geneid | 57799 |
---|---|
ensemblid | ENSG00000197562.10 |
hgncid | 18285 |
symbol | RAB40C |
name | RAB40C, member RAS oncogene family |
refseq_nuc | NM_021168.5 |
refseq_prot | NP_066991.3 |
ensembl_nuc | ENST00000248139.8 |
ensembl_prot | ENSP00000248139.3 |
mane_status | MANE Select |
chr | chr16 |
start | 590066 |
end | 629268 |
strand | + |
ver | v1.2 |
region | chr16:590066-629268 |
region5000 | chr16:585066-634268 |
regionname0 | RAB40C_chr16_590066_629268 |
regionname5000 | RAB40C_chr16_585066_634268 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 846 | 346 | 92 | 70 | 124 | 12 | 46 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
c0002 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
c0003 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
c0004 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
c0005 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1873 | 137 | 41 | 33 | 46 | 4 | 11 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0002 | 0/0 | 1873 | 105 | 3 | 25 | 56 | 3 | 18 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0003 | 0/0 | 1873 | 48 | 16 | 5 | 11 | 3 | 13 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0004 | 0/0 | 1870 | 10 | 8 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0005 | 0/0 | 1873 | 5 | 1 | 1 | 2 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0006 | 0/0 | 1873 | 5 | 4 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0007 | 0/0 | 1873 | 5 | 5 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0008 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0009 | 0/0 | 1873 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0010 | 0/0 | 1873 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0011 | 0/0 | 1873 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0012 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0013 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0014 | 0/0 | 1873 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0015 | 0/0 | 1873 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0016 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0017 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0018 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0019 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0020 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0021 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0022 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0023 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0024 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0025 | 0/0 | 1873 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0026 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0027 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0028 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0029 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0030 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0031 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0032 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0033 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
t0034 | 0/0 | 1873 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 846 | 346 | 92 | 70 | 124 | 12 | 46 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0003 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0004 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0005 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0002c0002 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2718 | 135 | 40 | 33 | 45 | 4 | 11 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0002 | 0/0 | 2718 | 105 | 3 | 25 | 56 | 3 | 18 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0003 | 0/0 | 2718 | 48 | 16 | 5 | 11 | 3 | 13 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0004 | 0/0 | 2715 | 10 | 8 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0005 | 0/0 | 2718 | 5 | 1 | 1 | 2 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0006 | 0/0 | 2718 | 5 | 4 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0007 | 0/0 | 2718 | 5 | 5 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0008 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0009 | 0/0 | 2718 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0010 | 0/0 | 2718 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0011 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0012 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0013 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0014 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0015 | 0/0 | 2718 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0016 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0017 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0018 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0019 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0020 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0021 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0022 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0025 | 0/0 | 2718 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0026 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0027 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0028 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0029 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0030 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0031 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0032 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0033 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0001t0034 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0003t0001 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0004t0023 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0001c0005t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
a0002c0002t0024 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | copy fasta | chr16 | 585066 | 634268 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0009g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0009g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0011g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0011g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0014g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0015g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0016g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0017g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0018g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0020g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0022g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0025g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0026g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0027g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0028g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0029g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0030g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0031g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0032g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0033g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0001t0034g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0004t0023g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0001c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
a0002c0002t0024g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0211 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00140 | hp2 | a0001 | c0001 | t0026 | g0010 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0231 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01255 | hp1 | a0001 | c0001 | t0015 | g0107 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01256 | hp1 | a0001 | c0001 | t0025 | g0007 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0008 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01884 | hp2 | a0001 | c0001 | t0031 | g0161 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0171 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02083 | hp1 | a0001 | c0001 | t0017 | g0240 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02132 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CDX | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0038 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02280 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0320 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02602 | hp1 | a0001 | c0001 | t0009 | g0316 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02622 | hp2 | a0001 | c0001 | t0033 | g0064 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0155 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0224 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02970 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02970 | hp2 | a0001 | c0001 | t0029 | g0188 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02976 | hp1 | a0001 | c0001 | t0034 | g0156 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03041 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03139 | hp2 | a0001 | c0001 | t0020 | g0034 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03195 | hp2 | a0001 | c0004 | t0023 | g0041 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0033 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0040 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03704 | hp1 | a0001 | c0001 | t0019 | g0003 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03704 | hp2 | a0001 | c0001 | t0009 | g0317 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18954 | hp1 | a0001 | c0001 | t0011 | g0302 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18961 | hp2 | a0001 | c0001 | t0014 | g0120 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18963 | hp2 | a0001 | c0001 | t0016 | g0321 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18971 | hp2 | a0001 | c0001 | t0011 | g0291 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18973 | hp2 | a0001 | c0001 | t0032 | g0020 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18982 | hp2 | a0001 | c0001 | t0030 | g0204 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19000 | hp2 | a0001 | c0001 | t0018 | g0091 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19001 | hp2 | a0002 | c0002 | t0024 | g0234 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19002 | hp1 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19043 | hp2 | a0001 | c0001 | t0021 | g0185 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19084 | hp2 | a0001 | c0005 | t0001 | g0056 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | ASW | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0255 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20805 | hp2 | a0001 | c0001 | t0027 | g0151 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | GIH | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | GIH | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0108 | REF | REF | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0126 | REF | REF | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:627519
|
G | T | 1 | a0002 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.743G>T | p.Gly248Val | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 969/2718 | 743/846 | 248/281 | chr16 | 627519 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:590315
|
G | T | 1 | a0001c0005 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.24G>T | p.Val8Val | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 250/2718 | 24/846 | 8/281 | chr16 | 590315 | ||
chr16:617212
|
C | T | 1 | a0001c0004 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.147C>T | p.Ile49Ile | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/6 | 373/2718 | 147/846 | 49/281 | chr16 | 617212 | ||
chr16:627511
|
C | T | 1 | a0001c0003 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.735C>T | p.Ser245Ser | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 961/2718 | 735/846 | 245/281 | chr16 | 627511 | ||
chr16:627517
|
C | G | 1 | a0002c0002 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.741C>G | p.Ala247Ala | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 967/2718 | 741/846 | 247/281 | chr16 | 627517 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:590087
|
T | A | 1 | a0001c0001t0005 | 5 | HG00738.hp1 HG02683.hp1 NA18982.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-205T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 205 | chr16 | 590087 | |||||
chr16:590131
|
C | A | 1 | a0001c0001t0016 | 1 | NA18963.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 161 | chr16 | 590131 | |||||
chr16:590138
|
G | A | 1 | a0001c0001t0017 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 154 | chr16 | 590138 | |||||
chr16:590186
|
G | A | 1 | a0001c0001t0018 | 1 | NA19000.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 106 | chr16 | 590186 | |||||
chr16:590192
|
A | G | 1 | a0001c0001t0034 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 100 | chr16 | 590192 | |||||
chr16:590245
|
G | A | 1 | a0001c0001t0008 | 2 | HG02258.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-47G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 47 | chr16 | 590245 | |||||
chr16:590265
|
C | CCGGCGCG others(9): Show |
1 | a0001c0001t0033 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18_-3dupGGCGCAGGC others(7): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 2 | INFO_REALIGN_3_PRIME | chr16 | 590265 | ||||
chr16:627629
|
T | C | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(12): Show | 134 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 7 | chr16 | 627629 | |||||
chr16:627740
|
G | A | 1 | a0001c0001t0009 | 2 | HG02602.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*118G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 118 | chr16 | 627740 | |||||
chr16:627770
|
C | G | 1 | a0001c0001t0013 | 2 | HG02970.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*148C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 148 | chr16 | 627770 | |||||
chr16:627770
|
C | T | 3 | a0001c0001t0004a0001c0001t0008a0001c0004t0023 | 13 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*148C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 148 | chr16 | 627770 | |||||
chr16:627854
|
G | T | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*232G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 232 | chr16 | 627854 | |||||
chr16:628020
|
G | A | 7 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(4): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*398G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 398 | chr16 | 628020 | |||||
chr16:628044
|
A | G | 1 | a0001c0001t0022 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 422 | chr16 | 628044 | |||||
chr16:628116
|
T | G | 1 | a0001c0001t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 494 | chr16 | 628116 | |||||
chr16:628174
|
G | C | 1 | a0001c0001t0019 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 552 | chr16 | 628174 | |||||
chr16:628264
|
C | G | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(3): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*642C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 642 | chr16 | 628264 | |||||
chr16:628304
|
G | A | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(3): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*682G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 682 | chr16 | 628304 | |||||
chr16:628336
|
CCTT | C | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(3): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*718delTTC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 716 | INFO_REALIGN_3_PRIME | chr16 | 628336 | ||||
chr16:628430
|
C | T | 1 | a0001c0001t0015 | 2 | HG01255.hp1 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*808C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 808 | chr16 | 628430 | |||||
chr16:628433
|
T | C | 1 | a0001c0001t0021 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 811 | chr16 | 628433 | |||||
chr16:628443
|
G | A | 1 | a0001c0001t0010 | 2 | HG02257.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 821 | chr16 | 628443 | |||||
chr16:628497
|
T | C | 1 | a0002c0002t0024 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*875T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 875 | chr16 | 628497 | |||||
chr16:628531
|
G | A | 1 | a0001c0001t0011 | 2 | NA18954.hp1 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*909G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 909 | chr16 | 628531 | |||||
chr16:628568
|
T | C | 1 | a0001c0001t0014 | 2 | NA18961.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*946T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 946 | chr16 | 628568 | |||||
chr16:628592
|
G | A | 1 | a0001c0001t0029 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*970G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 970 | chr16 | 628592 | |||||
chr16:628678
|
G | A | 1 | a0001c0001t0032 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1056G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1056 | chr16 | 628678 | |||||
chr16:628821
|
G | A | 1 | a0001c0001t0030 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1199 | chr16 | 628821 | |||||
chr16:628841
|
C | G | 2 | a0001c0001t0010a0001c0001t0020 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1219C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1219 | chr16 | 628841 | |||||
chr16:628843
|
C | T | 17 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(14): Show | 136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1221C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1221 | chr16 | 628843 | |||||
chr16:628877
|
C | T | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(3): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1255C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1255 | chr16 | 628877 | |||||
chr16:628879
|
T | C | 3 | a0001c0001t0006a0001c0001t0028a0001c0001t0031 | 7 | HG01884.hp2 HG01981.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1257T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1257 | chr16 | 628879 | |||||
chr16:628907
|
A | C | 1 | a0001c0001t0027 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1285 | chr16 | 628907 | |||||
chr16:628907
|
A | T | 1 | a0001c0001t0004 | 10 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1285A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1285 | chr16 | 628907 | |||||
chr16:628980
|
G | A | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(3): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1358G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1358 | chr16 | 628980 | |||||
chr16:629147
|
T | C | 1 | a0001c0001t0025 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1525 | chr16 | 629147 | |||||
chr16:629241
|
G | T | 1 | a0001c0001t0026 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1619 | chr16 | 629241 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:590440
|
C | T | 2 | a0001c0001t0002g0325a0001c0001t0002g0326 | 2 | HG00639.hp1 HG00741.hp1 |
splice_region_variant&intron_variant | LOW | c.142+7C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590440 | ||||||
chr16:590459
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019 | 4 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+26T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590459 | ||||||
chr16:590590
|
G | T | 1 | a0001c0001t0001g0324 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.142+157G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590590 | ||||||
chr16:590923
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.142+490C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590923 | ||||||
chr16:590949
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.142+516A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590949 | ||||||
chr16:590968
|
A | G | 1 | a0001c0001t0004g0322 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+535A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590968 | ||||||
chr16:591004
|
A | AGGAAGGT others(210): Show |
3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0032g0020 | 3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+606_142+822dup others(217): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 591004 | |||||
chr16:591004
|
A | T | 1 | a0001c0001t0016g0321 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+571A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591004 | ||||||
chr16:591044
|
A | G | 159 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(156): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.142+611A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591044 | ||||||
chr16:591098
|
G | A | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+665G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591098 | ||||||
chr16:591134
|
T | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | NA18981.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.142+701T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591134 | ||||||
chr16:591164
|
G | T | 159 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(156): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.142+731G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591164 | ||||||
chr16:591174
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142+741G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591174 | ||||||
chr16:591193
|
G | C | 1 | a0001c0001t0016g0321 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+760G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591193 | ||||||
chr16:591209
|
C | T | 13 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0004g0162others(10): Show | 13 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+776C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591209 | ||||||
chr16:591217
|
TCA | T | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+785_142+786del others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591217 | ||||||
chr16:591258
|
A | G | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+825A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591258 | ||||||
chr16:591260
|
G | A | 59 | a0001c0001t0001g0227a0001c0001t0002g0183a0001c0001t0003g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.142+827G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591260 | ||||||
chr16:591392
|
C | T | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+959C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591392 | ||||||
chr16:591445
|
G | T | 99 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(96): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.142+1012G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591445 | ||||||
