geneid | 126129 |
---|---|
ensemblid | ENSG00000169169.15 |
hgncid | 18540 |
symbol | CPT1C |
name | carnitine palmitoyltransferase 1C |
refseq_nuc | NM_001199753.2 |
refseq_prot | NP_001186682.1 |
ensembl_nuc | ENST00000598293.6 |
ensembl_prot | ENSP00000473028.1 |
mane_status | MANE Select |
chr | chr19 |
start | 49691116 |
end | 49713731 |
strand | + |
ver | v1.2 |
region | chr19:49691116-49713731 |
region5000 | chr19:49686116-49718731 |
regionname0 | CPT1C_chr19_49691116_49713731 |
regionname5000 | CPT1C_chr19_49686116_49718731 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 803 | 331 | 82 | 64 | 124 | 14 | 45 | 80 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002 | 0/0 | 328 | 16 | 2 | 7 | 6 | 0 | 1 | 4 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0003 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0004 | 0/0 | 803 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0005 | 0/0 | 803 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2412 | 308 | 80 | 50 | 122 | 12 | 42 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0002 | 0/0 | 2412 | 13 | 1 | 10 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0003 | 0/0 | 2413 | 13 | 2 | 4 | 6 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0004 | 0/0 | 2412 | 4 | 1 | 0 | 0 | 2 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0005 | 0/0 | 2413 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0006 | 0/0 | 2412 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0007 | 0/0 | 2413 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0008 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0009 | 0/0 | 2412 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0010 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0011 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
c0012 | 0/0 | 2412 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 435 | 209 | 41 | 40 | 93 | 10 | 24 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
t0002 | 0/1 | 435 | 92 | 21 | 31 | 25 | 4 | 10 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
t0003 | 0/0 | 435 | 40 | 20 | 1 | 11 | 0 | 8 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
t0004 | 0/0 | 435 | 4 | 0 | 0 | 0 | 0 | 4 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
t0005 | 0/0 | 435 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
t0006 | 0/0 | 435 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
t0007 | 0/0 | 435 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2412 | 308 | 80 | 50 | 122 | 12 | 42 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0002 | 0/0 | 2412 | 13 | 1 | 10 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0004 | 0/0 | 2412 | 4 | 1 | 0 | 0 | 2 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0006 | 0/0 | 2412 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0008 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0009 | 0/0 | 2412 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0012 | 0/0 | 2412 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0003 | 0/0 | 2413 | 13 | 2 | 4 | 6 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0005 | 0/0 | 2413 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0003c0007 | 0/0 | 2413 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0004c0011 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0005c0010 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2846 | 195 | 40 | 31 | 89 | 10 | 24 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0001t0002 | 0/1 | 2846 | 67 | 17 | 18 | 22 | 2 | 7 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0001t0003 | 0/0 | 2846 | 38 | 19 | 1 | 10 | 0 | 8 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0001t0004 | 0/0 | 2846 | 3 | 0 | 0 | 0 | 0 | 3 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0001t0005 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0001t0006 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0001t0007 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0002t0002 | 0/0 | 2846 | 13 | 1 | 10 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0004t0002 | 0/0 | 2846 | 4 | 1 | 0 | 0 | 2 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0006t0001 | 0/0 | 2846 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0008t0001 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0009t0001 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0001c0012t0001 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0003t0001 | 0/0 | 2847 | 6 | 0 | 4 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0003t0002 | 0/0 | 2847 | 4 | 1 | 0 | 3 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0003t0003 | 0/0 | 2847 | 2 | 1 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0003t0004 | 0/0 | 2847 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0002c0005t0002 | 0/0 | 2847 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0003c0007t0002 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0004c0011t0001 | 0/0 | 2846 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
a0005c0010t0001 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | copy fasta | chr19 | 49686116 | 49718731 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0006t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0006t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0008t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0009t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0001c0012t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0003t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0005t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0005t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0002c0005t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0003c0007t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0004c0011t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
a0005c0010t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0297 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | FIN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00423 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0267 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00735 | hp2 | a0002 | c0005 | t0002 | g0195 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00738 | hp2 | a0002 | c0003 | t0001 | g0230 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01081 | hp2 | a0005 | c0010 | t0001 | g0288 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0242 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01106 | hp1 | a0002 | c0005 | t0002 | g0205 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01175 | hp1 | a0001 | c0006 | t0001 | g0003 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0138 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01346 | hp1 | a0001 | c0008 | t0001 | g0013 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01496 | hp1 | a0002 | c0005 | t0002 | g0200 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01516 | hp2 | a0001 | c0004 | t0002 | g0203 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0142 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01975 | hp1 | a0001 | c0006 | t0001 | g0145 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02071 | hp2 | a0001 | c0012 | t0001 | g0221 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02293 | hp2 | a0001 | c0006 | t0001 | g0143 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02622 | hp2 | a0002 | c0003 | t0003 | g0099 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0232 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02738 | hp2 | a0001 | c0004 | t0002 | g0191 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02976 | hp2 | a0001 | c0004 | t0002 | g0193 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03209 | hp2 | a0004 | c0011 | t0001 | g0084 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03927 | hp2 | a0002 | c0003 | t0004 | g0311 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0310 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19005 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19062 | hp1 | a0002 | c0003 | t0002 | g0051 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19062 | hp2 | a0002 | c0003 | t0002 | g0055 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19066 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19082 | hp1 | a0002 | c0003 | t0003 | g0089 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | ASW | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ASW | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20805 | hp1 | a0001 | c0004 | t0002 | g0202 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | GIH | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | GIH | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02109 | hp1 | a0002 | c0003 | t0002 | g0210 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02109 | hp2 | a0003 | c0007 | t0002 | g0208 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0028 | REF | REF | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0281 | REF | REF | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49704737
|
T | C | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.721T>C | p.Tyr241His | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/20 | 1029/2846 | 721/2412 | 241/803 | chr19 | 49704737 | ||
chr19:49705086
|
A | AC | 2 | a0002a0003 | 17 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(14): Show |
frameshift_variant | HIGH | c.853dupC | p.Arg285fs | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 9/20 | 1162/2846 | 854/2412 | 285/803 | INFO_REALIGN_3_PRIME | chr19 | 49705086 | |
chr19:49708796
|
C | T | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1523C>T | p.Thr508Ile | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/20 | 1831/2846 | 1523/2412 | 508/803 | chr19 | 49708796 | ||
chr19:49712808
|
A | G | 1 | a0005 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.2092A>G | p.Asn698Asp | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 18/20 | 2400/2846 | 2092/2412 | 698/803 | chr19 | 49712808 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49701586
|
G | A | 4 | a0001c0002a0001c0004a0002c0005others(1): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
synonymous_variant | LOW | c.645G>A | p.Ser215Ser | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/20 | 953/2846 | 645/2412 | 215/803 | chr19 | 49701586 | ||
chr19:49705030
|
G | A | 1 | a0001c0008 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.795G>A | p.Thr265Thr | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 9/20 | 1103/2846 | 795/2412 | 265/803 | chr19 | 49705030 | ||
chr19:49705961
|
C | T | 1 | a0001c0012 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.1017C>T | p.Gly339Gly | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 11/20 | 1325/2846 | 1017/2412 | 339/803 | chr19 | 49705961 | ||
chr19:49706285
|
G | A | 1 | a0001c0009 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.1215G>A | p.Leu405Leu | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/20 | 1523/2846 | 1215/2412 | 405/803 | chr19 | 49706285 | ||
chr19:49706396
|
C | T | 4 | a0001c0002a0001c0004a0002c0005others(1): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
synonymous_variant | LOW | c.1326C>T | p.Ala442Ala | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/20 | 1634/2846 | 1326/2412 | 442/803 | chr19 | 49706396 | ||
chr19:49708767
|
C | T | 1 | a0001c0004 | 4 | HG01516.hp2 HG02738.hp2 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.1494C>T | p.Asp498Asp | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/20 | 1802/2846 | 1494/2412 | 498/803 | chr19 | 49708767 | ||
chr19:49708797
|
A | G | 1 | a0001c0006 | 3 | HG01175.hp1 HG01975.hp1 HG02293.hp2 |
synonymous_variant | LOW | c.1524A>G | p.Thr508Thr | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/20 | 1832/2846 | 1524/2412 | 508/803 | chr19 | 49708797 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49691142
|
G | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(8): Show | 137 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
5_prime_UTR_variant | MODIFIER | c.-282G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 1111 | chr19 | 49691142 | |||||
chr19:49691268
|
T | A | 1 | a0001c0001t0007 | 1 | NA19005.hp1 | 5_prime_UTR_variant | MODIFIER | c.-156T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 985 | chr19 | 49691268 | |||||
chr19:49691269
|
C | T | 1 | a0001c0001t0007 | 1 | NA19005.hp1 | 5_prime_UTR_variant | MODIFIER | c.-155C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 984 | chr19 | 49691269 | |||||
chr19:49691286
|
G | C | 3 | a0001c0001t0003a0001c0001t0005a0002c0003t0003 | 42 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 967 | chr19 | 49691286 | |||||
chr19:49713634
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(1): Show | 8 | HG02451.hp1 HG02630.hp2 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*29A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 20/20 | 29 | chr19 | 49713634 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49691376
|
GGGCCT | G | 17 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0020others(14): Show | 17 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.-84+39_-84+43delCC others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 49691376 | |||||
chr19:49691461
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-84+121A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | chr19 | 49691461 | ||||||
chr19:49691521
|
G | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01070.hp1 HG01433.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84+181G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | chr19 | 49691521 | ||||||
chr19:49691588
|
C | A | 97 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(94): Show | 103 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.-83-233C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | chr19 | 49691588 | ||||||
chr19:49691973
|
GGAGGAGG others(66): Show |
G | 8 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(5): Show | 9 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+166_-14-112del others(73): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr19 | 49691973 | |||||
chr19:49691982
|
G | A | 32 | a0001c0001t0002g0006a0001c0001t0002g0048a0001c0001t0002g0049others(29): Show | 33 | HG00423.hp2 HG00621.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15+93G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49691982 | ||||||
chr19:49692022
|
G | A | 8 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+133G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692022 | ||||||
chr19:49692055
|
G | A | 8 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(5): Show | 9 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+166G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692055 | ||||||
chr19:49692098
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-14-141G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692098 | ||||||
chr19:49692130
|
T | TGGGGCCT others(33): Show |
3 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326 | 3 | HG00609.hp1 NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-14-92_-14-53dupGG others(38): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr19 | 49692130 | |||||
chr19:49692198
|
G | A | 38 | a0001c0001t0003g0002a0001c0001t0003g0007a0001c0001t0003g0008others(35): Show | 42 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14-41G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692198 | ||||||
chr19:49692227
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-12T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692227 | ||||||
chr19:49692484
|
C | T | 19 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.141+91C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692484 | ||||||
chr19:49692513
|
T | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(197): Show | 209 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.141+120T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692513 | ||||||
chr19:49692514
|
T | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(197): Show | 209 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.141+121T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692514 | ||||||
chr19:49692612
|
C | T | 2 | a0001c0001t0002g0209a0002c0003t0002g0210 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.141+219C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692612 | ||||||
chr19:49692657
|
C | T | 2 | a0001c0002t0002g0207a0003c0007t0002g0208 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.141+264C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692657 | ||||||
chr19:49692743
|
C | CTGAGACA others(3): Show |
1 | a0001c0001t0001g0323 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141+352_141+361dup others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49692743 | |||||
chr19:49692908
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+515A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692908 | ||||||
chr19:49693169
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.141+776C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693169 | ||||||
chr19:49693173
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.141+780C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693173 | ||||||
chr19:49693194
|
C | T | 38 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(35): Show | 39 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+801C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693194 | ||||||
chr19:49693555
|
A | G | 13 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(10): Show | 13 | HG01109.hp1 HG01261.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+1162A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693555 | ||||||
chr19:49693599
|
T | C | 1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+1206T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693599 | ||||||
chr19:49693661
|
C | T | 17 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(14): Show | 17 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+1268C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693661 | ||||||
chr19:49693733
|
G | T | 11 | a0001c0001t0002g0009a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 12 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+1340G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693733 | ||||||
chr19:49693735
|
A | G | 153 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(150): Show | 161 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.141+1342A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693735 | ||||||
chr19:49693777
|
G | T | 1 | a0001c0001t0003g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.141+1384G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693777 | ||||||
chr19:49693966
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.141+1573G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693966 | ||||||
chr19:49694079
|
T | A | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0211others(3): Show | 6 | HG02015.hp1 HG02071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+1686T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694079 | ||||||
chr19:49694080
|
AAAATAAA others(4): Show |
A | 15 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(12): Show | 15 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+1695_141+1705d others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694080 | |||||
chr19:49694080
|
AAAATAAA others(8): Show |
A | 1 | a0001c0001t0002g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.141+1695_141+1709d others(17): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694080 | |||||
chr19:49694084
|
TAAA | T | 19 | a0001c0002t0002g0010a0001c0002t0002g0192a0001c0002t0002g0194others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+1695_141+1697d others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694084 | |||||
chr19:49694087
|
A | AAAAT | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0222others(3): Show | 6 | HG02071.hp2 HG02165.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+1729_141+1732d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | |||||
chr19:49694087
|
A | AT | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0002g0190 | 3 | HG01358.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141+1694_141+1695i others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694087 | ||||||
chr19:49694087
|
AAAAT | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG02080.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+1729_141+1732d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | |||||
chr19:49694087
|
AAAATAAA others(1): Show |
A | 36 | a0001c0001t0001g0035a0001c0001t0001g0315a0001c0001t0001g0316others(33): Show | 39 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+1725_141+1732d others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | |||||
chr19:49694087
|
AAAATAAA others(9): Show |
A | 79 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(76): Show | 83 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.141+1717_141+1732d others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | |||||
chr19:49694089
|
A | T | 1 | a0001c0001t0001g0323 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141+1696A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694089 | ||||||
chr19:49694091
|
T | A | 5 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(2): Show | 5 | HG01496.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1698T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694091 | ||||||
chr19:49694107
|
T | A | 1 | a0001c0001t0003g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141+1714T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694107 | ||||||
chr19:49694149
|
A | G | 148 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(145): Show | 156 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.141+1756A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694149 | ||||||
chr19:49694162
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.141+1769G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694162 | ||||||
chr19:49694338
|
A | AG | 5 | a0001c0001t0001g0224a0001c0001t0001g0315a0001c0001t0003g0108others(2): Show | 5 | HG02080.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1950dupG | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694338 | |||||
chr19:49694351
|
C | G | 1 | a0001c0001t0001g0323 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141+1958C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694351 | ||||||
chr19:49694360
|
G | C | 2 | a0001c0001t0003g0109a0001c0001t0003g0121 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.141+1967G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694360 | ||||||
chr19:49694415
|
A | T | 2 | a0001c0002t0002g0207a0003c0007t0002g0208 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.141+2022A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694415 | ||||||
chr19:49694575
|
G | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(33): Show | 37 | HG00558.hp2 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.141+2182G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694575 | ||||||
chr19:49694628
|
C | CA | 8 | a0001c0001t0001g0079a0001c0001t0001g0128a0001c0001t0001g0228others(5): Show | 8 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+2253dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694628 | |||||
chr19:49694628
|
CA | C | 16 | a0001c0001t0001g0040a0001c0001t0001g0126a0001c0001t0001g0314others(13): Show | 17 | HG00735.hp1 HG01071.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+2253delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694628 | |||||
chr19:49694646
|
A | G | 13 | a0001c0001t0002g0019a0001c0001t0002g0023a0001c0001t0002g0024others(10): Show | 13 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+2253A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694646 | ||||||
chr19:49694788
|
C | T | 37 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0002others(34): Show | 41 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+2395C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694788 | ||||||
chr19:49694865
|
G | A | 1 | a0002c0003t0001g0230 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.142-2461G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694865 | ||||||
chr19:49694923
|
G | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-2403G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694923 | ||||||
chr19:49695089
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142-2237C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695089 | ||||||
chr19:49695090
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-2236G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695090 | ||||||
chr19:49695144
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.142-2182A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695144 | ||||||
chr19:49695249
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.142-2077T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695249 | ||||||
chr19:49695278
|
A | AT | 50 | a0001c0001t0001g0164a0001c0001t0001g0186a0001c0001t0001g0214others(47): Show | 52 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-2026dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695278 | |||||
chr19:49695278
|
AT | A | 36 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 36 | HG00099.hp2 HG01070.hp1 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.142-2026delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695278 | |||||
chr19:49695446
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.142-1880G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695446 | ||||||
chr19:49695553
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-1773G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695553 | ||||||
chr19:49695584
|
C | CT | 14 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0229others(11): Show | 14 | HG00438.hp1 HG01168.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-1721dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695584 | |||||
chr19:49695584
|
CT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(101): Show | 110 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.142-1721delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695584 | |||||
chr19:49695584
|
CTT | C | 78 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0164others(75): Show | 81 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.142-1722_142-1721d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695584 | |||||
chr19:49695651
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0237a0001c0001t0001g0299 | 4 | HG02074.hp1 HG02129.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1675C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695651 | ||||||
chr19:49695709
|
A | AACACTAG others(10): Show |
1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.142-1616_142-1615i others(19): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695709 | |||||
chr19:49695728
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.142-1598C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695728 | ||||||
chr19:49695772
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.142-1554G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695772 | ||||||
chr19:49695880
|
C | CT | 42 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0022others(39): Show | 46 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.142-1438dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695880 | |||||
chr19:49695897
|
G | A | 11 | a0001c0001t0002g0020a0001c0001t0002g0024a0001c0001t0002g0025others(8): Show | 11 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.142-1429G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695897 | ||||||
chr19:49696283
|
G | C | 42 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0002others(39): Show | 46 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-1043G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696283 | ||||||
chr19:49696307
|
A | AT | 4 | a0001c0001t0002g0009a0001c0001t0002g0172a0001c0001t0002g0173others(1): Show | 5 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-1018dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696307 | |||||
chr19:49696320
|
T | C | 19 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(16): Show | 19 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-1006T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696320 | ||||||
chr19:49696344
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.142-982G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696344 | ||||||
chr19:49696359
|
G | A | 156 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(153): Show | 164 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.142-967G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696359 | ||||||
chr19:49696451
|
CTTTTCT | C | 39 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0002others(36): Show | 43 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-870_142-865del others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696451 | |||||
chr19:49696456
|
C | CT | 11 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-852dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696456 | |||||
chr19:49696456
|
CT | C | 57 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 58 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.142-852delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696456 | |||||
chr19:49696456
|
CTT | C | 62 | a0001c0001t0001g0164a0001c0001t0001g0309a0001c0001t0002g0005others(59): Show | 65 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.142-853_142-852del others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696456 | |||||
chr19:49696461
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.142-865T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696461 | ||||||
chr19:49696462
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.142-864T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696462 | ||||||
chr19:49696564
|
G | A | 16 | a0001c0001t0001g0164a0001c0001t0002g0050a0001c0001t0002g0052others(13): Show | 16 | HG00621.hp2 HG02129.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-762G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696564 | ||||||
chr19:49696628
|
T | C | 22 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0002g0010others(19): Show | 23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-698T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696628 | ||||||
chr19:49696636
|
CT | C | 133 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(130): Show | 140 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.142-677delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696636 | |||||
chr19:49696702
|
G | C | 22 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0002g0010others(19): Show | 23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-624G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696702 | ||||||
chr19:49696851
|
T | C | 22 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0002g0010others(19): Show | 23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-475T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696851 | ||||||
chr19:49697219
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.142-107C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49697219 | ||||||
chr19:49697500
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.281+35A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697500 | ||||||
chr19:49697691
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0294a0001c0001t0001g0314 | 3 | HG02040.hp1 HG02132.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.281+226C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697691 | ||||||
chr19:49697774
|
ATGGTGGC others(19): Show |
A | 1 | a0001c0001t0001g0246 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.281+310_281+335del others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697774 | ||||||
