geneid | 57697 |
---|---|
ensemblid | ENSG00000187790.12 |
hgncid | 23168 |
symbol | FANCM |
name | FA complementation group M |
refseq_nuc | NM_020937.4 |
refseq_prot | NP_065988.1 |
ensembl_nuc | ENST00000267430.10 |
ensembl_prot | ENSP00000267430.5 |
mane_status | MANE Select |
chr | chr14 |
start | 45135930 |
end | 45200890 |
strand | + |
ver | v1.2 |
region | chr14:45135930-45200890 |
region5000 | chr14:45130930-45205890 |
regionname0 | FANCM_chr14_45135930_45200890 |
regionname5000 | FANCM_chr14_45130930_45205890 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2048 | 113 | 24 | 22 | 42 | 5 | 19 | 31 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002 | 0/0 | 2048 | 37 | 35 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0003 | 0/0 | 2048 | 29 | 0 | 1 | 23 | 3 | 2 | 18 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0004 | 0/0 | 2048 | 10 | 9 | 0 | 1 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0005 | 0/0 | 2048 | 10 | 1 | 6 | 2 | 0 | 1 | 2 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0006 | 0/0 | 2048 | 5 | 2 | 1 | 0 | 1 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0007 | 0/0 | 2048 | 5 | 0 | 1 | 4 | 0 | 0 | 4 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0008 | 0/0 | 2048 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0009 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0010 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0011 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0012 | 0/0 | 2048 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0013 | 0/0 | 2048 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0014 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0015 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0016 | 0/0 | 2048 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0017 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0018 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0019 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0020 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0021 | 0/1 | 2048 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0022 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0023 | 0/0 | 2048 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0024 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0025 | 0/0 | 2048 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0026 | 0/0 | 2048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0027 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0028 | 0/0 | 2048 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 6147 | 113 | 24 | 22 | 42 | 5 | 19 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0002 | 0/0 | 6147 | 29 | 0 | 1 | 23 | 3 | 2 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0003 | 0/0 | 6147 | 14 | 12 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0004 | 0/0 | 6147 | 10 | 1 | 6 | 2 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0005 | 0/0 | 6147 | 10 | 9 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0006 | 0/0 | 6147 | 9 | 9 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0007 | 0/0 | 6147 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0008 | 0/0 | 6147 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0009 | 0/0 | 6147 | 5 | 0 | 1 | 4 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0010 | 0/0 | 6147 | 5 | 2 | 1 | 0 | 1 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0011 | 0/0 | 6147 | 3 | 3 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0012 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0013 | 0/0 | 6147 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0014 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0015 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0016 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0017 | 0/0 | 6147 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0018 | 0/0 | 6147 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0019 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0020 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0021 | 0/1 | 6147 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0022 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0023 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0024 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0025 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0026 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0027 | 0/0 | 6147 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0028 | 0/0 | 6147 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0029 | 0/0 | 6147 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0030 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0031 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0032 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0033 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
c0034 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 985 | 196 | 47 | 35 | 76 | 10 | 26 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0002 | 0/0 | 985 | 26 | 25 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0003 | 0/0 | 986 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0004 | 0/0 | 987 | 5 | 5 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0005 | 0/0 | 985 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0006 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0007 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
t0008 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6147 | 113 | 24 | 22 | 42 | 5 | 19 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0003 | 0/0 | 6147 | 14 | 12 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0006 | 0/0 | 6147 | 9 | 9 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0007 | 0/0 | 6147 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0008 | 0/0 | 6147 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0031 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0032 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0003c0002 | 0/0 | 6147 | 29 | 0 | 1 | 23 | 3 | 2 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0004c0005 | 0/0 | 6147 | 10 | 9 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0005c0004 | 0/0 | 6147 | 10 | 1 | 6 | 2 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0006c0010 | 0/0 | 6147 | 5 | 2 | 1 | 0 | 1 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0007c0009 | 0/0 | 6147 | 5 | 0 | 1 | 4 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0008c0011 | 0/0 | 6147 | 3 | 3 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0008c0025 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0009c0016 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0010c0015 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0011c0014 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0012c0012 | 0/0 | 6147 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0013c0013 | 0/0 | 6147 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0014c0034 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0015c0030 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0016c0029 | 0/0 | 6147 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0017c0033 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0018c0024 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0019c0026 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0020c0023 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0021c0021 | 0/1 | 6147 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0022c0019 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0023c0018 | 0/0 | 6147 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0024c0017 | 0/0 | 6147 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0025c0020 | 0/0 | 6147 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0026c0022 | 0/0 | 6147 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0027c0027 | 0/0 | 6147 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0028c0028 | 0/0 | 6147 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7131 | 113 | 24 | 22 | 42 | 5 | 19 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0003t0001 | 0/0 | 7131 | 4 | 3 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0003t0002 | 0/0 | 7131 | 10 | 9 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0006t0002 | 0/0 | 7131 | 9 | 9 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0007t0003 | 0/0 | 7132 | 6 | 6 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0008t0004 | 0/0 | 7133 | 5 | 5 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0008t0007 | 0/0 | 7133 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0031t0006 | 0/0 | 7115 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0002c0032t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0003c0002t0001 | 0/0 | 7131 | 29 | 0 | 1 | 23 | 3 | 2 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0004c0005t0001 | 0/0 | 7131 | 10 | 9 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0005c0004t0001 | 0/0 | 7131 | 10 | 1 | 6 | 2 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0006c0010t0001 | 0/0 | 7131 | 5 | 2 | 1 | 0 | 1 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0007c0009t0001 | 0/0 | 7131 | 5 | 0 | 1 | 4 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0008c0011t0002 | 0/0 | 7131 | 3 | 3 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0008c0025t0002 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0009c0016t0005 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0010c0015t0001 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0011c0014t0001 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0012c0012t0002 | 0/0 | 7131 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0013c0013t0001 | 0/0 | 7131 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0014c0034t0002 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0015c0030t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0016c0029t0001 | 0/0 | 7131 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0017c0033t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0018c0024t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0019c0026t0008 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0020c0023t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0021c0021t0001 | 0/1 | 7131 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0022c0019t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0023c0018t0001 | 0/0 | 7131 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0024c0017t0001 | 0/0 | 7131 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0025c0020t0001 | 0/0 | 7131 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0026c0022t0001 | 0/0 | 7131 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0027c0027t0001 | 0/0 | 7131 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
a0028c0028t0001 | 0/0 | 7131 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | copy fasta | chr14 | 45130930 | 45205890 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0006t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0007t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0008t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0031t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0002c0032t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0004c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0005c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0006c0010t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0007c0009t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0011t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0011t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0011t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0008c0025t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0009c0016t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0009c0016t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0010c0015t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0010c0015t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0011c0014t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0011c0014t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0012c0012t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0013c0013t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0013c0013t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0014c0034t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0015c0030t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0016c0029t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0017c0033t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0018c0024t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0019c0026t0008g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0020c0023t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0021c0021t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0022c0019t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0023c0018t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0024c0017t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0025c0020t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0026c0022t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0027c0027t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
a0028c0028t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0003 | c0002 | t0001 | g0188 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00323 | hp1 | a0003 | c0002 | t0001 | g0187 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00438 | hp1 | a0023 | c0018 | t0001 | g0026 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00558 | hp1 | a0003 | c0002 | t0001 | g0002 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00597 | hp1 | a0003 | c0002 | t0001 | g0191 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00609 | hp2 | a0003 | c0002 | t0001 | g0189 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG00673 | hp2 | a0003 | c0002 | t0001 | g0193 | EAS | CHS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01099 | hp1 | a0028 | c0028 | t0001 | g0079 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01106 | hp1 | a0006 | c0010 | t0001 | g0204 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0162 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01167 | hp1 | a0005 | c0004 | t0001 | g0112 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01169 | hp2 | a0005 | c0004 | t0001 | g0111 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01192 | hp1 | a0005 | c0004 | t0001 | g0023 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01243 | hp1 | a0005 | c0004 | t0001 | g0010 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01243 | hp2 | a0024 | c0017 | t0001 | g0035 | AMR | PUR | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01255 | hp1 | a0027 | c0027 | t0001 | g0109 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0172 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01358 | hp2 | a0003 | c0002 | t0001 | g0181 | AMR | CLM | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01516 | hp1 | a0006 | c0010 | t0001 | g0205 | EUR | IBS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0169 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01884 | hp2 | a0009 | c0016 | t0005 | g0208 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01891 | hp1 | a0011 | c0014 | t0001 | g0141 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01952 | hp2 | a0005 | c0004 | t0001 | g0010 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01993 | hp1 | a0005 | c0004 | t0001 | g0108 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02055 | hp1 | a0002 | c0003 | t0002 | g0142 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02055 | hp2 | a0026 | c0022 | t0001 | g0022 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02056 | hp2 | a0003 | c0002 | t0001 | g0201 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02132 | hp1 | a0016 | c0029 | t0001 | g0226 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02145 | hp2 | a0002 | c0032 | t0001 | g0209 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02257 | hp1 | a0002 | c0007 | t0003 | g0146 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0167 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02258 | hp1 | a0002 | c0008 | t0004 | g0173 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02258 | hp2 | a0008 | c0011 | t0002 | g0052 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02280 | hp2 | a0002 | c0006 | t0002 | g0213 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02293 | hp2 | a0007 | c0009 | t0001 | g0014 | AMR | PEL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02451 | hp1 | a0014 | c0034 | t0002 | g0139 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02615 | hp1 | a0019 | c0026 | t0008 | g0145 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02622 | hp1 | a0002 | c0006 | t0002 | g0215 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02630 | hp1 | a0002 | c0006 | t0002 | g0216 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02647 | hp1 | a0004 | c0005 | t0001 | g0161 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02717 | hp1 | a0004 | c0005 | t0001 | g0210 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02717 | hp2 | a0002 | c0003 | t0002 | g0225 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02723 | hp1 | a0004 | c0005 | t0001 | g0222 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02723 | hp2 | a0002 | c0007 | t0003 | g0149 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02809 | hp1 | a0004 | c0005 | t0001 | g0211 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02818 | hp1 | a0002 | c0031 | t0006 | g0160 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02818 | hp2 | a0002 | c0008 | t0004 | g0152 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02886 | hp1 | a0002 | c0008 | t0004 | g0151 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02886 | hp2 | a0002 | c0007 | t0003 | g0166 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02895 | hp1 | a0006 | c0010 | t0001 | g0138 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02895 | hp2 | a0012 | c0012 | t0002 | g0006 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02896 | hp2 | a0002 | c0003 | t0002 | g0153 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02897 | hp1 | a0012 | c0012 | t0002 | g0006 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0165 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02922 | hp2 | a0002 | c0003 | t0002 | g0223 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02965 | hp1 | a0002 | c0008 | t0007 | g0163 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02965 | hp2 | a0002 | c0003 | t0002 | g0221 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02976 | hp1 | a0008 | c0011 | t0002 | g0051 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02976 | hp2 | a0011 | c0014 | t0001 | g0140 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03017 | hp1 | a0003 | c0002 | t0001 | g0178 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03041 | hp1 | a0002 | c0006 | t0002 | g0218 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03098 | hp1 | a0004 | c0005 | t0001 | g0154 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03098 | hp2 | a0002 | c0006 | t0002 | g0219 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03139 | hp1 | a0015 | c0030 | t0001 | g0168 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03139 | hp2 | a0010 | c0015 | t0001 | g0198 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03195 | hp1 | a0002 | c0006 | t0002 | g0214 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03225 | hp2 | a0002 | c0006 | t0002 | g0212 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03239 | hp1 | a0003 | c0002 | t0001 | g0195 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03239 | hp2 | a0020 | c0023 | t0001 | g0078 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03453 | hp1 | a0002 | c0007 | t0003 | g0171 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03453 | hp2 | a0018 | c0024 | t0001 | g0144 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03486 | hp1 | a0002 | c0008 | t0004 | g0150 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03486 | hp2 | a0004 | c0005 | t0001 | g0157 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03516 | hp2 | a0002 | c0006 | t0002 | g0217 | AFR | ESN | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03540 | hp1 | a0002 | c0006 | t0002 | g0220 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03579 | hp2 | a0008 | c0025 | t0002 | g0136 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03831 | hp2 | a0005 | c0004 | t0001 | g0017 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03927 | hp2 | a0017 | c0033 | t0001 | g0190 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04199 | hp2 | a0006 | c0010 | t0001 | g0203 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04228 | hp1 | a0022 | c0019 | t0001 | g0019 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18522 | hp1 | a0004 | c0005 | t0001 | g0158 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18522 | hp2 | a0002 | c0003 | t0002 | g0155 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18906 | hp1 | a0006 | c0010 | t0001 | g0137 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18906 | hp2 | a0002 | c0007 | t0003 | g0148 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18939 | hp1 | a0013 | c0013 | t0001 | g0054 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18939 | hp2 | a0007 | c0009 | t0001 | g0015 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18940 | hp1 | a0003 | c0002 | t0001 | g0177 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18946 | hp2 | a0003 | c0002 | t0001 | g0002 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18952 | hp2 | a0003 | c0002 | t0001 | g0176 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18954 | hp2 | a0003 | c0002 | t0001 | g0185 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18964 | hp2 | a0003 | c0002 | t0001 | g0183 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18966 | hp1 | a0003 | c0002 | t0001 | g0002 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18966 | hp2 | a0007 | c0009 | t0001 | g0012 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18970 | hp1 | a0003 | c0002 | t0001 | g0182 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18974 | hp2 | a0007 | c0009 | t0001 | g0013 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18982 | hp2 | a0003 | c0002 | t0001 | g0186 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18984 | hp1 | a0003 | c0002 | t0001 | g0175 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18988 | hp1 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18991 | hp1 | a0003 | c0002 | t0001 | g0180 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18998 | hp1 | a0007 | c0009 | t0001 | g0016 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18999 | hp1 | a0003 | c0002 | t0001 | g0194 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA18999 | hp2 | a0013 | c0013 | t0001 | g0075 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19011 | hp1 | a0003 | c0002 | t0001 | g0192 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19030 | hp1 | a0009 | c0016 | t0005 | g0207 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19043 | hp1 | a0002 | c0008 | t0004 | g0143 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19043 | hp2 | a0005 | c0004 | t0001 | g0024 | AFR | LWK | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19063 | hp1 | a0003 | c0002 | t0001 | g0200 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19066 | hp1 | a0004 | c0005 | t0001 | g0179 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19067 | hp1 | a0003 | c0002 | t0001 | g0174 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19068 | hp2 | a0005 | c0004 | t0001 | g0099 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19072 | hp1 | a0003 | c0002 | t0001 | g0196 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19074 | hp2 | a0005 | c0004 | t0001 | g0110 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19078 | hp1 | a0003 | c0002 | t0001 | g0199 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19091 | hp1 | a0003 | c0002 | t0001 | g0202 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19240 | hp1 | a0002 | c0003 | t0002 | g0224 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA19240 | hp2 | a0002 | c0003 | t0002 | g0156 | AFR | YRI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20752 | hp1 | a0025 | c0020 | t0001 | g0106 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20805 | hp1 | a0003 | c0002 | t0001 | g0184 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02109 | hp2 | a0004 | c0005 | t0001 | g0164 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02486 | hp1 | a0010 | c0015 | t0001 | g0197 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG02559 | hp2 | a0004 | c0005 | t0001 | g0159 | AFR | ACB | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03471 | hp1 | a0008 | c0011 | t0002 | g0053 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0170 | AFR | MSL | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG06807 | hp1 | a0002 | c0007 | t0003 | g0147 | AFR | USA | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
homoSapiens_chm13v2 | hp1 | a0021 | c0021 | t0001 | g0105 | REF | REF | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | FANCM_chr14_45130930_45205890 | FANCM | chr14 | 45130930 | 45205890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45136260
|
A | G | 1 | a0006 | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.229A>G | p.Thr77Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 1/23 | 331/7131 | 229/6147 | 77/2048 | chr14 | 45136260 | ||
chr14:45137084
|
C | T | 11 | a0002a0003a0004others(8): Show | 91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
missense_variant | MODERATE | c.524C>T | p.Ser175Phe | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/23 | 626/7131 | 524/6147 | 175/2048 | chr14 | 45137084 | ||
chr14:45137184
|
A | G | 1 | a0028 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.624A>G | p.Ile208Met | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/23 | 726/7131 | 624/6147 | 208/2048 | chr14 | 45137184 | ||
chr14:45148951
|
C | G | 1 | a0009 | 2 | HG01884.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.874C>G | p.Pro292Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/23 | 976/7131 | 874/6147 | 292/2048 | chr14 | 45148951 | ||
chr14:45151518
|
C | T | 1 | a0014 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1040C>T | p.Pro347Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/23 | 1142/7131 | 1040/6147 | 347/2048 | chr14 | 45151518 | ||
chr14:45155391
|
T | G | 1 | a0012 | 2 | HG02895.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.1328T>G | p.Phe443Cys | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/23 | 1430/7131 | 1328/6147 | 443/2048 | chr14 | 45155391 | ||
chr14:45167125
|
A | G | 1 | a0027 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1964A>G | p.Asn655Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/23 | 2066/7131 | 1964/6147 | 655/2048 | chr14 | 45167125 | ||
chr14:45173134
|
A | G | 1 | a0013 | 2 | NA18939.hp1 NA18999.hp2 |
missense_variant | MODERATE | c.2240A>G | p.His747Arg | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/23 | 2342/7131 | 2240/6147 | 747/2048 | chr14 | 45173134 | ||
chr14:45173155
|
G | A | 1 | a0015 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2261G>A | p.Arg754Gln | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/23 | 2363/7131 | 2261/6147 | 754/2048 | chr14 | 45173155 | ||
chr14:45173187
|
A | G | 1 | a0017 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.2293A>G | p.Ile765Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/23 | 2395/7131 | 2293/6147 | 765/2048 | chr14 | 45173187 | ||
chr14:45175386
|
G | T | 17 | a0002a0003a0005others(14): Show | 105 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(102): Show |
missense_variant | MODERATE | c.2632G>T | p.Val878Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2734/7131 | 2632/6147 | 878/2048 | chr14 | 45175386 | ||
chr14:45175503
|
A | G | 2 | a0007a0016 | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
missense_variant | MODERATE | c.2749A>G | p.Ile917Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2851/7131 | 2749/6147 | 917/2048 | chr14 | 45175503 | ||
chr14:45175669
|
C | T | 1 | a0020 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.2915C>T | p.Thr972Ile | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3017/7131 | 2915/6147 | 972/2048 | chr14 | 45175669 | ||
chr14:45175794
|
G | T | 1 | a0010 | 2 | HG02486.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.3040G>T | p.Gly1014Cys | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3142/7131 | 3040/6147 | 1014/2048 | chr14 | 45175794 | ||
chr14:45176050
|
G | A | 1 | a0018 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.3296G>A | p.Arg1099His | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3398/7131 | 3296/6147 | 1099/2048 | chr14 | 45176050 | ||
chr14:45176512
|
A | G | 1 | a0026 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.3758A>G | p.Asn1253Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3860/7131 | 3758/6147 | 1253/2048 | chr14 | 45176512 | ||
chr14:45176581
|
C | T | 1 | a0021 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.3827C>T | p.Ser1276Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3929/7131 | 3827/6147 | 1276/2048 | chr14 | 45176581 | ||
chr14:45176617
|
A | G | 1 | a0019 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.3863A>G | p.Asn1288Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3965/7131 | 3863/6147 | 1288/2048 | chr14 | 45176617 | ||
chr14:45176674
|
A | G | 1 | a0011 | 2 | HG01891.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.3920A>G | p.Tyr1307Cys | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 4022/7131 | 3920/6147 | 1307/2048 | chr14 | 45176674 | ||
chr14:45181697
|
A | G | 4 | a0003a0005a0017others(1): Show | 41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
missense_variant | MODERATE | c.4378A>G | p.Ile1460Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/23 | 4480/7131 | 4378/6147 | 1460/2048 | chr14 | 45181697 | ||
chr14:45185264
|
A | C | 1 | a0010 | 2 | HG02486.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.4563A>C | p.Glu1521Asp | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/23 | 4665/7131 | 4563/6147 | 1521/2048 | chr14 | 45185264 | ||
chr14:45189246
|
A | G | 1 | a0025 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.5224A>G | p.Ile1742Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/23 | 5326/7131 | 5224/6147 | 1742/2048 | chr14 | 45189246 | ||
chr14:45196265
|
C | G | 5 | a0003a0005a0017others(2): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
missense_variant | MODERATE | c.5434C>G | p.Pro1812Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5536/7131 | 5434/6147 | 1812/2048 | chr14 | 45196265 | ||
chr14:45196266
|
C | T | 1 | a0023 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.5435C>T | p.Pro1812Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5537/7131 | 5435/6147 | 1812/2048 | chr14 | 45196266 | ||
chr14:45196458
|
A | G | 2 | a0024a0026 | 2 | HG01243.hp2 HG02055.hp2 |
missense_variant | MODERATE | c.5627A>G | p.Asn1876Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5729/7131 | 5627/6147 | 1876/2048 | chr14 | 45196458 | ||
chr14:45196487
|
C | T | 1 | a0019 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.5656C>T | p.His1886Tyr | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5758/7131 | 5656/6147 | 1886/2048 | chr14 | 45196487 | ||
chr14:45196515
|
G | A | 1 | a0022 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.5684G>A | p.Cys1895Tyr | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5786/7131 | 5684/6147 | 1895/2048 | chr14 | 45196515 | ||
chr14:45198775
|
T | G | 1 | a0009 | 2 | HG01884.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.5848T>G | p.Leu1950Val | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/23 | 5950/7131 | 5848/6147 | 1950/2048 | chr14 | 45198775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45151519
|
G | A | 2 | a0007c0009a0016c0029 | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
synonymous_variant | LOW | c.1041G>A | p.Pro347Pro | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/23 | 1143/7131 | 1041/6147 | 347/2048 | chr14 | 45151519 | ||
chr14:45175199
|
G | A | 2 | a0002c0007a0002c0008 | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
synonymous_variant | LOW | c.2445G>A | p.Ser815Ser | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2547/7131 | 2445/6147 | 815/2048 | chr14 | 45175199 | ||
chr14:45175424
|
T | C | 3 | a0002c0006a0008c0011a0012c0012 | 14 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.2670T>C | p.Phe890Phe | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 2772/7131 | 2670/6147 | 890/2048 | chr14 | 45175424 | ||
chr14:45176301
|
T | C | 1 | a0002c0031 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.3547T>C | p.Leu1183Leu | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/23 | 3649/7131 | 3547/6147 | 1183/2048 | chr14 | 45176301 | ||
chr14:45181467
|
C | T | 1 | a0002c0008 | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.4260C>T | p.Asp1420Asp | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 15/23 | 4362/7131 | 4260/6147 | 1420/2048 | chr14 | 45181467 | ||
chr14:45189164
|
G | A | 2 | a0002c0007a0010c0015 | 8 | HG02257.hp1 HG02486.hp1 HG02723.hp2 others(5): Show |
synonymous_variant | LOW | c.5142G>A | p.Ala1714Ala | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/23 | 5244/7131 | 5142/6147 | 1714/2048 | chr14 | 45189164 | ||
chr14:45189212
|
G | A | 1 | a0019c0026 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.5190G>A | p.Gln1730Gln | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/23 | 5292/7131 | 5190/6147 | 1730/2048 | chr14 | 45189212 | ||
chr14:45196408
|
T | C | 1 | a0002c0008 | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.5577T>C | p.Asn1859Asn | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/23 | 5679/7131 | 5577/6147 | 1859/2048 | chr14 | 45196408 | ||
chr14:45200002
|
T | C | 3 | a0002c0032a0006c0010a0019c0026 | 7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
synonymous_variant | LOW | c.6141T>C | p.Asp2047Asp | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 6243/7131 | 6141/6147 | 2047/2048 | chr14 | 45200002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45200151
|
TATAGAAA others(9): Show |
T | 1 | a0002c0031t0006 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145_*160delTAGAAA others(10): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 145 | INFO_REALIGN_3_PRIME | chr14 | 45200151 | ||||
chr14:45200240
|
G | A | 7 | a0002c0003t0002a0002c0006t0002a0008c0011t0002others(4): Show | 28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*232G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 232 | chr14 | 45200240 | |||||
chr14:45200254
|
T | C | 1 | a0002c0008t0007 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 246 | chr14 | 45200254 | |||||
chr14:45200260
|
A | AG | 3 | a0002c0007t0003a0002c0008t0004a0002c0008t0007 | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*254dupG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 255 | INFO_REALIGN_3_PRIME | chr14 | 45200260 | ||||
chr14:45200646
|
T | C | 1 | a0019c0026t0008 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 638 | chr14 | 45200646 | |||||
chr14:45200647
|
T | TG | 2 | a0002c0008t0004a0002c0008t0007 | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*643dupG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 644 | INFO_REALIGN_3_PRIME | chr14 | 45200647 | ||||
chr14:45200652
|
A | G | 2 | a0002c0008t0004a0002c0008t0007 | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*644A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 644 | chr14 | 45200652 | |||||
chr14:45200872
|
A | C | 1 | a0009c0016t0005 | 2 | HG01884.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*864A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 23/23 | 864 | chr14 | 45200872 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:45136615
|
C | T | 91 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(88): Show | 93 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.508+76C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 1/22 | chr14 | 45136615 | ||||||
chr14:45136772
|
A | T | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.508+233A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 1/22 | chr14 | 45136772 | ||||||
chr14:45137313
|
A | C | 1 | a0016c0029t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.681+72A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45137313 | ||||||
chr14:45137941
|
G | A | 2 | a0006c0010t0001g0137a0006c0010t0001g0138 | 2 | HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.681+700G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45137941 | ||||||
chr14:45137959
|
TA | T | 19 | a0002c0003t0002g0221a0002c0003t0002g0223a0002c0003t0002g0224others(16): Show | 19 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.681+720delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr14 | 45137959 | |||||
chr14:45138183
|
C | T | 64 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(61): Show | 66 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.681+942C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138183 | ||||||
chr14:45138262
|
G | C | 4 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(1): Show | 4 | HG02257.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+1021G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138262 | ||||||
chr14:45138321
|
T | A | 89 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(86): Show | 91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.681+1080T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138321 | ||||||