chr16:591471
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+1038T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591471 | ||||||
chr16:591486
|
C | G | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+1053C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591486 | ||||||
chr16:591486
|
C | T | 24 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+1053C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591486 | ||||||
chr16:591514
|
G | A | 1 | a0001c0001t0013g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142+1081G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591514 | ||||||
chr16:591544
|
C | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+1111C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591544 | ||||||
chr16:591582
|
C | G | 3 | a0001c0001t0012g0154a0001c0001t0012g0155a0001c0001t0034g0156 | 3 | HG02280.hp2 HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.142+1149C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591582 | ||||||
chr16:591587
|
C | G | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+1154C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591587 | ||||||
chr16:591596
|
C | CT | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0007g0157others(3): Show | 6 | HG02622.hp1 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+1177dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 591596 | |||||
chr16:591596
|
CT | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG00140.hp1 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1177delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 591596 | |||||
chr16:591702
|
C | G | 2 | a0001c0001t0003g0209a0001c0001t0003g0210 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142+1269C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591702 | ||||||
chr16:591744
|
A | T | 3 | a0001c0001t0006g0171a0001c0001t0006g0172a0001c0001t0006g0173 | 3 | HG01981.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.142+1311A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591744 | ||||||
chr16:591899
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0003g0210 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142+1466C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591899 | ||||||
chr16:591926
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.142+1493G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591926 | ||||||
chr16:591927
|
C | T | 1 | a0001c0001t0027g0151 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.142+1494C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591927 | ||||||
chr16:592062
|
G | C | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | NA18997.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.142+1629G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592062 | ||||||
chr16:592222
|
C | T | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+1789C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592222 | ||||||
chr16:592249
|
T | C | 194 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(191): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.142+1816T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592249 | ||||||
chr16:592610
|
T | C | 218 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0043others(215): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.142+2177T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592610 | ||||||
chr16:592761
|
G | A | 1 | a0001c0001t0033g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142+2328G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592761 | ||||||
chr16:592829
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.142+2396C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592829 | ||||||
chr16:592845
|
C | G | 3 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0016g0321 | 3 | HG02083.hp2 NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.142+2412C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592845 | ||||||
chr16:592910
|
T | A | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+2477T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592910 | ||||||
chr16:593027
|
C | T | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+2594C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593027 | ||||||
chr16:593064
|
G | A | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.142+2631G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593064 | ||||||
chr16:593090
|
G | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+2657G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593090 | ||||||
chr16:593098
|
C | T | 51 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0184others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.142+2665C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593098 | ||||||
chr16:593151
|
G | A | 18 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0004g0162others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+2718G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593151 | ||||||
chr16:593156
|
CAGCACAA | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0032g0020 | 3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+2724_142+2730d others(9): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593156 | ||||||
chr16:593236
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.142+2803G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593236 | ||||||
chr16:593264
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.142+2831A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593264 | ||||||
chr16:593318
|
G | T | 2 | a0001c0001t0009g0316a0001c0001t0009g0317 | 2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.142+2885G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593318 | ||||||
chr16:593338
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.142+2905G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593338 | ||||||
chr16:593402
|
G | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+2969G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593402 | ||||||
chr16:593760
|
G | T | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.142+3327G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593760 | ||||||
chr16:593873
|
A | G | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+3440A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593873 | ||||||
chr16:593894
|
G | A | 4 | a0001c0001t0005g0212a0001c0001t0005g0213a0001c0001t0005g0232others(1): Show | 4 | HG00738.hp1 NA18982.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3461G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593894 | ||||||
chr16:594048
|
C | T | 99 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(96): Show | 107 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.142+3615C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594048 | ||||||
chr16:594088
|
G | C | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+3655G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594088 | ||||||
chr16:594135
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.142+3702C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594135 | ||||||
chr16:594180
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.142+3747C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594180 | ||||||
chr16:594288
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0032g0020 | 3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+3855G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594288 | ||||||
chr16:594344
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.142+3911G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594344 | ||||||
chr16:594393
|
G | A | 29 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0184others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+3960G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594393 | ||||||
chr16:594438
|
G | A | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+4005G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594438 | ||||||
chr16:594494
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.142+4061C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594494 | ||||||
chr16:594502
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.142+4069C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594502 | ||||||
chr16:594612
|
C | G | 2 | a0001c0001t0008g0039a0001c0001t0008g0040 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+4179C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594612 | ||||||
chr16:594818
|
C | CT | 12 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0152others(9): Show | 12 | HG00673.hp2 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+4405dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 594818 | |||||
chr16:594818
|
CT | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0066a0001c0001t0001g0068others(6): Show | 9 | HG01070.hp2 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+4405delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 594818 | |||||
chr16:594824
|
T | TC | 55 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.142+4391_142+4392i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594824 | ||||||
chr16:594825
|
T | C | 2 | a0001c0001t0003g0190a0001c0001t0005g0232 | 2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.142+4392T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594825 | ||||||
chr16:594842
|
C | G | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+4409C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594842 | ||||||
chr16:594860
|
C | T | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.142+4427C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594860 | ||||||
chr16:594907
|
C | T | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+4474C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594907 | ||||||
chr16:595071
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG00733.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.142+4638G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595071 | ||||||
chr16:595148
|
T | A | 1 | a0001c0001t0003g0191 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.142+4715T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595148 | ||||||
chr16:595201
|
C | T | 6 | a0001c0001t0001g0144a0001c0001t0003g0184a0001c0001t0003g0189others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+4768C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595201 | ||||||
chr16:595243
|
G | C | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+4810G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595243 | ||||||
chr16:595371
|
G | A | 1 | a0001c0001t0017g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.142+4938G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595371 | ||||||
chr16:595382
|
G | C | 1 | a0001c0001t0003g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142+4949G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595382 | ||||||
chr16:595473
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+5040G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595473 | ||||||
chr16:595603
|
C | CT | 59 | a0001c0001t0001g0148a0001c0001t0001g0227a0001c0001t0001g0324others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.142+5187dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 595603 | |||||
chr16:595603
|
CT | C | 14 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0043others(11): Show | 14 | HG00323.hp2 HG00738.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.142+5187delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 595603 | |||||
chr16:595606
|
T | C | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+5173T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595606 | ||||||
chr16:595671
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0148 | 3 | HG02080.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.142+5238C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595671 | ||||||
chr16:595852
|
C | T | 7 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0205others(4): Show | 7 | HG01993.hp2 HG02148.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+5419C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595852 | ||||||
chr16:595968
|
C | T | 182 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(179): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.142+5535C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595968 | ||||||
chr16:595969
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0032g0020 | 3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+5536A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595969 | ||||||
chr16:595997
|
G | A | 21 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(18): Show | 21 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.142+5564G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595997 | ||||||
chr16:596233
|
C | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+5800C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596233 | ||||||
chr16:596246
|
G | A | 53 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(50): Show | 54 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.142+5813G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596246 | ||||||
chr16:596251
|
G | A | 1 | a0001c0001t0021g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+5818G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596251 | ||||||
chr16:596257
|
A | G | 16 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(13): Show | 16 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.142+5824A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596257 | ||||||
chr16:596336
|
G | A | 1 | a0001c0001t0021g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+5903G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596336 | ||||||
chr16:596388
|
G | A | 23 | a0001c0001t0001g0075a0001c0001t0001g0163a0001c0001t0001g0168others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.142+5955G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596388 | ||||||
chr16:596421
|
A | G | 122 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0002g0002others(119): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.142+5988A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596421 | ||||||
chr16:596452
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.142+6019C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596452 | ||||||
chr16:596473
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142+6040C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596473 | ||||||
chr16:596520
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+6087C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596520 | ||||||
chr16:596520
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.142+6087C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596520 | ||||||
chr16:596521
|
G | A | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+6088G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596521 | ||||||
chr16:596547
|
G | A | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+6114G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596547 | ||||||
chr16:596571
|
A | G | 100 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(97): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.142+6138A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596571 | ||||||
chr16:596606
|
T | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+6173T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596606 | ||||||
chr16:596639
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0018others(12): Show | 17 | HG00639.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.142+6206C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596639 | ||||||
chr16:596865
|
C | G | 80 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(77): Show | 81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.142+6432C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596865 | ||||||
chr16:597006
|
G | A | 97 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(94): Show | 105 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.142+6573G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597006 | ||||||
chr16:597094
|
A | G | 24 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+6661A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597094 | ||||||
chr16:597231
|
G | A | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+6798G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597231 | ||||||
chr16:597335
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.142+6902G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597335 | ||||||
chr16:597346
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142+6913A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597346 | ||||||
chr16:597383
|
G | A | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+6950G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597383 | ||||||
chr16:597438
|
A | G | 1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.142+7005A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597438 | ||||||
chr16:597506
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.142+7073C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597506 | ||||||
chr16:597519
|
C | A | 6 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+7086C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597519 | ||||||
chr16:597752
|
G | C | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+7319G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597752 | ||||||
chr16:597793
|
C | G | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+7360C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597793 | ||||||
chr16:597820
|
G | T | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+7387G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597820 | ||||||
chr16:597834
|
C | T | 1 | a0002c0002t0024g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.142+7401C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597834 | ||||||
chr16:597875
|
C | T | 2 | a0001c0001t0008g0039a0001c0001t0008g0040 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+7442C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597875 | ||||||
chr16:597937
|
C | CA | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0018others(113): Show | 122 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.142+7531dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | |||||
chr16:597937
|
C | CAA | 48 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0022others(45): Show | 51 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.142+7530_142+7531d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | |||||
chr16:597937
|
C | CAAA | 8 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0001t0002g0249others(5): Show | 8 | HG00438.hp2 HG01361.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+7529_142+7531d others(5): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | |||||
chr16:597937
|
CA | C | 21 | a0001c0001t0001g0129a0001c0001t0001g0227a0001c0001t0003g0014others(18): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+7531delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | |||||
chr16:597969
|
G | A | 1 | a0001c0001t0016g0321 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+7536G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597969 | ||||||
chr16:597975
|
A | G | 1 | a0001c0001t0016g0321 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+7542A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597975 | ||||||
chr16:598014
|
A | G | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+7581A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598014 | ||||||
chr16:598072
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+7639C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598072 | ||||||
chr16:598203
|
C | T | 15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00408.hp1 HG00544.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.142+7770C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598203 | ||||||
chr16:598376
|
CA | C | 184 | a0001c0001t0001g0025a0001c0001t0001g0129a0001c0001t0001g0141others(181): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.142+7958delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 598376 | |||||
chr16:598384
|
A | G | 1 | a0001c0001t0003g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+7951A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598384 | ||||||
chr16:598402
|
A | G | 4 | a0001c0001t0003g0184a0001c0001t0003g0189a0001c0001t0004g0186others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+7969A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598402 | ||||||
chr16:598515
|
T | C | 59 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.142+8082T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598515 | ||||||
chr16:598542
|
A | C | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.142+8109A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598542 | ||||||
chr16:598547
|
G | A | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.142+8114G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598547 | ||||||
chr16:598561
|
C | CA | 20 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0078others(17): Show | 20 | HG01109.hp2 HG01175.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.142+8147dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 598561 | |||||
chr16:598561
|
CA | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0127others(2): Show | 6 | HG01106.hp1 HG01168.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+8147delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 598561 | |||||
chr16:598575
|
A | G | 55 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.142+8142A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598575 | ||||||
chr16:598577
|
A | G | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.142+8144A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598577 | ||||||
chr16:598605
|
G | C | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.142+8172G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598605 | ||||||
chr16:598826
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.142+8393G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598826 | ||||||
chr16:598856
|
G | A | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+8423G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598856 | ||||||
chr16:598873
|
G | A | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+8440G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598873 | ||||||