chr19:49697835
|
A | G | 22 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0002g0010others(19): Show | 23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+370A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697835 | ||||||
chr19:49697998
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02965.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.281+533G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697998 | ||||||
chr19:49698049
|
C | CA | 25 | a0001c0001t0001g0011a0001c0001t0001g0079a0001c0001t0001g0085others(22): Show | 26 | HG00280.hp1 HG00423.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.281+606dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49698049 | |||||
chr19:49698049
|
CA | C | 29 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0001g0160others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.281+606delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49698049 | |||||
chr19:49698089
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.281+624G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698089 | ||||||
chr19:49698118
|
A | C | 1 | a0001c0001t0003g0008 | 2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.281+653A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698118 | ||||||
chr19:49698181
|
A | G | 4 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0107others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+716A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698181 | ||||||
chr19:49698501
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.281+1036A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698501 | ||||||
chr19:49698588
|
G | A | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.281+1123G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698588 | ||||||
chr19:49698603
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.281+1138C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698603 | ||||||
chr19:49698649
|
C | A | 14 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0023others(11): Show | 14 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.281+1184C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698649 | ||||||
chr19:49698662
|
C | CA | 47 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0125others(44): Show | 48 | HG00558.hp2 HG00609.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.281+1212dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49698662 | |||||
chr19:49698670
|
A | G | 22 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0002t0002g0010others(19): Show | 23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+1205A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698670 | ||||||
chr19:49698824
|
G | A | 13 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0023others(10): Show | 13 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.281+1359G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698824 | ||||||
chr19:49698893
|
A | G | 1 | a0001c0002t0002g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281+1428A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698893 | ||||||
chr19:49698898
|
C | T | 7 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+1433C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698898 | ||||||
chr19:49699180
|
T | G | 3 | a0001c0001t0001g0238a0001c0001t0001g0255a0001c0001t0001g0295 | 3 | HG02027.hp1 HG02056.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.282-1504T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699180 | ||||||
chr19:49699199
|
A | T | 11 | a0001c0001t0002g0009a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 12 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-1485A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699199 | ||||||
chr19:49699368
|
T | C | 4 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0107others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-1316T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699368 | ||||||
chr19:49699447
|
C | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282-1237C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699447 | ||||||
chr19:49699451
|
T | C | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.282-1233T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699451 | ||||||
chr19:49699457
|
T | TA | 40 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(37): Show | 43 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.282-1193dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
T | TAA | 33 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0140others(30): Show | 34 | HG00558.hp2 HG00621.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.282-1194_282-1193d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
T | TAAA | 20 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(17): Show | 20 | HG00438.hp2 HG01175.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.282-1195_282-1193d others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
T | TAAAA | 13 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0134others(10): Show | 13 | HG00609.hp2 HG01258.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.282-1196_282-1193d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
T | TAAAAA | 8 | a0001c0001t0002g0031a0001c0001t0002g0058a0001c0002t0002g0190others(5): Show | 8 | HG00741.hp1 HG01192.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-1197_282-1193d others(7): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
T | TAAAAAA | 6 | a0001c0001t0001g0253a0001c0001t0001g0256a0001c0002t0002g0010others(3): Show | 7 | HG00735.hp2 HG01069.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-1198_282-1193d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
T | TAAAAAAA others(11): Show |
1 | a0003c0007t0002g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.282-1210_282-1193d others(20): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TA | T | 60 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.282-1193delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAA | T | 33 | a0001c0001t0001g0161a0001c0001t0001g0177a0001c0001t0001g0180others(30): Show | 36 | HG01243.hp2 HG01346.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.282-1194_282-1193d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAAA | T | 10 | a0001c0001t0001g0123a0001c0001t0001g0175a0001c0001t0002g0009others(7): Show | 11 | HG00735.hp1 HG02083.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.282-1195_282-1193d others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAAAAAA | T | 13 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(10): Show | 13 | HG01070.hp1 HG01433.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.282-1198_282-1193d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.282-1203_282-1193d others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0030 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.282-1207_282-1193d others(17): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0001g0235 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.282-1211_282-1193d others(21): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699457
|
TAAAAAAA others(13): Show |
T | 2 | a0001c0001t0002g0209a0002c0003t0002g0210 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.282-1212_282-1193d others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | |||||
chr19:49699470
|
A | T | 1 | a0001c0001t0001g0291 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.282-1214A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699470 | ||||||
chr19:49699760
|
G | A | 11 | a0001c0001t0002g0009a0001c0001t0002g0165a0001c0001t0002g0166others(8): Show | 12 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-924G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699760 | ||||||
chr19:49699780
|
C | A | 1 | a0001c0001t0001g0319 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.282-904C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699780 | ||||||
chr19:49699796
|
T | C | 7 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-888T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699796 | ||||||
chr19:49699914
|
A | G | 7 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-770A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699914 | ||||||
chr19:49699932
|
C | CGA | 3 | a0001c0004t0002g0191a0001c0004t0002g0202a0001c0004t0002g0203 | 3 | HG01516.hp2 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.282-751_282-750dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699932 | |||||
chr19:49699966
|
T | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0300 | 2 | HG02135.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.282-718T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699966 | ||||||
chr19:49699976
|
G | C | 42 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0002g0021others(39): Show | 46 | HG00099.hp2 HG00280.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.282-708G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699976 | ||||||
chr19:49699985
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282-699C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699985 | ||||||
chr19:49700024
|
G | A | 4 | a0001c0001t0002g0009a0001c0001t0002g0172a0001c0001t0002g0173others(1): Show | 5 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-660G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700024 | ||||||
chr19:49700165
|
T | G | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.282-519T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700165 | ||||||
chr19:49700244
|
C | T | 1 | a0002c0003t0001g0230 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.282-440C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700244 | ||||||
chr19:49700257
|
C | CAA | 25 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0006others(22): Show | 27 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.282-424_282-423dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700257 | |||||
chr19:49700257
|
C | CAAA | 12 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0049others(9): Show | 12 | HG00423.hp2 HG00738.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-425_282-423dup others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700257 | |||||
chr19:49700262
|
C | A | 40 | a0001c0001t0001g0164a0001c0001t0001g0309a0001c0001t0002g0005others(37): Show | 42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.282-422C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700262 | ||||||
chr19:49700262
|
C | CA | 73 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0086others(70): Show | 77 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.282-411dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | |||||
chr19:49700262
|
C | CAA | 40 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(37): Show | 41 | HG00558.hp2 HG00609.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-412_282-411dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | |||||
chr19:49700262
|
CA | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(14): Show | 17 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.282-411delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | |||||
chr19:49700262
|
CAAA | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-413_282-411del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | |||||
chr19:49700267
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.282-417A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700267 | ||||||
chr19:49700296
|
T | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-388T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700296 | ||||||
chr19:49700328
|
G | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-356G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700328 | ||||||
chr19:49700334
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282-350G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700334 | ||||||
chr19:49700334
|
G | T | 5 | a0001c0001t0002g0166a0001c0001t0002g0168a0001c0001t0002g0169others(2): Show | 5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-350G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700334 | ||||||
chr19:49700427
|
G | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-257G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700427 | ||||||
chr19:49700660
|
C | A | 1 | a0001c0001t0001g0307 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.282-24C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700660 | ||||||
chr19:49700679
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG01169.hp2 | splice_region_variant&intron_variant | LOW | c.282-5C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700679 | ||||||
chr19:49700869
|
A | G | 15 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0083others(12): Show | 16 | HG00735.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.453+14A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49700869 | ||||||
chr19:49700944
|
G | A | 1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.453+89G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49700944 | ||||||
chr19:49700955
|
T | TCTCTCTC others(84): Show |
19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.453+109_453+199dup others(91): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49700955 | |||||
chr19:49700955
|
T | TCTCTCTC others(107): Show |
1 | a0001c0002t0002g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.453+139_453+140ins others(114): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49700955 | |||||
chr19:49700992
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.453+137T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49700992 | ||||||
chr19:49701008
|
CCTGGGTC others(15): Show |
C | 2 | a0001c0001t0001g0187a0001c0001t0003g0092 | 2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.453+178_453+199del others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701008 | |||||
chr19:49701024
|
C | CCT | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+176_453+177dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701024 | |||||
chr19:49701034
|
G | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+179G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701034 | ||||||
chr19:49701040
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+185T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701040 | ||||||
chr19:49701046
|
CCTCT | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+198_453+201del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701046 | |||||
chr19:49701052
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+197T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701052 | ||||||
chr19:49701058
|
T | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(47): Show | 52 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.453+203T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701058 | ||||||
chr19:49701064
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(47): Show | 52 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.453+209C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701064 | ||||||
chr19:49701065
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+210G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701065 | ||||||
chr19:49701066
|
T | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+211T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701066 | ||||||
chr19:49701070
|
C | CGACT | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+215_453+216ins others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701070 | ||||||
chr19:49701072
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+217C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701072 | ||||||
chr19:49701085
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+230A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701085 | ||||||
chr19:49701091
|
G | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-226G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701091 | ||||||
chr19:49701092
|
A | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-225A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701092 | ||||||
chr19:49701110
|
C | CCCCCCTC others(17): Show |
84 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(81): Show | 87 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.454-194_454-171dup others(24): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701110 | |||||
chr19:49701110
|
C | CCCCCCTC others(155): Show |
10 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0002g0019others(7): Show | 10 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.454-171_454-170ins others(162): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701110 | |||||
chr19:49701110
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(28): Show | 32 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.454-207C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701110 | ||||||
chr19:49701126
|
G | GGTCTCTG others(38): Show |
20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-162_454-161ins others(45): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701126 | |||||
chr19:49701181
|
T | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-136T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701181 | ||||||
chr19:49701200
|
G | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.454-117G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701200 | ||||||
chr19:49701730
|
C | A | 1 | a0001c0001t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.693+96C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701730 | ||||||
chr19:49701771
|
C | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+137C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701771 | ||||||
chr19:49701817
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.693+183A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701817 | ||||||
chr19:49701829
|
AT | A | 18 | a0001c0001t0001g0175a0001c0001t0001g0314a0001c0001t0002g0019others(15): Show | 18 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+196delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701829 | ||||||
chr19:49701859
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+225A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701859 | ||||||
chr19:49701860
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+226A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701860 | ||||||
chr19:49701865
|
ATAG | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+233_693+235del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701865 | |||||
chr19:49701870
|
G | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+236G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701870 | ||||||
chr19:49701877
|
T | A | 38 | a0001c0001t0001g0164a0001c0001t0001g0309a0001c0001t0002g0005others(35): Show | 40 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.693+243T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701877 | ||||||
chr19:49701879
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+245A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701879 | ||||||
chr19:49701880
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+246A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701880 | ||||||
chr19:49701886
|
ATATT | A | 38 | a0001c0001t0001g0164a0001c0001t0001g0309a0001c0001t0002g0005others(35): Show | 40 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.693+260_693+263del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701886 | |||||
chr19:49701899
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+265A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701899 | ||||||
chr19:49701901
|
T | C | 2 | a0001c0002t0002g0207a0003c0007t0002g0208 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.693+267T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701901 | ||||||
chr19:49701902
|
A | AT | 22 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(19): Show | 23 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.693+269dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701902 | |||||
chr19:49701902
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+268A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701902 | ||||||
chr19:49701912
|
A | ATATATAT others(312): Show |
1 | a0001c0002t0002g0199 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.693+281_693+282ins others(319): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701912 | |||||
chr19:49701912
|
A | ATATATAT others(312): Show |
16 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(13): Show | 17 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.693+281_693+282ins others(319): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701912 | |||||
chr19:49701916
|
T | A | 3 | a0001c0002t0002g0207a0001c0004t0002g0193a0003c0007t0002g0208 | 3 | HG02109.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+282T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701916 | ||||||
chr19:49701920
|
A | G | 3 | a0001c0002t0002g0207a0001c0004t0002g0193a0003c0007t0002g0208 | 3 | HG02109.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+286A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701920 | ||||||
chr19:49701923
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+289C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701923 | ||||||
chr19:49701925
|
A | T | 3 | a0001c0002t0002g0207a0001c0004t0002g0193a0003c0007t0002g0208 | 3 | HG02109.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+291A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701925 | ||||||
chr19:49701930
|
T | A | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+296T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701930 | ||||||
chr19:49701930
|
T | TTATTTAT others(263): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+296_693+297ins others(270): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701930 | ||||||
chr19:49701930
|
T | TTATTTAT others(306): Show |
2 | a0001c0002t0002g0207a0003c0007t0002g0208 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.693+296_693+297ins others(313): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701930 | ||||||
chr19:49701931
|
A | T | 59 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(56): Show | 61 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.693+297A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701931 | ||||||
chr19:49701936
|
T | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+302T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701936 | ||||||
chr19:49701936
|
T | TTATA | 88 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(85): Show | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.693+303_693+306dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701936 | |||||
chr19:49701938
|
A | T | 18 | a0001c0001t0003g0116a0001c0002t0002g0010a0001c0002t0002g0190others(15): Show | 19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+304A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701938 | ||||||
chr19:49701941
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+307A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701941 | ||||||
chr19:49701944
|
T | A | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+310T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701944 | ||||||
chr19:49701953
|
A | AATATAAA others(4): Show |
10 | a0001c0001t0001g0314a0001c0001t0002g0019a0001c0001t0002g0023others(7): Show | 10 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+324_693+325ins others(11): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701953 | |||||
chr19:49701953
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0141 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.693+325_693+326ins others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701953 | |||||
chr19:49701953
|
A | T | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+319A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701953 | ||||||
chr19:49701954
|
A | ATATATAA others(4): Show |
84 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(81): Show | 88 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.693+325_693+326ins others(11): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701954 | |||||
chr19:49701954
|
A | ATATATAA others(43): Show |
1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.693+325_693+326ins others(50): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701954 | |||||
chr19:49701954
|
A | ATATATAA others(43): Show |
7 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+325_693+326ins others(50): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701954 | |||||
chr19:49701956
|
A | T | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+322A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701956 | ||||||
chr19:49701958
|
AT | A | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+327delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701958 | |||||
chr19:49701961
|
T | A | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+327T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701961 | ||||||
chr19:49701966
|
A | T | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+332A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701966 | ||||||
chr19:49701969
|
A | AAT | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+336_693+337dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701969 | |||||
chr19:49701969
|
A | T | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+335A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701969 | ||||||
chr19:49701972
|
T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+338T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701972 | ||||||
chr19:49701977
|
A | T | 139 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(136): Show | 144 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.693+343A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701977 | ||||||
chr19:49701981
|
A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+347A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701981 | ||||||
chr19:49701982
|
A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+348A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701982 | ||||||
chr19:49701989
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+355A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701989 | ||||||
chr19:49701992
|
A | T | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+358A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701992 | ||||||
chr19:49701993
|
T | TATATA | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+359_693+360ins others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701993 | ||||||
chr19:49701998
|
A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+364A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701998 | ||||||
chr19:49701999
|
A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+365A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701999 | ||||||
chr19:49702001
|
A | G | 19 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0002g0021others(16): Show | 21 | HG00099.hp2 HG00280.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.693+367A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702001 | ||||||
chr19:49702003
|
A | T | 18 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(15): Show | 19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+369A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702003 | ||||||
chr19:49702004
|
T | TATATA | 18 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(15): Show | 19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+370_693+371ins others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702004 | ||||||
chr19:49702004
|
T | TTAAATAT others(64): Show |
1 | a0001c0001t0001g0038 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(71): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | |||||
chr19:49702004
|
T | TTAAATAT others(42): Show |
1 | a0001c0001t0002g0026 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(49): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | |||||
chr19:49702004
|
T | TTAAATAT others(69): Show |
1 | a0001c0001t0002g0023 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | |||||
chr19:49702004
|
T | TTAAATAT others(123): Show |
1 | a0001c0001t0002g0033 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(130): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | |||||
chr19:49702007
|
A | AATATATT others(97): Show |
1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.693+383_693+384ins others(104): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(15): Show |
5 | a0001c0001t0001g0187a0001c0001t0002g0032a0001c0001t0002g0034others(2): Show | 5 | HG00438.hp2 HG00544.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(40): Show |
5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01099.hp1 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(47): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(44): Show |
154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(51): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(69): Show |
7 | a0001c0001t0001g0130a0001c0001t0001g0220a0001c0001t0001g0252others(4): Show | 7 | HG01256.hp1 HG02040.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(94): Show |
5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0238others(2): Show | 5 | HG01099.hp2 HG01109.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(101): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(94): Show |
5 | a0001c0001t0002g0166a0001c0001t0002g0168a0001c0001t0002g0169others(2): Show | 5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(101): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(316): Show |
2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.693+391_693+392ins others(323): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(69): Show |
7 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0003g0002others(4): Show | 9 | HG02622.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | AATATATT others(127): Show |
1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(134): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | |||||
chr19:49702007
|
A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+373A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702007 | ||||||
chr19:49702009
|
T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+375T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702009 | ||||||
chr19:49702013
|
T | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+379T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702013 | ||||||
chr19:49702014
|
T | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+380T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702014 | ||||||
chr19:49702018
|
T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+384T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702018 | ||||||
chr19:49702021
|
TAAA | T | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+388_693+390del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702021 | ||||||
chr19:49702023
|
AATT | A | 50 | a0001c0001t0001g0131a0001c0001t0001g0149a0001c0001t0001g0159others(47): Show | 52 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.693+392_693+394del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702023 | |||||
chr19:49702024
|
A | ATAAATAT others(94): Show |
1 | a0001c0001t0005g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(101): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702024 | |||||
chr19:49702024
|
A | T | 1 | a0002c0003t0002g0051 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.693+390A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702024 | ||||||
chr19:49702025
|
T | TAAATATA others(63): Show |
1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(70): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(90): Show |
1 | a0004c0011t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(97): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(119): Show |