chr14:45138474
|
G | T | 19 | a0002c0003t0002g0221a0002c0003t0002g0223a0002c0003t0002g0224others(16): Show | 19 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.681+1233G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138474 | ||||||
chr14:45138904
|
G | C | 89 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(86): Show | 91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.681+1663G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45138904 | ||||||
chr14:45139400
|
T | C | 28 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(25): Show | 28 | HG01109.hp1 HG01358.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.682-1232T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139400 | ||||||
chr14:45139468
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682-1164T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139468 | ||||||
chr14:45139620
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.682-1012A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139620 | ||||||
chr14:45139932
|
C | T | 1 | a0003c0002t0001g0206 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.682-700C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139932 | ||||||
chr14:45139987
|
T | C | 89 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(86): Show | 91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.682-645T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139987 | ||||||
chr14:45139999
|
A | T | 17 | a0002c0003t0002g0221a0002c0003t0002g0223a0002c0003t0002g0224others(14): Show | 17 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-633A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45139999 | ||||||
chr14:45140194
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-438C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140194 | ||||||
chr14:45140227
|
G | GT | 9 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG01106.hp1 HG01516.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-394dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr14 | 45140227 | |||||
chr14:45140392
|
G | A | 5 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(2): Show | 5 | HG02293.hp2 NA18939.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-240G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140392 | ||||||
chr14:45140466
|
A | G | 89 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(86): Show | 91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.682-166A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140466 | ||||||
chr14:45140551
|
C | T | 1 | a0002c0008t0004g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.682-81C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 2/22 | chr14 | 45140551 | ||||||
chr14:45140801
|
G | A | 1 | a0003c0002t0001g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.759+92G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45140801 | ||||||
chr14:45141113
|
C | A | 4 | a0002c0008t0004g0150a0002c0008t0004g0151a0002c0008t0004g0152others(1): Show | 4 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+404C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141113 | ||||||
chr14:45141230
|
A | G | 2 | a0002c0003t0002g0142a0002c0008t0004g0143 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.759+521A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141230 | ||||||
chr14:45141287
|
C | CA | 40 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(37): Show | 40 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.759+599dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141287 | |||||
chr14:45141287
|
C | CAA | 25 | a0002c0003t0002g0153a0003c0002t0001g0002a0003c0002t0001g0174others(22): Show | 27 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.759+598_759+599dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141287 | |||||
chr14:45141287
|
CAAAAAAA others(2): Show |
C | 11 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(8): Show | 11 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+591_759+599del others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141287 | |||||
chr14:45141504
|
T | TCCTCCC | 84 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(81): Show | 86 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.759+803_759+808dup others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141504 | |||||
chr14:45141555
|
C | T | 1 | a0003c0002t0001g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.759+846C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141555 | ||||||
chr14:45141594
|
C | CT | 6 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0129others(3): Show | 6 | HG00438.hp1 HG00438.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+899dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141594 | |||||
chr14:45141774
|
G | C | 12 | a0002c0003t0002g0221a0002c0006t0002g0212a0002c0006t0002g0213others(9): Show | 12 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.759+1065G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141774 | ||||||
chr14:45141806
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.759+1097C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141806 | ||||||
chr14:45141834
|
C | T | 1 | a0016c0029t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.759+1125C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141834 | ||||||
chr14:45141836
|
GCCTCAGC others(2096): Show |
G | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.759+1154_759+3256d others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45141836 | |||||
chr14:45141880
|
T | C | 87 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(84): Show | 89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+1171T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141880 | ||||||
chr14:45141883
|
C | A | 29 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(26): Show | 31 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.759+1174C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45141883 | ||||||
chr14:45142057
|
T | C | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.759+1348T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142057 | ||||||
chr14:45142154
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.759+1445C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142154 | ||||||
chr14:45142278
|
C | T | 1 | a0016c0029t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.759+1569C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142278 | ||||||
chr14:45142308
|
C | CT | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.759+1615dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45142308 | |||||
chr14:45142308
|
CT | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0005c0004t0001g0017others(2): Show | 5 | HG01256.hp1 HG02132.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+1615delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45142308 | |||||
chr14:45142316
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.759+1607T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142316 | ||||||
chr14:45142489
|
G | A | 11 | a0002c0003t0002g0153a0002c0003t0002g0155a0002c0003t0002g0156others(8): Show | 11 | HG01109.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.759+1780G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142489 | ||||||
chr14:45142651
|
T | C | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+1942T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45142651 | ||||||
chr14:45143025
|
T | C | 87 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(84): Show | 89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+2316T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143025 | ||||||
chr14:45143058
|
T | G | 86 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(83): Show | 88 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.759+2349T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143058 | ||||||
chr14:45143072
|
G | A | 87 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(84): Show | 89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+2363G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143072 | ||||||
chr14:45143166
|
A | G | 1 | a0002c0032t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.759+2457A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143166 | ||||||
chr14:45143171
|
CT | C | 83 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(80): Show | 85 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.759+2479delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143171 | |||||
chr14:45143171
|
CTT | C | 5 | a0002c0003t0002g0153a0002c0003t0002g0165a0002c0006t0002g0212others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+2478_759+2479d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143171 | |||||
chr14:45143175
|
T | C | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+2466T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143175 | ||||||
chr14:45143244
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.759+2535T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143244 | ||||||
chr14:45143267
|
G | C | 2 | a0001c0001t0001g0034a0024c0017t0001g0035 | 2 | HG00323.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.759+2558G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143267 | ||||||
chr14:45143461
|
A | T | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+2752A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143461 | ||||||
chr14:45143505
|
A | G | 1 | a0002c0007t0003g0171 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.759+2796A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143505 | ||||||
chr14:45143690
|
A | AT | 63 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0117others(60): Show | 63 | HG00673.hp2 HG01106.hp1 HG01192.hp1 others(60): Show |
intron_variant | MODIFIER | c.759+3002dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143690 | |||||
chr14:45143690
|
A | ATT | 9 | a0001c0001t0001g0122a0002c0003t0001g0169a0002c0003t0001g0170others(6): Show | 9 | HG01109.hp1 HG01346.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.759+3001_759+3002d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45143690 | |||||
chr14:45143754
|
C | T | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.759+3045C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143754 | ||||||
chr14:45143817
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.759+3108C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143817 | ||||||
chr14:45143890
|
C | T | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+3181C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143890 | ||||||
chr14:45143971
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.759+3262C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143971 | ||||||
chr14:45143972
|
G | A | 12 | a0002c0003t0002g0153a0002c0003t0002g0155a0002c0003t0002g0156others(9): Show | 12 | HG01109.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+3263G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45143972 | ||||||
chr14:45144037
|
CT | C | 15 | a0002c0003t0002g0221a0002c0003t0002g0223a0002c0003t0002g0224others(12): Show | 15 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+3339delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144037 | |||||
chr14:45144192
|
T | C | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.759+3483T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144192 | ||||||
chr14:45144261
|
T | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 21 | HG01099.hp2 HG01261.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.759+3552T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144261 | ||||||
chr14:45144304
|
T | TC | 15 | a0002c0003t0002g0153a0002c0003t0002g0155a0002c0003t0002g0156others(12): Show | 15 | HG01109.hp1 HG02109.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.759+3599dupC | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144304 | |||||
chr14:45144309
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 196 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.759+3600T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144309 | ||||||
chr14:45144312
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.759+3603A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144312 | ||||||
chr14:45144349
|
C | T | 5 | a0001c0001t0001g0103a0004c0005t0001g0210a0004c0005t0001g0211others(2): Show | 5 | HG02132.hp1 HG02615.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+3640C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144349 | ||||||
chr14:45144352
|
CCTT | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(38): Show | 42 | HG01109.hp1 HG01261.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.759+3646_759+3648d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144352 | |||||
chr14:45144391
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.759+3682T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144391 | ||||||
chr14:45144741
|
G | T | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.759+4032G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144741 | ||||||
chr14:45144844
|
GCTGGTAC | G | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.760-3989_760-3983d others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45144844 | |||||
chr14:45144894
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.760-3943A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144894 | ||||||
chr14:45144955
|
G | A | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-3882G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45144955 | ||||||
chr14:45145229
|
T | C | 1 | a0018c0024t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-3608T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145229 | ||||||
chr14:45145230
|
C | CT | 5 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-3601dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45145230 | |||||
chr14:45145329
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.760-3508C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145329 | ||||||
chr14:45145357
|
C | G | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.760-3480C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145357 | ||||||
chr14:45145361
|
A | C | 15 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(12): Show | 15 | HG01358.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-3476A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145361 | ||||||
chr14:45145699
|
C | T | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.760-3138C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145699 | ||||||
chr14:45145744
|
G | GA | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-3090dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45145744 | |||||
chr14:45145828
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | NA18954.hp1 NA18968.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-3009G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145828 | ||||||
chr14:45145959
|
TGAGGCAG others(19): Show |
T | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-2872_760-2847d others(28): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45145959 | |||||
chr14:45145983
|
C | T | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-2854C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145983 | ||||||
chr14:45145988
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.760-2849G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45145988 | ||||||
chr14:45146007
|
C | T | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-2830C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146007 | ||||||
chr14:45146054
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0048others(2): Show | 7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-2783G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146054 | ||||||
chr14:45146072
|
G | A | 1 | a0007c0009t0001g0013 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.760-2765G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146072 | ||||||
chr14:45146129
|
T | TAC | 26 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(23): Show | 27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.760-2707_760-2706d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146129 | |||||
chr14:45146144
|
G | GGCA | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.760-2691_760-2689d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146144 | |||||
chr14:45146227
|
T | C | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-2610T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146227 | ||||||
chr14:45146238
|
C | G | 26 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(23): Show | 27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.760-2599C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146238 | ||||||
chr14:45146240
|
G | GA | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 146 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.760-2578dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146240 | |||||
chr14:45146240
|
G | GAA | 45 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0048others(42): Show | 47 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.760-2579_760-2578d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146240 | |||||
chr14:45146240
|
G | GAAA | 8 | a0003c0002t0001g0174a0003c0002t0001g0180a0003c0002t0001g0199others(5): Show | 9 | HG01192.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-2580_760-2578d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146240 | |||||
chr14:45146280
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.760-2557A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146280 | ||||||
chr14:45146331
|
C | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0096others(2): Show | 5 | HG02809.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-2506C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146331 | ||||||
chr14:45146428
|
A | G | 3 | a0002c0003t0001g0167a0002c0003t0001g0170a0015c0030t0001g0168 | 3 | HG02257.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.760-2409A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146428 | ||||||
chr14:45146433
|
T | G | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.760-2404T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146433 | ||||||
chr14:45146498
|
G | T | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.760-2339G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146498 | ||||||
chr14:45146574
|
A | G | 5 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-2263A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45146574 | ||||||
chr14:45146832
|
C | CA | 33 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(30): Show | 33 | HG00323.hp2 HG01106.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.760-1979dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | |||||
chr14:45146832
|