chr16:599132
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.142+8699C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599132 | ||||||
chr16:599173
|
G | T | 1 | a0001c0001t0002g0276 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.142+8740G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599173 | ||||||
chr16:599255
|
G | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+8822G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599255 | ||||||
chr16:599264
|
C | T | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+8831C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599264 | ||||||
chr16:599270
|
G | A | 2 | a0001c0001t0004g0186a0001c0001t0004g0187 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.142+8837G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599270 | ||||||
chr16:599272
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.142+8839G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599272 | ||||||
chr16:599308
|
C | G | 1 | a0001c0001t0003g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142+8875C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599308 | ||||||
chr16:599320
|
C | T | 2 | a0001c0001t0006g0031a0001c0001t0028g0033 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142+8887C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599320 | ||||||
chr16:599454
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+9021C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599454 | ||||||
chr16:599524
|
G | A | 3 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0195 | 3 | HG02280.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.142+9091G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599524 | ||||||
chr16:599555
|
TGTCAGCG others(35): Show |
T | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+9151_142+9192d others(44): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599555 | |||||
chr16:599588
|
C | T | 21 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0003g0160others(18): Show | 21 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.142+9155C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599588 | ||||||
chr16:599612
|
A | AGCAAGGT others(34): Show |
1 | a0001c0001t0007g0159 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142+9192_142+9193i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599612 | |||||
chr16:599618
|
G | A | 1 | a0001c0001t0010g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.142+9185G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599618 | ||||||
chr16:599626
|
A | C | 1 | a0001c0001t0002g0301 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+9193A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599626 | ||||||
chr16:599638
|
T | C | 189 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.142+9205T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599638 | ||||||
chr16:599640
|
A | G | 2 | a0001c0001t0002g0301a0001c0001t0007g0159 | 2 | HG01993.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+9207A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599640 | ||||||
chr16:599653
|
C | CGCAAGGT others(33): Show |
1 | a0001c0001t0002g0301 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+9220_142+9221i others(42): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599653 | ||||||
chr16:599654
|
A | AGCAAGGT others(34): Show |
3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0309 | 3 | NA18981.hp2 NA19054.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.142+9238_142+9239i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599654 | |||||
chr16:599654
|
A | AGCAAGGT others(75): Show |
98 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0002g0002others(95): Show | 106 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.142+9238_142+9239i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599654 | |||||
chr16:599654
|
A | AGCAAGGT others(75): Show |
1 | a0001c0001t0002g0300 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.142+9238_142+9239i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599654 | |||||
chr16:599654
|
A | C | 1 | a0001c0001t0002g0301 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+9221A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599654 | ||||||
chr16:599668
|
C | CCCTCGTG others(34): Show |
1 | a0001c0001t0002g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.142+9238_142+9239i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599668 | |||||
chr16:599672
|
T | C | 105 | a0001c0001t0001g0023a0001c0001t0001g0129a0001c0001t0002g0002others(102): Show | 113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.142+9239T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599672 | ||||||
chr16:599672
|
T | TGTGGCAT others(34): Show |
43 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(40): Show | 47 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.142+9275_142+9276i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(75): Show |
87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.142+9275_142+9276i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(116): Show |
1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.142+9275_142+9276i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(157): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0147 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142+9275_142+9276i others(166): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(75): Show |
1 | a0001c0001t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.142+9275_142+9276i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(75): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0074a0001c0001t0021g0185 | 4 | HG01167.hp2 HG01169.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+9549_142+9630d others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(34): Show |
14 | a0001c0001t0006g0031a0001c0001t0007g0037a0001c0001t0007g0157others(11): Show | 14 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.142+9261_142+9262i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(117): Show |
1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+9261_142+9262i others(126): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(75): Show |
2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+9261_142+9262i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
T | TGTGGCAT others(116): Show |
1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+9261_142+9262i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599672
|
TGTGGCAT others(34): Show |
T | 63 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+9590_142+9630d others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | |||||
chr16:599695
|
C | T | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+9262C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599695 | ||||||
chr16:599696
|
G | A | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+9263G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599696 | ||||||
chr16:599709
|
C | A | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+9276C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599709 | ||||||
chr16:599736
|
C | T | 63 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+9303C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599736 | ||||||
chr16:599750
|
C | A | 63 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(60): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+9317C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599750 | ||||||
chr16:599823
|
G | GGTTTTGT others(75): Show |
2 | a0001c0001t0008g0039a0001c0001t0008g0040 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+9471_142+9472i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599823 | |||||
chr16:599952
|
G | T | 24 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+9519G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599952 | ||||||
chr16:599983
|
G | GCAAGGTT others(34): Show |
3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+9590_142+9591i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599983 | |||||
chr16:600001
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.142+9568G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600001 | ||||||
chr16:600024
|
G | GCAAGGTT others(34): Show |
1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+9630_142+9631i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 600024 | |||||
chr16:600064
|
T | C | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+9631T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600064 | ||||||
chr16:600069
|
A | G | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+9636A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600069 | ||||||
chr16:600440
|
T | TTA | 52 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(49): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.142+10008_142+1000 others(6): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 600440 | |||||
chr16:600479
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142+10046A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600479 | ||||||
chr16:600554
|
C | G | 3 | a0001c0001t0006g0031a0001c0001t0007g0037a0001c0001t0028g0033 | 3 | HG03225.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142+10121C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600554 | ||||||
chr16:600562
|
C | G | 2 | a0001c0001t0002g0251a0001c0001t0002g0252 | 2 | NA18981.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.142+10129C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600562 | ||||||
chr16:600579
|
C | T | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+10146C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600579 | ||||||
chr16:600683
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+10250C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600683 | ||||||
chr16:600708
|
C | T | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+10275C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600708 | ||||||
chr16:600783
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142+10350C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600783 | ||||||
chr16:600788
|
G | A | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.142+10355G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600788 | ||||||
chr16:601065
|
C | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG02486.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+10632C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601065 | ||||||
chr16:601113
|
T | C | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+10680T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601113 | ||||||
chr16:601115
|
G | T | 186 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.142+10682G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601115 | ||||||
chr16:601137
|
C | G | 1 | a0001c0001t0007g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142+10704C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601137 | ||||||
chr16:601193
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.142+10760A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601193 | ||||||
chr16:601221
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142+10788G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601221 | ||||||
chr16:601279
|
G | C | 186 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.142+10846G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601279 | ||||||
chr16:601438
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+11005G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601438 | ||||||
chr16:601495
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.142+11062G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601495 | ||||||
chr16:601515
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.142+11082C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601515 | ||||||
chr16:601517
|
C | T | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+11084C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601517 | ||||||
chr16:601538
|
G | A | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+11105G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601538 | ||||||
chr16:601738
|
A | G | 8 | a0001c0001t0003g0190a0001c0001t0003g0202a0001c0001t0003g0203others(5): Show | 8 | NA18963.hp1 NA18967.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+11305A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601738 | ||||||
chr16:601785
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.142+11352G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601785 | ||||||
chr16:601815
|
T | TA | 80 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0043others(77): Show | 81 | HG00621.hp1 HG00621.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.142+11412dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601815
|
T | TAA | 13 | a0001c0001t0002g0016a0001c0001t0002g0111a0001c0001t0002g0278others(10): Show | 14 | HG00280.hp1 HG00673.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+11411_142+1141 others(6): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601815
|
T | TAAAAAAA others(18): Show |
1 | a0001c0001t0002g0301 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+11388_142+1141 others(29): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601815
|
T | TAAAAAAA others(20): Show |
2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01255.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.142+11386_142+1141 others(31): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601815
|
T | TAAAAAAA others(23): Show |
2 | a0001c0001t0002g0258a0001c0001t0002g0326 | 2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.142+11383_142+1141 others(34): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601815
|
T | TAAAAAAA others(25): Show |
1 | a0001c0001t0002g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.142+11412_142+1141 others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601815
|
TA | T | 83 | a0001c0001t0001g0025a0001c0001t0001g0168a0001c0001t0002g0002others(80): Show | 89 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.142+11412delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | |||||
chr16:601850
|
G | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+11417G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601850 | ||||||
chr16:601909
|
C | T | 1 | a0001c0001t0002g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.142+11476C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601909 | ||||||
chr16:601954
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0140 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142+11521C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601954 | ||||||
chr16:601960
|
T | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+11527T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601960 | ||||||
chr16:602045
|
C | G | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+11612C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602045 | ||||||
chr16:602195
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0116 | 2 | HG00621.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.142+11762T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602195 | ||||||
chr16:602214
|
G | A | 3 | a0001c0001t0012g0154a0001c0001t0012g0155a0001c0001t0021g0185 | 3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.142+11781G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602214 | ||||||
chr16:602218
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.142+11785T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602218 | ||||||
chr16:602228
|
C | T | 3 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0016g0321 | 3 | HG02083.hp2 NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.142+11795C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602228 | ||||||
chr16:602248
|
G | GT | 106 | a0001c0001t0001g0023a0001c0001t0001g0081a0001c0001t0002g0002others(103): Show | 114 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.142+11828dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 602248 | |||||
chr16:602268
|
G | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+11835G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602268 | ||||||
chr16:602572
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+12139G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602572 | ||||||
chr16:602618
|
A | G | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+12185A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602618 | ||||||
chr16:602623
|
A | G | 189 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.142+12190A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602623 | ||||||
chr16:602638
|
G | C | 2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+12205G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602638 | ||||||
chr16:602639
|
G | C | 2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+12206G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602639 | ||||||
chr16:602941
|
G | A | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+12508G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602941 | ||||||
chr16:602999
|
A | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+12566A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602999 | ||||||
chr16:603051
|
A | G | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+12618A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603051 | ||||||
chr16:603095
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+12662T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603095 | ||||||
chr16:603110
|
ATGTTCTG others(17): Show |
A | 1 | a0001c0001t0002g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.142+12681_142+1270 others(28): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 603110 | |||||
chr16:603265
|
T | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+12832T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603265 | ||||||
chr16:603298
|
A | AT | 6 | a0001c0001t0003g0211a0001c0001t0003g0216a0001c0001t0003g0221others(3): Show | 6 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+12868dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 603298 | |||||
chr16:603739
|
T | C | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+13306T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603739 | ||||||
chr16:603768
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.142+13335C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603768 | ||||||
chr16:603773
|
T | TCAGCCCC | 103 | a0001c0001t0001g0006a0001c0001t0002g0002a0001c0001t0002g0003others(100): Show | 112 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.142+13352_142+1335 others(11): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 603773 | |||||
chr16:603925
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-13283C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603925 | ||||||
chr16:604042
|
G | A | 1 | a0001c0001t0002g0314 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-13166G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604042 | ||||||
chr16:604061
|
C | CT | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-13133dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 604061 | |||||
chr16:604200
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0168 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.143-13008A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604200 | ||||||
chr16:604216
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.143-12992G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604216 | ||||||
chr16:604224
|
G | A | 186 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.143-12984G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604224 | ||||||
chr16:604238
|
AT | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(164): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.143-12959delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 604238 | |||||
chr16:604249
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.143-12959T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604249 | ||||||
chr16:604269
|
T | C | 2 | a0001c0001t0010g0035a0001c0001t0010g0038 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.143-12939T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604269 | ||||||
chr16:604280
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0050 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.143-12928C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604280 | ||||||
chr16:604297
|
G | T | 1 | a0001c0001t0001g0061 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.143-12911G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604297 | ||||||
chr16:604319
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.143-12889C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604319 | ||||||
chr16:604332
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.143-12876A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604332 | ||||||
chr16:604349
|
G | A | 14 | a0001c0001t0003g0190a0001c0001t0003g0192a0001c0001t0003g0197others(11): Show | 14 | HG01433.hp2 HG02129.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-12859G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604349 | ||||||
chr16:604425
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143-12783C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604425 | ||||||
chr16:604447
|
T | C | 1 | a0001c0001t0008g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-12761T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604447 | ||||||
chr16:604449
|
T | C | 1 | a0001c0001t0008g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-12759T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604449 | ||||||
chr16:604459
|
T | A | 2 | a0001c0001t0008g0039a0001c0001t0008g0040 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.143-12749T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604459 | ||||||
chr16:604491
|
CCTT | C | 24 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.143-12714_143-1271 others(7): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 604491 | |||||
chr16:604665
|
C | T | 1 | a0001c0001t0020g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.143-12543C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604665 | ||||||
chr16:604698
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-12510C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604698 | ||||||
chr16:604917
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.143-12291G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604917 | ||||||
chr16:605090