5 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(2): Show | 5 | HG02145.hp1 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(126): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(41): Show |
1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(48): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(68): Show |
1 | a0001c0001t0001g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(75): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(124): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(1): Show | 4 | HG01070.hp1 HG01433.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(131): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(93): Show |
1 | a0001c0001t0002g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(100): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(68): Show |
4 | a0001c0001t0002g0009a0001c0001t0002g0172a0001c0001t0002g0173others(1): Show | 5 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(75): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(39): Show |
1 | a0001c0001t0001g0123 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(46): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(66): Show |
1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(73): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(19): Show |
32 | a0001c0001t0001g0014a0001c0001t0001g0081a0001c0001t0001g0082others(29): Show | 33 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(48): Show |
6 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0075others(3): Show | 6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(55): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702025
|
T | TAAATATA others(19): Show |
3 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0102 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.693+391_693+392ins others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | ||||||
chr19:49702026
|
T | A | 62 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0037others(59): Show | 64 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.693+392T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702026 | ||||||
chr19:49702026
|
T | TATAA | 9 | a0001c0001t0001g0187a0001c0001t0002g0165a0001c0001t0002g0166others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+396_693+399dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702026 | |||||
chr19:49702030
|
A | T | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+396A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702030 | ||||||
chr19:49702032
|
T | TAA | 7 | a0001c0001t0001g0038a0001c0001t0002g0023a0001c0001t0002g0026others(4): Show | 7 | HG00438.hp2 HG00544.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+399_693+400ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702032 | |||||
chr19:49702034
|
T | A | 20 | a0001c0001t0001g0280a0001c0002t0002g0010a0001c0002t0002g0190others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+400T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702034 | ||||||
chr19:49702035
|
A | G | 6 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0075others(3): Show | 6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+401A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702035 | ||||||
chr19:49702035
|
A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+401A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702035 | ||||||
chr19:49702039
|
T | TTATTTAT others(43): Show |
3 | a0001c0001t0001g0262a0002c0003t0001g0245a0002c0003t0001g0267 | 3 | HG00544.hp2 HG01109.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.693+424_693+425ins others(50): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702039 | |||||
chr19:49702043
|
T | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+409T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702043 | ||||||
chr19:49702048
|
AATT | A | 3 | a0001c0001t0005g0105a0001c0001t0006g0069a0001c0001t0006g0070 | 3 | HG02451.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+417_693+419del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702048 | |||||
chr19:49702049
|
AT | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+417delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702049 | |||||
chr19:49702050
|
T | TATTTATA others(6): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+416_693+417ins others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702050 | ||||||
chr19:49702051
|
T | TATAA | 60 | a0001c0001t0001g0038a0001c0001t0001g0083a0001c0001t0001g0122others(57): Show | 63 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+421_693+424dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702051 | |||||
chr19:49702051
|
T | TATAAATA others(55): Show |
2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.693+424_693+425ins others(62): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702051 | |||||
chr19:49702051
|
T | TATAAATA others(26): Show |
1 | a0001c0001t0003g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.693+424_693+425ins others(33): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702051 | |||||
chr19:49702057
|
T | TAA | 6 | a0001c0001t0002g0019a0001c0001t0002g0023a0001c0001t0002g0025others(3): Show | 6 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+424_693+425ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702057 | |||||
chr19:49702057
|
T | TAAATATA others(76): Show |
1 | a0001c0001t0001g0314 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.693+424_693+425ins others(83): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702057 | |||||
chr19:49702060
|
A | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0007g0061 | 3 | HG02809.hp2 NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.693+426A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702060 | ||||||
chr19:49702060
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+426A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702060 | ||||||
chr19:49702068
|
T | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+434T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702068 | ||||||
chr19:49702074
|
A | T | 1 | a0001c0001t0005g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.693+440A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702074 | ||||||
chr19:49702075
|
T | G | 6 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0075others(3): Show | 6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+441T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702075 | ||||||
chr19:49702075
|
T | TATTTATA | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+441_693+442ins others(7): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702075 | ||||||
chr19:49702075
|
T | TATTTATA others(6): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+441_693+442ins others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702075 | ||||||
chr19:49702076
|
T | TATAA | 10 | a0001c0001t0001g0309a0001c0001t0002g0165a0001c0001t0002g0166others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+446_693+449dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | |||||
chr19:49702076
|
T | TATAAATA others(55): Show |
1 | a0002c0003t0002g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.693+449_693+450ins others(62): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | |||||
chr19:49702076
|
T | TATAAATA others(59): Show |
1 | a0001c0001t0001g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.693+449_693+450ins others(66): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | |||||
chr19:49702076
|
T | TATAAATA others(30): Show |
3 | a0001c0001t0005g0105a0001c0001t0006g0069a0001c0001t0006g0070 | 3 | HG02451.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+449_693+450ins others(37): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | |||||
chr19:49702076
|
T | TATAAATA others(63): Show |
9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(6): Show | 9 | HG01070.hp1 HG01433.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(70): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | |||||
chr19:49702080
|
A | AATAAATA others(1): Show |
6 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0075others(3): Show | 6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | |||||
chr19:49702080
|
A | AATAAATA others(30): Show |
1 | a0001c0001t0002g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.693+449_693+450ins others(37): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | |||||
chr19:49702080
|
A | AATAAATA others(201): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.693+449_693+450ins others(208): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | |||||
chr19:49702080
|
A | AATAAATA others(175): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0163 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.693+449_693+450ins others(182): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | |||||
chr19:49702080
|
A | AATAAATA others(55): Show |
30 | a0001c0001t0001g0164a0001c0001t0002g0005a0001c0001t0002g0006others(27): Show | 32 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(62): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | |||||
chr19:49702082
|
T | TAA | 8 | a0001c0001t0001g0314a0001c0001t0002g0019a0001c0001t0002g0023others(5): Show | 8 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702082 | |||||
chr19:49702084
|
T | A | 1 | a0001c0001t0004g0310 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.693+450T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702084 | ||||||
chr19:49702085
|
A | ATATTTAT others(76): Show |
1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.693+458_693+459ins others(83): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702085 | |||||
chr19:49702085
|
A | ATATTTAT others(22): Show |
1 | a0002c0003t0004g0311 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.693+475_693+503dup others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702085 | |||||
chr19:49702085
|
A | T | 42 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(39): Show | 44 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.693+451A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702085 | ||||||
chr19:49702085
|
ATATT | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(23): Show | 27 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+459_693+462del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702085 | |||||
chr19:49702089
|
T | A | 20 | a0001c0001t0004g0310a0001c0002t0002g0010a0001c0002t0002g0190others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+455T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702089 | ||||||
chr19:49702093
|
T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+459T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702093 | ||||||
chr19:49702098
|
A | T | 19 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(16): Show | 20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+464A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702098 | ||||||
chr19:49702099
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0189 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.693+465A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702099 | ||||||
chr19:49702099
|
A | T | 1 | a0001c0001t0003g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.693+465A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702099 | ||||||
chr19:49702100
|
T | G | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0007g0061 | 3 | HG02809.hp2 NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.693+466T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | ||||||
chr19:49702100
|
T | TAAATATA others(72): Show |
1 | a0001c0002t0002g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.693+466_693+467ins others(79): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | ||||||
chr19:49702100
|
T | TAAATATA others(82): Show |
15 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0194others(12): Show | 16 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+466_693+467ins others(89): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | ||||||
chr19:49702100
|
T | TAAATATA others(96): Show |
2 | a0001c0002t0002g0207a0003c0007t0002g0208 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.693+466_693+467ins others(103): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | ||||||
chr19:49702100
|
T | TAAATATT others(4): Show |
1 | a0002c0005t0002g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.693+466_693+467ins others(11): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | ||||||
chr19:49702101
|
T | TATAA | 52 | a0001c0001t0001g0038a0001c0001t0001g0079a0001c0001t0001g0080others(49): Show | 55 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.693+471_693+474dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702101
|
T | TATAAATA others(30): Show |
2 | a0001c0001t0002g0057a0001c0001t0007g0061 | 2 | HG02809.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.693+474_693+475ins others(37): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702101
|
T | TATAAATA others(62): Show |
1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+474_693+475ins others(69): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702101
|
T | TATAAATA others(92): Show |
1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.693+474_693+475ins others(99): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702101
|
T | TATAAATA others(92): Show |
1 | a0004c0011t0001g0084 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.693+474_693+475ins others(99): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702101
|
T | TATAAATA others(134): Show |
1 | a0001c0001t0002g0025 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.693+474_693+475ins others(141): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702101
|
T | TATAAATA others(84): Show |
1 | a0001c0001t0001g0309 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.693+474_693+475ins others(91): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | |||||
chr19:49702109
|
T | A | 32 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(29): Show | 32 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.693+475T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702109 | ||||||
chr19:49702110
|
ATATT | A | 15 | a0001c0001t0001g0137a0001c0001t0001g0251a0001c0001t0001g0252others(12): Show | 15 | HG00544.hp2 HG00609.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.693+488_693+491del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702110 | |||||
chr19:49702114
|
T | A | 52 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(49): Show | 53 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.693+480T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702114 | ||||||
chr19:49702114
|
T | TTATTTAT others(99): Show |
1 | a0001c0001t0002g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.693+487_693+488ins others(106): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | |||||
chr19:49702114
|
T | TTATTTAT others(155): Show |
1 | a0001c0001t0001g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.693+487_693+488ins others(162): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | |||||
chr19:49702114
|
T | TTATTTAT others(22): Show |
1 | a0001c0001t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.693+522_693+550dup others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | |||||
chr19:49702114
|
T | TTATTTAT others(51): Show |
2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.693+522_693+523ins others(58): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | |||||
chr19:49702117
|
T | TAA | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0194others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+483_693+484ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702117 | ||||||
chr19:49702118
|
T | A | 18 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(15): Show | 19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+484T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702118 | ||||||
chr19:49702118
|
T | TTATAAAT others(31): Show |