C | CAAA | 5 | a0006c0010t0001g0137a0006c0010t0001g0203a0006c0010t0001g0204others(2): Show | 5 | HG01106.hp1 HG01891.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-1981_760-1979d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | |||||
chr14:45146832
|
CA | C | 36 | a0001c0001t0001g0047a0001c0001t0001g0094a0001c0001t0001g0095others(33): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.760-1979delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | |||||
chr14:45146832
|
CAAAA | C | 9 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(6): Show | 9 | HG02055.hp1 HG02717.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-1982_760-1979d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | |||||
chr14:45146832
|
CAAAAA | C | 16 | a0002c0003t0002g0221a0002c0006t0002g0213a0002c0006t0002g0214others(13): Show | 17 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.760-1983_760-1979d others(7): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45146832 | |||||
chr14:45147148
|
T | C | 108 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(105): Show | 112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.760-1689T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147148 | ||||||
chr14:45147265
|
C | G | 2 | a0005c0004t0001g0111a0005c0004t0001g0112 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.760-1572C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147265 | ||||||
chr14:45147467
|
G | T | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.760-1370G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147467 | ||||||
chr14:45147482
|
T | G | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.760-1355T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147482 | ||||||
chr14:45147529
|
C | T | 3 | a0006c0010t0001g0203a0006c0010t0001g0204a0006c0010t0001g0205 | 3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.760-1308C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147529 | ||||||
chr14:45147538
|
C | G | 1 | a0003c0002t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.760-1299C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147538 | ||||||
chr14:45147551
|
G | A | 5 | a0003c0002t0001g0175a0003c0002t0001g0182a0003c0002t0001g0183others(2): Show | 5 | NA18964.hp2 NA18970.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-1286G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147551 | ||||||
chr14:45147582
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.760-1255C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147582 | ||||||
chr14:45147582
|
C | T | 1 | a0003c0002t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.760-1255C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147582 | ||||||
chr14:45147791
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0063 | 2 | HG02109.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.760-1046G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147791 | ||||||
chr14:45147865
|
G | C | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.760-972G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147865 | ||||||
chr14:45147887
|
G | T | 37 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(34): Show | 40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.760-950G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147887 | ||||||
chr14:45147897
|
G | GC | 15 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0046others(12): Show | 15 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.760-930dupC | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45147897 | |||||
chr14:45147897
|
G | GCC | 17 | a0002c0003t0002g0221a0002c0006t0002g0212a0002c0006t0002g0213others(14): Show | 18 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.760-931_760-930dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45147897 | |||||
chr14:45147905
|
C | A | 10 | a0002c0031t0006g0160a0004c0005t0001g0154a0004c0005t0001g0157others(7): Show | 10 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-932C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147905 | ||||||
chr14:45147905
|
C | G | 6 | a0002c0032t0001g0209a0006c0010t0001g0137a0006c0010t0001g0138others(3): Show | 6 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.760-932C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147905 | ||||||
chr14:45147906
|
C | A | 11 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(8): Show | 11 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.760-931C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147906 | ||||||
chr14:45147907
|
C | A | 33 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(30): Show | 36 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.760-930C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147907 | ||||||
chr14:45147907
|
C | CA | 14 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 14 | HG00323.hp2 HG00597.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.760-921dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45147907 | |||||
chr14:45147907
|
C | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0092others(1): Show | 4 | HG02015.hp2 NA18994.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-930C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147907 | ||||||
chr14:45147908
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.760-929A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147908 | ||||||
chr14:45147977
|
C | A | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.760-860C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45147977 | ||||||
chr14:45148049
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.760-788T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148049 | ||||||
chr14:45148151
|
C | T | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.760-686C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148151 | ||||||
chr14:45148198
|
A | AACAC | 5 | a0002c0007t0003g0166a0002c0007t0003g0171a0003c0002t0001g0185others(2): Show | 5 | HG02886.hp2 HG03453.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-638_760-637ins others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | |||||
chr14:45148198
|
A | AACACAC | 3 | a0003c0002t0001g0199a0003c0002t0001g0200a0019c0026t0008g0145 | 3 | HG02615.hp1 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.760-638_760-637ins others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | |||||
chr14:45148198
|
A | AACACACA others(1): Show |
22 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(19): Show | 24 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.760-638_760-637ins others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | |||||
chr14:45148198
|
A | AACACACA others(3): Show |
5 | a0003c0002t0001g0181a0003c0002t0001g0189a0005c0004t0001g0010others(2): Show | 6 | HG00609.hp2 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.760-638_760-637ins others(10): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | |||||
chr14:45148198
|
A | AACACACA others(5): Show |
1 | a0005c0004t0001g0017 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.760-638_760-637ins others(12): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | |||||
chr14:45148198
|
A | AACACACA others(7): Show |
1 | a0017c0033t0001g0190 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.760-638_760-637ins others(14): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148198 | |||||
chr14:45148200
|
A | AAC | 13 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0045others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.760-603_760-602dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACAC | 12 | a0001c0001t0001g0098a0001c0001t0001g0120a0002c0003t0001g0167others(9): Show | 12 | HG01106.hp1 HG01358.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-605_760-602dup others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACACAC | 10 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-607_760-602dup others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACACACA others(1): Show |
3 | a0004c0005t0001g0210a0004c0005t0001g0211a0018c0024t0001g0144 | 3 | HG02717.hp1 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.760-609_760-602dup others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACACACA others(3): Show |
5 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(2): Show | 5 | HG02055.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-611_760-602dup others(10): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACACACA others(5): Show |
14 | a0002c0006t0002g0212a0002c0006t0002g0213a0002c0006t0002g0214others(11): Show | 14 | HG02132.hp1 HG02280.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.760-613_760-602dup others(12): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACACACA others(7): Show |
9 | a0002c0003t0002g0162a0002c0003t0002g0223a0002c0003t0002g0224others(6): Show | 10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-615_760-602dup others(14): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | AACACACA others(9): Show |
4 | a0002c0003t0002g0221a0002c0003t0002g0225a0008c0011t0002g0053others(1): Show | 4 | HG02717.hp2 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-617_760-602dup others(16): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
A | C | 40 | a0002c0007t0003g0166a0002c0007t0003g0171a0003c0002t0001g0002others(37): Show | 43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.760-637A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148200 | ||||||
chr14:45148200
|
AAC | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0117a0021c0021t0001g0105 | 3 | HG02647.hp2 HG03927.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.760-603_760-602del others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148200
|
AACAC | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 5 | HG01261.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-605_760-602del others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr14 | 45148200 | |||||
chr14:45148514
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.760-323G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148514 | ||||||
chr14:45148561
|
T | C | 3 | a0005c0004t0001g0111a0005c0004t0001g0112a0027c0027t0001g0109 | 3 | HG01167.hp1 HG01169.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.760-276T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148561 | ||||||
chr14:45148731
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.760-106T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 3/22 | chr14 | 45148731 | ||||||
chr14:45149107
|
A | G | 1 | a0025c0020t0001g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.918+112A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149107 | ||||||
chr14:45149142
|
G | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0119 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.918+147G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149142 | ||||||
chr14:45149157
|
T | C | 1 | a0003c0002t0001g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.918+162T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149157 | ||||||
chr14:45149285
|
G | GCA | 14 | a0001c0001t0001g0067a0001c0001t0001g0101a0001c0001t0001g0102others(11): Show | 14 | HG01169.hp1 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.918+313_918+314dup others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | |||||
chr14:45149285
|
G | GCACA | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+311_918+314dup others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | |||||
chr14:45149285
|
GCA | G | 37 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(34): Show | 40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.918+313_918+314del others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | |||||
chr14:45149285
|
GCACACA | G | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+309_918+314del others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149285 | |||||
chr14:45149331
|
A | C | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+336A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149331 | ||||||
chr14:45149484
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0048others(2): Show | 7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+489A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149484 | ||||||
chr14:45149512
|
A | G | 1 | a0011c0014t0001g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.918+517A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149512 | ||||||
chr14:45149541
|
A | G | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+546A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149541 | ||||||
chr14:45149717
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.918+722T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45149717 | ||||||
chr14:45149804
|
T | TACA | 37 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(34): Show | 40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.918+829_918+831dup others(3): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr14 | 45149804 | |||||
chr14:45150014
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+1019A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150014 | ||||||
chr14:45150036
|
A | C | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.918+1041A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150036 | ||||||
chr14:45150574
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.919-823T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150574 | ||||||
chr14:45150586
|
C | T | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.919-811C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150586 | ||||||
chr14:45150637
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.919-760A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150637 | ||||||
chr14:45150727
|
A | G | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.919-670A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150727 | ||||||
chr14:45150814
|
C | T | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-583C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150814 | ||||||
chr14:45150926
|
G | A | 2 | a0002c0006t0002g0217a0002c0006t0002g0219 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919-471G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45150926 | ||||||
chr14:45151055
|
T | A | 1 | a0002c0006t0002g0213 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.919-342T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45151055 | ||||||
chr14:45151104
|
A | G | 7 | a0002c0032t0001g0209a0006c0010t0001g0137a0006c0010t0001g0138others(4): Show | 7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.919-293A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45151104 | ||||||
chr14:45151116
|
G | A | 9 | a0002c0031t0006g0160a0004c0005t0001g0154a0004c0005t0001g0157others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.919-281G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 4/22 | chr14 | 45151116 | ||||||
chr14:45151840
|
G | T | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1050+312G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45151840 | ||||||
chr14:45151912
|
T | TA | 15 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0068others(12): Show | 15 | HG01261.hp1 HG02056.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1050+406dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45151912 | |||||
chr14:45151912
|
TA | T | 33 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0085others(30): Show | 33 | HG01109.hp1 HG01256.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1050+406delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45151912 | |||||
chr14:45151912
|
TAA | T | 12 | a0002c0003t0002g0221a0002c0006t0002g0212a0002c0006t0002g0213others(9): Show | 13 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1050+405_1050+406d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45151912 | |||||
chr14:45151930
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1050+402A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45151930 | ||||||
chr14:45151991
|
T | C | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1050+463T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45151991 | ||||||
chr14:45152009
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1050+481T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152009 | ||||||
chr14:45152032
|
C | CT | 5 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050+518dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45152032 | |||||
chr14:45152032
|
CT | C | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1050+518delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr14 | 45152032 | |||||
chr14:45152065
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1050+537A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152065 | ||||||
chr14:45152315
|
T | C | 108 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(105): Show | 112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1050+787T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152315 | ||||||
chr14:45152475
|
G | A | 1 | a0005c0004t0001g0099 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1050+947G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152475 | ||||||
chr14:45152557
|
G | A | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1050+1029G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45152557 | ||||||
chr14:45153062
|
T | C | 35 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(32): Show | 35 | HG01106.hp1 HG01358.hp1 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.1051-858T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153062 | ||||||
chr14:45153354
|
A | C | 26 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(23): Show | 27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1051-566A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153354 | ||||||
chr14:45153355
|
A | G | 108 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(105): Show | 112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1051-565A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153355 | ||||||
chr14:45153616
|
A | G | 37 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(34): Show | 40 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1051-304A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 5/22 | chr14 | 45153616 | ||||||
chr14:45154084
|
T | C | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1183+32T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154084 | ||||||
chr14:45154211
|
G | A | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+159G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154211 | ||||||
chr14:45154257
|
T | C | 40 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(37): Show | 43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1183+205T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154257 | ||||||
chr14:45154270
|
G | C | 1 | a0002c0008t0007g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1183+218G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154270 | ||||||