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.143-12118C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605090 | ||||||
chr16:605173
|
C | T | 3 | a0001c0001t0012g0154a0001c0001t0012g0155a0001c0001t0021g0185 | 3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.143-12035C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605173 | ||||||
chr16:605184
|
C | T | 23 | a0001c0001t0001g0074a0001c0001t0003g0190a0001c0001t0003g0191others(20): Show | 23 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-12024C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605184 | ||||||
chr16:605262
|
T | G | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-11946T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605262 | ||||||
chr16:605266
|
A | C | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.143-11942A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605266 | ||||||
chr16:605338
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0086a0001c0001t0001g0105others(2): Show | 5 | HG01167.hp1 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-11870G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605338 | ||||||
chr16:605396
|
A | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-11812A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605396 | ||||||
chr16:605417
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0100others(6): Show | 10 | HG01106.hp1 HG01243.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-11791G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605417 | ||||||
chr16:605425
|
A | C | 1 | a0001c0001t0002g0260 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.143-11783A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605425 | ||||||
chr16:605430
|
G | A | 20 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0003g0160others(17): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.143-11778G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605430 | ||||||
chr16:605452
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-11756C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605452 | ||||||
chr16:605615
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.143-11593C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605615 | ||||||
chr16:605646
|
C | T | 2 | a0001c0001t0004g0186a0001c0001t0004g0187 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.143-11562C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605646 | ||||||
chr16:605652
|
G | A | 27 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(24): Show | 27 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.143-11556G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605652 | ||||||
chr16:605686
|
T | C | 30 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0184others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-11522T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605686 | ||||||
chr16:605734
|
C | G | 1 | a0001c0001t0002g0298 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.143-11474C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605734 | ||||||
chr16:605763
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.143-11445C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605763 | ||||||
chr16:605781
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.143-11427G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605781 | ||||||
chr16:605809
|
G | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0244others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-11399G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605809 | ||||||
chr16:605985
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-11223C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605985 | ||||||
chr16:606033
|
T | C | 189 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(186): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.143-11175T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606033 | ||||||
chr16:606065
|
T | A | 1 | a0001c0001t0002g0260 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.143-11143T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606065 | ||||||
chr16:606105
|
T | C | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-11103T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606105 | ||||||
chr16:606236
|
A | ACAGTCCT others(59): Show |
3 | a0001c0001t0012g0154a0001c0001t0012g0155a0001c0001t0021g0185 | 3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.143-10907_143-1090 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606236 | |||||
chr16:606302
|
A | ACAGTCCT others(59): Show |
11 | a0001c0001t0001g0063a0001c0001t0001g0115a0001c0001t0002g0004others(8): Show | 13 | HG01081.hp2 HG02132.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-10801_143-1073 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606302 | |||||
chr16:606302
|
A | G | 9 | a0001c0001t0001g0049a0001c0001t0002g0297a0001c0001t0003g0196others(6): Show | 9 | HG00408.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-10906A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606302 | ||||||
chr16:606331
|
G | GGTTTCCC others(59): Show |
1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-10812_143-1081 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606331 | |||||
chr16:606368
|
G | GCAGTCCT others(59): Show |
51 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0184others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-10775_143-1077 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606368 | |||||
chr16:606434
|
G | A | 56 | a0001c0001t0001g0049a0001c0001t0001g0227a0001c0001t0003g0014others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-10774G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606434 | ||||||
chr16:606434
|
G | GCAGTCCT others(59): Show |
259 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.143-10736_143-1073 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606434 | |||||
chr16:606434
|
G | GCAGTCCT others(125): Show |
1 | a0001c0001t0002g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.143-10736_143-1073 others(136): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606434 | |||||
chr16:606484
|
A | G | 2 | a0001c0001t0003g0218a0001c0001t0003g0229 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-10724A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606484 | ||||||
chr16:606487
|
T | C | 1 | a0001c0001t0003g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.143-10721T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606487 | ||||||
chr16:606539
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.143-10669G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606539 | ||||||
chr16:606624
|
A | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0245 | 2 | HG01943.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.143-10584A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606624 | ||||||
chr16:606625
|
T | C | 1 | a0001c0001t0010g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-10583T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606625 | ||||||
chr16:606703
|
G | A | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.143-10505G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606703 | ||||||
chr16:606818
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.143-10390G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606818 | ||||||
chr16:606842
|
G | T | 59 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-10366G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606842 | ||||||
chr16:606862
|
G | A | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-10346G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606862 | ||||||
chr16:606879
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143-10329G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606879 | ||||||
chr16:606985
|
G | A | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.143-10223G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606985 | ||||||
chr16:606997
|
C | G | 59 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-10211C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606997 | ||||||
chr16:607073
|
G | C | 59 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-10135G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607073 | ||||||
chr16:607087
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-10121C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607087 | ||||||
chr16:607446
|
T | C | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-9762T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607446 | ||||||
chr16:607459
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.143-9749C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607459 | ||||||
chr16:607466
|
A | G | 60 | a0001c0001t0001g0125a0001c0001t0001g0227a0001c0001t0003g0014others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.143-9742A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607466 | ||||||
chr16:607501
|
C | CA | 10 | a0001c0001t0001g0071a0001c0001t0001g0074a0001c0001t0001g0100others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-9692dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 607501 | |||||
chr16:607501
|
C | CAA | 54 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.143-9693_143-9692d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 607501 | |||||
chr16:607501
|
CA | C | 28 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0124others(25): Show | 28 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.143-9692delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 607501 | |||||
chr16:607517
|
C | A | 54 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.143-9691C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607517 | ||||||
chr16:607517
|
C | G | 5 | a0001c0001t0003g0184a0001c0001t0003g0189a0001c0001t0003g0218others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-9691C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607517 | ||||||
chr16:607531
|
C | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG02486.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-9677C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607531 | ||||||
chr16:607532
|
G | A | 1 | a0001c0001t0010g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143-9676G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607532 | ||||||
chr16:607552
|
G | C | 191 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(188): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.143-9656G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607552 | ||||||
chr16:607575
|
G | A | 1 | a0001c0001t0010g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-9633G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607575 | ||||||
chr16:607646
|
G | C | 1 | a0001c0001t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9562G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607646 | ||||||
chr16:607651
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9557C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607651 | ||||||
chr16:607653
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9555C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607653 | ||||||
chr16:607658
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9550G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607658 | ||||||
chr16:607745
|
C | T | 1 | a0001c0001t0010g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-9463C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607745 | ||||||
chr16:607746
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.143-9462G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607746 | ||||||
chr16:607954
|
C | G | 1 | a0001c0001t0010g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-9254C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607954 | ||||||
chr16:607972
|
G | C | 1 | a0001c0001t0002g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.143-9236G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607972 | ||||||
chr16:607988
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0194 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.143-9220C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607988 | ||||||
chr16:608038
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-9170C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608038 | ||||||
chr16:608201
|
G | C | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-9007G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608201 | ||||||
chr16:608252
|
C | T | 1 | a0001c0001t0012g0154 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-8956C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608252 | ||||||
chr16:608271
|
G | T | 39 | a0001c0001t0001g0065a0001c0001t0002g0289a0001c0001t0003g0014others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.143-8937G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608271 | ||||||
chr16:608326
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-8882C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608326 | ||||||
chr16:608330
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.143-8878C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608330 | ||||||
chr16:609022
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.143-8186T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609022 | ||||||
chr16:609057
|
G | C | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-8151G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609057 | ||||||
chr16:609172
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.143-8036C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609172 | ||||||
chr16:609339
|
GGGGGACA others(8): Show |
G | 2 | a0001c0001t0001g0139a0001c0001t0010g0035 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.143-7854_143-7840d others(17): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 609339 | |||||
chr16:609403
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0140 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.143-7805C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609403 | ||||||
chr16:609469
|
C | T | 55 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.143-7739C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609469 | ||||||
chr16:609543
|
A | G | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-7665A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609543 | ||||||
chr16:609576
|
G | A | 2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-7632G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609576 | ||||||
chr16:609739
|
G | A | 1 | a0001c0001t0029g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.143-7469G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609739 | ||||||
chr16:609852
|
G | A | 21 | a0001c0001t0003g0160a0001c0001t0004g0162a0001c0001t0004g0164others(18): Show | 21 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-7356G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609852 | ||||||
chr16:609873
|
G | C | 1 | a0001c0001t0010g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143-7335G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609873 | ||||||
chr16:609874
|
G | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-7334G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609874 | ||||||
chr16:610020
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-7188C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610020 | ||||||
chr16:610060
|
A | G | 2 | a0001c0001t0003g0216a0001c0001t0003g0231 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.143-7148A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610060 | ||||||
chr16:610086
|
G | C | 1 | a0001c0001t0005g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-7122G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610086 | ||||||
chr16:610285
|
T | G | 1 | a0001c0001t0002g0247 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.143-6923T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610285 | ||||||
chr16:610303
|
G | A | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-6905G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610303 | ||||||
chr16:610325
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0057 | 2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.143-6883G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610325 | ||||||
chr16:610362
|
AC | A | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-6844delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 610362 | |||||
chr16:610491
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143-6717G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610491 | ||||||
chr16:610493
|
C | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-6715C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610493 | ||||||
chr16:610997
|
C | T | 1 | a0001c0001t0008g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-6211C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610997 | ||||||
chr16:610998
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0053 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.143-6210G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610998 | ||||||
chr16:611059
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.143-6149C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611059 | ||||||
chr16:611080
|
C | T | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-6128C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611080 | ||||||
chr16:611109
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-6099C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611109 | ||||||
chr16:611137
|
G | A | 4 | a0001c0001t0006g0031a0001c0001t0007g0037a0001c0001t0028g0033others(1): Show | 4 | HG01884.hp2 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-6071G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611137 | ||||||
chr16:611142
|
T | C | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-6066T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611142 | ||||||
chr16:611335
|
T | C | 199 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0044others(196): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.143-5873T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611335 | ||||||
chr16:611361
|
G | C | 2 | a0001c0001t0008g0040a0001c0004t0023g0041 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-5847G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611361 | ||||||
chr16:611395
|
T | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-5813T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611395 | ||||||
chr16:611439
|
A | G | 189 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.143-5769A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611439 | ||||||
chr16:611451
|
A | G | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-5757A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611451 | ||||||
chr16:611572
|
G | A | 3 | a0001c0001t0003g0192a0001c0001t0003g0200a0001c0001t0003g0201 | 3 | NA18940.hp1 NA18974.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.143-5636G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611572 | ||||||
chr16:611595
|
CGGGACAG others(509): Show |
C | 2 | a0001c0001t0003g0218a0001c0001t0003g0229 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-5543_143-5028d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611595 | |||||
chr16:611595
|
CGGGACAG others(543): Show |
C | 1 | a0001c0001t0003g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.143-5543_143-4994d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611595 | |||||
chr16:611628
|
CAGGGACA others(441): Show |
C | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-5543_143-5096d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611628 | |||||
chr16:611662
|
CAGAGACA others(407): Show |
C | 24 | a0001c0001t0003g0160a0001c0001t0004g0162a0001c0001t0004g0164others(21): Show | 24 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-5543_143-5130d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611662 | |||||
chr16:611665
|
A | G | 160 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0227others(157): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.143-5543A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611665 | ||||||
chr16:611665
|
AGACAGCC others(27): Show |
A | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.143-5486_143-5453d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611665 | |||||
chr16:611730
|
CAGGGACA others(957): Show |
C | 1 | a0001c0001t0005g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143-5452_143-4489d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611730 | |||||
chr16:611746
|
GGCCTGTA others(62): Show |
G | 50 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(47): Show | 51 | HG00280.hp1 HG00673.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.143-5452_143-5384d others(71): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611746 | |||||
chr16:611756
|
T | A | 111 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(108): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.143-5452T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611756 | ||||||
chr16:611764
|
CAGGGACA others(923): Show |
C | 51 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-5408_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611764 | |||||
chr16:611780
|
GGCCTGTA others(28): Show |
G | 1 | a0001c0001t0002g0296 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.143-5408_143-5374d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611780 | |||||
chr16:611780
|
GGCCTGTA others(236): Show |
G | 15 | a0001c0001t0002g0002a0001c0001t0002g0244a0001c0001t0002g0246others(12): Show | 15 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-5408_143-5166d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611780 | |||||
chr16:611798
|
CA | C | 34 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(31): Show | 35 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.143-5408delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611798 | |||||
chr16:611798
|
CAAGGGAC others(889): Show |
C | 2 | a0001c0001t0003g0184a0001c0001t0007g0320 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.143-5408_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611798 | |||||
chr16:611799
|
AAGGGACA others(63): Show |
A | 8 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(5): Show | 8 | HG00408.hp2 HG00639.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-5408_143-5339d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611799 | ||||||
chr16:611799
|
AAGGGACA others(98): Show |