1 | a0001c0001t0001g0149 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.693+487_693+488ins others(38): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702118 | |||||
chr19:49702122
|
T | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+488T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702122 | ||||||
chr19:49702128
|
A | T | 9 | a0001c0001t0001g0038a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG00735.hp1 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+494A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702128 | ||||||
chr19:49702129
|
T | TA | 18 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(15): Show | 19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+495_693+496ins others(1): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702129 | ||||||
chr19:49702129
|
T | TATATCTA others(110): Show |
1 | a0002c0005t0002g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.693+495_693+496ins others(117): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702129 | ||||||
chr19:49702129
|
T | TATATCTA others(124): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+495_693+496ins others(131): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702129 | ||||||
chr19:49702134
|
A | AATATATA others(14): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0256 | 2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.693+503_693+504ins others(21): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702134 | |||||
chr19:49702134
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+500A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702134 | ||||||
chr19:49702136
|
T | A | 1 | a0001c0002t0002g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.693+502T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702136 | ||||||
chr19:49702138
|
A | AAT | 18 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0194others(15): Show | 19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+511_693+512dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702138 | |||||
chr19:49702138
|
A | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(30): Show | 34 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.693+504A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702138 | ||||||
chr19:49702143
|
A | ATATT | 62 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(59): Show | 64 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.693+517_693+520dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | |||||
chr19:49702143
|
A | ATATTTAT others(113): Show |
1 | a0001c0001t0003g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693+550_693+551ins others(120): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | |||||
chr19:49702143
|
A | ATATTTAT others(142): Show |
1 | a0001c0001t0003g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.693+550_693+551ins others(149): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | |||||
chr19:49702143
|
A | ATATTTAT others(22): Show |
1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.693+537_693+538ins others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | |||||
chr19:49702143
|
A | ATATTTAT others(59): Show |
5 | a0001c0001t0001g0127a0001c0001t0002g0009a0001c0001t0002g0172others(2): Show | 6 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+520_693+521ins others(66): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | |||||
chr19:49702143
|
A | ATATTTAT others(88): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG01255.hp1 HG01884.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+520_693+521ins others(95): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | |||||
chr19:49702143
|
A | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(30): Show | 34 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.693+509A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702143 | ||||||
chr19:49702163
|
A | AATAAATA others(51): Show |
1 | a0001c0001t0002g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.693+550_693+551ins others(58): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702163 | |||||
chr19:49702163
|
A | AATAAATA others(22): Show |
5 | a0001c0001t0001g0314a0001c0001t0002g0019a0001c0001t0002g0023others(2): Show | 5 | HG00544.hp1 HG00642.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+550_693+551ins others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702163 | |||||
chr19:49702163
|
A | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0209others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+529A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702163 | ||||||
chr19:49702163
|
A | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+529A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702163 | ||||||
chr19:49702171
|
T | A | 1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.693+537T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702171 | ||||||
chr19:49702180
|
T | TTA | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+553_693+554dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702180 | |||||
chr19:49702299
|
T | A | 1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+665T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702299 | ||||||
chr19:49702307
|
C | G | 1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+673C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702307 | ||||||
chr19:49702308
|
A | C | 1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+674A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702308 | ||||||
chr19:49702309
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+675A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702309 | ||||||
chr19:49702310
|
A | T | 1 | a0001c0001t0002g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+676A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702310 | ||||||
chr19:49702347
|
A | G | 21 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(18): Show | 22 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.693+713A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702347 | ||||||
chr19:49702399
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+765C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702399 | ||||||
chr19:49702414
|
TCAAGACC others(8): Show |
T | 1 | a0001c0001t0001g0326 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.693+784_693+798del others(15): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702414 | |||||
chr19:49702491
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+857A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702491 | ||||||
chr19:49702512
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+878C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702512 | ||||||
chr19:49702513
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.693+879G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702513 | ||||||
chr19:49702525
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+891C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702525 | ||||||
chr19:49702608
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.693+974A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702608 | ||||||
chr19:49702630
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+996A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702630 | ||||||
chr19:49702638
|
G | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1004G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702638 | ||||||
chr19:49702638
|
G | GA | 8 | a0001c0001t0001g0226a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+1015dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702638 | |||||
chr19:49702641
|
A | AAC | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1008_693+1009i others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702641 | |||||
chr19:49702643
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1009A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702643 | ||||||
chr19:49702824
|
G | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1190G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702824 | ||||||
chr19:49702833
|
G | A | 3 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0107 | 3 | HG02572.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.693+1199G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702833 | ||||||
chr19:49702921
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0180 | 2 | HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.693+1287C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702921 | ||||||
chr19:49702936
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1302A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702936 | ||||||
chr19:49702974
|
G | A | 25 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.693+1340G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702974 | ||||||
chr19:49703055
|
G | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1421G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703055 | ||||||
chr19:49703070
|
T | TAC | 8 | a0001c0001t0001g0226a0001c0001t0001g0236a0001c0001t0002g0174others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+1465_693+1466d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | |||||
chr19:49703070
|
TAC | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(160): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.693+1465_693+1466d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | |||||
chr19:49703070
|
TACAC | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(121): Show | 129 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.693+1463_693+1466d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | |||||
chr19:49703070
|
TACACAC | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(3): Show | 6 | HG01070.hp1 HG01433.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+1461_693+1466d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | |||||
chr19:49703121
|
T | TTCCC | 18 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(15): Show | 20 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+1503_693+1506d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703121 | |||||
chr19:49703121
|
TTCCC | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1503_693+1506d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703121 | |||||
chr19:49703237
|
TCTCA | T | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-1469_694-1466d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703237 | |||||
chr19:49703248
|
C | T | 34 | a0001c0001t0001g0164a0001c0001t0002g0005a0001c0001t0002g0041others(31): Show | 35 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.694-1462C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703248 | ||||||
chr19:49703326
|
C | T | 1 | a0002c0003t0001g0242 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.694-1384C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703326 | ||||||
chr19:49703345
|
A | T | 1 | a0002c0003t0001g0242 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.694-1365A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703345 | ||||||
chr19:49703350
|
C | CTT | 25 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-1346_694-1345d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703350 | |||||
chr19:49703369
|
T | G | 25 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-1341T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703369 | ||||||
chr19:49703372
|
T | C | 5 | a0001c0001t0002g0020a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG00280.hp2 HG01169.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-1338T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703372 | ||||||
chr19:49703390
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694-1320T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703390 | ||||||
chr19:49703391
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694-1319G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703391 | ||||||
chr19:49703392
|
G | A | 34 | a0001c0001t0001g0164a0001c0001t0002g0005a0001c0001t0002g0041others(31): Show | 35 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.694-1318G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703392 | ||||||
chr19:49703491
|
A | G | 69 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(66): Show | 71 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.694-1219A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703491 | ||||||
chr19:49703496
|
C | T | 1 | a0002c0003t0002g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.694-1214C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703496 | ||||||
chr19:49703500
|
C | CTCTT | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-1194_694-1191d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703500 | |||||
chr19:49703563
|
T | TCCTC | 17 | a0001c0001t0001g0004a0001c0001t0001g0222a0001c0001t0001g0223others(14): Show | 18 | HG00597.hp2 HG02027.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-1115_694-1112d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
T | TCCTCCCT others(1): Show |
7 | a0001c0001t0001g0238a0001c0001t0002g0029a0001c0001t0002g0031others(4): Show | 8 | HG00280.hp2 HG02056.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1119_694-1112d others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
T | TCCTCCCT others(5): Show |
11 | a0001c0001t0001g0131a0001c0001t0001g0140a0001c0001t0001g0147others(8): Show | 11 | HG01169.hp2 HG01891.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.694-1123_694-1112d others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
T | TCCTCCCT others(9): Show |
14 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0141others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.694-1127_694-1112d others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
T | TCCTCCCT others(13): Show |
5 | a0001c0001t0001g0081a0001c0001t0002g0027a0001c0001t0002g0028others(2): Show | 5 | HG03669.hp2 HG04204.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-1131_694-1112d others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
T | TCCTCCCT others(17): Show |
6 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0003g0092others(3): Show | 6 | HG00099.hp2 HG00280.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-1135_694-1112d others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
T | TCCTCCCT others(21): Show |
1 | a0001c0001t0003g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.694-1139_694-1112d others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
TCCTC | T | 21 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(18): Show | 23 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.694-1115_694-1112d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
TCCTCCCT others(1): Show |
T | 16 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-1119_694-1112d others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703563
|
TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.694-1123_694-1112d others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | |||||
chr19:49703568
|
C | T | 35 | a0001c0001t0001g0164a0001c0001t0002g0050a0001c0001t0002g0052others(32): Show | 36 | HG00621.hp2 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.694-1142C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703568 | ||||||
chr19:49703587
|
C | CCTTCCCT others(13): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694-1122_694-1121i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | |||||
chr19:49703587
|
C | CCTTCCCT others(17): Show |
3 | a0001c0002t0002g0198a0001c0002t0002g0207a0003c0007t0002g0208 | 3 | HG01192.hp2 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.694-1122_694-1121i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | |||||
chr19:49703587
|
C | CCTTCCCT others(21): Show |
4 | a0001c0002t0002g0190a0001c0002t0002g0196a0001c0004t0002g0203others(1): Show | 4 | HG01074.hp2 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-1122_694-1121i others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | |||||
chr19:49703587
|
C | CCTTCCCT others(25): Show |