chr14:45154273
|
C | T | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1183+221C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154273 | ||||||
chr14:45154378
|
GC | G | 12 | a0003c0002t0001g0174a0003c0002t0001g0176a0003c0002t0001g0180others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1184-318delC | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154378 | ||||||
chr14:45154398
|
T | TA | 20 | a0001c0001t0001g0045a0001c0001t0001g0100a0001c0001t0001g0129others(17): Show | 21 | HG01106.hp1 HG01106.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1184-281dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr14 | 45154398 | |||||
chr14:45154398
|
TA | T | 45 | a0001c0001t0001g0030a0001c0001t0001g0090a0001c0001t0001g0095others(42): Show | 48 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1184-281delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr14 | 45154398 | |||||
chr14:45154466
|
A | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0083 | 3 | HG02056.hp1 HG02129.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1184-231A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 6/22 | chr14 | 45154466 | ||||||
chr14:45155178
|
A | C | 26 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(23): Show | 27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1310-195A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155178 | ||||||
chr14:45155234
|
T | A | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1310-139T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155234 | ||||||
chr14:45155286
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0048others(2): Show | 7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1310-87A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155286 | ||||||
chr14:45155305
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1310-68A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | chr14 | 45155305 | ||||||
chr14:45155330
|
G | GA | 26 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(23): Show | 27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1310-36dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr14 | 45155330 | |||||
chr14:45155485
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1396+26G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155485 | ||||||
chr14:45155491
|
C | T | 1 | a0002c0006t0002g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1396+32C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155491 | ||||||
chr14:45155596
|
CA | C | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1396+139delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45155596 | |||||
chr14:45155738
|
G | A | 35 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(32): Show | 35 | HG01106.hp1 HG01358.hp1 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.1396+279G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155738 | ||||||
chr14:45155747
|
C | T | 1 | a0006c0010t0001g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1396+288C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155747 | ||||||
chr14:45155888
|
TA | T | 108 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(105): Show | 112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1396+431delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45155888 | |||||
chr14:45155980
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1396+521A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155980 | ||||||
chr14:45155987
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1396+528A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45155987 | ||||||
chr14:45156190
|
T | G | 1 | a0004c0005t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1396+731T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156190 | ||||||
chr14:45156668
|
C | T | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1396+1209C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156668 | ||||||
chr14:45156788
|
T | A | 2 | a0009c0016t0005g0207a0009c0016t0005g0208 | 2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1396+1329T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156788 | ||||||
chr14:45156802
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1396+1343C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156802 | ||||||
chr14:45156872
|
T | G | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1396+1413T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45156872 | ||||||
chr14:45156916
|
C | CA | 39 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0046others(36): Show | 39 | HG01106.hp1 HG01516.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1396+1479dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45156916 | |||||
chr14:45156916
|
C | CAA | 22 | a0002c0003t0001g0169a0002c0003t0001g0170a0002c0003t0001g0172others(19): Show | 22 | HG01109.hp1 HG01358.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1396+1478_1396+147 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45156916 | |||||
chr14:45156916
|
CA | C | 5 | a0001c0001t0001g0114a0002c0006t0002g0215a0003c0002t0001g0178others(2): Show | 5 | HG02622.hp1 HG02976.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396+1479delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45156916 | |||||
chr14:45157025
|
T | C | 1 | a0002c0008t0004g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1396+1566T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157025 | ||||||
chr14:45157036
|
A | G | 6 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+1577A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157036 | ||||||
chr14:45157071
|
A | C | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+1612A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157071 | ||||||
chr14:45157071
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1396+1612A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157071 | ||||||
chr14:45157535
|
G | C | 1 | a0002c0003t0002g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1397-1561G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157535 | ||||||
chr14:45157764
|
C | T | 3 | a0006c0010t0001g0203a0006c0010t0001g0204a0006c0010t0001g0205 | 3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1397-1332C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157764 | ||||||
chr14:45157903
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0081a0001c0001t0001g0135others(1): Show | 4 | HG00438.hp1 HG00609.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-1193A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157903 | ||||||
chr14:45157925
|
C | G | 106 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(103): Show | 110 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1397-1171C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45157925 | ||||||
chr14:45158111
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1397-985T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158111 | ||||||
chr14:45158344
|
C | A | 1 | a0004c0005t0001g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1397-752C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158344 | ||||||
chr14:45158405
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1397-691G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158405 | ||||||
chr14:45158439
|
G | A | 1 | a0011c0014t0001g0140 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1397-657G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158439 | ||||||
chr14:45158459
|
C | T | 1 | a0003c0002t0001g0002 | 3 | HG00558.hp1 NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1397-637C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158459 | ||||||
chr14:45158607
|
T | G | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1397-489T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158607 | ||||||
chr14:45158947
|
T | C | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1397-149T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45158947 | ||||||
chr14:45159021
|
G | A | 1 | a0007c0009t0001g0014 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1397-75G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45159021 | ||||||
chr14:45159038
|
T | G | 109 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(106): Show | 113 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1397-58T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45159038 | ||||||
chr14:45159080
|
TTA | T | 40 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(37): Show | 43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1397-3_1397-2delTA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | 45159080 | |||||
chr14:45159084
|
A | G | 1 | a0002c0032t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1397-12A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 8/22 | chr14 | 45159084 | ||||||
chr14:45159346
|
T | G | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+66T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159346 | ||||||
chr14:45159427
|
A | C | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1581+147A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159427 | ||||||
chr14:45159461
|
A | C | 1 | a0002c0006t0002g0219 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1581+181A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159461 | ||||||
chr14:45159515
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1581+235G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159515 | ||||||
chr14:45159547
|
T | G | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+267T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159547 | ||||||
chr14:45159550
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1581+270C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159550 | ||||||
chr14:45159572
|
C | T | 208 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 217 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1581+292C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159572 | ||||||
chr14:45159654
|
A | G | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+374A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159654 | ||||||
chr14:45159800
|
A | C | 13 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1581+520A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159800 | ||||||
chr14:45159815
|
T | C | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+535T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159815 | ||||||
chr14:45159819
|
G | C | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+539G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159819 | ||||||
chr14:45159912
|
A | G | 1 | a0004c0005t0001g0211 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1581+632A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45159912 | ||||||
chr14:45160002
|
G | GT | 10 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0096others(7): Show | 10 | HG01346.hp2 HG01993.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1581+739dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160002 | |||||
chr14:45160002
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1581+722G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160002 | ||||||
chr14:45160002
|
GTT | G | 59 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(56): Show | 60 | HG00609.hp2 HG01106.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.1581+738_1581+739d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160002 | |||||
chr14:45160002
|
GTTT | G | 35 | a0002c0031t0006g0160a0003c0002t0001g0002a0003c0002t0001g0174others(32): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1581+737_1581+739d others(5): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160002 | |||||
chr14:45160004
|
T | G | 1 | a0002c0003t0002g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1581+724T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160004 | ||||||
chr14:45160037
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1581+757G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160037 | ||||||
chr14:45160096
|
G | A | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581+816G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160096 | ||||||
chr14:45160241
|
G | A | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1581+961G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160241 | ||||||
chr14:45160268
|
A | T | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+988A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160268 | ||||||
chr14:45160290
|
G | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02145.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1581+1010G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160290 | ||||||
chr14:45160305
|
T | G | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+1025T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160305 | ||||||
chr14:45160318
|
CT | C | 18 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0001g0056others(15): Show | 18 | HG00323.hp1 HG00323.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1581+1054delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr14 | 45160318 | |||||
chr14:45160480
|
G | A | 27 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(24): Show | 28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1581+1200G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160480 | ||||||
chr14:45160491
|
T | A | 1 | a0002c0003t0002g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1581+1211T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160491 | ||||||
chr14:45160567
|
C | T | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1581+1287C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160567 | ||||||
chr14:45160623
|
C | T | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+1343C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160623 | ||||||
chr14:45160658
|
T | C | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1581+1378T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160658 | ||||||
chr14:45160708
|
A | T | 1 | a0005c0004t0001g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1581+1428A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45160708 | ||||||
chr14:45161128
|
A | G | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+1848A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161128 | ||||||
chr14:45161153
|
C | T | 2 | a0003c0002t0001g0174a0003c0002t0001g0193 | 2 | HG00673.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1581+1873C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161153 | ||||||
chr14:45161191
|
C | T | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1581+1911C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161191 | ||||||
chr14:45161319
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1581+2039T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161319 | ||||||
chr14:45161369
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1581+2089G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161369 | ||||||
chr14:45161378
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0098a0001c0001t0001g0113 | 3 | HG03669.hp2 NA19005.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1581+2098G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161378 | ||||||
chr14:45161506
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1581+2226C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161506 | ||||||
chr14:45161595
|
A | G | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1581+2315A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161595 | ||||||
chr14:45161768
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0059 | 2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1581+2488C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161768 | ||||||
chr14:45161817
|
A | G | 1 | a0019c0026t0008g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1581+2537A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45161817 | ||||||
chr14:45162015
|
T | A | 1 | a0003c0002t0001g0194 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1582-2344T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162015 | ||||||
chr14:45162124
|
G | A | 1 | a0014c0034t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1582-2235G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162124 | ||||||
chr14:45162616
|
A | G | 2 | a0001c0001t0001g0080a0028c0028t0001g0079 | 2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1582-1743A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162616 | ||||||
chr14:45162752
|
A | G | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1607A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162752 | ||||||
chr14:45162828
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0059 | 2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1582-1531A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162828 | ||||||
chr14:45162847
|
G | A | 6 | a0002c0032t0001g0209a0006c0010t0001g0137a0006c0010t0001g0138others(3): Show | 6 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1512G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162847 | ||||||
chr14:45162869
|
T | G | 8 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1582-1490T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162869 | ||||||
chr14:45162881
|
C | G | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1478C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45162881 | ||||||
chr14:45163002
|
CCGA | C | 38 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(35): Show | 41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1582-1356_1582-135 others(7): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163002 | ||||||
chr14:45163013
|
C | T | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582-1346C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163013 | ||||||
chr14:45163137
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0048others(2): Show | 7 | HG00639.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.1582-1222G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163137 | ||||||
chr14:45163238
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG00639.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1582-1121G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163238 | ||||||
chr14:45163299
|
A | T | 1 | a0005c0004t0001g0108 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1582-1060A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163299 | ||||||
chr14:45163383
|
A | T | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1582-976A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163383 | ||||||
chr14:45163485
|
T | G | 1 | a0001c0001t0001g0009 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1582-874T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163485 | ||||||
chr14:45163610
|
T | C | 1 | a0018c0024t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1582-749T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45163610 | ||||||