A | 1 | a0001c0001t0002g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.143-5408_143-5304d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611799 | ||||||
chr16:611813
|
T | C | 33 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(30): Show | 34 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.143-5395T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611813 | ||||||
chr16:611815
|
C | G | 33 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(30): Show | 34 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.143-5393C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611815 | ||||||
chr16:611867
|
CACGGGAC others(202): Show |
C | 3 | a0001c0001t0002g0247a0001c0001t0002g0300a0001c0001t0032g0020 | 3 | HG00280.hp2 HG01361.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.143-5339_143-5131d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611867 | |||||
chr16:611868
|
AC | A | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(76): Show | 84 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.143-5339delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611868 | ||||||
chr16:611902
|
CACGGGAC others(167): Show |
C | 18 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(15): Show | 18 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-5304_143-5131d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611902 | |||||
chr16:611903
|
AC | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(67): Show | 74 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.143-5304delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611903 | ||||||
chr16:611904
|
CGGGACAG others(27): Show |
C | 1 | a0001c0001t0027g0151 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-5269_143-5236d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611904 | |||||
chr16:611905
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.143-5303G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611905 | ||||||
chr16:611906
|
G | A | 1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-5302G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611906 | ||||||
chr16:611927
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.143-5281G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611927 | ||||||
chr16:611937
|
CAGGGACA others(28): Show |
C | 1 | a0001c0001t0002g0235 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.143-5222_143-5188d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611937 | |||||
chr16:611963
|
A | T | 13 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(10): Show | 13 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-5245A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611963 | ||||||
chr16:611971
|
CA | C | 68 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(65): Show | 72 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.143-5235delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611971 | |||||
chr16:611971
|
CAAGGGAC others(98): Show |
C | 1 | a0001c0001t0011g0291 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.143-5235_143-5131d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611971 | |||||
chr16:611972
|
A | AGGGACAG others(26): Show |
1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-5236_143-5235i others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611972 | ||||||
chr16:611988
|
GGCCTGTA others(28): Show |
G | 41 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(38): Show | 41 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.143-5200_143-5166d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611988 | |||||
chr16:611997
|
A | G | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-5211A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611997 | ||||||
chr16:611998
|
A | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0306 | 2 | HG03654.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.143-5210A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611998 | ||||||
chr16:612006
|
CA | C | 18 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0015others(15): Show | 19 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.143-5200delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612006 | |||||
chr16:612006
|
CAAGGGAC others(63): Show |
C | 12 | a0001c0001t0002g0016a0001c0001t0002g0182a0001c0001t0002g0183others(9): Show | 12 | HG01943.hp1 HG02683.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-5200_143-5131d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612006 | |||||
chr16:612021
|
T | C | 7 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(4): Show | 7 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-5187T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612021 | ||||||
chr16:612023
|
T | C | 14 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(11): Show | 14 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-5185T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612023 | ||||||
chr16:612023
|
T | G | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5185T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612023 | ||||||
chr16:612023
|
TGCCTGTA others(96): Show |
T | 1 | a0001c0001t0002g0288 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.143-5142_143-5040d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612023 | |||||
chr16:612024
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.143-5184G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612024 | ||||||
chr16:612033
|
A | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5175A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612033 | ||||||
chr16:612066
|
C | A | 72 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(69): Show | 76 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.143-5142C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612066 | ||||||
chr16:612067
|
A | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(38): Show | 41 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.143-5141A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612067 | ||||||
chr16:612075
|
CA | C | 60 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(57): Show | 62 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.143-5131delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612075 | |||||
chr16:612076
|
A | AAGGGACA others(27): Show |
3 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG00099.hp1 HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.143-4868_143-4835d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612076 | |||||
chr16:612076
|
AAGGGACA others(27): Show |
A | 5 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0103others(2): Show | 5 | HG01243.hp2 HG02080.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4868_143-4835d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612076 | |||||
chr16:612076
|
AAGGGACA others(61): Show |
A | 2 | a0001c0001t0001g0046a0001c0005t0001g0056 | 2 | NA18943.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.143-4902_143-4835d others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612076 | |||||
chr16:612077
|
A | C | 14 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(11): Show | 14 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-5131A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612077 | ||||||
chr16:612090
|
C | T | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5118C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612090 | ||||||
chr16:612092
|
G | C | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5116G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612092 | ||||||
chr16:612100
|
G | A | 2 | a0001c0001t0002g0258a0001c0001t0002g0301 | 2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.143-5108G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612100 | ||||||
chr16:612102
|
A | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0182a0001c0001t0002g0183others(8): Show | 11 | HG01943.hp1 HG02683.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-5106A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612102 | ||||||
chr16:612111
|
A | AC | 14 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(11): Show | 14 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-5097_143-5096i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612111 | ||||||
chr16:612122
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.143-5086C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612122 | ||||||
chr16:612124
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.143-5084C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612124 | ||||||
chr16:612126
|
G | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.143-5082G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612126 | ||||||
chr16:612136
|
A | T | 19 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(16): Show | 19 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-5072A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612136 | ||||||
chr16:612145
|
A | AC | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5063_143-5062i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612145 | ||||||
chr16:612158
|
C | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0182a0001c0001t0002g0183others(8): Show | 11 | HG01943.hp1 HG02683.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-5050C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612158 | ||||||
chr16:612160
|
G | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0182a0001c0001t0002g0183others(8): Show | 11 | HG01943.hp1 HG02683.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-5048G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612160 | ||||||
chr16:612170
|
A | T | 2 | a0001c0001t0002g0247a0001c0001t0002g0300 | 2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.143-5038A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612170 | ||||||
chr16:612178
|
C | CA | 9 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(6): Show | 9 | HG00738.hp2 HG01978.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-5029dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612178 | |||||
chr16:612179
|
A | AC | 51 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(48): Show | 52 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-5029_143-5028i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612179 | ||||||
chr16:612179
|
AGGGACAG others(26): Show |
A | 3 | a0001c0001t0002g0242a0001c0001t0002g0260a0001c0001t0002g0295 | 3 | HG01261.hp1 NA18966.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.143-5028_143-4996d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612179 | ||||||
chr16:612179
|
AGGGACAG others(60): Show |
A | 2 | a0001c0001t0002g0304a0001c0001t0002g0308 | 2 | NA18974.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.143-5028_143-4962d others(69): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612179 | ||||||
chr16:612192
|
C | T | 26 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(23): Show | 27 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.143-5016C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612192 | ||||||
chr16:612194
|
G | C | 19 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(16): Show | 19 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-5014G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612194 | ||||||
chr16:612194
|
G | GGCCTGTA others(28): Show |
1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-4995_143-4994i others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612194 | |||||
chr16:612194
|
G | T | 8 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(5): Show | 8 | HG00738.hp2 HG01978.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-5014G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612194 | ||||||
chr16:612203
|
A | C | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-5005A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612203 | ||||||
chr16:612204
|
A | T | 16 | a0001c0001t0002g0002a0001c0001t0002g0244a0001c0001t0002g0246others(13): Show | 16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-5004A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612204 | ||||||
chr16:612213
|
A | AC | 54 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(51): Show | 55 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.143-4995_143-4994i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612213 | ||||||
chr16:612226
|
C | T | 5 | a0001c0001t0002g0242a0001c0001t0002g0247a0001c0001t0002g0260others(2): Show | 5 | HG00280.hp2 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4982C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612226 | ||||||
chr16:612228
|
G | C | 2 | a0001c0001t0002g0247a0001c0001t0002g0300 | 2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.143-4980G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612228 | ||||||
chr16:612228
|
G | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0260a0001c0001t0002g0295 | 3 | HG01261.hp1 NA18966.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.143-4980G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612228 | ||||||
chr16:612237
|
A | C | 9 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0239others(6): Show | 9 | HG00738.hp2 HG01978.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-4971A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612237 | ||||||
chr16:612246
|
C | CA | 15 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0015others(12): Show | 16 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4961dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612246 | |||||
chr16:612247
|
A | AC | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0016others(29): Show | 32 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.143-4961_143-4960i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612247 | ||||||
chr16:612247
|
AGGGACAG others(94): Show |
A | 2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-4960_143-4860d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612247 | ||||||
chr16:612260
|
C | T | 24 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(21): Show | 24 | HG00544.hp1 HG00639.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-4948C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612260 | ||||||
chr16:612262
|
G | C | 16 | a0001c0001t0002g0002a0001c0001t0002g0244a0001c0001t0002g0246others(13): Show | 16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4946G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612262 | ||||||
chr16:612262
|
G | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0255others(5): Show | 8 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-4946G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612262 | ||||||
chr16:612271
|
A | C | 3 | a0001c0001t0002g0242a0001c0001t0002g0260a0001c0001t0002g0295 | 3 | HG01261.hp1 NA18966.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.143-4937A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612271 | ||||||
chr16:612272
|
ATCAAGAG others(95): Show |
A | 2 | a0001c0001t0002g0255a0001c0001t0002g0281 | 2 | NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.143-4892_143-4791d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612272 | |||||
chr16:612280
|
C | CA | 24 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0016others(21): Show | 24 | HG00280.hp1 HG00408.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-4927dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612280 | |||||
chr16:612281
|
A | AC | 21 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(18): Show | 21 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4927_143-4926i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612281 | ||||||
chr16:612281
|
AGGGACAG others(26): Show |
A | 21 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0021others(18): Show | 21 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-4926_143-4894d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612281 | ||||||
chr16:612281
|
AGGGACAG others(60): Show |
A | 1 | a0001c0001t0008g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-4926_143-4860d others(69): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612281 | ||||||
chr16:612284
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4924G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612284 | ||||||
chr16:612294
|
C | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0016others(18): Show | 21 | HG00280.hp1 HG00408.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-4914C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612294 | ||||||
chr16:612296
|
G | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0016others(18): Show | 21 | HG00280.hp1 HG00408.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-4912G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612296 | ||||||
chr16:612296
|
GGCCTGTA others(130): Show |
G | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0254others(1): Show | 4 | HG02300.hp2 HG04115.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-4858_143-4722d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612296 | |||||
chr16:612305
|
A | C | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0304others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-4903A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612305 | ||||||
chr16:612306
|
ATCAAGAG others(61): Show |
A | 17 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0180others(14): Show | 17 | HG00280.hp1 HG01070.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.143-4858_143-4791d others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612306 | |||||
chr16:612314
|
C | CA | 16 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0016others(13): Show | 16 | HG00639.hp1 HG01081.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-4893dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612314 | |||||
chr16:612315
|
A | AC | 16 | a0001c0001t0002g0002a0001c0001t0002g0244a0001c0001t0002g0246others(13): Show | 16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4893_143-4892i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612315 | ||||||
chr16:612315
|
AGGGACAG others(26): Show |
A | 4 | a0001c0001t0002g0247a0001c0001t0002g0265a0001c0001t0002g0268others(1): Show | 4 | HG00280.hp2 HG01071.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-4892_143-4860d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612315 | ||||||
chr16:612315
|
AGGGACAG others(129): Show |
A | 1 | a0001c0001t0008g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4892_143-4757d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612315 | ||||||
chr16:612328
|
C | T | 31 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(28): Show | 31 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-4880C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612328 | ||||||
chr16:612330
|
G | T | 30 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(27): Show | 30 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-4878G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612330 | ||||||
chr16:612330
|
GGCCTGTA others(96): Show |
G | 1 | a0001c0001t0002g0237 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.143-4834_143-4732d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612330 | |||||
chr16:612339
|
A | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0261a0001c0001t0002g0277others(1): Show | 4 | HG00408.hp2 HG02027.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-4869A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612339 | ||||||
chr16:612340
|
ATCAAGAG others(27): Show |
A | 25 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(22): Show | 25 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.143-4834_143-4801d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612340 | |||||
chr16:612348
|
C | CA | 23 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(20): Show | 23 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-4859dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612348 | |||||
chr16:612349
|
A | AC | 16 | a0001c0001t0002g0002a0001c0001t0002g0244a0001c0001t0002g0246others(13): Show | 16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4859_143-4858i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612349 | ||||||
chr16:612349
|
A | C | 5 | a0001c0001t0002g0247a0001c0001t0002g0300a0001c0001t0008g0039others(2): Show | 5 | HG00280.hp2 HG01361.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-4859A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612349 | ||||||
chr16:612349
|
AGGGACAG others(26): Show |
A | 1 | a0001c0001t0002g0261 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-4858_143-4826d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612349 | ||||||
chr16:612362
|
C | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(18): Show | 21 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4846C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612362 | ||||||
chr16:612364
|
G | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(18): Show | 21 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4844G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612364 | ||||||
chr16:612373
|
A | C | 5 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(2): Show | 5 | NA18966.hp2 NA18981.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4835A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612373 | ||||||
chr16:612374
|
T | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(59): Show | 64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.143-4834T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612374 | ||||||
chr16:612374
|
TTCAAGAG others(407): Show |
T | 28 | a0001c0001t0002g0235a0001c0001t0003g0160a0001c0001t0004g0162others(25): Show | 28 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.143-4651_143-4238d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612374 | |||||
chr16:612382
|
C | CA | 5 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(2): Show | 5 | NA18966.hp2 NA18981.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4825dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612382 | |||||
chr16:612383
|
AGGGACAG others(97): Show |
A | 1 | a0001c0001t0002g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143-4790_143-4687d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612383 | |||||
chr16:612392
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.143-4816C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612392 | ||||||
chr16:612398
|
GGCCTGTA others(28): Show |
G | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0277 | 3 | HG01081.hp2 HG02027.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.143-4790_143-4756d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612398 | |||||
