geneid | 10841 |
---|---|
ensemblid | ENSG00000160282.15 |
hgncid | 3974 |
symbol | FTCD |
name | formimidoyltransferase cyclodeaminase |
refseq_nuc | NM_206965.2 |
refseq_prot | NP_996848.1 |
ensembl_nuc | ENST00000397746.8 |
ensembl_prot | ENSP00000380854.3 |
mane_status | MANE Select |
chr | chr21 |
start | 46136779 |
end | 46155579 |
strand | - |
ver | v1.2 |
region | chr21:46136779-46155579 |
region5000 | chr21:46131779-46160579 |
regionname0 | FTCD_chr21_46136779_46155579 |
regionname5000 | FTCD_chr21_46131779_46160579 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 181 | 57 | 41 | 46 | 12 | 23 | 32 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002 | 0/0 | 541 | 20 | 2 | 3 | 12 | 0 | 3 | 7 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003 | 0/0 | 541 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0004 | 0/0 | 541 | 4 | 1 | 1 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0005 | 0/0 | 541 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0006 | 0/0 | 541 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0007 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0008 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0009 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0010 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0011 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0012 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0013 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0014 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0015 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0016 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0017 | 0/0 | 541 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1626 | 73 | 24 | 25 | 12 | 4 | 7 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0002 | 1/0 | 1626 | 60 | 21 | 13 | 9 | 6 | 10 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0003 | 0/0 | 1626 | 28 | 4 | 2 | 19 | 0 | 3 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0004 | 0/0 | 1626 | 11 | 1 | 1 | 5 | 2 | 2 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0005 | 0/0 | 1626 | 7 | 0 | 2 | 4 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0006 | 0/0 | 1626 | 6 | 1 | 1 | 4 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0007 | 0/0 | 1626 | 5 | 4 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0008 | 0/0 | 1626 | 4 | 1 | 1 | 0 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0009 | 0/0 | 1626 | 3 | 0 | 0 | 3 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0010 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0011 | 0/0 | 1626 | 2 | 0 | 0 | 0 | 0 | 2 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0012 | 0/0 | 1626 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0013 | 0/0 | 1626 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0014 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0015 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0016 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0017 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0018 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0019 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0020 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0021 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0022 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0023 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0024 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0025 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0026 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0027 | 0/0 | 1673 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0028 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0029 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0030 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0031 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0032 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0033 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0034 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0035 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
c0036 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 265 | 105 | 27 | 37 | 25 | 3 | 12 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0002 | 1/0 | 265 | 61 | 27 | 7 | 7 | 6 | 13 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0003 | 0/0 | 265 | 21 | 5 | 2 | 10 | 0 | 4 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0004 | 0/0 | 265 | 11 | 0 | 3 | 7 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0005 | 0/0 | 265 | 9 | 0 | 0 | 9 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0006 | 0/0 | 265 | 7 | 7 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0007 | 0/0 | 265 | 7 | 4 | 1 | 0 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0008 | 0/0 | 265 | 5 | 0 | 0 | 4 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
t0009 | 0/0 | 265 | 4 | 0 | 0 | 2 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1626 | 73 | 24 | 25 | 12 | 4 | 7 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002 | 1/0 | 1626 | 60 | 21 | 13 | 9 | 6 | 10 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0003 | 0/0 | 1626 | 28 | 4 | 2 | 19 | 0 | 3 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0004 | 0/0 | 1626 | 11 | 1 | 1 | 5 | 2 | 2 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0010 | 0/0 | 1626 | 3 | 3 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0021 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0022 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0025 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0031 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0032 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0035 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0005 | 0/0 | 1626 | 7 | 0 | 2 | 4 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0006 | 0/0 | 1626 | 6 | 1 | 1 | 4 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0009 | 0/0 | 1626 | 3 | 0 | 0 | 3 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0011 | 0/0 | 1626 | 2 | 0 | 0 | 0 | 0 | 2 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0016 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0018 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0007 | 0/0 | 1626 | 5 | 4 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0014 | 0/0 | 1626 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0015 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0034 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0004c0008 | 0/0 | 1626 | 4 | 1 | 1 | 0 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0005c0012 | 0/0 | 1626 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0005c0017 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0006c0013 | 0/0 | 1626 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0007c0036 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0008c0019 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0009c0020 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0010c0026 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0011c0029 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0012c0028 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0013c0030 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0014c0027 | 0/0 | 1673 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0015c0023 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0016c0033 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0017c0024 | 0/0 | 1626 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1890 | 55 | 15 | 22 | 9 | 2 | 6 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0001t0002 | 0/0 | 1890 | 3 | 2 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0001t0004 | 0/0 | 1890 | 6 | 0 | 3 | 2 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0001t0006 | 0/0 | 1890 | 3 | 3 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0001t0007 | 0/0 | 1890 | 4 | 4 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0001t0008 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0001t0009 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002t0001 | 0/0 | 1890 | 23 | 6 | 9 | 4 | 1 | 3 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002t0002 | 1/0 | 1890 | 27 | 11 | 4 | 1 | 4 | 6 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002t0004 | 0/0 | 1890 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002t0006 | 0/0 | 1890 | 4 | 4 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002t0008 | 0/0 | 1890 | 2 | 0 | 0 | 1 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0002t0009 | 0/0 | 1890 | 2 | 0 | 0 | 1 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0003t0002 | 0/0 | 1890 | 3 | 1 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0003t0003 | 0/0 | 1890 | 16 | 3 | 2 | 8 | 0 | 3 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0003t0005 | 0/0 | 1890 | 8 | 0 | 0 | 8 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0003t0008 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0004t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0004t0002 | 0/0 | 1890 | 9 | 1 | 1 | 3 | 2 | 2 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0004t0008 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0010t0002 | 0/0 | 1890 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0010t0003 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0021t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0022t0003 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0025t0002 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0031t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0032t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0001c0035t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0005t0001 | 0/0 | 1890 | 7 | 0 | 2 | 4 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0006t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0006t0002 | 0/0 | 1890 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0006t0004 | 0/0 | 1890 | 3 | 0 | 0 | 3 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0009t0003 | 0/0 | 1890 | 2 | 0 | 0 | 2 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0009t0005 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0011t0002 | 0/0 | 1890 | 2 | 0 | 0 | 0 | 0 | 2 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0016t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0002c0018t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0007t0002 | 0/0 | 1890 | 5 | 4 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0014t0001 | 0/0 | 1890 | 2 | 1 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0015t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0003c0034t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0004c0008t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0004c0008t0007 | 0/0 | 1890 | 3 | 0 | 1 | 0 | 2 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0005c0012t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0005c0012t0009 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0005c0017t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0006c0013t0001 | 0/0 | 1890 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0007c0036t0001 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0008c0019t0001 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0009c0020t0003 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0010c0026t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0011c0029t0001 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0012c0028t0001 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0013c0030t0001 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0014c0027t0002 | 0/0 | 1937 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0015c0023t0002 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0016c0033t0002 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
a0017c0024t0001 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | copy fasta | chr21 | 46131779 | 46160579 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0002t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0003t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0004t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0010t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0010t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0010t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0021t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0022t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0025t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0031t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0032t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0001c0035t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0005t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0006t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0006t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0006t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0006t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0006t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0009t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0009t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0009t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0011t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0011t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0016t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0002c0018t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0007t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0007t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0007t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0007t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0007t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0014t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0014t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0015t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0003c0034t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0004c0008t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0004c0008t0007g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0004c0008t0007g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0004c0008t0007g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0005c0012t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0005c0012t0009g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0005c0017t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0006c0013t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0007c0036t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0008c0019t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0009c0020t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0010c0026t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0011c0029t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0012c0028t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0013c0030t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0014c0027t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0015c0023t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0016c0033t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
a0017c0024t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0102 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0017 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00140 | hp2 | a0004 | c0008 | t0007 | g0079 | EUR | GBR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00280 | hp1 | a0001 | c0004 | t0002 | g0069 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0206 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0061 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00323 | hp2 | a0001 | c0004 | t0002 | g0148 | EUR | FIN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00423 | hp1 | a0005 | c0012 | t0009 | g0014 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00423 | hp2 | a0001 | c0003 | t0005 | g0221 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00438 | hp2 | a0002 | c0006 | t0001 | g0099 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00544 | hp1 | a0001 | c0004 | t0002 | g0149 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00544 | hp2 | a0002 | c0009 | t0003 | g0088 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00558 | hp1 | a0010 | c0026 | t0001 | g0033 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00558 | hp2 | a0002 | c0005 | t0001 | g0066 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00609 | hp1 | a0005 | c0012 | t0001 | g0027 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00639 | hp2 | a0001 | c0004 | t0002 | g0178 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00673 | hp1 | a0002 | c0009 | t0005 | g0205 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00673 | hp2 | a0001 | c0003 | t0008 | g0210 | EAS | CHS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00733 | hp1 | a0002 | c0005 | t0001 | g0146 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00738 | hp1 | a0004 | c0008 | t0007 | g0063 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01069 | hp1 | a0002 | c0005 | t0001 | g0194 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01069 | hp2 | a0006 | c0013 | t0001 | g0004 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01071 | hp1 | a0006 | c0013 | t0001 | g0004 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01081 | hp1 | a0002 | c0006 | t0002 | g0029 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01167 | hp2 | a0003 | c0014 | t0001 | g0118 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01168 | hp2 | a0001 | c0003 | t0003 | g0070 | AMR | PUR | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01517 | hp1 | a0004 | c0008 | t0007 | g0015 | EUR | IBS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01517 | hp2 | a0001 | c0001 | t0009 | g0094 | EUR | IBS | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01884 | hp2 | a0003 | c0007 | t0002 | g0136 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01943 | hp2 | a0008 | c0019 | t0001 | g0057 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01975 | hp1 | a0001 | c0003 | t0003 | g0174 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01978 | hp1 | a0003 | c0007 | t0002 | g0138 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02027 | hp2 | a0002 | c0006 | t0004 | g0201 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02040 | hp1 | a0001 | c0003 | t0005 | g0214 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02040 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02132 | hp1 | a0001 | c0003 | t0005 | g0217 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02132 | hp2 | a0001 | c0004 | t0002 | g0031 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02135 | hp1 | a0012 | c0028 | t0001 | g0009 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02135 | hp2 | a0001 | c0001 | t0008 | g0211 | EAS | KHV | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02165 | hp2 | a0001 | c0003 | t0003 | g0089 | EAS | CDX | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02258 | hp1 | a0003 | c0007 | t0002 | g0135 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0139 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02280 | hp1 | a0001 | c0032 | t0001 | g0182 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02451 | hp1 | a0001 | c0031 | t0001 | g0184 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0120 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02630 | hp2 | a0001 | c0010 | t0002 | g0199 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02717 | hp1 | a0003 | c0007 | t0002 | g0077 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02723 | hp2 | a0001 | c0003 | t0003 | g0134 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02818 | hp1 | a0002 | c0006 | t0002 | g0183 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02886 | hp1 | a0001 | c0004 | t0002 | g0141 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0111 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02897 | hp2 | a0001 | c0002 | t0006 | g0083 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0081 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02922 | hp2 | a0001 | c0003 | t0003 | g0110 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02965 | hp1 | a0003 | c0015 | t0002 | g0007 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02970 | hp1 | a0001 | c0035 | t0002 | g0191 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03017 | hp2 | a0001 | c0004 | t0002 | g0030 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03130 | hp2 | a0003 | c0014 | t0001 | g0137 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0128 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03453 | hp2 | a0002 | c0018 | t0002 | g0129 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03486 | hp1 | a0009 | c0020 | t0003 | g0130 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03491 | hp2 | a0001 | c0003 | t0003 | g0092 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0095 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03516 | hp1 | a0015 | c0023 | t0002 | g0179 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ESN | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03540 | hp2 | a0001 | c0010 | t0003 | g0114 | AFR | GWD | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03579 | hp1 | a0013 | c0030 | t0001 | g0172 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03579 | hp2 | a0001 | c0002 | t0006 | g0082 | AFR | MSL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03654 | hp1 | a0017 | c0024 | t0001 | g0150 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03654 | hp2 | a0001 | c0002 | t0008 | g0219 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03669 | hp1 | a0001 | c0003 | t0003 | g0020 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0145 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03688 | hp1 | a0002 | c0005 | t0001 | g0011 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03942 | hp1 | a0007 | c0036 | t0001 | g0024 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG03942 | hp2 | a0002 | c0011 | t0002 | g0098 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04115 | hp1 | a0016 | c0033 | t0002 | g0164 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0147 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04184 | hp1 | a0001 | c0022 | t0003 | g0193 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04184 | hp2 | a0014 | c0027 | t0002 | g0073 | SAS | BEB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04204 | hp2 | a0001 | c0004 | t0002 | g0100 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04228 | hp1 | a0002 | c0011 | t0002 | g0062 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | STU | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18612 | hp2 | a0011 | c0029 | t0001 | g0090 | EAS | CHB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18943 | hp1 | a0001 | c0003 | t0005 | g0215 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18943 | hp2 | a0002 | c0006 | t0004 | g0202 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18944 | hp2 | a0001 | c0002 | t0009 | g0046 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18945 | hp1 | a0002 | c0005 | t0001 | g0067 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18945 | hp2 | a0001 | c0003 | t0003 | g0051 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18947 | hp1 | a0001 | c0003 | t0005 | g0218 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18947 | hp2 | a0001 | c0002 | t0008 | g0220 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18952 | hp1 | a0002 | c0005 | t0001 | g0026 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18952 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0034 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18966 | hp2 | a0002 | c0009 | t0003 | g0068 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18970 | hp1 | a0001 | c0003 | t0005 | g0213 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18971 | hp1 | a0001 | c0003 | t0003 | g0075 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18971 | hp2 | a0001 | c0003 | t0005 | g0212 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18973 | hp2 | a0001 | c0002 | t0004 | g0204 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18980 | hp1 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18980 | hp2 | a0001 | c0003 | t0003 | g0105 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18983 | hp1 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18984 | hp1 | a0001 | c0002 | t0004 | g0207 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18984 | hp2 | a0005 | c0017 | t0001 | g0060 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18990 | hp1 | a0002 | c0005 | t0001 | g0028 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA18990 | hp2 | a0002 | c0016 | t0001 | g0025 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19000 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19005 | hp2 | a0001 | c0003 | t0005 | g0216 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19043 | hp2 | a0001 | c0010 | t0002 | g0200 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19064 | hp1 | a0001 | c0004 | t0008 | g0222 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19064 | hp2 | a0001 | c0025 | t0002 | g0032 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19066 | hp1 | a0002 | c0006 | t0004 | g0203 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19066 | hp2 | a0001 | c0003 | t0003 | g0074 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19240 | hp1 | a0001 | c0003 | t0003 | g0106 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20129 | hp1 | a0004 | c0008 | t0001 | g0168 | AFR | ASW | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0170 | AFR | ASW | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0175 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20752 | hp2 | a0001 | c0002 | t0009 | g0155 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0044 | EUR | TSI | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | GIH | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02109 | hp1 | a0003 | c0034 | t0002 | g0117 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02109 | hp2 | a0001 | c0021 | t0001 | g0180 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG02559 | hp2 | a0001 | c0002 | t0006 | g0123 | AFR | ACB | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG06807 | hp1 | a0003 | c0007 | t0002 | g0078 | AFR | USA | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | USA | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0159 | REF | REF | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0080 | REF | REF | FTCD_chr21_46131779_46160579 | FTCD | chr21 | 46131779 | 46160579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:46137283
|
GCACGTTG others(26): Show |
G | 1 | a0012 | 1 | HG02135.hp1 | conservative_inframe_deletion | MODERATE | c.1462_1494delGAGATG others(27): Show |
p.Glu488_Val498del | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/14 | 1550/1890 | 1462/1626 | 488/541 | chr21 | 46137283 | ||
chr21:46138542
|
C | T | 1 | a0006 | 2 | HG01069.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.1409G>A | p.Arg470Gln | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1465/1890 | 1409/1626 | 470/541 | chr21 | 46138542 | ||
chr21:46138587
|
G | A | 1 | a0013 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1364C>T | p.Ala455Val | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1420/1890 | 1364/1626 | 455/541 | chr21 | 46138587 | ||
chr21:46138614
|
C | T | 3 | a0005a0011a0012 | 5 | HG00423.hp1 HG00609.hp1 HG02135.hp1 others(2): Show |
missense_variant | MODERATE | c.1337G>A | p.Arg446Gln | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1393/1890 | 1337/1626 | 446/541 | chr21 | 46138614 | ||
chr21:46138638
|
G | A | 1 | a0004 | 4 | HG00140.hp2 HG00738.hp1 HG01517.hp1 others(1): Show |
missense_variant | MODERATE | c.1313C>T | p.Ala438Val | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1369/1890 | 1313/1626 | 438/541 | chr21 | 46138638 | ||
chr21:46145471
|
C | CGAAGCCT others(40): Show |
1 | a0014 | 1 | HG04184.hp2 | frameshift_variant&stop_gained | HIGH | c.1159_1205dupCTGGAC others(41): Show |
p.Ala403fs | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/14 | 1261/1890 | 1205/1626 | 402/541 | chr21 | 46145471 | ||
chr21:46150186
|
T | A | 1 | a0015 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.839A>T | p.Asp280Val | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/14 | 895/1890 | 839/1626 | 280/541 | chr21 | 46150186 | ||
chr21:46151562
|
T | C | 1 | a0016 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.632A>G | p.Asp211Gly | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 688/1890 | 632/1626 | 211/541 | chr21 | 46151562 | ||
chr21:46151571
|
C | T | 1 | a0010 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.623G>A | p.Arg208His | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 679/1890 | 623/1626 | 208/541 | chr21 | 46151571 | ||
chr21:46151725
|
C | A | 1 | a0017 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.469G>T | p.Asp157Tyr | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 525/1890 | 469/1626 | 157/541 | chr21 | 46151725 | ||
chr21:46151896
|
T | A | 1 | a0003 | 9 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(6): Show |
missense_variant | MODERATE | c.452A>T | p.Lys151Met | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 508/1890 | 452/1626 | 151/541 | chr21 | 46151896 | ||
chr21:46151941
|
C | T | 1 | a0009 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.407G>A | p.Arg136Gln | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 463/1890 | 407/1626 | 136/541 | chr21 | 46151941 | ||
chr21:46151944
|
C | T | 1 | a0008 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.404G>A | p.Arg135His | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 460/1890 | 404/1626 | 135/541 | chr21 | 46151944 | ||
chr21:46152973
|
C | T | 2 | a0002a0005 | 23 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(20): Show |
missense_variant | MODERATE | c.301G>A | p.Val101Met | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/14 | 357/1890 | 301/1626 | 101/541 | chr21 | 46152973 | ||
chr21:46154293
|
C | A | 1 | a0007 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.94G>T | p.Gly32Cys | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/14 | 150/1890 | 94/1626 | 32/541 | chr21 | 46154293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:46137308
|
G | A | 8 | a0001c0003a0001c0010a0001c0022others(5): Show | 43 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(40): Show |
synonymous_variant | LOW | c.1470C>T | p.Gly490Gly | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/14 | 1526/1890 | 1470/1626 | 490/541 | chr21 | 46137308 | ||
chr21:46138559
|
G | C | 21 | a0001c0001a0001c0010a0001c0021others(18): Show | 107 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(104): Show |
synonymous_variant | LOW | c.1392C>G | p.Ala464Ala | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/14 | 1448/1890 | 1392/1626 | 464/541 | chr21 | 46138559 | ||
chr21:46145866
|
G | C | 4 | a0001c0031a0003c0007a0003c0014others(1): Show | 9 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(6): Show |
synonymous_variant | LOW | c.1050C>G | p.Arg350Arg | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/14 | 1106/1890 | 1050/1626 | 350/541 | chr21 | 46145866 | ||
chr21:46145929
|
G | C | 1 | a0001c0032 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.987C>G | p.Arg329Arg | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/14 | 1043/1890 | 987/1626 | 329/541 | chr21 | 46145929 | ||
chr21:46146315
|
G | A | 1 | a0003c0014 | 2 | HG01167.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.919C>T | p.Leu307Leu | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/14 | 975/1890 | 919/1626 | 307/541 | chr21 | 46146315 | ||
chr21:46151714
|
G | T | 1 | a0001c0025 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.480C>A | p.Pro160Pro | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/14 | 536/1890 | 480/1626 | 160/541 | chr21 | 46151714 | ||
chr21:46151931
|
C | T | 7 | a0001c0004a0001c0021a0001c0022others(4): Show | 18 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(15): Show |
synonymous_variant | LOW | c.417G>A | p.Pro139Pro | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/14 | 473/1890 | 417/1626 | 139/541 | chr21 | 46151931 | ||
chr21:46154168
|
G | A | 1 | a0001c0035 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.219C>T | p.Ile73Ile | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/14 | 275/1890 | 219/1626 | 73/541 | chr21 | 46154168 | ||
chr21:46155488
|
C | T | 1 | a0003c0015 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.36G>A | p.Ser12Ser | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/14 | 92/1890 | 36/1626 | 12/541 | chr21 | 46155488 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:46136855
|
G | A | 2 | a0001c0001t0006a0001c0002t0006 | 7 | HG02257.hp2 HG02559.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*132C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 132 | chr21 | 46136855 | |||||
chr21:46136879
|
C | T | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(26): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*108G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 108 | chr21 | 46136879 | |||||
chr21:46136895
|
C | T | 10 | a0001c0001t0009a0001c0002t0009a0001c0003t0003others(7): Show | 34 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*92G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 92 | chr21 | 46136895 | |||||
chr21:46136968
|
G | A | 2 | a0001c0001t0007a0004c0008t0007 | 7 | HG00140.hp2 HG00738.hp1 HG01517.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*19C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 14/14 | 19 | chr21 | 46136968 | |||||
chr21:46155556
|
G | A | 9 | a0001c0001t0004a0001c0001t0008a0001c0002t0004others(6): Show | 25 | HG00280.hp2 HG00423.hp2 HG00673.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/14 | 33 | chr21 | 46155556 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:46137152
|
C | A | 2 | a0001c0001t0001g0166a0007c0036t0001g0024 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1540-79G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/13 | chr21 | 46137152 | ||||||
chr21:46137160
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(216): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1539+79T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/13 | chr21 | 46137160 | ||||||
chr21:46137204
|
G | A | 3 | a0004c0008t0007g0015a0004c0008t0007g0063a0004c0008t0007g0079 | 3 | HG00140.hp2 HG00738.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1539+35C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 13/13 | chr21 | 46137204 | ||||||
chr21:46137466
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0188 | 2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1444-132G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137466 | ||||||
chr21:46137499
|
C | T | 4 | a0001c0002t0002g0113a0001c0002t0002g0147a0003c0015t0002g0007others(1): Show | 4 | HG02965.hp1 HG03516.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444-165G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137499 | ||||||
chr21:46137554
|
G | A | 10 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0001t0002g0140others(7): Show | 10 | HG02257.hp2 HG02559.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444-220C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137554 | ||||||
chr21:46137585
|
G | A | 2 | a0004c0008t0007g0063a0004c0008t0007g0079 | 2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1444-251C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137585 | ||||||
chr21:46137614
|
A | C | 2 | a0001c0002t0002g0091a0001c0004t0002g0031 | 2 | HG00438.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1444-280T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137614 | ||||||
chr21:46137619
|
CAA | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 132 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1444-287_1444-286d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137619 | ||||||
chr21:46137737
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1444-403C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137737 | ||||||
chr21:46137739
|
G | A | 1 | a0005c0012t0009g0014 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1444-405C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137739 | ||||||
chr21:46137741
|
C | CTTTCCTA others(23): Show |
1 | a0001c0002t0002g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1444-437_1444-408d others(32): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137741 | ||||||
chr21:46137741
|
C | T | 1 | a0004c0008t0007g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1444-407G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137741 | ||||||
chr21:46137808
|
A | G | 1 | a0002c0005t0001g0194 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1444-474T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137808 | ||||||
chr21:46137849
|
