | 37 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.2974+850_2974+852d others(5): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123145692 | |||||
chr8:123145708
|
G | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(85): Show | 89 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2974+853G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145708 | ||||||
chr8:123145723
|
T | C | 2 | a0001c0005t0001g0298a0001c0013t0001g0272 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2974+868T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123145723 | ||||||
chr8:123145871
|
C | CT | 96 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0155others(93): Show | 97 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2974+1032dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123145871 | |||||
chr8:123146067
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0154 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2974+1212G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146067 | ||||||
chr8:123146133
|
G | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2974+1278G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146133 | ||||||
chr8:123146149
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(74): Show | 78 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2974+1294C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146149 | ||||||
chr8:123146162
|
G | A | 3 | a0001c0003t0001g0268a0007c0014t0001g0076a0007c0014t0001g0077 | 3 | HG00735.hp1 HG02145.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2974+1307G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146162 | ||||||
chr8:123146286
|
ACT | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2974+1432_2974+143 others(6): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146286 | ||||||
chr8:123146289
|
T | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2974+1434T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146289 | ||||||
chr8:123146303
|
G | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2974+1448G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146303 | ||||||
chr8:123146322
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0153 | 2 | HG00738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2974+1467C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146322 | ||||||
chr8:123146326
|
A | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(85): Show | 89 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2974+1471A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146326 | ||||||
chr8:123146368
|
C | A | 2 | a0001c0004t0001g0096a0001c0004t0001g0166 | 2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2974+1513C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146368 | ||||||
chr8:123146511
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2974+1656A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146511 | ||||||
chr8:123146571
|
G | A | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2974+1716G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146571 | ||||||
chr8:123146960
|
C | T | 17 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0256others(14): Show | 19 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.2974+2105C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146960 | ||||||
chr8:123146998
|
C | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0277others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2974+2143C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123146998 | ||||||
chr8:123147102
|
CT | C | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2974+2249delT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123147102 | |||||
chr8:123147163
|
T | TG | 5 | a0001c0005t0001g0298a0001c0013t0001g0272a0006c0011t0001g0078others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2974+2309dupG | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123147163 | |||||
chr8:123147164
|
G | GT | 45 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(42): Show | 47 | HG00423.hp1 HG00673.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2974+2320dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123147164 | |||||
chr8:123147461
|
C | T | 1 | a0003c0010t0001g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2975-2575C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147461 | ||||||
chr8:123147528
|
ATAGAGAA others(3): Show |
A | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2505_2975-249 others(14): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123147528 | |||||
chr8:123147542
|
G | C | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2494G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147542 | ||||||
chr8:123147544
|
A | C | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2492A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147544 | ||||||
chr8:123147558
|
T | A | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2478T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147558 | ||||||
chr8:123147561
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(29): Show | 33 | HG00423.hp2 HG00544.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2975-2475G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147561 | ||||||
chr8:123147562
|
T | A | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2474T>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147562 | ||||||
chr8:123147563
|
C | G | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2473C>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147563 | ||||||
chr8:123147566
|
C | T | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-2470C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147566 | ||||||
chr8:123147739
|
A | C | 1 | a0003c0010t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2975-2297A>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147739 | ||||||
chr8:123147851
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0009c0023t0001g0066 | 3 | HG01099.hp2 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2975-2185G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147851 | ||||||
chr8:123147867
|
C | T | 9 | a0001c0004t0001g0015a0001c0004t0001g0023a0001c0004t0001g0024others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2975-2169C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147867 | ||||||
chr8:123147903
|
A | G | 2 | a0001c0004t0001g0096a0001c0004t0001g0166 | 2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2975-2133A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123147903 | ||||||
chr8:123148076
|
A | G | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2975-1960A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148076 | ||||||
chr8:123148126
|
C | CA | 44 | a0001c0001t0001g0171a0001c0001t0001g0263a0001c0001t0001g0276others(41): Show | 46 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2975-1895dupA | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123148126 | |||||
chr8:123148148
|
C | T | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2975-1888C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148148 | ||||||