8 | a0001c0002t0002g0010a0001c0002t0002g0192a0001c0002t0002g0199others(5): Show | 9 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.694-1122_694-1121i others(34): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | |||||
chr19:49703587
|
C | CCTTCCCT others(29): Show |
2 | a0001c0002t0002g0197a0002c0005t0002g0200 | 2 | HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.694-1122_694-1121i others(38): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | |||||
chr19:49703587
|
C | CCTTCCCT others(33): Show |
2 | a0001c0002t0002g0194a0002c0005t0002g0195 | 2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.694-1122_694-1121i others(42): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | |||||
chr19:49703591
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-1119C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703591 | ||||||
chr19:49703595
|
C | CCCTCCCT others(17): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0139a0001c0001t0002g0171 | 3 | HG03453.hp2 NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(13): Show |
6 | a0001c0001t0001g0135a0001c0001t0001g0151a0001c0001t0001g0155others(3): Show | 7 | HG00558.hp2 HG00735.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(21): Show |
1 | a0001c0001t0002g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.694-1112_694-1111i others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(9): Show |
17 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 18 | HG00609.hp2 HG01175.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(13): Show |
1 | a0001c0001t0002g0053 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(17): Show |
7 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(4): Show | 8 | HG00642.hp1 HG01168.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(5): Show |
4 | a0001c0001t0001g0153a0001c0001t0002g0172a0001c0001t0002g0173others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(13): Show |
1 | a0001c0001t0002g0043 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(17): Show |
7 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0065others(4): Show | 7 | HG00423.hp2 HG02055.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(21): Show |
1 | a0001c0001t0002g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.694-1112_694-1111i others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(1): Show |
7 | a0001c0001t0001g0136a0001c0001t0002g0165a0001c0001t0002g0167others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(13): Show |
9 | a0001c0001t0001g0164a0001c0001t0002g0050a0001c0001t0002g0052others(6): Show | 9 | HG02129.hp1 HG02135.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTCCCT others(17): Show |
1 | a0001c0001t0002g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTT | 3 | a0001c0001t0001g0159a0001c0001t0001g0211a0001c0001t0001g0326 | 3 | HG00609.hp1 HG02015.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.694-1093_694-1090d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTTCCT others(13): Show |
4 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0075others(1): Show | 4 | HG02683.hp1 NA18951.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1109_694-1090d others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | CCCTTCCT others(17): Show |
2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.694-1113_694-1090d others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | |||||
chr19:49703595
|
C | T | 37 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(34): Show | 40 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.694-1115C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703595 | ||||||
chr19:49703599
|
T | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0113 | 3 | HG03491.hp1 HG03492.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.694-1111T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703599 | ||||||
chr19:49703787
|
T | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-923T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703787 | ||||||
chr19:49703793
|
T | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-917T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703793 | ||||||
chr19:49703908
|
G | C | 233 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0036others(230): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.694-802G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703908 | ||||||
chr19:49703948
|
A | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-762A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703948 | ||||||
chr19:49703949
|
C | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-761C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703949 | ||||||
chr19:49703958
|
C | T | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-752C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703958 | ||||||
chr19:49703960
|
A | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-750A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703960 | ||||||
chr19:49703963
|
G | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-747G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703963 | ||||||
chr19:49703967
|
G | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-743G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703967 | ||||||
chr19:49703969
|
G | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-741G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703969 | ||||||
chr19:49703971
|
C | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-739C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703971 | ||||||
chr19:49703972
|
A | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-738A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703972 | ||||||
chr19:49703974
|
A | T | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-736A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703974 | ||||||
chr19:49703976
|
G | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-734G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703976 | ||||||
chr19:49703979
|
C | A | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-731C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703979 | ||||||
chr19:49703980
|
C | A | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-730C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703980 | ||||||
chr19:49703983
|
T | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-727T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703983 | ||||||
chr19:49703984
|
T | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-726T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703984 | ||||||
chr19:49703986
|
T | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-724T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703986 | ||||||
chr19:49703987
|
T | A | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-723T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703987 | ||||||
chr19:49703988
|
T | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-722T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703988 | ||||||
chr19:49703992
|
T | A | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-718T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703992 | ||||||
chr19:49703996
|
A | T | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-714A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703996 | ||||||
chr19:49703997
|
C | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-713C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703997 | ||||||
chr19:49703999
|
A | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-711A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703999 | ||||||
chr19:49704001
|
A | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-709A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704001 | ||||||
chr19:49704006
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.694-704C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704006 | ||||||
chr19:49704007
|
A | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-703A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704007 | ||||||
chr19:49704008
|
A | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-702A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704008 | ||||||
chr19:49704009
|
A | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-701A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704009 | ||||||
chr19:49704024
|
C | G | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-686C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704024 | ||||||
chr19:49704025
|
A | T | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-685A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704025 | ||||||
chr19:49704026
|
G | A | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-684G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704026 | ||||||
chr19:49704028
|
T | C | 1 | a0002c0003t0003g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-682T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704028 | ||||||
chr19:49704149
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.694-561T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704149 | ||||||
chr19:49704253
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.694-457C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704253 | ||||||
chr19:49704266
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694-444G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704266 | ||||||
chr19:49704296
|
C | T | 2 | a0001c0002t0002g0199a0002c0005t0002g0200 | 2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.694-414C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704296 | ||||||
chr19:49704301
|
A | G | 25 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-409A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704301 | ||||||
chr19:49704328
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG01261.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-382C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704328 | ||||||
chr19:49704329
|
G | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-381G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704329 | ||||||
chr19:49704406
|
A | G | 2 | a0001c0002t0002g0192a0001c0002t0002g0196 | 2 | HG01074.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.694-304A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704406 | ||||||
chr19:49704460
|
C | A | 2 | a0001c0001t0002g0073a0002c0003t0002g0067 | 2 | HG00423.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.694-250C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704460 | ||||||
chr19:49704462
|
T | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-248T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704462 | ||||||
chr19:49704512
|
G | A | 2 | a0001c0001t0002g0073a0002c0003t0002g0067 | 2 | HG00423.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.694-198G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704512 | ||||||
chr19:49704517
|
A | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-193A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704517 | ||||||
chr19:49704583
|
G | T | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-127G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704583 | ||||||
chr19:49704902
|
AT | A | 40 | a0001c0001t0001g0164a0001c0001t0001g0309a0001c0001t0002g0005others(37): Show | 42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.772-104delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704902 | ||||||
chr19:49704923
|
G | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.772-84G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704923 | ||||||
chr19:49704931
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.772-76C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704931 | ||||||
chr19:49704956
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.772-51G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704956 | ||||||
chr19:49704997
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0256 | 2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.772-10T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704997 | ||||||
chr19:49705370
|
C | T | 14 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0003g0007others(11): Show | 16 | HG00099.hp2 HG00280.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.964+72C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705370 | ||||||
chr19:49705453
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0275a0001c0001t0001g0283others(4): Show | 8 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.964+155A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705453 | ||||||
chr19:49705492
|
G | A | 38 | a0001c0001t0001g0164a0001c0001t0001g0309a0001c0001t0002g0005others(35): Show | 40 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.964+194G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705492 | ||||||
chr19:49705658
|
C | G | 1 | a0001c0002t0002g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.965-251C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705658 | ||||||
chr19:49705685
|
C | G | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.965-224C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705685 | ||||||
chr19:49705685
|
C | T | 5 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0053others(2): Show | 5 | HG02129.hp1 NA18942.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-224C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705685 | ||||||
chr19:49705686
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.965-223G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705686 | ||||||
chr19:49705701
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.965-208A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705701 | ||||||
chr19:49705750
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.965-159C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705750 | ||||||
chr19:49705838
|
T | G | 49 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(46): Show | 52 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.965-71T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705838 | ||||||
chr19:49705881
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0307 | 2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.965-28C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705881 | ||||||
chr19:49706177
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1161-54G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 11/19 | chr19 | 49706177 | ||||||
chr19:49706472
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1343+59C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706472 | ||||||
chr19:49706476
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1343+63G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706476 | ||||||
chr19:49706482
|
T | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(17): Show | 21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1343+69T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706482 | ||||||
chr19:49706608
|
A | G | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1343+195A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706608 | ||||||
chr19:49706688
|
C | A | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+275C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706688 | ||||||
chr19:49706690
|
C | A | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+277C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706690 | ||||||
chr19:49706691
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+278A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706691 | ||||||
chr19:49706692
|
G | C | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+279G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706692 | ||||||
chr19:49706695
|
A | C | 1 | a0001c0001t0001g0265 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+282A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706695 | ||||||
chr19:49706749
|