chr14:45164096
|
C | G | 1 | a0001c0001t0001g0008 | 2 | NA18970.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1582-263C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164096 | ||||||
chr14:45164127
|
G | A | 1 | a0004c0005t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1582-232G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164127 | ||||||
chr14:45164215
|
C | G | 109 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(106): Show | 113 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1582-144C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164215 | ||||||
chr14:45164225
|
A | G | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1582-134A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164225 | ||||||
chr14:45164319
|
A | G | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1582-40A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 9/22 | chr14 | 45164319 | ||||||
chr14:45164595
|
CA | C | 27 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(24): Show | 28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1788+31delA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164595 | ||||||
chr14:45164711
|
C | T | 3 | a0006c0010t0001g0203a0006c0010t0001g0204a0006c0010t0001g0205 | 3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1788+146C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164711 | ||||||
chr14:45164736
|
G | A | 1 | a0003c0002t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1788+171G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164736 | ||||||
chr14:45164873
|
G | T | 10 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(7): Show | 10 | HG02109.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1788+308G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164873 | ||||||
chr14:45164907
|
T | A | 1 | a0005c0004t0001g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1788+342T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45164907 | ||||||
chr14:45164960
|
CTAAA | C | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1788+399_1788+402d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr14 | 45164960 | |||||
chr14:45165296
|
G | A | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1788+731G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165296 | ||||||
chr14:45165296
|
G | T | 17 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(14): Show | 17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1788+731G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165296 | ||||||
chr14:45165360
|
A | C | 2 | a0003c0002t0001g0002a0003c0002t0001g0201 | 4 | HG00558.hp1 HG02056.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1788+795A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165360 | ||||||
chr14:45165373
|
C | G | 1 | a0001c0001t0001g0060 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1788+808C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165373 | ||||||
chr14:45165415
|
G | A | 1 | a0003c0002t0001g0002 | 3 | HG00558.hp1 NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1788+850G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165415 | ||||||
chr14:45165483
|
G | C | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1788+918G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165483 | ||||||
chr14:45165534
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 7 | HG01261.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+969C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165534 | ||||||
chr14:45165557
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1788+992A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165557 | ||||||
chr14:45165611
|
T | C | 6 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1788+1046T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165611 | ||||||
chr14:45165947
|
A | G | 23 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(20): Show | 23 | HG01358.hp1 HG01884.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.1789-1003A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45165947 | ||||||
chr14:45166111
|
C | T | 1 | a0002c0032t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1789-839C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166111 | ||||||
chr14:45166155
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1789-795G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166155 | ||||||
chr14:45166277
|
G | A | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1789-673G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166277 | ||||||
chr14:45166534
|
C | A | 1 | a0002c0003t0002g0224 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1789-416C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166534 | ||||||
chr14:45166669
|
A | T | 2 | a0002c0006t0002g0216a0002c0006t0002g0218 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1789-281A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166669 | ||||||
chr14:45166766
|
A | G | 3 | a0002c0003t0001g0167a0002c0003t0001g0170a0015c0030t0001g0168 | 3 | HG02257.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1789-184A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166766 | ||||||
chr14:45166777
|
C | CA | 15 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0062others(12): Show | 15 | HG01952.hp1 HG02055.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1789-154dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr14 | 45166777 | |||||
chr14:45166777
|
C | CAA | 15 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(12): Show | 15 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1789-155_1789-154d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr14 | 45166777 | |||||
chr14:45166904
|
A | G | 1 | a0002c0003t0001g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789-46A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 10/22 | chr14 | 45166904 | ||||||
chr14:45167268
|
A | G | 1 | a0002c0007t0003g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2002+105A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167268 | ||||||
chr14:45167304
|
G | A | 99 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(96): Show | 103 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.2002+141G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167304 | ||||||
chr14:45167564
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2002+401A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167564 | ||||||
chr14:45167580
|
T | C | 7 | a0002c0031t0006g0160a0007c0009t0001g0012a0007c0009t0001g0013others(4): Show | 7 | HG02132.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+417T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167580 | ||||||
chr14:45167885
|
A | G | 17 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(14): Show | 17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2002+722A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167885 | ||||||
chr14:45167984
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0008c0025t0002g0136 | 3 | HG03491.hp2 HG03492.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2002+821C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167984 | ||||||
chr14:45167997
|
G | A | 7 | a0002c0031t0006g0160a0007c0009t0001g0012a0007c0009t0001g0013others(4): Show | 7 | HG02132.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+834G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45167997 | ||||||
chr14:45168007
|
A | T | 1 | a0003c0002t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2002+844A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45168007 | ||||||
chr14:45168149
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 7 | HG01261.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2002+986A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45168149 | ||||||
chr14:45168771
|
C | CATAGTAT others(23): Show |
2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2002+1621_2002+165 others(34): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45168771 | |||||
chr14:45168784
|
T | TTATATAT others(23): Show |
2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2002+1626_2002+165 others(34): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45168784 | |||||
chr14:45168946
|
C | CAG | 110 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(107): Show | 114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2003-1642_2003-164 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45168946 | |||||
chr14:45169026
|
A | G | 1 | a0004c0005t0001g0179 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2003-1563A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169026 | ||||||
chr14:45169057
|
G | A | 11 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(8): Show | 11 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2003-1532G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169057 | ||||||
chr14:45169264
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2003-1325C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169264 | ||||||
chr14:45169383
|
G | GT | 62 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(59): Show | 66 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2003-1194dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45169383 | |||||
chr14:45169383
|
G | GTT | 5 | a0003c0002t0001g0175a0003c0002t0001g0182a0003c0002t0001g0194others(2): Show | 5 | NA18970.hp1 NA18984.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2003-1195_2003-119 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr14 | 45169383 | |||||
chr14:45169410
|
T | A | 3 | a0001c0001t0001g0135a0002c0032t0001g0209a0023c0018t0001g0026 | 3 | HG00438.hp1 HG02145.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2003-1179T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169410 | ||||||
chr14:45169432
|
C | A | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.2003-1157C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169432 | ||||||
chr14:45169484
|
C | T | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2003-1105C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169484 | ||||||
chr14:45169591
|
G | C | 4 | a0002c0008t0004g0150a0002c0008t0004g0151a0002c0008t0004g0152others(1): Show | 4 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003-998G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169591 | ||||||
chr14:45169616
|
G | T | 1 | a0003c0002t0001g0194 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2003-973G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45169616 | ||||||
chr14:45170128
|
A | T | 17 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(14): Show | 17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2003-461A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45170128 | ||||||
chr14:45170170
|
G | T | 1 | a0002c0032t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2003-419G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45170170 | ||||||
chr14:45170333
|
C | G | 6 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003-256C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 11/22 | chr14 | 45170333 | ||||||
chr14:45170777
|
T | C | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2160+31T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45170777 | ||||||
chr14:45170782
|
C | G | 26 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(23): Show | 27 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.2160+36C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45170782 | ||||||
chr14:45170985
|
CTG | C | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.2160+242_2160+243d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45170985 | |||||
chr14:45171090
|
A | G | 9 | a0002c0006t0002g0213a0002c0006t0002g0220a0002c0032t0001g0209others(6): Show | 9 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2160+344A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171090 | ||||||
chr14:45171147
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2160+401T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171147 | ||||||
chr14:45171169
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2160+423G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171169 | ||||||
chr14:45171202
|
A | C | 41 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(38): Show | 44 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2160+456A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171202 | ||||||
chr14:45171294
|
AATTATGC others(4): Show |
A | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2160+551_2160+561d others(13): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171294 | |||||
chr14:45171325
|
A | AT | 7 | a0002c0003t0002g0162a0007c0009t0001g0012a0007c0009t0001g0013others(4): Show | 7 | HG01109.hp1 HG02132.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2160+589dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171325 | |||||
chr14:45171354
|
A | G | 110 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(107): Show | 114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2160+608A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171354 | ||||||
chr14:45171447
|
A | G | 1 | a0002c0007t0003g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2160+701A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171447 | ||||||
chr14:45171485
|
C | T | 1 | a0018c0024t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2160+739C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171485 | ||||||
chr14:45171642
|
C | T | 7 | a0002c0031t0006g0160a0007c0009t0001g0012a0007c0009t0001g0013others(4): Show | 7 | HG02132.hp1 HG02293.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2160+896C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171642 | ||||||
chr14:45171691
|
T | TTG | 2 | a0001c0001t0001g0096a0018c0024t0001g0144 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2160+976_2160+977d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | |||||
chr14:45171691
|
TTG | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 157 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.2160+976_2160+977d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | |||||
chr14:45171691
|
TTGTG | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0125a0002c0003t0002g0221others(1): Show | 4 | HG01516.hp2 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2160+974_2160+977d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | |||||
chr14:45171691
|
TTGTGTG | T | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2160+972_2160+977d others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | |||||
chr14:45171691
|
TTGTGTGT others(7): Show |
T | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.2160+964_2160+977d others(16): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr14 | 45171691 | |||||
chr14:45171692
|
TGTGTGTG | T | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2160+947_2160+953d others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171692 | ||||||
chr14:45171811
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2160+1065A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45171811 | ||||||
chr14:45172401
|
C | T | 6 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2161-654C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172401 | ||||||
chr14:45172511
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0059 | 2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2161-544C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172511 | ||||||
chr14:45172653
|
T | C | 17 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(14): Show | 17 | HG01358.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2161-402T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172653 | ||||||
chr14:45172705
|
A | G | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2161-350A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 12/22 | chr14 | 45172705 | ||||||
chr14:45173303
|
C | A | 1 | a0002c0008t0004g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2316+93C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173303 | ||||||
chr14:45173469
|
C | G | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2316+259C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173469 | ||||||
chr14:45173535
|
T | C | 1 | a0005c0004t0001g0017 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2316+325T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173535 | ||||||
chr14:45173805
|
C | T | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2316+595C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173805 | ||||||
chr14:45173806
|
G | A | 7 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2316+596G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173806 | ||||||
chr14:45173827
|
G | C | 1 | a0002c0003t0002g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2316+617G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173827 | ||||||
chr14:45173852
|
T | G | 1 | a0006c0010t0001g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2316+642T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45173852 | ||||||
chr14:45174057
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2316+847C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174057 | ||||||
chr14:45174095
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2316+885A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174095 | ||||||
chr14:45174158
|
AG | A | 38 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(35): Show | 41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2317-911delG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 45174158 | |||||
chr14:45174168
|
C | T | 2 | a0006c0010t0001g0137a0006c0010t0001g0138 | 2 | HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2317-903C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174168 | ||||||
chr14:45174385
|
T | TA | 32 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0069others(29): Show | 32 | HG01346.hp2 HG01358.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.2317-672dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 45174385 | |||||
chr14:45174400
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2317-671C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174400 | ||||||
chr14:45174429
|
T | C | 6 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2317-642T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174429 | ||||||
chr14:45174635
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2317-436T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174635 | ||||||
chr14:45174665
|
T | TGAAAGAG others(242): Show |
1 | a0001c0001t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2317-392_2317-391i others(251): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr14 | 45174665 | |||||
chr14:45174822
|
A | G | 1 | a0002c0008t0004g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2317-249A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174822 | ||||||