CCT | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1444-517_1444-516d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137849 | ||||||
chr21:46137936
|
A | T | 1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1443+572T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137936 | ||||||
chr21:46137937
|
C | G | 1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1443+571G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137937 | ||||||
chr21:46137966
|
G | A | 38 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0037others(35): Show | 40 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1443+542C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137966 | ||||||
chr21:46137980
|
T | C | 3 | a0004c0008t0007g0015a0004c0008t0007g0063a0004c0008t0007g0079 | 3 | HG00140.hp2 HG00738.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1443+528A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46137980 | ||||||
chr21:46138059
|
A | G | 1 | a0001c0002t0008g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1443+449T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138059 | ||||||
chr21:46138071
|
T | C | 1 | a0001c0002t0002g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1443+437A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138071 | ||||||
chr21:46138083
|
G | A | 2 | a0001c0010t0002g0199a0001c0010t0002g0200 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1443+425C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138083 | ||||||
chr21:46138111
|
G | A | 1 | a0001c0002t0002g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1443+397C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138111 | ||||||
chr21:46138137
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1443+371G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138137 | ||||||
chr21:46138214
|
A | C | 13 | a0001c0001t0001g0104a0001c0001t0009g0094a0001c0002t0002g0113others(10): Show | 13 | HG00639.hp2 HG00642.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1443+294T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138214 | ||||||
chr21:46138235
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1443+273C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138235 | ||||||
chr21:46138266
|
G | C | 1 | a0015c0023t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1443+242C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138266 | ||||||
chr21:46138316
|
G | A | 2 | a0001c0002t0002g0121a0001c0002t0002g0190 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1443+192C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138316 | ||||||
chr21:46138349
|
G | A | 1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1443+159C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138349 | ||||||
chr21:46138372
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1443+136G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138372 | ||||||
chr21:46138375
|
C | T | 1 | a0001c0004t0008g0222 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1443+133G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138375 | ||||||
chr21:46138430
|
G | A | 1 | a0001c0002t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1443+78C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 12/13 | chr21 | 46138430 | ||||||
chr21:46138672
|
A | G | 80 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0125others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1305-26T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138672 | ||||||
chr21:46138675
|
A | G | 19 | a0001c0001t0001g0101a0001c0001t0001g0142a0001c0001t0002g0140others(16): Show | 19 | HG00438.hp2 HG00639.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1305-29T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138675 | ||||||
chr21:46138677
|
A | G | 66 | a0001c0001t0001g0093a0001c0001t0001g0125a0001c0001t0001g0132others(63): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.1305-31T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138677 | ||||||
chr21:46138800
|
C | T | 1 | a0001c0003t0005g0218 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1304+80G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138800 | ||||||
chr21:46138801
|
A | G | 1 | a0001c0010t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1304+79T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138801 | ||||||
chr21:46138854
|
C | T | 1 | a0001c0002t0002g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1304+26G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138854 | ||||||
chr21:46138855
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1304+25C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 11/13 | chr21 | 46138855 | ||||||
chr21:46138983
|
T | C | 1 | a0001c0001t0004g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1261-60A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46138983 | ||||||
chr21:46138990
|
C | T | 2 | a0001c0002t0002g0147a0002c0006t0001g0099 | 2 | HG00438.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1261-67G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46138990 | ||||||
chr21:46139080
|
A | G | 95 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(92): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1261-157T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139080 | ||||||
chr21:46139148
|
G | A | 6 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(3): Show | 6 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1261-225C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139148 | ||||||
chr21:46139287
|
G | A | 1 | a0001c0035t0002g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1261-364C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139287 | ||||||
chr21:46139417
|
G | A | 1 | a0001c0002t0004g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1261-494C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139417 | ||||||
chr21:46139434
|
G | A | 2 | a0001c0001t0009g0094a0001c0002t0009g0155 | 2 | HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1261-511C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139434 | ||||||
chr21:46139466
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1261-543G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139466 | ||||||
chr21:46139480
|
C | T | 1 | a0003c0015t0002g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1261-557G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139480 | ||||||
chr21:46139505
|
G | A | 39 | a0001c0001t0009g0094a0001c0002t0001g0076a0001c0002t0001g0096others(36): Show | 39 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1261-582C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139505 | ||||||
chr21:46139664
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1261-741G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139664 | ||||||
chr21:46139696
|
G | A | 33 | a0001c0001t0002g0048a0001c0001t0008g0211a0001c0002t0001g0042others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1261-773C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139696 | ||||||
chr21:46139827
|
C | T | 1 | a0001c0003t0003g0074 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1261-904G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139827 | ||||||
chr21:46139833
|
C | A | 14 | a0001c0002t0001g0043a0001c0002t0002g0044a0001c0002t0002g0072others(11): Show | 14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-910G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139833 | ||||||
chr21:46139856
|
G | A | 2 | a0001c0001t0009g0094a0001c0002t0009g0155 | 2 | HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1261-933C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139856 | ||||||
chr21:46139861
|
G | A | 33 | a0001c0001t0002g0048a0001c0001t0008g0211a0001c0002t0001g0042others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1261-938C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139861 | ||||||
chr21:46139932
|
G | A | 2 | a0001c0003t0003g0070a0002c0009t0005g0205 | 2 | HG00673.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1261-1009C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46139932 | ||||||
chr21:46140029
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(166): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1261-1106C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140029 | ||||||
chr21:46140031
|
G | A | 3 | a0001c0004t0002g0030a0001c0004t0002g0069a0001c0004t0002g0148 | 3 | HG00280.hp1 HG00323.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1261-1108C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140031 | ||||||
chr21:46140084
|
G | A | 7 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(4): Show | 8 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1261-1161C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140084 | ||||||
chr21:46140116
|
C | T | 2 | a0002c0006t0004g0202a0002c0006t0004g0203 | 2 | NA18943.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1261-1193G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140116 | ||||||
chr21:46140148
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1261-1225G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140148 | ||||||
chr21:46140264
|
G | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(137): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1261-1341C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140264 | ||||||
chr21:46140283
|
A | G | 4 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1360T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140283 | ||||||
chr21:46140283
|
ACAGGGAA others(194): Show |
A | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-1561_1261-136 others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140283 | ||||||
chr21:46140296
|
A | G | 32 | a0001c0001t0002g0048a0001c0001t0008g0211a0001c0002t0001g0042others(29): Show | 33 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1261-1373T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140296 | ||||||
chr21:46140359
|
TC | T | 5 | a0001c0001t0002g0140a0001c0001t0006g0124a0001c0001t0006g0126others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-1437delG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140359 | ||||||
chr21:46140360
|
C | CCCCCGTC others(43): Show |
199 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(196): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1261-1487_1261-143 others(54): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140360 | ||||||
chr21:46140408
|
A | ACTCCCCG others(143): Show |
1 | a0001c0004t0002g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1261-1486_1261-148 others(154): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140408 | ||||||
chr21:46140410
|
T | TC | 5 | a0001c0001t0002g0140a0001c0001t0006g0124a0001c0001t0006g0126others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-1488dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140410 | ||||||
chr21:46140415
|
G | A | 1 | a0001c0001t0006g0124 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1261-1492C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140415 | ||||||
chr21:46140425
|
G | A | 7 | a0001c0001t0002g0140a0001c0001t0006g0124a0001c0001t0006g0126others(4): Show | 7 | HG01978.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1261-1502C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140425 | ||||||
chr21:46140435
|
CAGGGAGT others(93): Show |
C | 4 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1612_1261-151 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140435 | ||||||
chr21:46140442
|
T | TGTAAACC others(93): Show |
1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1261-1520_1261-151 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140442 | ||||||
chr21:46140442
|
T | TGTAAACC others(143): Show |
1 | a0003c0007t0002g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1261-1520_1261-151 others(154): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140442 | ||||||
chr21:46140484
|
G | A | 1 | a0001c0004t0002g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1261-1561C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140484 | ||||||
chr21:46140525
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1602C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140525 | ||||||
chr21:46140527
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1604T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140527 | ||||||
chr21:46140529
|
T | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1606A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140529 | ||||||
chr21:46140535
|
G | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-1612C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140535 | ||||||
chr21:46140610
|
TC | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1688delG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140610 | ||||||
chr21:46140619
|
C | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1696G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140619 | ||||||
chr21:46140620
|
A | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1697T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140620 | ||||||
chr21:46140628
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1705C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140628 | ||||||
chr21:46140630
|
G | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1707C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140630 | ||||||
chr21:46140636
|
C | CAGGGAGT others(193): Show |
1 | a0002c0005t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1261-1714_1261-171 others(204): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140636 | ||||||
chr21:46140636
|
C | CAGGGAGT others(193): Show |
94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(91): Show | 99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1261-1714_1261-171 others(204): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140636 | ||||||
chr21:46140643
|
T | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1720A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140643 | ||||||
chr21:46140651
|
C | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(153): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1261-1728G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140651 | ||||||
chr21:46140661
|
T | TCCTCGTC others(194): Show |
7 | a0001c0002t0001g0084a0001c0002t0001g0115a0001c0002t0001g0116others(4): Show | 7 | HG00140.hp2 HG00738.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-1739_1261-173 others(205): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140661 | ||||||
chr21:46140664
|
C | T | 2 | a0001c0001t0001g0169a0002c0006t0004g0201 | 2 | HG00140.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1261-1741G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140664 | ||||||
chr21:46140677
|
C | T | 4 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1754G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140677 | ||||||
chr21:46140693
|
T | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1770A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140693 | ||||||
chr21:46140703
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1780A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140703 | ||||||
chr21:46140719
|
T | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1796A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140719 | ||||||
chr21:46140719
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1796A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140719 | ||||||
chr21:46140720
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1797C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140720 | ||||||
chr21:46140728
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1805T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140728 | ||||||
chr21:46140730
|
T | G | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1807A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140730 | ||||||
chr21:46140743
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1820G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140743 | ||||||
chr21:46140753
|
C | CCCAGCAC others(343): Show |
1 | a0002c0006t0004g0201 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1261-1831_1261-183 others(354): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140753 | ||||||
chr21:46140753
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1261-1830G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140753 | ||||||
chr21:46140764
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1841G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140764 | ||||||
chr21:46140769
|
C | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1846G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140769 | ||||||
chr21:46140770
|
A | G | 18 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1261-1847T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140770 | ||||||
chr21:46140770
|
ACCTTCAC others(43): Show |
A | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1897_1261-184 others(54): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140770 | ||||||
chr21:46140777
|
C | T | 3 | a0001c0002t0002g0002a0001c0010t0002g0199a0001c0010t0002g0200 | 4 | HG02630.hp2 HG02723.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-1854G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140777 | ||||||
chr21:46140778
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1855C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140778 | ||||||
chr21:46140780
|
G | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(13): Show | 16 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1261-1857C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140780 | ||||||
chr21:46140793
|
C | T | 2 | a0001c0001t0001g0142a0002c0006t0004g0201 | 2 | HG02027.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1261-1870G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140793 | ||||||
chr21:46140803
|
T | C | 9 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(6): Show | 9 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-1880A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140803 | ||||||
chr21:46140811
|
T | TCCCCGTC others(345): Show |
1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1261-1889_1261-188 others(356): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140811 | ||||||
chr21:46140819
|
A | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(23): Show | 26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1896T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140819 | ||||||
chr21:46140819
|