chr16:612398
|
GGCCTGTA others(236): Show |
G | 2 | a0001c0001t0002g0278a0001c0001t0034g0156 | 2 | HG01978.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.143-4790_143-4548d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612398 | |||||
chr16:612405
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00099.hp1 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-4803A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612405 | ||||||
chr16:612407
|
A | C | 62 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(59): Show | 65 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.143-4801A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612407 | ||||||
chr16:612416
|
CA | C | 11 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(8): Show | 11 | HG00408.hp2 HG00738.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-4790delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612416 | |||||
chr16:612417
|
AAGGGACA others(63): Show |
A | 5 | a0001c0001t0002g0015a0001c0001t0002g0284a0001c0001t0002g0295others(2): Show | 5 | HG00639.hp1 HG02273.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4790_143-4721d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612417 | ||||||
chr16:612418
|
A | C | 1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-4790A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612418 | ||||||
chr16:612431
|
T | C | 74 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(71): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.143-4777T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612431 | ||||||
chr16:612433
|
C | G | 74 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(71): Show | 77 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.143-4775C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612433 | ||||||
chr16:612433
|
C | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0244a0001c0001t0002g0246others(18): Show | 21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4775C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612433 | ||||||
chr16:612461
|
C | T | 2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-4747C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612461 | ||||||
chr16:612465
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4743C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612465 | ||||||
chr16:612467
|
G | T | 1 | a0001c0001t0008g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4741G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612467 | ||||||
chr16:612476
|
A | C | 22 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(19): Show | 22 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.143-4732A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612476 | ||||||
chr16:612485
|
CACGGGAC others(202): Show |
C | 3 | a0001c0001t0002g0242a0001c0001t0002g0253a0001c0001t0002g0260 | 3 | HG01261.hp1 NA19001.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.143-4721_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612485 | |||||
chr16:612485
|
CACGGGAC others(236): Show |
C | 1 | a0001c0001t0002g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.143-4721_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612485 | |||||
chr16:612486
|
AC | A | 74 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(71): Show | 80 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.143-4721delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612486 | ||||||
chr16:612487
|
C | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(20): Show | 23 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.143-4721C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612487 | ||||||
chr16:612496
|
C | CGCCTTTG others(27): Show |
1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-4709_143-4708i others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612496 | |||||
chr16:612496
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4712C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612496 | ||||||
chr16:612511
|
A | C | 2 | a0001c0001t0008g0040a0001c0004t0023g0041 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-4697A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612511 | ||||||
chr16:612520
|
CACGGGAC others(167): Show |
C | 1 | a0001c0001t0002g0308 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.143-4686_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612520 | |||||
chr16:612521
|
AC | A | 98 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 106 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.143-4686delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612521 | ||||||
chr16:612522
|
C | A | 2 | a0001c0001t0008g0040a0001c0004t0023g0041 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-4686C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612522 | ||||||
chr16:612555
|
CACGGGAC others(132): Show |
C | 1 | a0001c0001t0002g0004 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.143-4651_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612555 | |||||
chr16:612556
|
AC | A | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-4651delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612556 | ||||||
chr16:612590
|
CAGGGACA others(97): Show |
C | 11 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0015others(8): Show | 11 | HG00408.hp2 HG00639.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-4582_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612590 | |||||
chr16:612590
|
CAGGGACA others(131): Show |
C | 1 | a0001c0001t0002g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.143-4582_143-4445d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612590 | |||||
chr16:612624
|
CA | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(18): Show | 21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4582delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612624 | |||||
chr16:612624
|
CAAGGGAC others(63): Show |
C | 66 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(63): Show | 69 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.143-4582_143-4513d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612624 | |||||
chr16:612624
|
CAAGGGAC others(97): Show |
C | 5 | a0001c0001t0002g0003a0001c0001t0002g0254a0001c0001t0002g0276others(2): Show | 5 | HG02027.hp1 HG02300.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-4582_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612624 | |||||
chr16:612639
|
T | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(18): Show | 21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4569T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612639 | ||||||
chr16:612641
|
T | G | 21 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(18): Show | 21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4567T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612641 | ||||||
chr16:612659
|
CAGGGACA others(407): Show |
C | 3 | a0001c0001t0003g0218a0001c0001t0003g0220a0001c0001t0003g0229 | 3 | HG03688.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-4539_143-4126d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612659 | |||||
chr16:612669
|
T | C | 34 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0054others(31): Show | 34 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.143-4539T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612669 | ||||||
chr16:612684
|
C | A | 23 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(20): Show | 23 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.143-4524C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612684 | ||||||
chr16:612693
|
CA | C | 23 | a0001c0001t0002g0002a0001c0001t0002g0237a0001c0001t0002g0244others(20): Show | 23 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.143-4513delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612693 | |||||
chr16:612694
|
AAGGGACA others(27): Show |
A | 1 | a0001c0001t0027g0151 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-4410_143-4377d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612694 | |||||
chr16:612720
|
A | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4488A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612720 | ||||||
chr16:612754
|
A | T | 1 | a0001c0001t0002g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.143-4454A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612754 | ||||||
chr16:612773
|
G | A | 2 | a0001c0001t0002g0283a0001c0001t0002g0293 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.143-4435G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612773 | ||||||
chr16:612776
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4432C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612776 | ||||||
chr16:612778
|
G | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4430G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612778 | ||||||
chr16:612788
|
A | T | 159 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(156): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.143-4420A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612788 | ||||||
chr16:612832
|
A | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4376A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612832 | ||||||
chr16:612841
|
C | T | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-4367C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612841 | ||||||
chr16:612845
|
T | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4363T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612845 | ||||||
chr16:612847
|
C | G | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4361C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612847 | ||||||
chr16:612936
|
C | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4272C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612936 | ||||||
chr16:612946
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.143-4262G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612946 | ||||||
chr16:612949
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4259C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612949 | ||||||
chr16:612951
|
G | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4257G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612951 | ||||||
chr16:612976
|
A | T | 1 | a0001c0001t0007g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.143-4232A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612976 | ||||||
chr16:612980
|
G | A | 101 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(98): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-4228G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612980 | ||||||
chr16:612994
|
A | C | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4214A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612994 | ||||||
chr16:612994
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.143-4214A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612994 | ||||||
chr16:613004
|
AAGGGACA others(27): Show |
A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4190_143-4157d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 613004 | |||||
chr16:613063
|
CATCAAGA others(28): Show |
C | 55 | a0001c0001t0001g0073a0001c0001t0001g0227a0001c0001t0003g0014others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.143-4099_143-4065d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 613063 | |||||
chr16:613098
|
A | C | 3 | a0001c0001t0003g0218a0001c0001t0003g0220a0001c0001t0003g0229 | 3 | HG03688.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-4110A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613098 | ||||||
chr16:613127
|
CTGTAGAA others(160): Show |
C | 2 | a0001c0001t0013g0024a0001c0001t0013g0036 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-4050_143-3884d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 613127 | |||||
chr16:613136
|
CAA | C | 3 | a0001c0001t0006g0171a0001c0001t0006g0172a0001c0001t0006g0173 | 3 | HG01981.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.143-4071_143-4070d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613136 | ||||||
chr16:613193
|
A | G | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-4015A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613193 | ||||||
chr16:613218
|
G | T | 24 | a0001c0001t0003g0160a0001c0001t0004g0162a0001c0001t0004g0164others(21): Show | 24 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-3990G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613218 | ||||||
chr16:613294
|
T | G | 2 | a0001c0001t0003g0218a0001c0001t0003g0229 | 2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-3914T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613294 | ||||||
chr16:613319
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.143-3889C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613319 | ||||||
chr16:613389
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.143-3819G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613389 | ||||||
chr16:613395
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-3813G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613395 | ||||||
chr16:613430
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0002g0298 | 2 | HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.143-3778C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613430 | ||||||
chr16:613431
|
G | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-3777G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613431 | ||||||
chr16:613546
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.143-3662G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613546 | ||||||
chr16:613687
|
G | A | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-3521G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613687 | ||||||
chr16:613841
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.143-3367T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613841 | ||||||
chr16:613880
|
G | A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-3328G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613880 | ||||||
chr16:614013
|
A | AGATGGTG others(24): Show |
1 | a0001c0001t0005g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143-3181_143-3151d others(33): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614013 | |||||
chr16:614037
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.143-3171C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614037 | ||||||
chr16:614105
|
C | T | 4 | a0001c0001t0002g0256a0001c0001t0007g0157a0001c0001t0007g0158others(1): Show | 4 | HG02622.hp1 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-3103C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614105 | ||||||
chr16:614160
|
A | ATCCCGAT others(54): Show |
1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-3031_143-3030i others(63): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614160 | |||||
chr16:614176
|
GC | G | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-3030delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614176 | |||||
chr16:614179
|
G | T | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-3029G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614179 | ||||||
chr16:614186
|
A | G | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-3022A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614186 | ||||||
chr16:614189
|
G | A | 1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-3019G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614189 | ||||||
chr16:614196
|
T | G | 187 | a0001c0001t0001g0006a0001c0001t0001g0227a0001c0001t0002g0002others(184): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.143-3012T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614196 | ||||||
chr16:614207
|
G | GC | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-3000dupC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614207 | |||||
chr16:614216
|
G | A | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2992G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614216 | ||||||
chr16:614217
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.143-2991C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614217 | ||||||
chr16:614219
|
G | A | 1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2989G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614219 | ||||||
chr16:614219
|
G | T | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2989G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614219 | ||||||
chr16:614221
|
A | G | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2987A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614221 | ||||||
chr16:614225
|
C | T | 1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2983C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614225 | ||||||
chr16:614240
|
T | A | 1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2968T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614240 | ||||||
chr16:614245
|
C | T | 1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2963C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614245 | ||||||
chr16:614246
|
T | TACCACAT others(81): Show |
1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2959_143-2958i others(90): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614246 | |||||
chr16:614246
|
T | TACCACAT others(81): Show |
23 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(20): Show | 23 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-2959_143-2958i others(90): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614246 | |||||
chr16:614246
|
T | TACCACAT others(81): Show |
32 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(29): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-2959_143-2958i others(90): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614246 | |||||
chr16:614278
|
A | G | 1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2930A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614278 | ||||||
chr16:614281
|
A | G | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2927A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614281 | ||||||
chr16:614299
|
G | GC | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2908dupC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614299 | |||||
chr16:614308
|
G | A | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2900G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614308 | ||||||
chr16:614341
|
G | A | 57 | a0001c0001t0001g0227a0001c0001t0002g0269a0001c0001t0003g0014others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2867G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614341 | ||||||
chr16:614351
|
G | A | 1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-2857G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614351 | ||||||
chr16:614405
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.143-2803C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614405 | ||||||
chr16:614428
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2780C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614428 | ||||||
chr16:614429
|
C | T | 2 | a0001c0001t0002g0257a0001c0001t0032g0020 | 2 | HG03669.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.143-2779C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614429 | ||||||
chr16:614492
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2716C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614492 | ||||||
chr16:614493
|
ATCCCGAT others(24): Show |
A | 1 | a0001c0001t0001g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.143-2696_143-2666d others(33): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614493 | |||||
chr16:614497
|
C | T | 1 | a0001c0005t0001g0056 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.143-2711C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614497 | ||||||
chr16:614551
|
G | A | 56 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2657G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614551 | ||||||
chr16:614555
|
C | T | 5 | a0001c0001t0008g0039a0001c0001t0008g0040a0001c0001t0013g0024others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-2653C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614555 | ||||||
chr16:614556
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2652G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614556 | ||||||
chr16:614580
|
G | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2628G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614580 | ||||||
chr16:614582
|
A | G | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2626A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614582 | ||||||
chr16:614587
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2621G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614587 | ||||||
chr16:614611
|
A | ACATCCCA others(116): Show |
2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.143-2591_143-2590i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | |||||
chr16:614611
|
A | ACATCCCA others(116): Show |
52 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(49): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.143-2591_143-2590i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | |||||
chr16:614611
|
A | ACATCCCA others(116): Show |
1 | a0001c0001t0003g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.143-2591_143-2590i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | |||||
chr16:614611
|
A | ACATCCCG others(116): Show |
1 | a0001c0001t0005g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2475_143-2474i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | |||||
chr16:614611
|
A | G | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2597A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614611 | ||||||
chr16:614647
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.143-2561C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614647 | ||||||
chr16:614797
|
G | A | 1 | a0001c0001t0006g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-2411G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614797 | ||||||
chr16:614802
|
G | A | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-2406G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614802 | ||||||
chr16:614825
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143-2383C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614825 | ||||||
chr16:614915
|
A | G | 1 | a0001c0001t0009g0317 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143-2293A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614915 | ||||||
chr16:615185
|