chr14:45174926
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2317-145G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174926 | ||||||
chr14:45174977
|
A | G | 1 | a0003c0002t0001g0182 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2317-94A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 13/22 | chr14 | 45174977 | ||||||
chr14:45176983
|
T | G | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.4222+7T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45176983 | ||||||
chr14:45177059
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4222+83T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177059 | ||||||
chr14:45177140
|
TAGATTTA others(73): Show |
T | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4222+167_4222+246d others(82): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45177140 | |||||
chr14:45177310
|
C | T | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4222+334C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177310 | ||||||
chr14:45177456
|
G | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4222+480G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177456 | ||||||
chr14:45177856
|
A | G | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4222+880A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177856 | ||||||
chr14:45177920
|
C | T | 3 | a0002c0003t0001g0167a0002c0003t0001g0170a0015c0030t0001g0168 | 3 | HG02257.hp2 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4222+944C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177920 | ||||||
chr14:45177941
|
G | A | 40 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(37): Show | 43 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.4222+965G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45177941 | ||||||
chr14:45178108
|
C | A | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222+1132C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178108 | ||||||
chr14:45178150
|
A | G | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222+1174A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178150 | ||||||
chr14:45178245
|
A | G | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4222+1269A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178245 | ||||||
chr14:45178368
|
G | T | 1 | a0020c0023t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4222+1392G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178368 | ||||||
chr14:45178603
|
T | C | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4222+1627T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178603 | ||||||
chr14:45178908
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4222+1932A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178908 | ||||||
chr14:45178928
|
A | G | 110 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(107): Show | 114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4222+1952A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45178928 | ||||||
chr14:45179068
|
A | G | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4222+2092A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179068 | ||||||
chr14:45179375
|
T | C | 1 | a0003c0002t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4223-2055T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179375 | ||||||
chr14:45179396
|
C | T | 1 | a0002c0007t0003g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4223-2034C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179396 | ||||||
chr14:45179460
|
C | G | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1970C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179460 | ||||||
chr14:45179484
|
T | C | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1946T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179484 | ||||||
chr14:45179522
|
A | G | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1908A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179522 | ||||||
chr14:45179541
|
G | T | 1 | a0002c0008t0004g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4223-1889G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179541 | ||||||
chr14:45179561
|
CT | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 167 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.4223-1849delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45179561 | |||||
chr14:45179561
|
CTT | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0133a0002c0006t0002g0218others(10): Show | 13 | HG02056.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4223-1850_4223-184 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45179561 | |||||
chr14:45179561
|
CTTTTTTT others(4): Show |
C | 8 | a0002c0006t0002g0213a0002c0006t0002g0220a0002c0032t0001g0209others(5): Show | 8 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.4223-1859_4223-184 others(15): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45179561 | |||||
chr14:45179565
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0050 | 2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.4223-1865T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179565 | ||||||
chr14:45179604
|
C | G | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4223-1826C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179604 | ||||||
chr14:45179710
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4223-1720T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179710 | ||||||
chr14:45179840
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4223-1590G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179840 | ||||||
chr14:45179935
|
T | C | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1495T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45179935 | ||||||
chr14:45180141
|
A | G | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4223-1289A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180141 | ||||||
chr14:45180149
|
A | G | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4223-1281A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180149 | ||||||
chr14:45180300
|
GCA | G | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4223-1129_4223-112 others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180300 | ||||||
chr14:45180432
|
G | GT | 8 | a0001c0001t0001g0080a0002c0032t0001g0209a0006c0010t0001g0137others(5): Show | 8 | HG01099.hp1 HG01106.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.4223-987dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr14 | 45180432 | |||||
chr14:45180478
|
G | C | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4223-952G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180478 | ||||||
chr14:45180497
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4223-933A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180497 | ||||||
chr14:45180749
|
A | G | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4223-681A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180749 | ||||||
chr14:45180774
|
T | G | 4 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0015others(1): Show | 4 | NA18939.hp2 NA18966.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.4223-656T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180774 | ||||||
chr14:45180815
|
A | T | 1 | a0021c0021t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4223-615A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180815 | ||||||
chr14:45180827
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4223-603C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180827 | ||||||
chr14:45180861
|
A | G | 2 | a0010c0015t0001g0197a0010c0015t0001g0198 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4223-569A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180861 | ||||||
chr14:45180955
|
A | G | 14 | a0002c0003t0002g0221a0002c0006t0002g0212a0002c0006t0002g0213others(11): Show | 15 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4223-475A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45180955 | ||||||
chr14:45181196
|
A | T | 7 | a0002c0032t0001g0209a0006c0010t0001g0137a0006c0010t0001g0138others(4): Show | 7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4223-234A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45181196 | ||||||
chr14:45181330
|
C | T | 14 | a0002c0003t0002g0221a0002c0006t0002g0212a0002c0006t0002g0213others(11): Show | 15 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4223-100C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45181330 | ||||||
chr14:45181366
|
G | C | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4223-64G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 14/22 | chr14 | 45181366 | ||||||
chr14:45181601
|
A | G | 2 | a0002c0006t0002g0216a0002c0006t0002g0218 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4318-36A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 15/22 | chr14 | 45181601 | ||||||
chr14:45181610
|
G | A | 101 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(98): Show | 105 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.4318-27G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 15/22 | chr14 | 45181610 | ||||||
chr14:45182065
|
A | G | 3 | a0003c0002t0001g0186a0003c0002t0001g0192a0003c0002t0001g0199 | 3 | NA18982.hp2 NA19011.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.4386+360A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182065 | ||||||
chr14:45182224
|
A | G | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4386+519A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182224 | ||||||
chr14:45182256
|
A | AT | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4386+552dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr14 | 45182256 | |||||
chr14:45182433
|
G | A | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4386+728G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182433 | ||||||
chr14:45182478
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 189 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.4386+773G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182478 | ||||||
chr14:45182535
|
T | G | 1 | a0002c0032t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4386+830T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182535 | ||||||
chr14:45182629
|
C | T | 1 | a0002c0032t0001g0209 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4386+924C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182629 | ||||||
chr14:45182762
|
G | A | 109 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(106): Show | 113 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.4387-1012G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182762 | ||||||
chr14:45182783
|
TTGTA | T | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4387-987_4387-984d others(6): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr14 | 45182783 | |||||
chr14:45182853
|
C | T | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4387-921C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182853 | ||||||
chr14:45182885
|
A | G | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4387-889A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45182885 | ||||||
chr14:45183106
|
T | C | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4387-668T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183106 | ||||||
chr14:45183116
|
G | C | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4387-658G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183116 | ||||||
chr14:45183735
|
A | T | 12 | a0003c0002t0001g0174a0003c0002t0001g0176a0003c0002t0001g0180others(9): Show | 12 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.4387-39A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183735 | ||||||
chr14:45183770
|
A | T | 1 | a0005c0004t0001g0112 | 1 | HG01167.hp1 | splice_region_variant&intron_variant | LOW | c.4387-4A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 16/22 | chr14 | 45183770 | ||||||
chr14:45184529
|
G | A | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4515+627G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184529 | ||||||
chr14:45184660
|
C | CA | 8 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0043others(5): Show | 8 | HG01192.hp2 HG02056.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4516-538dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184660 | |||||
chr14:45184660
|
C | CAAAAAAA | 10 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(7): Show | 10 | HG02257.hp1 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.4516-544_4516-538d others(9): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184660 | |||||
chr14:45184674
|
A | AC | 27 | a0002c0003t0002g0153a0002c0003t0002g0155a0002c0003t0002g0156others(24): Show | 28 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.4516-543_4516-542i others(3): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184674 | ||||||
chr14:45184674
|
A | C | 52 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(49): Show | 55 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.4516-543A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184674 | ||||||
chr14:45184776
|
C | CT | 23 | a0001c0001t0001g0018a0001c0001t0001g0135a0002c0003t0002g0221others(20): Show | 24 | HG02056.hp1 HG02132.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.4516-427dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184776 | |||||
chr14:45184866
|
C | T | 8 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.4516-351C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184866 | ||||||
chr14:45184894
|
T | C | 100 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(97): Show | 104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.4516-323T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184894 | ||||||
chr14:45184940
|
A | AT | 5 | a0001c0001t0001g0066a0001c0001t0001g0121a0001c0001t0001g0125others(2): Show | 5 | HG02145.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4516-262dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184940 | |||||
chr14:45184940
|
AT | A | 51 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(48): Show | 54 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.4516-262delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45184940 | |||||
chr14:45184982
|
A | G | 1 | a0002c0008t0004g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4516-235A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45184982 | ||||||
chr14:45185054
|
T | C | 7 | a0002c0032t0001g0209a0006c0010t0001g0137a0006c0010t0001g0138others(4): Show | 7 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4516-163T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | chr14 | 45185054 | ||||||
chr14:45185207
|
TCTTA | T | 110 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(107): Show | 114 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(111): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.4516-5_4516-2delCT others(2): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr14 | 45185207 | |||||
chr14:45185703
|
A | G | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4672+330A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185703 | ||||||
chr14:45185705
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4672+332A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185705 | ||||||
chr14:45185775
|
T | A | 1 | a0003c0002t0001g0194 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4672+402T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185775 | ||||||
chr14:45185848
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4672+475T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45185848 | ||||||
chr14:45186164
|
G | A | 1 | a0003c0002t0001g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4672+791G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186164 | ||||||
chr14:45186190
|
T | A | 3 | a0002c0003t0002g0223a0002c0003t0002g0224a0002c0003t0002g0225 | 3 | HG02717.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4672+817T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186190 | ||||||
chr14:45186343
|
A | G | 41 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(38): Show | 44 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.4672+970A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186343 | ||||||
chr14:45186689
|
A | G | 1 | a0023c0018t0001g0026 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4673-1092A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186689 | ||||||
chr14:45186866
|
A | C | 1 | a0018c0024t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4673-915A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45186866 | ||||||
chr14:45187096
|
A | G | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4673-685A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187096 | ||||||
chr14:45187209
|
CT | C | 28 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0027others(25): Show | 28 | HG00438.hp2 HG01106.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.4673-559delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr14 | 45187209 | |||||
chr14:45187243
|
T | C | 27 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(24): Show | 28 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.4673-538T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187243 | ||||||
chr14:45187314
|
T | TA | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.4673-458dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr14 | 45187314 | |||||
chr14:45187341
|
T | A | 1 | a0002c0003t0001g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4673-440T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187341 | ||||||
chr14:45187351
|
C | T | 12 | a0003c0002t0001g0002a0003c0002t0001g0177a0003c0002t0001g0181others(9): Show | 15 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.4673-430C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187351 | ||||||
chr14:45187422
|
C | T | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4673-359C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187422 | ||||||
chr14:45187441
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4673-340T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187441 | ||||||
chr14:45187447
|
T | A | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4673-334T>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187447 | ||||||
chr14:45187547
|
G | A | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4673-234G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187547 | ||||||
chr14:45187596
|
C | G | 5 | a0006c0010t0001g0137a0006c0010t0001g0138a0006c0010t0001g0203others(2): Show | 5 | HG01106.hp1 HG01516.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4673-185C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187596 | ||||||
chr14:45187704
|
TAGATTGA others(7): Show |
T | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4673-76_4673-63del others(14): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187704 | ||||||
chr14:45187719
|