A | T | 1 | a0002c0006t0004g0201 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1261-1896T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140819 | ||||||
chr21:46140819
|
AGCCTTCA others(43): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1261-1946_1261-189 others(54): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140819 | ||||||
chr21:46140820
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(23): Show | 26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1897C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140820 | ||||||
chr21:46140828
|
A | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(23): Show | 26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1905T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140828 | ||||||
chr21:46140830
|
T | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(23): Show | 26 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1261-1907A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140830 | ||||||
chr21:46140832
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1909G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140832 | ||||||
chr21:46140835
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1912T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140835 | ||||||
chr21:46140842
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1919C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140842 | ||||||
chr21:46140843
|
C | CGTAAACC others(93): Show |
136 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(133): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1261-1921_1261-192 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140843 | ||||||
chr21:46140843
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1261-1920G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140843 | ||||||
chr21:46140849
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1926G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140849 | ||||||
chr21:46140853
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1930A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140853 | ||||||
chr21:46140859
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1936T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140859 | ||||||
chr21:46140866
|
G | GTCTGCCT others(93): Show |
1 | a0001c0031t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1261-1944_1261-194 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140866 | ||||||
chr21:46140869
|
T | A | 10 | a0001c0001t0001g0142a0001c0001t0001g0181a0001c0001t0001g0185others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1261-1946A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140869 | ||||||
chr21:46140869
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1946A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140869 | ||||||
chr21:46140870
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1947C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140870 | ||||||
chr21:46140876
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1953T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140876 | ||||||
chr21:46140886
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1963G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140886 | ||||||
chr21:46140893
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1970G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140893 | ||||||
chr21:46140903
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1980A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140903 | ||||||
chr21:46140915
|
C | T | 37 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(34): Show | 37 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1261-1992G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140915 | ||||||
chr21:46140916
|
G | GTCCACCT others(93): Show |
1 | a0001c0001t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1261-1994_1261-199 others(104): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46140916 | ||||||
chr21:46141021
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-2098G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141021 | ||||||
chr21:46141031
|
C | T | 1 | a0001c0010t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1261-2108G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141031 | ||||||
chr21:46141032
|
C | T | 136 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0101others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1261-2109G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141032 | ||||||
chr21:46141091
|
T | G | 66 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0142others(63): Show | 66 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1261-2168A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141091 | ||||||
chr21:46141112
|
A | AACATAAA others(5): Show |
1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1261-2201_1261-219 others(16): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141112 | ||||||
chr21:46141124
|
TTCC | T | 14 | a0001c0002t0001g0043a0001c0002t0002g0044a0001c0002t0002g0072others(11): Show | 14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-2204_1261-220 others(7): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141124 | ||||||
chr21:46141127
|
C | T | 104 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0101others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1261-2204G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141127 | ||||||
chr21:46141225
|
ACTCCTGG others(7): Show |
A | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-2316_1261-230 others(18): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141225 | ||||||
chr21:46141258
|
C | T | 1 | a0003c0007t0002g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1261-2335G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141258 | ||||||
chr21:46141270
|
G | A | 1 | a0001c0001t0004g0223 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1261-2347C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141270 | ||||||
chr21:46141303
|
A | AT | 8 | a0001c0001t0001g0133a0001c0001t0002g0140a0001c0002t0001g0177others(5): Show | 9 | HG00738.hp1 HG01517.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-2381dupA | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141303 | ||||||
chr21:46141303
|
AT | A | 65 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0142others(62): Show | 65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1261-2381delA | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141303 | ||||||
chr21:46141356
|
A | T | 1 | a0002c0018t0002g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1261-2433T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141356 | ||||||
chr21:46141357
|
G | C | 14 | a0001c0002t0001g0043a0001c0002t0002g0044a0001c0002t0002g0072others(11): Show | 14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-2434C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141357 | ||||||
chr21:46141403
|
T | C | 66 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0142others(63): Show | 66 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1261-2480A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141403 | ||||||
chr21:46141405
|
C | A | 1 | a0001c0001t0002g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1261-2482G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141405 | ||||||
chr21:46141615
|
C | G | 1 | a0002c0006t0001g0099 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1261-2692G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141615 | ||||||
chr21:46141625
|
A | G | 6 | a0001c0001t0001g0012a0001c0002t0002g0102a0001c0002t0002g0161others(3): Show | 6 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-2702T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141625 | ||||||
chr21:46141653
|
A | G | 1 | a0001c0002t0001g0160 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1261-2730T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141653 | ||||||
chr21:46141716
|
T | TAA | 14 | a0001c0002t0001g0043a0001c0002t0002g0044a0001c0002t0002g0072others(11): Show | 14 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-2795_1261-279 others(6): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141716 | ||||||
chr21:46141802
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-2879A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141802 | ||||||
chr21:46141812
|
G | A | 48 | a0001c0001t0001g0101a0001c0001t0001g0142a0001c0001t0001g0181others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1261-2889C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141812 | ||||||
chr21:46141886
|
T | C | 30 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0142others(27): Show | 30 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1261-2963A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141886 | ||||||
chr21:46141914
|
G | C | 10 | a0001c0003t0002g0081a0001c0031t0001g0184a0003c0007t0002g0077others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-2991C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141914 | ||||||
chr21:46141957
|
G | T | 48 | a0001c0001t0001g0093a0001c0001t0001g0132a0001c0001t0001g0133others(45): Show | 49 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1261-3034C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46141957 | ||||||
chr21:46142039
|
G | C | 1 | a0001c0001t0009g0094 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1261-3116C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142039 | ||||||
chr21:46142059
|
G | A | 1 | a0002c0018t0002g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1261-3136C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142059 | ||||||
chr21:46142091
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1261-3168T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142091 | ||||||
chr21:46142094
|
GTAAA | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-3175_1261-317 others(8): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142094 | ||||||
chr21:46142276
|
G | GAGCTCTT others(66): Show |
9 | a0001c0001t0001g0142a0001c0001t0001g0181a0001c0001t0001g0185others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+3140_1260+314 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | ||||||
chr21:46142276
|
G | GAGCTCTT others(139): Show |
1 | a0001c0002t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1260+3140_1260+314 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | ||||||
chr21:46142276
|
G | GAGCTCTT others(139): Show |
1 | a0001c0010t0002g0200 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1260+3140_1260+314 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | ||||||
chr21:46142276
|
GAGCTCTT others(66): Show |
G | 6 | a0001c0001t0001g0035a0001c0002t0002g0061a0001c0002t0009g0046others(3): Show | 6 | HG00323.hp1 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+3068_1260+314 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142276 | ||||||
chr21:46142292
|
C | CGCGTCGG others(212): Show |
3 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171 | 3 | HG02257.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1260+3124_1260+312 others(223): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142292 | ||||||
chr21:46142292
|
C | CGCGTCGG others(285): Show |
1 | a0001c0002t0006g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1260+3124_1260+312 others(296): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142292 | ||||||
chr21:46142305
|
G | A | 1 | a0001c0010t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1260+3112C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142305 | ||||||
chr21:46142318
|
G | C | 61 | a0001c0001t0001g0012a0001c0001t0001g0142a0001c0001t0001g0181others(58): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1260+3099C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142318 | ||||||
chr21:46142319
|
G | A | 33 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(30): Show | 33 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1260+3098C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142319 | ||||||
chr21:46142319
|
G | C | 4 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+3098C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142319 | ||||||
chr21:46142319
|
G | GTGAGGCC others(67): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1260+3097_1260+309 others(78): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142319 | ||||||
chr21:46142329
|
A | AGACCTTC others(140): Show |
1 | a0001c0002t0008g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(151): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142329
|
A | AGACCTTC others(139): Show |
1 | a0001c0002t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142329
|
A | AGACCTTC others(139): Show |
1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142329
|
A | AGACCTTC others(66): Show |
2 | a0001c0001t0001g0133a0013c0030t0001g0172 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+3015_1260+308 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142329
|
A | AGACCTTC others(285): Show |
1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+3087_1260+308 others(296): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142329
|
A | AGACCTTC others(67): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0132 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1260+3087_1260+308 others(78): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142329
|
A | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0142a0001c0001t0001g0144others(59): Show | 62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+3088T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142329 | ||||||
chr21:46142346
|
C | G | 35 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+3071G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142346 | ||||||
chr21:46142347
|
A | ATAAGCTC others(212): Show |
2 | a0001c0002t0002g0161a0001c0002t0002g0162 | 2 | HG00733.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1260+3069_1260+307 others(223): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | ||||||
chr21:46142347
|
A | ATAAGCTC others(139): Show |
2 | a0002c0006t0002g0183a0002c0018t0002g0129 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+3069_1260+307 others(150): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | ||||||
chr21:46142347
|
A | ATAAGCTC others(66): Show |
1 | a0006c0013t0001g0004 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1260+2997_1260+306 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | ||||||
chr21:46142347
|
A | T | 35 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+3070T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | ||||||
chr21:46142347
|
ATAAGCTC others(66): Show |
A | 1 | a0001c0003t0005g0212 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1260+2997_1260+306 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142347 | ||||||
chr21:46142391
|
C | T | 2 | a0001c0002t0002g0121a0001c0002t0002g0139 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1260+3026G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142391 | ||||||
chr21:46142392
|
G | A | 4 | a0001c0002t0009g0046a0001c0003t0005g0213a0001c0003t0005g0215others(1): Show | 4 | NA18943.hp1 NA18944.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+3025C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142392 | ||||||
chr21:46142398
|
C | G | 2 | a0001c0002t0002g0121a0001c0002t0002g0139 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1260+3019G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142398 | ||||||
chr21:46142419
|
G | C | 35 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+2998C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142419 | ||||||
chr21:46142420
|
T | A | 35 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(32): Show | 35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1260+2997A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142420 | ||||||
chr21:46142420
|
T | TTAAGCTC others(66): Show |
2 | a0001c0001t0001g0166a0007c0036t0001g0024 | 2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1260+2996_1260+299 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142420 | ||||||
chr21:46142464
|
C | CGTGAGGC others(66): Show |
6 | a0001c0001t0001g0196a0001c0002t0001g0116a0001c0004t0002g0030others(3): Show | 6 | HG00140.hp2 HG00738.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+2952_1260+295 others(77): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142464 | ||||||
chr21:46142464
|
C | G | 61 | a0001c0001t0001g0012a0001c0001t0001g0093a0001c0001t0001g0132others(58): Show | 61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1260+2953G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142464 | ||||||
chr21:46142465
|
G | A | 1 | a0001c0002t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1260+2952C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142465 | ||||||
chr21:46142475
|
C | A | 10 | a0001c0002t0001g0177a0001c0031t0001g0184a0002c0018t0002g0129others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260+2942G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142475 | ||||||
chr21:46142483
|
G | A | 9 | a0001c0002t0001g0177a0001c0031t0001g0184a0003c0007t0002g0077others(6): Show | 9 | HG01167.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+2934C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142483 | ||||||
chr21:46142503
|
T | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0142others(33): Show | 36 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1260+2914A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142503 | ||||||
chr21:46142503
|
T | TACAGGTG others(67): Show |
1 | a0001c0002t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1260+2913_1260+291 others(78): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142503 | ||||||
chr21:46142523
|
G | C | 2 | a0001c0002t0004g0204a0002c0006t0004g0201 | 2 | HG02027.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1260+2894C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142523 | ||||||
chr21:46142531
|
C | T | 1 | a0001c0004t0002g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1260+2886G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142531 | ||||||
chr21:46142538
|
C | G | 17 | a0001c0001t0001g0133a0001c0001t0002g0140a0001c0001t0008g0211others(14): Show | 18 | HG00099.hp2 HG00639.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1260+2879G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142538 | ||||||
chr21:46142567
|