C | T | 2 | a0001c0001t0009g0316a0001c0001t0009g0317 | 2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.143-2023C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615185 | ||||||
chr16:615266
|
A | G | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-1942A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615266 | ||||||
chr16:615305
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-1903C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615305 | ||||||
chr16:615323
|
A | G | 57 | a0001c0001t0001g0227a0001c0001t0002g0292a0001c0001t0003g0014others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-1885A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615323 | ||||||
chr16:615405
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.143-1803C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615405 | ||||||
chr16:615439
|
C | T | 1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-1769C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615439 | ||||||
chr16:615606
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.143-1602G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615606 | ||||||
chr16:615625
|
G | A | 21 | a0001c0001t0003g0160a0001c0001t0004g0162a0001c0001t0004g0164others(18): Show | 21 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-1583G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615625 | ||||||
chr16:615732
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(40): Show | 47 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.143-1476C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615732 | ||||||
chr16:615777
|
C | T | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.143-1431C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615777 | ||||||
chr16:615811
|
A | C | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-1397A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615811 | ||||||
chr16:615860
|
G | T | 1 | a0001c0001t0005g0233 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.143-1348G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615860 | ||||||
chr16:615877
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-1331G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615877 | ||||||
chr16:615886
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0066others(14): Show | 17 | HG00140.hp2 HG00733.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.143-1322C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615886 | ||||||
chr16:615891
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.143-1317G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615891 | ||||||
chr16:615957
|
A | G | 1 | a0001c0001t0031g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-1251A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615957 | ||||||
chr16:616028
|
C | T | 1 | a0001c0001t0007g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.143-1180C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616028 | ||||||
chr16:616149
|
A | G | 186 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(183): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.143-1059A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616149 | ||||||
chr16:616151
|
C | G | 57 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-1057C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616151 | ||||||
chr16:616255
|
C | CA | 11 | a0001c0001t0001g0044a0001c0001t0001g0065a0001c0001t0001g0081others(8): Show | 11 | HG01891.hp1 HG02083.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-938dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616255 | |||||
chr16:616273
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143-935C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616273 | ||||||
chr16:616320
|
C | T | 11 | a0001c0001t0003g0160a0001c0001t0006g0031a0001c0001t0007g0037others(8): Show | 11 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-888C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616320 | ||||||
chr16:616333
|
T | TTTTA | 91 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(88): Show | 99 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.143-844_143-841dup others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | |||||
chr16:616333
|
T | TTTTATTT others(1): Show |
126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 136 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.143-848_143-841dup others(8): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | |||||
chr16:616333
|
T | TTTTATTT others(5): Show |
22 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0094others(19): Show | 22 | HG00099.hp2 HG01074.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.143-852_143-841dup others(12): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | |||||
chr16:616333
|
T | TTTTATTT others(9): Show |
29 | a0001c0001t0003g0014a0001c0001t0003g0174a0001c0001t0003g0176others(26): Show | 30 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-856_143-841dup others(16): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | |||||
chr16:616333
|
T | TTTTATTT others(13): Show |
11 | a0001c0001t0003g0175a0001c0001t0003g0177a0001c0001t0003g0179others(8): Show | 11 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-860_143-841dup others(20): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | |||||
chr16:616382
|
A | G | 199 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0044others(196): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.143-826A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616382 | ||||||
chr16:616393
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-815C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616393 | ||||||
chr16:616474
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-734G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616474 | ||||||
chr16:616482
|
G | C | 37 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(34): Show | 38 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.143-726G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616482 | ||||||
chr16:616517
|
T | G | 185 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(182): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.143-691T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616517 | ||||||
chr16:616528
|
C | T | 19 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(16): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.143-680C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616528 | ||||||
chr16:616584
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-624C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616584 | ||||||
chr16:616686
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143-522G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616686 | ||||||
chr16:616709
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.143-499C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616709 | ||||||
chr16:617108
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.143-100G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617108 | ||||||
chr16:617110
|
G | A | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.143-98G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617110 | ||||||
chr16:617158
|
G | A | 1 | a0001c0001t0002g0271 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.143-50G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617158 | ||||||
chr16:617177
|
C | T | 4 | a0001c0001t0002g0016a0001c0001t0002g0264a0001c0001t0002g0278others(1): Show | 5 | HG00280.hp1 HG01074.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-31C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617177 | ||||||
chr16:617203
|
C | T | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.143-5C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617203 | ||||||
chr16:617311
|
A | G | 24 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(21): Show | 24 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.203+43A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617311 | ||||||
chr16:617345
|
C | T | 1 | a0001c0001t0010g0035 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.203+77C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617345 | ||||||
chr16:617396
|
C | G | 24 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(21): Show | 24 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.203+128C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617396 | ||||||
chr16:617440
|
GTCTGGGA others(44): Show |
G | 1 | a0001c0001t0003g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.203+173_203+223del others(51): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617440 | ||||||
chr16:617457
|
C | A | 1 | a0001c0001t0003g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.203+189C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617457 | ||||||
chr16:617467
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.203+199G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617467 | ||||||
chr16:617490
|
A | G | 60 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.203+222A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617490 | ||||||
chr16:617513
|
A | G | 59 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.203+245A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617513 | ||||||
chr16:617554
|
A | G | 17 | a0001c0001t0003g0160a0001c0001t0004g0162a0001c0001t0004g0164others(14): Show | 17 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.203+286A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617554 | ||||||
chr16:617583
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.203+315C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617583 | ||||||
chr16:617628
|
AG | A | 109 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(106): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.203+362delG | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 617628 | |||||
chr16:617791
|
T | A | 33 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.204-409T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617791 | ||||||
chr16:617799
|
C | T | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.204-401C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617799 | ||||||
chr16:617849
|
GA | G | 24 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(21): Show | 24 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.204-339delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 617849 | |||||
chr16:618034
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.204-166G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618034 | ||||||
chr16:618099
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0195 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.204-101C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618099 | ||||||
chr16:618165
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204-35A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618165 | ||||||
chr16:618173
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.204-27G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618173 | ||||||
chr16:618185
|
C | T | 1 | a0001c0001t0010g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.204-15C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618185 | ||||||
chr16:618274
|
C | T | 2 | a0001c0001t0011g0291a0001c0001t0011g0302 | 2 | NA18954.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.264+14C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618274 | ||||||
chr16:618297
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.264+37G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618297 | ||||||
chr16:618443
|
A | G | 190 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(187): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.264+183A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618443 | ||||||
chr16:618451
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.264+191A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618451 | ||||||
chr16:618540
|
G | GGGTGTAC others(603): Show |
1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.264+347_264+956dup others(610): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618540 | |||||
chr16:618540
|
GGGTGTAC others(728): Show |
G | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264+397_264+1131de others(1): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618540 | |||||
chr16:618563
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.264+303T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618563 | ||||||
chr16:618606
|
G | A | 1 | a0001c0001t0012g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.264+346G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618606 | ||||||
chr16:618672
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.264+412C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618672 | ||||||
chr16:618685
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.264+425G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618685 | ||||||
chr16:618711
|
CAG | C | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+452_264+453del others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618711 | ||||||
chr16:618718
|
A | T | 1 | a0001c0001t0003g0191 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.264+458A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618718 | ||||||
chr16:618722
|
G | GTA | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+463_264+464ins others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618722 | |||||
chr16:618751
|
A | G | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+491A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618751 | ||||||
chr16:618752
|
C | G | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+492C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618752 | ||||||
chr16:618843
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.264+583A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618843 | ||||||
chr16:618854
|
T | C | 1 | a0001c0001t0003g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.264+594T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618854 | ||||||
chr16:618885
|
A | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0313 | 3 | HG01261.hp2 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.264+625A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618885 | ||||||
chr16:618902
|
T | G | 27 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(24): Show | 27 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.264+642T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618902 | ||||||
chr16:618907
|
T | TGTG | 189 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(186): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.264+648_264+650dup others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618907 | |||||
chr16:618930
|
G | T | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+670G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618930 | ||||||
chr16:618971
|
G | A | 3 | a0001c0001t0012g0154a0001c0001t0012g0155a0001c0001t0021g0185 | 3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.264+711G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618971 | ||||||
chr16:618975
|
T | G | 27 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(24): Show | 27 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.264+715T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618975 | ||||||
chr16:619073
|
C | CGGCCATG others(116): Show |
1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+852_264+853ins others(123): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619073 | |||||
chr16:619074
|
G | A | 2 | a0001c0001t0010g0035a0001c0001t0010g0038 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+814G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619074 | ||||||
chr16:619153
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.264+893T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619153 | ||||||
chr16:619259
|
AGT | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | NA18940.hp1 NA18979.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+1007_264+1008d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619259 | |||||
chr16:619268
|
G | GCAGGTGT others(360): Show |
1 | a0001c0001t0003g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.264+1061_264+1062i others(369): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619268 | |||||
chr16:619274
|
GTGGTGTA others(118): Show |
G | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+1020_264+1144d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619274 | |||||
chr16:619283
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(6): Show | 9 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+1023T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619283 | ||||||
chr16:619342
|
C | G | 1 | a0001c0001t0003g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.264+1082C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619342 | ||||||
chr16:619416
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+1156C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619416 | ||||||
chr16:619480
|
G | T | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+1220G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619480 | ||||||
chr16:619708
|
T | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0028others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.264+1448T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619708 | ||||||
chr16:619784
|
C | A | 5 | a0001c0001t0007g0320a0001c0001t0010g0035a0001c0001t0010g0038others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+1524C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619784 | ||||||
chr16:619857
|
G | T | 55 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.264+1597G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619857 | ||||||
chr16:619865
|
A | G | 5 | a0001c0001t0001g0227a0001c0001t0003g0215a0001c0001t0003g0218others(2): Show | 5 | HG01074.hp2 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1605A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619865 | ||||||
chr16:619872
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0129 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.264+1612G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619872 | ||||||
chr16:619961
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.264+1701C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619961 | ||||||
chr16:619995
|
G | A | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+1735G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619995 | ||||||
chr16:620097
|
A | G | 1 | a0001c0001t0002g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.264+1837A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620097 | ||||||
chr16:620117
|
T | C | 203 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0044others(200): Show | 213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.264+1857T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620117 | ||||||
chr16:620122
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0189 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.264+1862C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620122 | ||||||
chr16:620133
|
G | T | 1 | a0001c0001t0002g0283 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.264+1873G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620133 | ||||||
chr16:620168
|
A | G | 190 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(187): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.264+1908A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620168 | ||||||
chr16:620336
|
TGAGCCGA others(28): Show |
T | 4 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034others(1): Show | 4 | HG02257.hp2 HG03139.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+2079_264+2113d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620336 | |||||
chr16:620341
|
C | T | 1 | a0001c0001t0013g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264+2081C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620341 | ||||||
chr16:620371
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+2111C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620371 | ||||||
chr16:620391
|
C | CA | 6 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 6 | HG00621.hp2 HG02083.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+2140dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620391 | |||||
chr16:620470
|
C | A | 7 | a0001c0001t0004g0162a0001c0001t0004g0164a0001c0001t0004g0165others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+2210C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620470 | ||||||
chr16:620522
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+2262C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620522 | ||||||
chr16:620596
|
AGGCTCCA others(27): Show |
A | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+2345_264+2378d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620596 | |||||
chr16:620605
|
T | C | 194 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(191): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.264+2345T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620605 | ||||||
chr16:620626
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.264+2366C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620626 | ||||||
chr16:620664
|
CGGGCTCC others(27): Show |
C | 2 | a0001c0001t0002g0069a0001c0001t0018g0091 | 2 | NA18988.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.264+2434_264+2467d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620664 | |||||
chr16:620692
|
CCCCGATG others(29): Show |
C | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+2435_264+2470d others(38): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620692 | |||||
chr16:620693
|
C | CCCGACGG others(28): Show |
1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.264+2437_264+2438i others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620693 | |||||
chr16:620698
|
T | C | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.264+2438T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620698 | ||||||
chr16:620698
|
T | TGGGCTCC others(28): Show |
1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+2534_264+2568d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620698 | |||||
chr16:620698
|
TGGGCTCC others(28): Show |
T | 72 | a0001c0001t0001g0108a0001c0001t0001g0227a0001c0001t0003g0014others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.264+2534_264+2568d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620698 | |||||
chr16:620710