C | T | 17 | a0001c0002t0002g0010a0001c0002t0002g0190a0001c0002t0002g0192others(14): Show | 18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1343+336C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706749 | ||||||
chr19:49706909
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1343+496C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706909 | ||||||
chr19:49707049
|
C | T | 1 | a0001c0002t0002g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1344-469C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707049 | ||||||
chr19:49707084
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0066 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1344-434G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707084 | ||||||
chr19:49707216
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1344-302C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707216 | ||||||
chr19:49707240
|
G | A | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344-278G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707240 | ||||||
chr19:49707241
|
C | A | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344-277C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707241 | ||||||
chr19:49707244
|
C | T | 3 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0101 | 3 | HG02970.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1344-274C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707244 | ||||||
chr19:49707285
|
C | G | 6 | a0001c0001t0001g0159a0001c0001t0002g0009a0001c0001t0002g0031others(3): Show | 7 | HG00735.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344-233C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707285 | ||||||
chr19:49707331
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1344-187C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707331 | ||||||
chr19:49707355
|
G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0319 | 3 | HG01106.hp2 HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1344-163G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707355 | ||||||
chr19:49707387
|
G | C | 3 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0101 | 3 | HG02970.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1344-131G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707387 | ||||||
chr19:49707724
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1449+101C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49707724 | ||||||
chr19:49707895
|
C | T | 1 | a0001c0001t0003g0120 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1449+272C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49707895 | ||||||
chr19:49707929
|
G | A | 1 | a0001c0002t0002g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1449+306G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49707929 | ||||||
chr19:49708002
|
C | CA | 22 | a0001c0001t0001g0016a0001c0001t0001g0085a0001c0001t0001g0128others(19): Show | 23 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1449+404dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | |||||
chr19:49708002
|
CA | C | 30 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(27): Show | 31 | HG00558.hp1 HG00621.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1449+404delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | |||||
chr19:49708002
|
CAA | C | 7 | a0001c0001t0001g0037a0001c0001t0002g0049a0001c0002t0002g0207others(4): Show | 7 | HG01070.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1449+403_1449+404d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | |||||
chr19:49708002
|
CAAAAA | C | 27 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(24): Show | 29 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1449+400_1449+404d others(7): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | |||||
chr19:49708022
|
A | G | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+399A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708022 | ||||||
chr19:49708227
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0086 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1450-496G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708227 | ||||||
chr19:49708291
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1450-432C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708291 | ||||||
chr19:49708310
|
A | C | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450-413A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708310 | ||||||
chr19:49708338
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0250 | 2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.1450-385A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708338 | ||||||
chr19:49708584
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(26): Show | 30 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1450-139G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708584 | ||||||
chr19:49708662
|
G | A | 3 | a0001c0004t0002g0191a0001c0004t0002g0202a0001c0004t0002g0203 | 3 | HG01516.hp2 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1450-61G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708662 | ||||||
chr19:49708715
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.1450-8G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708715 | ||||||
chr19:49708945
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1566+106A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49708945 | ||||||
chr19:49708995
|
C | T | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+156C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49708995 | ||||||
chr19:49709031
|
C | T | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+192C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709031 | ||||||
chr19:49709366
|
G | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1566+527G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709366 | ||||||
chr19:49709386
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1566+547C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709386 | ||||||
chr19:49709555
|
A | AT | 17 | a0001c0001t0001g0185a0001c0001t0001g0265a0001c0001t0001g0315others(14): Show | 17 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1566+733dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709555 | |||||
chr19:49709555
|
AT | A | 40 | a0001c0001t0001g0164a0001c0001t0001g0234a0001c0001t0001g0309others(37): Show | 42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1566+733delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709555 | |||||
chr19:49709767
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1567-553G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709767 | ||||||
chr19:49709855
|
A | AT | 11 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0163others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1567-455dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709855 | |||||
chr19:49709855
|
A | ATT | 19 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0175others(16): Show | 21 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567-456_1567-455d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709855 | |||||
chr19:49709910
|
G | A | 6 | a0001c0002t0002g0207a0001c0004t0002g0191a0001c0004t0002g0193others(3): Show | 6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-410G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709910 | ||||||
chr19:49709976
|
A | G | 2 | a0001c0001t0004g0231a0001c0001t0004g0232 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1567-344A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709976 | ||||||
chr19:49710075
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1567-245C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710075 | ||||||
chr19:49710084
|
G | A | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1567-236G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710084 | ||||||
chr19:49710139
|
C | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0102 | 2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1567-181C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710139 | ||||||
chr19:49710241
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1567-79C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710241 | ||||||
chr19:49710921
|
G | A | 7 | a0001c0001t0005g0091a0001c0002t0002g0207a0001c0004t0002g0191others(4): Show | 7 | HG01516.hp2 HG02109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1866+64G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49710921 | ||||||
chr19:49711151
|
T | C | 1 | a0001c0001t0003g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1866+294T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711151 | ||||||
chr19:49711167
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1866+310T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711167 | ||||||
chr19:49711210
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0002g0209 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1866+353C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711210 | ||||||
chr19:49711260
|
A | AT | 100 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0124others(97): Show | 105 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1866+421dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr19 | 49711260 | |||||
chr19:49711260
|
A | ATT | 43 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(40): Show | 44 | HG00423.hp2 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1866+420_1866+421d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr19 | 49711260 | |||||
chr19:49711296
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1866+439G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711296 | ||||||
chr19:49711298
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0003g0088 | 3 | HG02615.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1866+441G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711298 | ||||||
chr19:49711359
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1867-450G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711359 | ||||||
chr19:49711396
|
T | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(131): Show | 140 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1867-413T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711396 | ||||||
chr19:49711424
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1867-385A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711424 | ||||||
chr19:49711567
|
A | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(38): Show | 42 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1867-242A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711567 | ||||||
chr19:49711580
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1867-229G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711580 | ||||||
chr19:49711611
|
G | A | 44 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0309others(41): Show | 47 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1867-198G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711611 | ||||||
chr19:49711644
|
A | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(27): Show | 31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1867-165A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711644 | ||||||
chr19:49712010
|
G | A | 5 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0004g0310others(2): Show | 5 | HG02630.hp2 HG02735.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019+49G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712010 | ||||||
chr19:49712081
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(34): Show | 38 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.2019+120G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712081 | ||||||
chr19:49712110
|
A | T | 1 | a0001c0001t0001g0277 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2019+149A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712110 | ||||||
chr19:49712117
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2019+156C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712117 | ||||||
chr19:49712203
|
T | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(35): Show | 39 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.2019+242T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712203 | ||||||
chr19:49712343
|
C | CA | 11 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0001g0183others(8): Show | 11 | HG00621.hp2 HG01261.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.2020-377dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0005g0105a0001c0001t0006g0069 | 2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2020-387_2020-377d others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0006g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2019+387_2020-377d others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0140 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2019+386_2020-377d others(15): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(7): Show |
18 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0134others(15): Show | 19 | HG01175.hp1 HG01975.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2019+385_2020-377d others(16): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0144others(3): Show | 6 | HG02015.hp1 HG02080.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+384_2020-377d others(17): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0150others(1): Show | 4 | HG00558.hp2 HG00609.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+383_2020-377d others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712343
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2020-377_2020-376i others(19): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | |||||
chr19:49712385
|
G | A | 1 | a0001c0006t0001g0145 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2020-351G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712385 | ||||||
chr19:49712446
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2020-290A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712446 | ||||||
chr19:49712483
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(12): Show | 16 | HG00423.hp2 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.2020-253G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712483 | ||||||
chr19:49712510
|
G | A | 1 | a0002c0003t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2020-226G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712510 | ||||||
chr19:49712545
|
CGTGGGT | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0130others(34): Show | 38 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.2020-183_2020-178d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712545 | |||||
chr19:49712700
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0237a0001c0001t0001g0299others(1): Show | 5 | HG02056.hp1 HG02074.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.2020-36C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712700 | ||||||
chr19:49712861
|
T | TG | 329 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(326): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2133+15dupG | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr19 | 49712861 | |||||
chr19:49713130
|
C | T | 1 | a0001c0001t0001g0017 | 2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2226+66C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | chr19 | 49713130 | ||||||
chr19:49713185
|
A | AGGAGTCC others(67): Show |
1 | a0001c0001t0001g0259 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2226+156_2227-127d others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr19 | 49713185 | |||||
chr19:49713185
|
AGGAGTCC others(30): Show |
A | 2 | a0001c0002t0002g0198a0002c0003t0001g0142 | 2 | HG01192.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.2227-163_2227-127d others(39): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr19 | 49713185 | |||||
chr19:49713314
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0256 | 2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2227-106T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | chr19 | 49713314 |