G | A | 2 | a0002c0006t0002g0183a0002c0018t0002g0129 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+2850C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142567 | ||||||
chr21:46142640
|
G | A | 1 | a0003c0014t0001g0118 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260+2777C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142640 | ||||||
chr21:46142646
|
T | C | 71 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1260+2771A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142646 | ||||||
chr21:46142651
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1260+2766A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142651 | ||||||
chr21:46142670
|
A | T | 82 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1260+2747T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142670 | ||||||
chr21:46142680
|
A | G | 67 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0103others(64): Show | 67 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1260+2737T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142680 | ||||||
chr21:46142691
|
G | A | 1 | a0001c0003t0008g0210 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1260+2726C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142691 | ||||||
chr21:46142692
|
A | G | 71 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1260+2725T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142692 | ||||||
chr21:46142718
|
T | C | 82 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1260+2699A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142718 | ||||||
chr21:46142721
|
C | T | 9 | a0001c0001t0001g0133a0001c0001t0002g0140a0001c0002t0001g0177others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+2696G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142721 | ||||||
chr21:46142722
|
G | C | 7 | a0001c0001t0001g0101a0001c0001t0001g0181a0001c0001t0001g0185others(4): Show | 7 | HG01433.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+2695C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142722 | ||||||
chr21:46142753
|
C | T | 52 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0001g0132others(49): Show | 54 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1260+2664G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142753 | ||||||
chr21:46142800
|
C | CG | 1 | a0001c0002t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+2616_1260+261 others(5): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142800 | ||||||
chr21:46142801
|
A | T | 1 | a0001c0002t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+2616T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142801 | ||||||
chr21:46142807
|
C | A | 1 | a0001c0002t0001g0005 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+2610G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142807 | ||||||
chr21:46142877
|
G | C | 71 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1260+2540C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142877 | ||||||
chr21:46142891
|
G | A | 1 | a0001c0022t0003g0193 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1260+2526C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142891 | ||||||
chr21:46142911
|
A | T | 1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+2506T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46142911 | ||||||
chr21:46143070
|
G | C | 7 | a0001c0001t0002g0140a0001c0002t0002g0121a0001c0002t0002g0139others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+2347C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143070 | ||||||
chr21:46143152
|
G | T | 1 | a0001c0002t0008g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1260+2265C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143152 | ||||||
chr21:46143252
|
G | A | 1 | a0001c0002t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1260+2165C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143252 | ||||||
chr21:46143431
|
C | G | 23 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0181others(20): Show | 23 | HG01433.hp1 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1260+1986G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143431 | ||||||
chr21:46143446
|
C | T | 69 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1260+1971G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143446 | ||||||
chr21:46143449
|
T | C | 69 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0125others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1260+1968A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143449 | ||||||
chr21:46143675
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1260+1742G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143675 | ||||||
chr21:46143710
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+1707G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143710 | ||||||
chr21:46143723
|
G | C | 11 | a0001c0001t0001g0101a0001c0001t0001g0181a0001c0001t0001g0187others(8): Show | 11 | HG01433.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+1694C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143723 | ||||||
chr21:46143756
|
T | G | 1 | a0001c0003t0005g0221 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1260+1661A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143756 | ||||||
chr21:46143779
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1260+1638G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143779 | ||||||
chr21:46143853
|
C | A | 1 | a0007c0036t0001g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1260+1564G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46143853 | ||||||
chr21:46144033
|
T | A | 1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+1384A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144033 | ||||||
chr21:46144044
|
A | G | 2 | a0001c0002t0002g0121a0001c0002t0002g0139 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1260+1373T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144044 | ||||||
chr21:46144048
|
G | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0142a0001c0001t0001g0144others(15): Show | 18 | HG00099.hp1 HG00438.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1260+1369C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144048 | ||||||
chr21:46144196
|
C | T | 1 | a0001c0002t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1260+1221G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144196 | ||||||
chr21:46144277
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1260+1140A>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144277 | ||||||
chr21:46144408
|
A | C | 1 | a0001c0003t0003g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260+1009T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144408 | ||||||
chr21:46144444
|
CT | C | 5 | a0001c0001t0001g0144a0001c0002t0002g0102a0001c0002t0008g0219others(2): Show | 5 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+972delA | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144444 | ||||||
chr21:46144447
|
T | C | 1 | a0001c0010t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1260+970A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144447 | ||||||
chr21:46144451
|
T | C | 1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+966A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144451 | ||||||
chr21:46144453
|
T | TCCCCCTC others(703): Show |
1 | a0001c0010t0003g0114 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1260+963_1260+964i others(712): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144453 | ||||||
chr21:46144466
|
C | CCCCTCTC others(740): Show |
1 | a0005c0012t0009g0014 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1260+950_1260+951i others(749): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144466 | ||||||
chr21:46144472
|
C | CTCCCCCC others(714): Show |
1 | a0001c0001t0001g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1260+944_1260+945i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | ||||||
chr21:46144472
|
C | CTCCCCCC others(712): Show |
1 | a0001c0001t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1260+944_1260+945i others(721): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | ||||||
chr21:46144472
|
C | CTCCCCCC others(711): Show |
4 | a0001c0001t0001g0085a0002c0005t0001g0194a0004c0008t0007g0015others(1): Show | 4 | HG00140.hp2 HG01069.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+944_1260+945i others(720): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | ||||||
chr21:46144472
|
C | CTCCCCCC others(714): Show |
1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1260+944_1260+945i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | ||||||
chr21:46144472
|
C | CTCCCCCC others(713): Show |
5 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0009g0155others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+944_1260+945i others(722): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | ||||||
chr21:46144472
|
C | CTCCCCCC others(716): Show |
1 | a0001c0001t0001g0064 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1260+944_1260+945i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144472 | ||||||
chr21:46144473
|
T | TC | 151 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(148): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1260+943dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144473 | ||||||
chr21:46144477
|
C | T | 1 | a0005c0012t0009g0014 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1260+940G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144477 | ||||||
chr21:46144478
|
C | CA | 38 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1260+938_1260+939i others(3): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144478 | ||||||
chr21:46144478
|
C | G | 1 | a0005c0012t0009g0014 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1260+939G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144478 | ||||||
chr21:46144483
|
C | CTCCCCTT others(721): Show |
1 | a0001c0003t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1260+933_1260+934i others(730): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144483 | ||||||
chr21:46144485
|
T | C | 1 | a0001c0003t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1260+932A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCCTT others(737): Show |
1 | a0001c0001t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(746): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTCC others(663): Show |
1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(672): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
1 | a0001c0001t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(730): Show |
1 | a0002c0011t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(739): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(698): Show |
1 | a0001c0001t0008g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(707): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(734): Show |
1 | a0002c0006t0004g0202 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(743): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(727): Show |
1 | a0001c0001t0001g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
1 | a0002c0005t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(735): Show |
1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(744): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(687): Show |
1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(696): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(716): Show |
1 | a0001c0002t0001g0153 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(751): Show |
1 | a0001c0001t0001g0013 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(760): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(723): Show |
2 | a0001c0002t0001g0005a0001c0002t0002g0061 | 3 | HG00323.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(722): Show |
1 | a0004c0008t0001g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(731): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(723): Show |
1 | a0001c0001t0001g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
1 | a0001c0001t0001g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
1 | a0002c0006t0004g0201 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
1 | a0001c0001t0004g0223 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(727): Show |
1 | a0001c0001t0007g0022 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
1 | a0001c0001t0004g0209 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
2 | a0002c0005t0001g0028a0002c0016t0001g0025 | 2 | NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
38 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(35): Show | 40 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(723): Show |
3 | a0001c0001t0001g0058a0001c0001t0004g0006a0001c0002t0001g0154 | 4 | HG01433.hp2 HG01496.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(714): Show |
1 | a0001c0001t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(716): Show |
1 | a0001c0035t0002g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(715): Show |
4 | a0001c0002t0001g0152a0001c0002t0001g0173a0001c0002t0001g0175others(1): Show | 4 | HG01256.hp1 HG01975.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(724): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(716): Show |
1 | a0013c0030t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(699): Show |
1 | a0001c0001t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(708): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(727): Show |
1 | a0001c0001t0001g0052 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(723): Show |
1 | a0001c0001t0001g0037 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(738): Show |
1 | a0001c0001t0001g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(747): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0001c0001t0001g0167 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0127a0001c0001t0001g0131 | 3 | HG00642.hp2 HG01258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(714): Show |
2 | a0001c0002t0002g0107a0003c0034t0002g0117 | 2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(734): Show |
1 | a0001c0002t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(743): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(716): Show |
1 | a0003c0007t0002g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(714): Show |
1 | a0003c0015t0002g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(713): Show |
5 | a0001c0031t0001g0184a0003c0007t0002g0078a0003c0007t0002g0135others(2): Show | 5 | HG01167.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(722): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(716): Show |
1 | a0003c0007t0002g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(712): Show |
1 | a0003c0007t0002g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(721): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(705): Show |
1 | a0001c0003t0002g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(714): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(738): Show |
1 | a0001c0002t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(747): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(740): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0186 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(749): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0001c0003t0002g0010 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(699): Show |
1 | a0001c0001t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(708): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(766): Show |
1 | a0012c0028t0001g0009 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(775): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(733): Show |
1 | a0001c0025t0002g0032 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(742): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(732): Show |
1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(741): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(732): Show |
7 | a0001c0001t0001g0012a0001c0002t0001g0043a0001c0002t0002g0044others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(741): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(732): Show |
1 | a0001c0002t0002g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(741): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0001c0003t0003g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0001c0003t0005g0216 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0001c0002t0001g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
1 | a0001c0002t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(723): Show |
1 | a0001c0003t0005g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(732): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0009c0020t0003g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(725): Show |
1 | a0002c0009t0003g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(734): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
20 | a0001c0002t0001g0096a0001c0002t0002g0113a0001c0003t0003g0008others(17): Show | 20 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(744): Show |
1 | a0001c0002t0006g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(753): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
1 | a0001c0003t0002g0157 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(722): Show |
4 | a0001c0002t0001g0109a0001c0002t0001g0112a0001c0003t0003g0110others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(731): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(679): Show |
1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(688): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(677): Show |
4 | a0001c0002t0002g0121a0001c0002t0002g0139a0001c0004t0002g0141others(1): Show | 4 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(686): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(713): Show |
1 | a0001c0004t0002g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(722): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(729): Show |
2 | a0001c0002t0001g0049a0016c0033t0002g0164 | 2 | HG00639.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(738): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(729): Show |
1 | a0002c0011t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(738): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(728): Show |
14 | a0001c0001t0002g0048a0001c0002t0001g0042a0001c0002t0001g0160others(11): Show | 15 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(737): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(726): Show |
1 | a0001c0004t0008g0222 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(735): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(729): Show |