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0002g0259 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.264+2450C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620710 | ||||||
chr16:620712
|
G | A | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.264+2452G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620712 | ||||||
chr16:620724
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0051others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+2464C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620724 | ||||||
chr16:620727
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.264+2467C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620727 | ||||||
chr16:620730
|
C | T | 1 | a0001c0001t0006g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.264+2470C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620730 | ||||||
chr16:620733
|
C | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+2473C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620733 | ||||||
chr16:620765
|
C | T | 16 | a0001c0001t0004g0162a0001c0001t0004g0164a0001c0001t0004g0165others(13): Show | 16 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.264+2505C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620765 | ||||||
chr16:620794
|
C | A | 5 | a0001c0001t0003g0178a0001c0001t0003g0202a0001c0001t0003g0206others(2): Show | 5 | HG03098.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+2534C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620794 | ||||||
chr16:620795
|
CCCGCCGA others(27): Show |
C | 5 | a0001c0001t0003g0178a0001c0001t0003g0202a0001c0001t0003g0206others(2): Show | 5 | HG03098.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+2538_264+2571d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620795 | |||||
chr16:620853
|
A | G | 3 | a0001c0001t0006g0031a0001c0001t0007g0037a0001c0001t0028g0033 | 3 | HG03225.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.264+2593A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620853 | ||||||
chr16:620895
|
G | C | 1 | a0001c0001t0002g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.264+2635G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620895 | ||||||
chr16:620934
|
T | A | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264+2674T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620934 | ||||||
chr16:620964
|
G | T | 22 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(19): Show | 22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+2704G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620964 | ||||||
chr16:620998
|
C | T | 2 | a0001c0001t0002g0283a0001c0001t0002g0293 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.264+2738C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620998 | ||||||
chr16:621209
|
G | A | 1 | a0001c0001t0002g0294 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+2949G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621209 | ||||||
chr16:621211
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0195 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.264+2951C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621211 | ||||||
chr16:621233
|
C | G | 1 | a0001c0001t0002g0271 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.264+2973C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621233 | ||||||
chr16:621245
|
G | A | 58 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.264+2985G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621245 | ||||||
chr16:621257
|
GTC | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+3002_264+3003d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 621257 | |||||
chr16:621415
|
TA | T | 4 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034others(1): Show | 4 | HG02257.hp2 HG03139.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+3156delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621415 | ||||||
chr16:621451
|
G | A | 3 | a0001c0001t0012g0154a0001c0001t0012g0155a0001c0001t0021g0185 | 3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.264+3191G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621451 | ||||||
chr16:621453
|
G | T | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+3193G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621453 | ||||||
chr16:621502
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.264+3242C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621502 | ||||||
chr16:621527
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.264+3267C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621527 | ||||||
chr16:621556
|
C | T | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+3296C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621556 | ||||||
chr16:621653
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.264+3393C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621653 | ||||||
chr16:621682
|
A | G | 196 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(193): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.264+3422A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621682 | ||||||
chr16:621906
|
G | A | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.265-3526G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621906 | ||||||
chr16:621914
|
G | C | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-3518G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621914 | ||||||
chr16:621919
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG03491.hp1 HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.265-3513G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621919 | ||||||
chr16:621939
|
G | A | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-3493G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621939 | ||||||
chr16:621987
|
A | G | 7 | a0001c0001t0002g0004a0001c0001t0002g0237a0001c0001t0002g0238others(4): Show | 9 | HG01081.hp2 NA18945.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-3445A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621987 | ||||||
chr16:622040
|
G | A | 119 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(116): Show | 127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.265-3392G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622040 | ||||||
chr16:622243
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-3189C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622243 | ||||||
chr16:622244
|
G | A | 2 | a0001c0001t0010g0035a0001c0001t0010g0038 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.265-3188G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622244 | ||||||
chr16:622284
|
G | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0286 | 2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.265-3148G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622284 | ||||||
chr16:622328
|
A | G | 1 | a0001c0001t0002g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.265-3104A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622328 | ||||||
chr16:622361
|
C | G | 31 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0051others(28): Show | 32 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.265-3071C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622361 | ||||||
chr16:622406
|
ACGT | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0051others(7): Show | 11 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.265-3024_265-3022d others(5): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 622406 | |||||
chr16:622412
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.265-3020G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622412 | ||||||
chr16:622469
|
G | A | 13 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0196others(10): Show | 13 | HG01074.hp2 HG01106.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.265-2963G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622469 | ||||||
chr16:622478
|
T | C | 2 | a0001c0001t0002g0263a0001c0001t0002g0288 | 2 | NA19007.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.265-2954T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622478 | ||||||
chr16:622484
|
C | G | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-2948C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622484 | ||||||
chr16:622506
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.265-2926C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622506 | ||||||
chr16:622507
|
G | A | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.265-2925G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622507 | ||||||
chr16:622548
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.265-2884G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622548 | ||||||
chr16:622598
|
C | T | 1 | a0001c0001t0034g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-2834C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622598 | ||||||
chr16:622627
|
G | C | 48 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0174others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.265-2805G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622627 | ||||||
chr16:622661
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.265-2771G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622661 | ||||||
chr16:622662
|
C | T | 1 | a0001c0001t0002g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.265-2770C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622662 | ||||||
chr16:622799
|
T | C | 194 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0044others(191): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.265-2633T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622799 | ||||||
chr16:622919
|
C | T | 1 | a0001c0001t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.265-2513C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622919 | ||||||
chr16:622972
|
G | A | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.265-2460G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622972 | ||||||
chr16:622991
|
C | T | 3 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0016g0321 | 3 | HG02083.hp2 NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.265-2441C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622991 | ||||||
chr16:623044
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0315 | 2 | HG00280.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.265-2388G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623044 | ||||||
chr16:623060
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.265-2372C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623060 | ||||||
chr16:623158
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.265-2274G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623158 | ||||||
chr16:623167
|
A | G | 3 | a0001c0001t0007g0157a0001c0001t0007g0158a0001c0001t0007g0159 | 3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.265-2265A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623167 | ||||||
chr16:623200
|
C | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0127a0001c0001t0001g0150 | 4 | HG01106.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-2232C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623200 | ||||||
chr16:623277
|
C | T | 106 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(103): Show | 114 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.265-2155C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623277 | ||||||
chr16:623371
|
C | T | 1 | a0001c0001t0012g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265-2061C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623371 | ||||||
chr16:623376
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.265-2056G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623376 | ||||||
chr16:623383
|
C | G | 2 | a0001c0001t0002g0286a0001c0001t0032g0020 | 2 | HG03490.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.265-2049C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623383 | ||||||
chr16:623398
|
C | T | 13 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0003g0176others(10): Show | 13 | HG01884.hp1 HG02280.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.265-2034C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623398 | ||||||
chr16:623430
|
G | A | 95 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0044others(92): Show | 98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.265-2002G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623430 | ||||||
chr16:623454
|
C | T | 36 | a0001c0001t0002g0017a0001c0001t0002g0022a0001c0001t0002g0244others(33): Show | 37 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.265-1978C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623454 | ||||||
chr16:623465
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-1967C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623465 | ||||||
chr16:623515
|
A | G | 1 | a0001c0001t0003g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.265-1917A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623515 | ||||||
chr16:623537
|
C | T | 1 | a0001c0001t0029g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.265-1895C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623537 | ||||||
chr16:623577
|
C | A | 24 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.265-1855C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623577 | ||||||
chr16:623584
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.265-1848C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623584 | ||||||
chr16:623596
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.265-1836G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623596 | ||||||
chr16:623636
|
C | CA | 14 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0068others(11): Show | 14 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-1780dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 623636 | |||||
chr16:623636
|
CA | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0168a0001c0001t0002g0021others(3): Show | 6 | HG01993.hp1 HG01993.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-1780delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 623636 | |||||
chr16:623793
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.265-1639A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623793 | ||||||
chr16:623948
|
A | T | 1 | a0001c0001t0002g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.265-1484A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623948 | ||||||
chr16:624006
|
C | G | 1 | a0001c0001t0002g0270 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.265-1426C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624006 | ||||||
chr16:624024
|
T | C | 105 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(102): Show | 113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-1408T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624024 | ||||||
chr16:624029
|
C | T | 105 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(102): Show | 113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-1403C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624029 | ||||||
chr16:624060
|
G | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0252 | 2 | NA18981.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.265-1372G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624060 | ||||||
chr16:624090
|
C | T | 2 | a0001c0001t0002g0275a0001c0001t0002g0276 | 2 | NA18988.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.265-1342C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624090 | ||||||
chr16:624205
|
C | A | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.265-1227C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624205 | ||||||
chr16:624424
|
G | A | 195 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(192): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.265-1008G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624424 | ||||||
chr16:624565
|
T | TA | 3 | a0001c0001t0001g0124a0001c0001t0002g0325a0002c0002t0024g0234 | 3 | HG00741.hp1 NA18957.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.265-862dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 624565 | |||||
chr16:624571
|
C | T | 1 | a0001c0001t0032g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-861C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624571 | ||||||
chr16:624601
|
C | T | 24 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0211others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.265-831C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624601 | ||||||
chr16:624737
|
G | A | 105 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(102): Show | 113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-695G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624737 | ||||||
chr16:624770
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.265-662G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624770 | ||||||
chr16:625067
|
C | A | 15 | a0001c0001t0002g0017a0001c0001t0002g0021a0001c0001t0002g0022others(12): Show | 16 | HG00639.hp1 HG00741.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.265-365C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625067 | ||||||
chr16:625087
|
AC | A | 126 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(123): Show | 134 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.265-344delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625087 | ||||||
chr16:625101
|
C | T | 8 | a0001c0001t0003g0160a0001c0001t0006g0031a0001c0001t0006g0171others(5): Show | 8 | HG01884.hp2 HG01981.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.265-331C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625101 | ||||||
chr16:625215
|
G | A | 127 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(124): Show | 135 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.265-217G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625215 | ||||||
chr16:625281
|
G | C | 18 | a0001c0001t0004g0162a0001c0001t0004g0164a0001c0001t0004g0165others(15): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.265-151G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625281 | ||||||
chr16:625310
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.265-122C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625310 | ||||||
chr16:625617
|
C | A | 18 | a0001c0001t0004g0162a0001c0001t0004g0164a0001c0001t0004g0165others(15): Show | 18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+108C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625617 | ||||||
chr16:625680
|
T | C | 195 | a0001c0001t0001g0227a0001c0001t0002g0002a0001c0001t0002g0003others(192): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.342+171T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625680 | ||||||
chr16:625709
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0129 | 2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.343-190C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625709 | ||||||
chr16:625712
|
C | T | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.343-187C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625712 | ||||||
chr16:625776
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.343-123G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625776 | ||||||
chr16:625863
|
C | T | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.343-36C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625863 | ||||||
chr16:625874
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG02257.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.343-25C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625874 | ||||||
chr16:626155
|
C | T | 1 | a0001c0004t0023g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.565+34C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626155 | ||||||
chr16:626180
|
A | G | 1 | a0001c0001t0007g0320 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.565+59A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626180 | ||||||
chr16:626184
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565+63A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626184 | ||||||
chr16:626216
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.565+95G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626216 | ||||||
chr16:626239
|
G | A | 2 | a0001c0001t0010g0038a0001c0001t0020g0034 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.565+118G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626239 | ||||||
chr16:626257
|
C | G | 1 | a0002c0002t0024g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.565+136C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626257 | ||||||
chr16:626261
|
G | C | 65 | a0001c0001t0001g0227a0001c0001t0003g0014a0001c0001t0003g0160others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.565+140G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626261 | ||||||
chr16:626325
|
G | A | 3 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0195 | 3 | HG02280.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.565+204G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626325 | ||||||
chr16:626492
|
G | A | 31 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0003g0176others(28): Show | 31 | HG01433.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+371G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626492 | ||||||
chr16:626686
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565+565C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626686 | ||||||
chr16:626735
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.566-607C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626735 | ||||||
chr16:626795
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.566-547G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626795 | ||||||
chr16:626898
|
A | G | 1 | a0001c0001t0029g0188 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.566-444A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626898 | ||||||
chr16:626989
|
C | T | 75 | a0001c0001t0001g0101a0001c0001t0002g0315a0001c0001t0003g0014others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.566-353C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626989 | ||||||
chr16:627000
|
T | A | 3 | a0001c0001t0010g0035a0001c0001t0010g0038a0001c0001t0020g0034 | 3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.566-342T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 627000 | ||||||
chr16:627020
|
G | T | 125 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(122): Show | 133 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.566-322G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 627020 | ||||||
chr16:627191
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566-151G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 627191 |