T | C | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4673-62T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 18/22 | chr14 | 45187719 | ||||||
chr14:45188104
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4779+217C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | chr14 | 45188104 | ||||||
chr14:45188298
|
C | G | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4779+411C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | chr14 | 45188298 | ||||||
chr14:45188386
|
A | AT | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4780-408dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr14 | 45188386 | |||||
chr14:45188621
|
A | G | 1 | a0021c0021t0001g0105 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4780-181A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | chr14 | 45188621 | ||||||
chr14:45188754
|
GTTAA | G | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.4780-45_4780-42del others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr14 | 45188754 | |||||
chr14:45189385
|
A | T | 3 | a0006c0010t0001g0203a0006c0010t0001g0204a0006c0010t0001g0205 | 3 | HG01106.hp1 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.5340+23A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189385 | ||||||
chr14:45189511
|
A | T | 5 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5340+149A>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189511 | ||||||
chr14:45189588
|
A | G | 28 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(25): Show | 29 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5340+226A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189588 | ||||||
chr14:45189756
|
G | A | 1 | a0002c0003t0002g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5340+394G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189756 | ||||||
chr14:45189837
|
G | A | 38 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(35): Show | 41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.5340+475G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45189837 | ||||||
chr14:45190044
|
G | A | 6 | a0002c0032t0001g0209a0006c0010t0001g0137a0006c0010t0001g0138others(3): Show | 6 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.5340+682G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190044 | ||||||
chr14:45190194
|
T | C | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+832T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190194 | ||||||
chr14:45190268
|
A | G | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5340+906A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190268 | ||||||
chr14:45190408
|
C | G | 8 | a0002c0006t0002g0213a0002c0006t0002g0220a0002c0032t0001g0209others(5): Show | 8 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5340+1046C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190408 | ||||||
chr14:45190637
|
T | C | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5340+1275T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45190637 | ||||||
chr14:45191396
|
A | G | 99 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(96): Show | 103 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.5340+2034A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191396 | ||||||
chr14:45191557
|
G | C | 107 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(104): Show | 111 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.5340+2195G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191557 | ||||||
chr14:45191582
|
AATAG | A | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5340+2224_5340+222 others(8): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45191582 | |||||
chr14:45191636
|
G | T | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+2274G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191636 | ||||||
chr14:45191832
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0083 | 3 | HG02056.hp1 HG02129.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.5340+2470A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191832 | ||||||
chr14:45191873
|
T | C | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+2511T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191873 | ||||||
chr14:45191880
|
A | G | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5340+2518A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191880 | ||||||
chr14:45191954
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.5340+2592G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191954 | ||||||
chr14:45191955
|
C | A | 1 | a0004c0005t0001g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5340+2593C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45191955 | ||||||
chr14:45192173
|
C | T | 1 | a0004c0005t0001g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5340+2811C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192173 | ||||||
chr14:45192215
|
T | C | 1 | a0020c0023t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5340+2853T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192215 | ||||||
chr14:45192229
|
A | C | 12 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5340+2867A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192229 | ||||||
chr14:45192527
|
C | T | 8 | a0002c0006t0002g0213a0002c0006t0002g0220a0002c0032t0001g0209others(5): Show | 8 | HG01106.hp1 HG01516.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.5340+3165C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192527 | ||||||
chr14:45192585
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5340+3223G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192585 | ||||||
chr14:45192599
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0096others(2): Show | 5 | HG02809.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.5340+3237C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192599 | ||||||
chr14:45192602
|
C | A | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5340+3240C>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192602 | ||||||
chr14:45192609
|
C | G | 2 | a0004c0005t0001g0210a0004c0005t0001g0211 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5340+3247C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192609 | ||||||
chr14:45192629
|
C | G | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5340+3267C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192629 | ||||||
chr14:45192638
|
A | G | 100 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(97): Show | 104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.5340+3276A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192638 | ||||||
chr14:45192980
|
G | A | 6 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-3192G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45192980 | ||||||
chr14:45193065
|
A | G | 1 | a0002c0008t0007g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5341-3107A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193065 | ||||||
chr14:45193122
|
T | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(28): Show | 35 | HG00323.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.5341-3050T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193122 | ||||||
chr14:45193311
|
C | T | 39 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(36): Show | 42 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.5341-2861C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193311 | ||||||
chr14:45193374
|
T | C | 108 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(105): Show | 112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.5341-2798T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193374 | ||||||
chr14:45193384
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5341-2788G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193384 | ||||||
chr14:45193386
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5341-2786T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193386 | ||||||
chr14:45193388
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5341-2784C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193388 | ||||||
chr14:45193390
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5341-2782T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193390 | ||||||
chr14:45193436
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0117 | 3 | HG01255.hp2 HG01516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.5341-2736A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193436 | ||||||
chr14:45193561
|
G | A | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5341-2611G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193561 | ||||||
chr14:45193762
|
GT | G | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-2399delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45193762 | |||||
chr14:45193906
|
G | A | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-2266G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193906 | ||||||
chr14:45193933
|
A | G | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5341-2239A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45193933 | ||||||
chr14:45194263
|
T | C | 9 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.5341-1909T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194263 | ||||||
chr14:45194298
|
G | A | 1 | a0003c0002t0001g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5341-1874G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194298 | ||||||
chr14:45194316
|
C | CA | 8 | a0001c0001t0001g0030a0001c0001t0001g0059a0002c0003t0001g0167others(5): Show | 8 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.5341-1847dupA | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45194316 | |||||
chr14:45194625
|
G | A | 112 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0096others(109): Show | 116 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.5341-1547G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194625 | ||||||
chr14:45194630
|
A | G | 1 | a0026c0022t0001g0022 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5341-1542A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194630 | ||||||
chr14:45194631
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5341-1541C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194631 | ||||||
chr14:45194718
|
G | A | 1 | a0023c0018t0001g0026 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5341-1454G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194718 | ||||||
chr14:45194812
|
C | CT | 9 | a0001c0001t0001g0025a0001c0001t0001g0095a0002c0006t0002g0217others(6): Show | 9 | HG00438.hp2 HG01167.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.5341-1343dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45194812 | |||||
chr14:45194812
|
CT | C | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-1343delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr14 | 45194812 | |||||
chr14:45194839
|
C | T | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-1333C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194839 | ||||||
chr14:45194842
|
C | T | 5 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5341-1330C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194842 | ||||||
chr14:45194847
|
C | T | 40 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(37): Show | 41 | HG01106.hp1 HG01109.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.5341-1325C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194847 | ||||||
chr14:45194855
|
A | G | 1 | a0002c0031t0006g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5341-1317A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194855 | ||||||
chr14:45194894
|
T | C | 5 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.5341-1278T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194894 | ||||||
chr14:45194896
|
C | T | 4 | a0002c0008t0004g0150a0002c0008t0004g0151a0002c0008t0004g0152others(1): Show | 4 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.5341-1276C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194896 | ||||||
chr14:45194946
|
A | G | 1 | a0004c0005t0001g0154 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5341-1226A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45194946 | ||||||
chr14:45195060
|
T | C | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-1112T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195060 | ||||||
chr14:45195128
|
G | A | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5341-1044G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195128 | ||||||
chr14:45195325
|
A | G | 2 | a0003c0002t0001g0177a0003c0002t0001g0206 | 2 | NA18940.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.5341-847A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195325 | ||||||
chr14:45195431
|
T | G | 1 | a0002c0006t0002g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5341-741T>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195431 | ||||||
chr14:45195518
|
C | G | 108 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(105): Show | 112 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.5341-654C>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195518 | ||||||
chr14:45195598
|
T | C | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5341-574T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195598 | ||||||
chr14:45195626
|
A | G | 1 | a0008c0025t0002g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5341-546A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195626 | ||||||
chr14:45195711
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0040 | 3 | HG01099.hp2 HG01256.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5341-461T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195711 | ||||||
chr14:45195861
|
G | A | 1 | a0016c0029t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5341-311G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195861 | ||||||
chr14:45195953
|
C | T | 1 | a0004c0005t0001g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5341-219C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45195953 | ||||||
chr14:45196109
|
G | A | 6 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.5341-63G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45196109 | ||||||
chr14:45196153
|
G | A | 1 | a0002c0008t0004g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5341-19G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 20/22 | chr14 | 45196153 | ||||||
chr14:45196639
|
T | C | 6 | a0007c0009t0001g0012a0007c0009t0001g0013a0007c0009t0001g0014others(3): Show | 6 | HG02132.hp1 HG02293.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.5716+92T>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45196639 | ||||||
chr14:45197226
|
A | G | 1 | a0024c0017t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5716+679A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197226 | ||||||
chr14:45197294
|
G | T | 107 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(104): Show | 111 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.5716+747G>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197294 | ||||||
chr14:45197315
|
C | T | 6 | a0002c0007t0003g0146a0002c0007t0003g0147a0002c0007t0003g0148others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5716+768C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197315 | ||||||
chr14:45197335
|
A | G | 1 | a0011c0014t0001g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5716+788A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197335 | ||||||
chr14:45197396
|
C | T | 1 | a0011c0014t0001g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5716+849C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197396 | ||||||
chr14:45197418
|
C | T | 1 | a0002c0003t0002g0156 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5716+871C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197418 | ||||||
chr14:45197470
|
G | GT | 6 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.5716+935dupT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197470 | |||||
chr14:45197470
|
GT | G | 87 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(84): Show | 91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.5716+935delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197470 | |||||
chr14:45197767
|
CT | C | 92 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(89): Show | 96 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.5717-863delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197767 | |||||
chr14:45197767
|
CTT | C | 6 | a0002c0003t0001g0167a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 6 | HG01358.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.5717-864_5717-863d others(4): Show |
FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr14 | 45197767 | |||||
chr14:45197785
|
AT | A | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.5717-858delT | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197785 | ||||||
chr14:45197854
|
C | T | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5717-790C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197854 | ||||||
chr14:45197898
|
A | G | 6 | a0002c0008t0004g0143a0002c0008t0004g0150a0002c0008t0004g0151others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.5717-746A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45197898 | ||||||
chr14:45198029
|
AG | A | 38 | a0003c0002t0001g0002a0003c0002t0001g0174a0003c0002t0001g0175others(35): Show | 41 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.5717-614delG | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45198029 | ||||||
chr14:45198545
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0059 | 2 | NA18960.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.5717-99A>G | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 21/22 | chr14 | 45198545 | ||||||
chr14:45199024
|
G | A | 2 | a0011c0014t0001g0140a0011c0014t0001g0141 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6008+89G>A | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199024 | ||||||
chr14:45199140
|
G | C | 1 | a0002c0003t0002g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6008+205G>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199140 | ||||||
chr14:45199172
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6008+237C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199172 | ||||||
chr14:45199385
|
C | T | 8 | a0004c0005t0001g0154a0004c0005t0001g0157a0004c0005t0001g0158others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.6008+450C>T | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199385 | ||||||
chr14:45199455
|
A | C | 28 | a0002c0003t0002g0142a0002c0003t0002g0153a0002c0003t0002g0155others(25): Show | 29 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.6009-415A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199455 | ||||||
chr14:45199618
|
A | C | 2 | a0002c0006t0002g0216a0002c0006t0002g0218 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.6009-252A>C | FANCM | ENSG00000187790.12 | transcript | ENST00000267430.10 | protein_coding | 22/22 | chr14 | 45199618 |