1 | a0001c0004t0002g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(738): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(684): Show |
1 | a0015c0023t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(693): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(753): Show |
1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(762): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(751): Show |
5 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(760): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(717): Show |
5 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(726): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(719): Show |
1 | a0001c0002t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(728): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(697): Show |
1 | a0001c0022t0003g0193 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(706): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(706): Show |
1 | a0002c0006t0001g0099 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(715): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(696): Show |
4 | a0001c0001t0009g0094a0001c0002t0008g0220a0001c0003t0005g0212others(1): Show | 4 | HG00738.hp1 HG01517.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(705): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(716): Show |
3 | a0001c0002t0002g0003a0001c0002t0002g0017a0001c0002t0002g0190 | 4 | HG00099.hp2 HG02809.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(725): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(765): Show |
1 | a0002c0018t0002g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(774): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(765): Show |
1 | a0002c0006t0002g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(774): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(762): Show |
2 | a0001c0002t0002g0102a0001c0002t0008g0219 | 2 | HG00099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(771): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(763): Show |
1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(772): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(727): Show |
2 | a0001c0010t0002g0199a0001c0010t0002g0200 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1260+931_1260+932i others(736): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
1 | a0001c0001t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(721): Show |
1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(730): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(743): Show |
1 | a0001c0002t0006g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1260+931_1260+932i others(752): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(719): Show |
1 | a0001c0001t0001g0151 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(728): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(714): Show |
1 | a0001c0002t0001g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(723): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(720): Show |
1 | a0001c0002t0004g0207 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(729): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(722): Show |
1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(731): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(717): Show |
1 | a0001c0002t0002g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(726): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TCCCCTTT others(724): Show |
1 | a0001c0002t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1260+931_1260+932i others(733): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144485
|
T | TGTCTCC | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0085others(11): Show | 15 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1260+931_1260+932i others(8): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144485 | ||||||
chr21:46144492
|
T | TCCCCCCT others(728): Show |
1 | a0002c0005t0001g0026 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1260+924_1260+925i others(737): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144492 | ||||||
chr21:46144493
|
C | CCCCCCTC others(741): Show |
1 | a0001c0002t0006g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1260+923_1260+924i others(750): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144493 | ||||||
chr21:46144528
|
C | T | 4 | a0001c0004t0002g0100a0002c0011t0002g0062a0002c0011t0002g0098others(1): Show | 4 | HG03942.hp2 HG04115.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+889G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144528 | ||||||
chr21:46144528
|
CCT | C | 6 | a0001c0001t0002g0140a0001c0002t0002g0121a0001c0002t0002g0139others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+887_1260+888d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144528 | ||||||
chr21:46144536
|
C | T | 24 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(21): Show | 25 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1260+881G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144536 | ||||||
chr21:46144550
|
CCT | C | 25 | a0001c0001t0002g0048a0001c0002t0001g0042a0001c0002t0001g0049others(22): Show | 26 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1260+865_1260+866d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144550 | ||||||
chr21:46144600
|
CCT | C | 95 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0085others(92): Show | 97 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.1260+815_1260+816d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144600 | ||||||
chr21:46144600
|
CCTCT | C | 5 | a0001c0001t0001g0144a0001c0002t0002g0102a0001c0002t0008g0219others(2): Show | 5 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+813_1260+816d others(6): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144600 | ||||||
chr21:46144606
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+811A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144606 | ||||||
chr21:46144611
|
G | C | 1 | a0001c0001t0002g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1260+806C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144611 | ||||||
chr21:46144611
|
G | T | 6 | a0001c0002t0002g0121a0001c0002t0002g0139a0001c0004t0002g0141others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+806C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144611 | ||||||
chr21:46144630
|
T | TC | 6 | a0001c0001t0001g0052a0001c0001t0001g0108a0001c0002t0002g0145others(3): Show | 6 | HG00544.hp1 HG00642.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+786dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144630 | ||||||
chr21:46144644
|
TCCTCCCC others(12): Show |
T | 1 | a0002c0005t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1260+754_1260+772d others(21): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144644 | ||||||
chr21:46144657
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1260+760A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144657 | ||||||
chr21:46144658
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1260+759G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144658 | ||||||
chr21:46144751
|
C | G | 10 | a0001c0003t0002g0081a0001c0031t0001g0184a0003c0007t0002g0077others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260+666G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144751 | ||||||
chr21:46144782
|
GAACTGCT others(46): Show |
G | 1 | a0002c0016t0001g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+582_1260+634d others(55): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144782 | ||||||
chr21:46144818
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1260+599A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144818 | ||||||
chr21:46144856
|
A | C | 1 | a0002c0016t0001g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+561T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144856 | ||||||
chr21:46144857
|
C | T | 1 | a0002c0016t0001g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+560G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144857 | ||||||
chr21:46144859
|
C | A | 1 | a0002c0016t0001g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260+558G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144859 | ||||||
chr21:46144998
|
G | C | 129 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0103others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1260+419C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46144998 | ||||||
chr21:46145072
|
GC | G | 5 | a0001c0001t0001g0144a0001c0002t0002g0102a0001c0002t0008g0219others(2): Show | 5 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+344delG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46145072 | ||||||
chr21:46145279
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1260+138C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | 46145279 | ||||||
chr21:46145631
|
G | A | 3 | a0001c0003t0003g0020a0001c0003t0003g0092a0001c0003t0003g0095 | 3 | HG03491.hp2 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1099-53C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145631 | ||||||
chr21:46145733
|
C | CCGTGCCC others(513): Show |
1 | a0001c0001t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1098+84_1098+85ins others(520): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145733 | ||||||
chr21:46145735
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1098+83A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(197): Show |
1 | a0015c0023t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(204): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(510): Show |
3 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03130.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(517): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(214): Show |
4 | a0001c0001t0002g0140a0001c0002t0002g0121a0001c0004t0002g0141others(1): Show | 4 | HG00639.hp2 HG01884.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(221): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(513): Show |
1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(520): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(511): Show |
1 | a0001c0001t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(518): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(196): Show |
1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(203): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(224): Show |
3 | a0001c0001t0001g0125a0001c0001t0001g0142a0001c0001t0001g0186 | 3 | HG02280.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(231): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(249): Show |
1 | a0001c0002t0002g0161 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(256): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCC others(250): Show |
4 | a0001c0002t0002g0162a0001c0004t0002g0030a0001c0004t0002g0069others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+82_1098+83ins others(257): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145735
|
T | TGCCCTCG others(423): Show |
1 | a0001c0002t0002g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1098+82_1098+83ins others(430): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145735 | ||||||
chr21:46145753
|
G | GCCCTTCC others(250): Show |
2 | a0003c0014t0001g0118a0003c0014t0001g0137 | 2 | HG01167.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1098+64_1098+65ins others(257): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145753 | ||||||
chr21:46145756
|
C | CTTCCCCC others(265): Show |
1 | a0001c0001t0001g0064 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(272): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(247): Show |
1 | a0006c0013t0001g0004 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(254): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(264): Show |
4 | a0001c0001t0001g0085a0002c0005t0001g0194a0004c0008t0007g0015others(1): Show | 4 | HG00140.hp2 HG01069.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(271): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(265): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0195 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(272): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(248): Show |
1 | a0001c0002t0009g0155 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(255): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(240): Show |
4 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0002g0087others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(247): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(248): Show |
1 | a0001c0001t0001g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(255): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0001c0001t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(270): Show |
1 | a0001c0001t0007g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(277): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(266): Show |
1 | a0001c0002t0002g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(273): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(312): Show |
11 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0001g0132others(8): Show | 11 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(319): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(270): Show |
1 | a0001c0002t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(277): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(265): Show |
1 | a0001c0001t0001g0151 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(272): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(250): Show |
3 | a0001c0001t0001g0071a0001c0001t0001g0104a0014c0027t0002g0073 | 3 | HG00642.hp2 HG04184.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(257): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(267): Show |
57 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(54): Show | 61 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(392): Show |
1 | a0002c0005t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(399): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0001c0001t0004g0223 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(405): Show |
1 | a0001c0002t0002g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(412): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0001c0001t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0001c0001t0001g0131 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0002c0016t0001g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0007c0036t0001g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(285): Show |
1 | a0001c0001t0004g0209 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(292): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(269): Show |
1 | a0001c0001t0001g0059 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(276): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(192): Show |
1 | a0001c0002t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(199): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(269): Show |
1 | a0001c0001t0001g0041 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(276): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(268): Show |
1 | a0005c0012t0009g0014 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(351): Show |
5 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+61_1098+62ins others(358): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | CTTCCCCC others(408): Show |
1 | a0001c0002t0002g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1098+61_1098+62ins others(415): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145756
|
C | G | 7 | a0001c0001t0002g0140a0001c0002t0002g0120a0001c0002t0002g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+62G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145756 | ||||||
chr21:46145757
|
T | TTCCCCCC others(300): Show |
1 | a0001c0002t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1098+60_1098+61ins others(307): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | ||||||
chr21:46145757
|
T | TTCCCCCT others(225): Show |
1 | a0003c0007t0002g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1098+60_1098+61ins others(232): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | ||||||
chr21:46145757
|
T | TTCCCCCT others(298): Show |
1 | a0001c0002t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1098+60_1098+61ins others(305): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | ||||||
chr21:46145757
|
T | TTCCCCCT others(224): Show |
6 | a0001c0003t0002g0081a0001c0031t0001g0184a0003c0007t0002g0078others(3): Show | 6 | HG01978.hp1 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+60_1098+61ins others(231): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | ||||||
chr21:46145757
|
T | TTCCCCCT others(241): Show |
13 | a0001c0001t0008g0211a0001c0001t0009g0094a0001c0002t0002g0003others(10): Show | 14 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+60_1098+61ins others(248): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145757 | ||||||
chr21:46145758
|
T | C | 9 | a0001c0001t0001g0125a0001c0001t0001g0142a0001c0001t0001g0181others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+60A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145758
|
T | TCCCCCTC others(264): Show |
1 | a0001c0001t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(271): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145758
|
T | TCCCCCTC others(408): Show |
2 | a0002c0006t0002g0183a0002c0018t0002g0129 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+59_1098+60ins others(415): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145758
|
T | TCCCCCTC others(441): Show |
1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(448): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145758
|
T | TCCCCCTC others(424): Show |
1 | a0001c0002t0002g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(431): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145758
|
T | TCCCCCTC others(226): Show |
1 | a0003c0007t0002g0077 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(233): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145758
|
T | TCCCCCTC others(427): Show |
1 | a0001c0002t0008g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1098+59_1098+60ins others(434): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145758 | ||||||
chr21:46145763
|
C | CCTCCCCG others(247): Show |
1 | a0001c0001t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1098+54_1098+55ins others(254): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145763 | ||||||