chr8:123148232
|
G | A | 2 | a0001c0005t0001g0040a0001c0024t0001g0037 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2975-1804G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148232 | ||||||
chr8:123148239
|
G | C | 2 | a0001c0002t0001g0085a0001c0002t0001g0086 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2975-1797G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148239 | ||||||
chr8:123148286
|
C | T | 9 | a0001c0004t0001g0015a0001c0004t0001g0023a0001c0004t0001g0024others(6): Show | 9 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.2975-1750C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148286 | ||||||
chr8:123148438
|
G | A | 3 | a0006c0011t0001g0078a0006c0011t0001g0079a0006c0011t0001g0080 | 3 | HG02486.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2975-1598G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148438 | ||||||
chr8:123148532
|
G | GT | 5 | a0001c0005t0001g0298a0001c0013t0001g0272a0006c0011t0001g0078others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2975-1502dupT | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123148532 | |||||
chr8:123148688
|
G | A | 4 | a0001c0003t0001g0046a0001c0003t0001g0048a0001c0003t0001g0050others(1): Show | 4 | NA18955.hp1 NA18985.hp2 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.2975-1348G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148688 | ||||||
chr8:123148814
|
C | T | 13 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0005t0001g0004others(10): Show | 15 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2975-1222C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148814 | ||||||
chr8:123148988
|
A | G | 83 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0137others(80): Show | 87 | HG00323.hp1 HG00673.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.2975-1048A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123148988 | ||||||
chr8:123149131
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG02922.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2975-905G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149131 | ||||||
chr8:123149170
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2975-866C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149170 | ||||||
chr8:123149231
|
TCC | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0162others(73): Show | 77 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2975-801_2975-800d others(4): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | 123149231 | |||||
chr8:123149388
|
G | A | 2 | a0001c0003t0001g0065a0002c0006t0001g0316 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2975-648G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149388 | ||||||
chr8:123149585
|
G | T | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-451G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149585 | ||||||
chr8:123149730
|
T | C | 4 | a0001c0003t0001g0146a0001c0009t0001g0069a0001c0009t0001g0070others(1): Show | 4 | HG02809.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2975-306T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149730 | ||||||
chr8:123149740
|
C | A | 31 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0002t0001g0035others(28): Show | 31 | HG00642.hp2 HG00741.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.2975-296C>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149740 | ||||||
chr8:123149758
|
G | T | 1 | a0002c0025t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2975-278G>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149758 | ||||||
chr8:123149827
|
A | T | 1 | a0001c0002t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2975-209A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149827 | ||||||
chr8:123149832
|
G | A | 1 | a0011c0021t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2975-204G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 20/21 | chr8 | 123149832 | ||||||
chr8:123150330
|
A | G | 1 | a0004c0007t0001g0033 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3067+202A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150330 | ||||||
chr8:123150483
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3067+355G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150483 | ||||||
chr8:123150501
|
T | C | 1 | a0001c0004t0001g0177 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3067+373T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150501 | ||||||
chr8:123150556
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3067+428C>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150556 | ||||||
chr8:123150578
|
T | C | 1 | a0001c0005t0001g0036 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3067+450T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150578 | ||||||
chr8:123150632
|
A | G | 1 | a0001c0024t0001g0037 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3067+504A>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150632 | ||||||
chr8:123150721
|
T | G | 2 | a0001c0009t0001g0069a0001c0009t0001g0070 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3067+593T>G | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150721 | ||||||
chr8:123150816
|
G | C | 1 | a0001c0002t0001g0236 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3067+688G>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150816 | ||||||
chr8:123150850
|
T | C | 2 | a0001c0004t0001g0143a0001c0004t0001g0144 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3067+722T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150850 | ||||||
chr8:123150891
|
A | T | 4 | a0001c0003t0001g0006a0001c0003t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02165.hp2 NA18949.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.3067+763A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123150891 | ||||||
chr8:123151137
|
T | TGGTTATT others(11): Show |
75 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(72): Show | 79 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.3068-659_3068-658i others(20): Show |
TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | 123151137 | |||||
chr8:123151274
|
A | T | 1 | a0001c0002t0001g0174 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3068-532A>T | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123151274 | ||||||
chr8:123151381
|
T | C | 13 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0005t0001g0004others(10): Show | 15 | HG00323.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3068-425T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123151381 | ||||||
chr8:123151439
|
G | A | 78 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(75): Show | 82 | HG00323.hp1 HG00673.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.3068-367G>A | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123151439 | ||||||
chr8:123151744
|
T | C | 2 | a0007c0014t0001g0076a0007c0014t0001g0077 | 2 | HG00735.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.3068-62T>C | TBC1D31 | ENSG00000156787.17 | transcript | ENST00000287380.6 | protein_coding | 21/21 | chr8 | 123151744 |