chr21:46145764
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1098+54A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145764 | ||||||
chr21:46145764
|
T | TCCCCGCC others(266): Show |
1 | a0001c0001t0001g0052 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1098+53_1098+54ins others(273): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145764 | ||||||
chr21:46145767
|
C | CCCGCCCT others(287): Show |
1 | a0001c0004t0002g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(294): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(285): Show |
1 | a0002c0011t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(292): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(365): Show |
1 | a0001c0003t0003g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(372): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(367): Show |
1 | a0002c0009t0003g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(374): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(365): Show |
1 | a0001c0002t0004g0207 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(372): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(184): Show |
2 | a0001c0010t0002g0199a0001c0010t0002g0200 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(191): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(366): Show |
27 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0109others(24): Show | 27 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(373): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(308): Show |
1 | a0001c0003t0005g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(315): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(367): Show |
1 | a0001c0002t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(374): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(234): Show |
1 | a0001c0002t0002g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(241): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(267): Show |
1 | a0001c0002t0002g0002 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(308): Show |
3 | a0001c0003t0003g0070a0001c0003t0005g0221a0001c0004t0001g0165 | 3 | HG00423.hp2 HG01168.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(315): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(176): Show |
1 | a0002c0006t0004g0203 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(183): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(287): Show |
1 | a0001c0002t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(294): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(234): Show |
2 | a0001c0001t0001g0133a0001c0002t0001g0177 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(241): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(267): Show |
6 | a0001c0001t0002g0048a0001c0002t0001g0160a0001c0004t0002g0016others(3): Show | 6 | HG02040.hp2 HG02132.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+50_1098+51ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(267): Show |
1 | a0001c0002t0001g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(274): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(284): Show |
1 | a0002c0011t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(291): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(177): Show |
1 | a0002c0006t0004g0202 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(184): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(286): Show |
1 | a0016c0033t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(293): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(268): Show |
1 | a0001c0004t0002g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(275): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(367): Show |
1 | a0001c0003t0003g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(374): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145767
|
C | CCGCCCTC others(369): Show |
1 | a0009c0020t0003g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+50_1098+51ins others(376): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145767 | ||||||
chr21:46145773
|
T | TCCCCCCA others(252): Show |
1 | a0002c0005t0001g0028 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1098+44_1098+45ins others(259): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145773 | ||||||
chr21:46145773
|
T | TCCCCCCC others(368): Show |
1 | a0001c0002t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1098+44_1098+45ins others(375): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145773 | ||||||
chr21:46145803
|
T | TC | 6 | a0001c0001t0001g0036a0001c0001t0007g0019a0001c0002t0002g0050others(3): Show | 6 | HG00544.hp2 HG01517.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+14dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 9/13 | chr21 | 46145803 | ||||||
chr21:46145961
|
G | A | 2 | a0002c0006t0002g0183a0002c0018t0002g0129 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.969-14C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46145961 | ||||||
chr21:46145962
|
C | A | 2 | a0002c0006t0002g0183a0002c0018t0002g0129 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.969-15G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46145962 | ||||||
chr21:46146046
|
G | A | 2 | a0001c0002t0002g0161a0001c0002t0002g0162 | 2 | HG00733.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.969-99C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146046 | ||||||
chr21:46146080
|
A | AC | 3 | a0001c0001t0001g0195a0001c0002t0002g0120a0001c0003t0005g0212 | 3 | HG02451.hp2 NA18971.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.969-134dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146080 | ||||||
chr21:46146122
|
G | T | 23 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(20): Show | 24 | HG00438.hp2 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.968+144C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146122 | ||||||
chr21:46146172
|
A | T | 1 | a0002c0009t0005g0205 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.968+94T>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146172 | ||||||
chr21:46146176
|
G | A | 16 | a0001c0001t0001g0108a0001c0001t0001g0156a0001c0001t0001g0196others(13): Show | 17 | HG00099.hp2 HG00738.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.968+90C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 8/13 | chr21 | 46146176 | ||||||
chr21:46146373
|
C | T | 1 | a0001c0022t0003g0193 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.907-46G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146373 | ||||||
chr21:46146404
|
A | C | 2 | a0001c0002t0002g0120a0001c0021t0001g0180 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.907-77T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146404 | ||||||
chr21:46146405
|
C | A | 1 | a0001c0021t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.907-78G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146405 | ||||||
chr21:46146406
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.907-79G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146406 | ||||||
chr21:46146418
|
C | T | 2 | a0001c0003t0003g0106a0001c0003t0003g0110 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.907-91G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146418 | ||||||
chr21:46146431
|
G | A | 22 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(19): Show | 23 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.907-104C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146431 | ||||||
chr21:46146476
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-149C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146476 | ||||||
chr21:46146477
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-150G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146477 | ||||||
chr21:46146478
|
A | AC | 12 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0144others(9): Show | 12 | HG00609.hp1 HG01109.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.907-152dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146478 | ||||||
chr21:46146478
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-151T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146478 | ||||||
chr21:46146488
|
T | G | 39 | a0001c0002t0001g0076a0001c0002t0001g0096a0001c0002t0001g0097others(36): Show | 39 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.907-161A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146488 | ||||||
chr21:46146529
|
A | C | 1 | a0001c0002t0002g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.907-202T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146529 | ||||||
chr21:46146556
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.907-229T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146556 | ||||||
chr21:46146754
|
C | G | 3 | a0001c0031t0001g0184a0003c0007t0002g0077a0003c0007t0002g0078 | 3 | HG02451.hp1 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.907-427G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146754 | ||||||
chr21:46146881
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.907-554T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146881 | ||||||
chr21:46146912
|
G | C | 1 | a0004c0008t0007g0063 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.907-585C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146912 | ||||||
chr21:46146914
|
G | A | 21 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(18): Show | 22 | HG00099.hp2 HG00438.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.907-587C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46146914 | ||||||
chr21:46147037
|
T | TCATTCGA others(67): Show |
1 | a0001c0004t0002g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.907-784_907-711dup others(74): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147037 | ||||||
chr21:46147231
|
C | G | 1 | a0012c0028t0001g0009 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.907-904G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147231 | ||||||
chr21:46147265
|
C | T | 6 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0002t0001g0115others(3): Show | 6 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-938G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147265 | ||||||
chr21:46147289
|
G | GA | 142 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0021others(139): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.907-963dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147289 | ||||||
chr21:46147289
|
G | GAA | 16 | a0001c0001t0001g0125a0001c0001t0001g0158a0001c0001t0001g0186others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.907-964_907-963dup others(2): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147289 | ||||||
chr21:46147296
|
A | C | 1 | a0001c0003t0005g0213 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.907-969T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147296 | ||||||
chr21:46147354
|
C | T | 2 | a0001c0010t0002g0199a0001c0010t0002g0200 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.907-1027G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147354 | ||||||
chr21:46147407
|
G | C | 1 | a0001c0004t0002g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.907-1080C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147407 | ||||||
chr21:46147412
|
AG | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0108a0001c0002t0002g0047others(2): Show | 5 | HG00323.hp1 HG00558.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-1086delC | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147412 | ||||||
chr21:46147446
|
G | C | 22 | a0001c0001t0002g0048a0001c0002t0001g0042a0001c0002t0001g0049others(19): Show | 23 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.907-1119C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147446 | ||||||
chr21:46147534
|
C | A | 1 | a0001c0002t0004g0207 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.907-1207G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147534 | ||||||
chr21:46147574
|
G | T | 1 | a0001c0002t0004g0207 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.907-1247C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147574 | ||||||
chr21:46147619
|
C | T | 1 | a0001c0003t0002g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.907-1292G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147619 | ||||||
chr21:46147714
|
G | A | 46 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0004g0006others(43): Show | 47 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.907-1387C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147714 | ||||||
chr21:46147734
|
C | CAAGACCA others(4): Show |
1 | a0001c0025t0002g0032 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.907-1418_907-1408d others(13): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147734 | ||||||
chr21:46147774
|
T | TA | 8 | a0001c0001t0006g0171a0001c0002t0001g0049a0001c0002t0001g0076others(5): Show | 8 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-1448dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147774 | ||||||
chr21:46147933
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.907-1606C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147933 | ||||||
chr21:46147942
|
C | CA | 7 | a0001c0001t0001g0159a0001c0001t0002g0143a0001c0002t0002g0087others(4): Show | 7 | HG01109.hp2 HG02132.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.907-1616dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147942 | ||||||
chr21:46147942
|
CA | C | 49 | a0001c0001t0001g0064a0001c0001t0001g0108a0001c0001t0001g0131others(46): Show | 50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.907-1616delT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147942 | ||||||
chr21:46147942
|
CAA | C | 9 | a0001c0001t0001g0142a0001c0031t0001g0184a0003c0007t0002g0077others(6): Show | 9 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.907-1617_907-1616d others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147942 | ||||||
chr21:46147958
|
A | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-1631T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46147958 | ||||||
chr21:46148239
|
C | T | 7 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0002t0002g0102others(4): Show | 7 | HG00099.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+1880G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148239 | ||||||
chr21:46148381
|
T | C | 4 | a0001c0001t0007g0018a0001c0001t0007g0019a0001c0001t0007g0022others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1738A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148381 | ||||||
chr21:46148618
|
C | G | 1 | a0013c0030t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.906+1501G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148618 | ||||||
chr21:46148623
|
G | C | 3 | a0001c0001t0001g0131a0002c0006t0002g0183a0002c0018t0002g0129 | 3 | HG02818.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.906+1496C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148623 | ||||||
chr21:46148722
|
T | C | 1 | a0014c0027t0002g0073 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.906+1397A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148722 | ||||||
chr21:46148728
|
T | G | 1 | a0001c0002t0006g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.906+1391A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148728 | ||||||
chr21:46148761
|
G | GAACAGTT others(6): Show |
1 | a0001c0002t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.906+1345_906+1357d others(15): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46148761 | ||||||
chr21:46149048
|
GA | G | 4 | a0001c0001t0001g0133a0001c0002t0002g0091a0001c0002t0002g0147others(1): Show | 4 | HG00438.hp1 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+1070delT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149048 | ||||||
chr21:46149083
|
G | A | 11 | a0001c0002t0001g0043a0001c0002t0002g0017a0001c0002t0002g0044others(8): Show | 11 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+1036C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149083 | ||||||
chr21:46149117
|
G | A | 58 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0144others(55): Show | 60 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.906+1002C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149117 | ||||||
chr21:46149157
|
A | G | 13 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(10): Show | 13 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+962T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149157 | ||||||
chr21:46149227
|
G | A | 43 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0144others(40): Show | 45 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.906+892C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149227 | ||||||
chr21:46149393
|
A | C | 1 | a0001c0001t0001g0035 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.906+726T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149393 | ||||||
chr21:46149453
|
CACAA | C | 2 | a0001c0002t0002g0121a0001c0002t0002g0139 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.906+662_906+665del others(4): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149453 | ||||||
chr21:46149457
|
A | G | 1 | a0001c0003t0003g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.906+662T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149457 | ||||||
chr21:46149507
|
C | T | 13 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(10): Show | 13 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+612G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149507 | ||||||
chr21:46149728
|
C | T | 1 | a0001c0002t0002g0017 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.906+391G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149728 | ||||||
chr21:46149813
|
TGGAGGTG others(6): Show |
T | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906+293_906+305del others(13): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149813 | ||||||
chr21:46149938
|
C | CA | 6 | a0001c0001t0001g0053a0001c0001t0001g0065a0001c0002t0002g0045others(3): Show | 6 | HG01261.hp2 HG02027.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+180dupT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46149938 | ||||||
chr21:46150104
|
G | A | 5 | a0001c0001t0006g0124a0001c0001t0006g0126a0001c0001t0006g0171others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+15C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46150104 | ||||||
chr21:46150106
|
C | T | 1 | a0002c0005t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.906+13G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 7/13 | chr21 | 46150106 | ||||||
chr21:46150270
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.775-20C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150270 | ||||||
chr21:46150272
|
C | T | 2 | a0001c0010t0002g0199a0001c0010t0002g0200 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.775-22G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150272 | ||||||
chr21:46150273
|
A | AC | 5 | a0001c0001t0001g0187a0001c0002t0002g0047a0001c0003t0003g0092others(2): Show | 5 | HG00280.hp1 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-24dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150273 | ||||||
chr21:46150352
|
G | A | 22 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(19): Show | 24 | HG00438.hp2 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.774+36C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 6/13 | chr21 | 46150352 | ||||||
chr21:46150553
|
G | T | 1 | a0002c0009t0005g0205 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.637-28C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150553 | ||||||
chr21:46150631
|
G | A | 1 | a0001c0002t0009g0046 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.637-106C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150631 | ||||||
chr21:46150638
|
G | C | 13 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(10): Show | 13 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.637-113C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150638 | ||||||
chr21:46150718
|
G | A | 1 | a0001c0001t0009g0094 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.637-193C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150718 | ||||||
chr21:46150738
|
A | G | 62 | a0001c0001t0001g0108a0001c0001t0001g0125a0001c0001t0001g0131others(59): Show | 64 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.637-213T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150738 | ||||||
chr21:46150751
|
C | CCCG | 11 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0001t0006g0124others(8): Show | 11 | HG01109.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-229_637-227dup others(3): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150751 | ||||||
chr21:46150856
|
T | TC | 4 | a0001c0002t0002g0087a0001c0003t0002g0010a0001c0032t0001g0182others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-332dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150856 | ||||||
chr21:46150859
|
C | A | 1 | a0015c0023t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637-334G>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150859 | ||||||
chr21:46150860
|
A | C | 1 | a0015c0023t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637-335T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150860 | ||||||
chr21:46150927
|
G | T | 1 | a0001c0004t0002g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.637-402C>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150927 | ||||||
chr21:46150954
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.637-429G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46150954 | ||||||
chr21:46151060
|
G | C | 2 | a0001c0002t0002g0147a0002c0006t0001g0099 | 2 | HG00438.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.636+498C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151060 | ||||||
chr21:46151090
|
C | T | 1 | a0002c0005t0001g0194 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.636+468G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151090 | ||||||
chr21:46151248
|
G | A | 33 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0001t0002g0048others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.636+310C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151248 | ||||||
chr21:46151261
|
C | T | 13 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(10): Show | 15 | HG00438.hp2 HG00738.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+297G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151261 | ||||||
chr21:46151262
|
G | A | 2 | a0001c0002t0002g0121a0001c0002t0002g0139 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.636+296C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151262 | ||||||
chr21:46151295
|
T | C | 22 | a0001c0001t0001g0108a0001c0001t0008g0211a0001c0001t0009g0094others(19): Show | 24 | HG00438.hp2 HG00738.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.636+263A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151295 | ||||||
chr21:46151307
|
G | C | 4 | a0001c0004t0002g0141a0001c0004t0002g0178a0001c0021t0001g0180others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+251C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151307 | ||||||
chr21:46151392
|
T | TC | 7 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0108others(4): Show | 7 | HG00642.hp1 HG01978.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.636+165dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151392 | ||||||
chr21:46151454
|
G | A | 1 | a0001c0002t0002g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.636+104C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151454 | ||||||
chr21:46151469
|
C | CA | 222 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(219): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.636+88_636+89insT | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151469 | ||||||
chr21:46151475
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.636+83C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151475 | ||||||
chr21:46151508
|
C | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0185a0001c0001t0001g0187others(3): Show | 6 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+50G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151508 | ||||||
chr21:46151515
|
G | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0142others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.636+43C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 5/13 | chr21 | 46151515 | ||||||
chr21:46151753
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.457-16G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/13 | chr21 | 46151753 | ||||||
chr21:46151787
|
G | GC | 6 | a0001c0001t0001g0052a0001c0001t0001g0163a0001c0002t0002g0087others(3): Show | 6 | HG00438.hp1 HG00642.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-51dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/13 | chr21 | 46151787 | ||||||
chr21:46151871
|
G | A | 5 | a0001c0001t0001g0181a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+21C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 4/13 | chr21 | 46151871 | ||||||
chr21:46151997
|
C | T | 1 | a0001c0002t0002g0002 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.368-17G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46151997 | ||||||
chr21:46152013
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.368-33C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152013 | ||||||
chr21:46152029
|
C | G | 1 | a0002c0005t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.368-49G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152029 | ||||||
chr21:46152068
|
G | GTCCCCCC others(8): Show |
1 | a0001c0003t0003g0070 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.368-89_368-88insGT others(13): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152068 | ||||||
chr21:46152119
|
T | G | 7 | a0001c0001t0002g0140a0001c0002t0002g0121a0001c0002t0002g0139others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-139A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152119 | ||||||
chr21:46152330
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.368-350C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152330 | ||||||
chr21:46152342
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.368-362C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152342 | ||||||
chr21:46152349
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.368-369G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152349 | ||||||
chr21:46152382
|
G | A | 4 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0002g0087others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-402C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152382 | ||||||
chr21:46152409
|
ATGACCGT others(32): Show |
A | 2 | a0001c0004t0001g0165a0003c0034t0002g0117 | 2 | HG02109.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.367+459_368-430del others(39): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152409 | ||||||
chr21:46152480
|
C | T | 1 | a0001c0031t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367+427G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152480 | ||||||
chr21:46152486
|
C | T | 1 | a0001c0002t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.367+421G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152486 | ||||||
chr21:46152531
|
C | T | 1 | a0001c0031t0001g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367+376G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152531 | ||||||
chr21:46152755
|
T | C | 1 | a0004c0008t0007g0079 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.367+152A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152755 | ||||||
chr21:46152879
|
A | G | 4 | a0001c0004t0002g0178a0001c0021t0001g0180a0003c0015t0002g0007others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+28T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 3/13 | chr21 | 46152879 | ||||||
chr21:46153048
|
G | A | 4 | a0001c0001t0001g0142a0001c0002t0002g0003a0001c0002t0002g0190others(1): Show | 5 | HG02280.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-13C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153048 | ||||||
chr21:46153104
|
C | T | 3 | a0001c0002t0002g0119a0001c0002t0002g0120a0003c0015t0002g0007 | 3 | HG02451.hp2 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.239-69G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153104 | ||||||
chr21:46153176
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.239-141T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153176 | ||||||
chr21:46153209
|
T | C | 7 | a0001c0001t0001g0142a0001c0002t0002g0190a0001c0004t0002g0141others(4): Show | 7 | HG00639.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-174A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153209 | ||||||
chr21:46153314
|
C | G | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.239-279G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153314 | ||||||
chr21:46153315
|
G | C | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.239-280C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153315 | ||||||
chr21:46153374
|
T | G | 22 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(19): Show | 23 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.239-339A>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153374 | ||||||
chr21:46153424
|
G | C | 29 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0131others(26): Show | 30 | HG01109.hp2 HG01167.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.239-389C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153424 | ||||||
chr21:46153526
|
G | A | 6 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0006g0124others(3): Show | 6 | HG01258.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-491C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153526 | ||||||
chr21:46153545
|
G | A | 1 | a0001c0002t0008g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.239-510C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153545 | ||||||
chr21:46153555
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0055others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.239-520C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153555 | ||||||
chr21:46153596
|
A | AC | 4 | a0001c0001t0001g0181a0001c0002t0002g0119a0001c0003t0003g0092others(1): Show | 4 | HG02027.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+552dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153596 | ||||||
chr21:46153636
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(149): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.238+513T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153636 | ||||||
chr21:46153782
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(91): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.238+367G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153782 | ||||||
chr21:46153784
|
A | G | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0002t0001g0084others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.238+365T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153784 | ||||||
chr21:46153793
|
T | C | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.238+356A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153793 | ||||||
chr21:46153795
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.238+354G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153795 | ||||||
chr21:46153930
|
G | A | 20 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(17): Show | 21 | HG01167.hp2 HG01884.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.238+219C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153930 | ||||||
chr21:46153941
|
G | A | 3 | a0001c0002t0002g0119a0001c0002t0002g0120a0001c0002t0002g0121 | 3 | HG01884.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.238+208C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153941 | ||||||
chr21:46153949
|
C | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0002t0001g0084 | 3 | HG01167.hp1 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.238+200G>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153949 | ||||||
chr21:46153973
|
A | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(184): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.238+176T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 2/13 | chr21 | 46153973 | ||||||
chr21:46154392
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-60G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154392 | ||||||
chr21:46154393
|
T | C | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-61A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154393 | ||||||
chr21:46154407
|
A | G | 3 | a0002c0005t0001g0066a0002c0005t0001g0067a0002c0009t0003g0068 | 3 | HG00558.hp2 NA18945.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.55-75T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154407 | ||||||
chr21:46154411
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0002t0001g0084 | 3 | HG01167.hp1 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.55-79G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154411 | ||||||
chr21:46154501
|
G | GC | 5 | a0001c0001t0001g0192a0001c0001t0002g0143a0001c0002t0008g0220others(2): Show | 5 | HG00423.hp2 HG02257.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-170dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154501 | ||||||
chr21:46154512
|
A | C | 1 | a0001c0002t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55-180T>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154512 | ||||||
chr21:46154538
|
A | AG | 49 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0021others(46): Show | 51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.55-207dupC | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154538 | ||||||
chr21:46154549
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0021others(167): Show | 176 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.55-217T>C | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154549 | ||||||
chr21:46154593
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0002t0001g0084 | 3 | HG01167.hp1 HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.55-261G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154593 | ||||||
chr21:46154594
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.55-262C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154594 | ||||||
chr21:46154625
|
C | T | 1 | a0002c0005t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.55-293G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154625 | ||||||
chr21:46154657
|
C | T | 3 | a0001c0002t0006g0082a0001c0002t0006g0083a0001c0003t0002g0081 | 3 | HG02897.hp2 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.55-325G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154657 | ||||||
chr21:46154679
|
A | AC | 7 | a0001c0001t0001g0167a0001c0001t0007g0022a0001c0003t0002g0010others(4): Show | 7 | HG01261.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-348dupG | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154679 | ||||||
chr21:46154858
|
C | T | 1 | a0001c0003t0002g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55-526G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154858 | ||||||
chr21:46154885
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(166): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.55-553C>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154885 | ||||||
chr21:46154922
|
G | A | 24 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0158others(21): Show | 26 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.54+548C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46154922 | ||||||
chr21:46155046
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(66): Show | 71 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.54+424C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155046 | ||||||
chr21:46155115
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(166): Show | 175 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.54+355C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155115 | ||||||
chr21:46155284
|
C | T | 1 | a0002c0011t0002g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.54+186G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155284 | ||||||
chr21:46155323
|
T | C | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(5): Show | 8 | HG01069.hp1 HG01361.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+147A>G | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155323 | ||||||
chr21:46155346
|
G | A | 1 | a0001c0002t0002g0061 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54+124C>T | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155346 | ||||||
chr21:46155373
|
C | T | 1 | a0001c0003t0003g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.54+97G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155373 | ||||||
chr21:46155458
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.54+12G>A | FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 1/13 | chr21 | 46155458 |