geneid | 83593 |
---|---|
ensemblid | ENSG00000266094.8 |
hgncid | 17609 |
symbol | RASSF5 |
name | Ras association domain family member 5 |
refseq_nuc | NM_182663.4 |
refseq_prot | NP_872604.1 |
ensembl_nuc | ENST00000579436.7 |
ensembl_prot | ENSP00000462099.1 |
mane_status | MANE Select |
chr | chr1 |
start | 206507531 |
end | 206589448 |
strand | + |
ver | v1.2 |
region | chr1:206507531-206589448 |
region5000 | chr1:206502531-206594448 |
regionname0 | RASSF5_chr1_206507531_206589448 |
regionname5000 | RASSF5_chr1_206502531_206594448 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 418 | 328 | 87 | 63 | 134 | 10 | 32 | 98 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002 | 0/0 | 418 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0003 | 0/0 | 418 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0004 | 0/0 | 418 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0005 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0006 | 0/0 | 418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0007 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0008 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1257 | 253 | 58 | 48 | 111 | 6 | 29 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0002 | 0/0 | 1257 | 42 | 13 | 6 | 21 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0003 | 1/0 | 1257 | 13 | 1 | 6 | 0 | 2 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0004 | 0/0 | 1257 | 12 | 12 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0005 | 0/0 | 1257 | 7 | 7 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0006 | 0/0 | 1257 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0007 | 0/0 | 1257 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0008 | 0/0 | 1257 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0009 | 0/0 | 1257 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0010 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0011 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0012 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0013 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0014 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0015 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
c0016 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2543 | 92 | 13 | 27 | 37 | 1 | 12 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0002 | 0/0 | 2543 | 64 | 9 | 10 | 40 | 3 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0003 | 0/0 | 2543 | 64 | 15 | 11 | 26 | 2 | 10 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0004 | 0/0 | 2543 | 23 | 3 | 1 | 17 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0005 | 0/0 | 2543 | 20 | 4 | 9 | 2 | 2 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0006 | 0/0 | 2543 | 15 | 12 | 1 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0007 | 0/0 | 2543 | 10 | 10 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0008 | 0/0 | 2543 | 10 | 0 | 0 | 10 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0009 | 0/0 | 2543 | 9 | 9 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0010 | 0/0 | 2543 | 6 | 0 | 0 | 3 | 0 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0011 | 0/0 | 2543 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0012 | 0/0 | 2543 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0013 | 0/0 | 2543 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0014 | 0/0 | 2543 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0015 | 0/0 | 2543 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0016 | 0/0 | 2543 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0017 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0018 | 0/0 | 2543 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0019 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0020 | 0/0 | 2543 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0021 | 0/0 | 2543 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0022 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0023 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0024 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0025 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0026 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0027 | 0/0 | 2543 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0028 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0029 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0030 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
t0031 | 0/0 | 2543 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1257 | 253 | 58 | 48 | 111 | 6 | 29 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002 | 0/0 | 1257 | 42 | 13 | 6 | 21 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0003 | 1/0 | 1257 | 13 | 1 | 6 | 0 | 2 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004 | 0/0 | 1257 | 12 | 12 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0007 | 0/0 | 1257 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0008 | 0/0 | 1257 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0010 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0016 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0005 | 0/0 | 1257 | 7 | 7 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0013 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0003c0006 | 0/0 | 1257 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0004c0009 | 0/0 | 1257 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0005c0012 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0006c0014 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0007c0015 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0008c0011 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3799 | 76 | 10 | 23 | 32 | 1 | 9 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0002 | 0/0 | 3799 | 55 | 7 | 9 | 35 | 2 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0003 | 0/0 | 3799 | 57 | 10 | 10 | 25 | 2 | 10 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0004 | 0/0 | 3799 | 2 | 1 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0005 | 0/0 | 3799 | 7 | 3 | 1 | 1 | 1 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0006 | 0/0 | 3799 | 12 | 9 | 1 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0007 | 0/0 | 3799 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0008 | 0/0 | 3799 | 10 | 0 | 0 | 10 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0009 | 0/0 | 3799 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0010 | 0/0 | 3799 | 6 | 0 | 0 | 3 | 0 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0011 | 0/0 | 3799 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0012 | 0/0 | 3799 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0013 | 0/0 | 3799 | 3 | 2 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0014 | 0/0 | 3799 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0016 | 0/0 | 3799 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0017 | 0/0 | 3809 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0018 | 0/0 | 3799 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0019 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0021 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0025 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0029 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0001t0031 | 0/0 | 3799 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0001 | 0/0 | 3799 | 4 | 0 | 3 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0002 | 0/0 | 3799 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0003 | 0/0 | 3799 | 3 | 2 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0004 | 0/0 | 3799 | 20 | 1 | 1 | 16 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0006 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0009 | 0/0 | 3799 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0015 | 0/0 | 3799 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0020 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0022 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0026 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0002t0027 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0003t0001 | 1/0 | 3799 | 2 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0003t0002 | 0/0 | 3799 | 2 | 1 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0003t0005 | 0/0 | 3799 | 9 | 0 | 6 | 0 | 1 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0003 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0005 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0006 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0007 | 0/0 | 3799 | 6 | 6 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0013 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0024 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0004t0030 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0007t0002 | 0/0 | 3799 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0007t0011 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0007t0023 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0008t0005 | 0/0 | 3799 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0010t0003 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0001c0016t0002 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0005t0001 | 0/0 | 3799 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0005t0003 | 0/0 | 3799 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0005t0007 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0005t0028 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0002c0013t0004 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0003c0006t0001 | 0/0 | 3799 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0003c0006t0005 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0004c0009t0001 | 0/0 | 3799 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0005c0012t0002 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0006c0014t0001 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0007c0015t0001 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
a0008c0011t0006 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | copy fasta | chr1 | 206502531 | 206594448 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0014g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0016g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0016g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0018g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0019g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0021g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0025g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0029g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0031g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0015g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0015g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0020g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0022g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0026g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0027g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0007g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0024g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0030g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0023g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0008t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0008t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0010t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0016t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0028g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0013t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0004c0009t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0004c0009t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0005c0012t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0006c0014t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0007c0015t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0008c0011t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0225 | EUR | GBR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00099 | hp2 | a0001 | c0002 | t0004 | g0262 | EUR | GBR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00323 | hp1 | a0001 | c0003 | t0005 | g0240 | EUR | FIN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0284 | EUR | FIN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00438 | hp2 | a0007 | c0015 | t0001 | g0259 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00558 | hp2 | a0001 | c0001 | t0008 | g0168 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00609 | hp2 | a0001 | c0002 | t0027 | g0205 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00738 | hp1 | a0001 | c0003 | t0005 | g0235 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00741 | hp2 | a0001 | c0003 | t0005 | g0237 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01069 | hp2 | a0006 | c0014 | t0001 | g0080 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0183 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01081 | hp1 | a0001 | c0003 | t0005 | g0234 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01081 | hp2 | a0001 | c0001 | t0021 | g0058 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01099 | hp1 | a0001 | c0003 | t0005 | g0236 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0032 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01109 | hp2 | a0001 | c0001 | t0013 | g0049 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01168 | hp1 | a0001 | c0003 | t0005 | g0220 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01169 | hp2 | a0001 | c0003 | t0005 | g0181 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01243 | hp1 | a0001 | c0007 | t0002 | g0222 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0319 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01258 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01346 | hp1 | a0001 | c0002 | t0020 | g0119 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0211 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0232 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0212 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0296 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0197 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0295 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0233 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01884 | hp2 | a0001 | c0004 | t0007 | g0001 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0314 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01952 | hp2 | a0001 | c0008 | t0005 | g0107 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01978 | hp2 | a0001 | c0008 | t0005 | g0106 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02055 | hp1 | a0001 | c0002 | t0022 | g0315 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02056 | hp1 | a0003 | c0006 | t0001 | g0115 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02056 | hp2 | a0001 | c0002 | t0004 | g0068 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02074 | hp1 | a0001 | c0002 | t0004 | g0110 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02129 | hp1 | a0001 | c0001 | t0008 | g0144 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0170 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02132 | hp1 | a0001 | c0001 | t0010 | g0074 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0242 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0202 | EAS | CDX | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | CDX | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02258 | hp1 | a0001 | c0004 | t0007 | g0001 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02280 | hp1 | a0001 | c0004 | t0024 | g0020 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02451 | hp1 | a0002 | c0013 | t0004 | g0210 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02615 | hp2 | a0002 | c0005 | t0028 | g0209 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02622 | hp1 | a0001 | c0002 | t0009 | g0159 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02622 | hp2 | a0002 | c0005 | t0007 | g0190 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0161 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0071 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0289 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0309 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02717 | hp2 | a0001 | c0004 | t0013 | g0104 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0033 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02735 | hp2 | a0001 | c0003 | t0005 | g0231 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02809 | hp1 | a0001 | c0002 | t0009 | g0186 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02818 | hp1 | a0001 | c0004 | t0007 | g0105 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02895 | hp1 | a0002 | c0005 | t0001 | g0184 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02895 | hp2 | a0001 | c0002 | t0009 | g0007 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02897 | hp2 | a0002 | c0005 | t0001 | g0185 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02922 | hp1 | a0001 | c0001 | t0029 | g0247 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02922 | hp2 | a0002 | c0005 | t0001 | g0189 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02965 | hp1 | a0001 | c0002 | t0015 | g0321 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02965 | hp2 | a0001 | c0004 | t0030 | g0043 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02970 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0316 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02976 | hp1 | a0001 | c0002 | t0026 | g0040 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0160 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03041 | hp1 | a0008 | c0011 | t0006 | g0313 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03041 | hp2 | a0001 | c0007 | t0002 | g0223 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0322 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03098 | hp2 | a0002 | c0005 | t0003 | g0187 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0117 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03209 | hp2 | a0001 | c0004 | t0003 | g0102 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03239 | hp2 | a0001 | c0001 | t0031 | g0229 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03453 | hp1 | a0001 | c0004 | t0006 | g0019 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0162 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03486 | hp1 | a0001 | c0007 | t0023 | g0224 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03486 | hp2 | a0001 | c0002 | t0009 | g0007 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03490 | hp1 | a0004 | c0009 | t0001 | g0294 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03492 | hp2 | a0004 | c0009 | t0001 | g0042 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03516 | hp2 | a0001 | c0004 | t0005 | g0018 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03654 | hp1 | a0001 | c0001 | t0010 | g0324 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0306 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03669 | hp1 | a0001 | c0001 | t0018 | g0288 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0238 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0213 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0219 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03710 | hp1 | a0001 | c0003 | t0005 | g0057 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0312 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0178 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0002 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18906 | hp2 | a0002 | c0005 | t0003 | g0188 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18948 | hp1 | a0001 | c0001 | t0016 | g0304 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18952 | hp2 | a0001 | c0001 | t0019 | g0089 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18954 | hp1 | a0001 | c0002 | t0004 | g0101 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0264 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18966 | hp2 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18971 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18978 | hp1 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18979 | hp2 | a0001 | c0001 | t0016 | g0303 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18981 | hp2 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0154 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18984 | hp1 | a0001 | c0001 | t0008 | g0142 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18985 | hp2 | a0001 | c0016 | t0002 | g0133 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18986 | hp1 | a0001 | c0010 | t0003 | g0268 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18986 | hp2 | a0003 | c0006 | t0001 | g0113 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18990 | hp1 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18993 | hp1 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18998 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18999 | hp2 | a0001 | c0002 | t0004 | g0218 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19000 | hp2 | a0001 | c0002 | t0004 | g0176 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19004 | hp1 | a0003 | c0006 | t0001 | g0123 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19007 | hp1 | a0003 | c0006 | t0005 | g0114 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19007 | hp2 | a0001 | c0002 | t0004 | g0175 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0138 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19011 | hp2 | a0001 | c0002 | t0004 | g0173 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0199 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19030 | hp1 | a0001 | c0004 | t0007 | g0001 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0050 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0327 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19067 | hp2 | a0001 | c0001 | t0008 | g0151 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19084 | hp2 | a0001 | c0002 | t0004 | g0171 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19086 | hp1 | a0001 | c0002 | t0004 | g0169 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19086 | hp2 | a0001 | c0001 | t0017 | g0044 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19091 | hp1 | a0005 | c0012 | t0002 | g0191 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0182 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20129 | hp1 | a0001 | c0002 | t0015 | g0244 | AFR | ASW | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20129 | hp2 | a0001 | c0004 | t0007 | g0103 | AFR | ASW | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0200 | SAS | GIH | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | GIH | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0002 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02559 | hp2 | a0001 | c0002 | t0009 | g0243 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03471 | hp2 | a0001 | c0007 | t0011 | g0221 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG06807 | hp1 | a0001 | c0004 | t0007 | g0001 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0217 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0086 | REF | REF | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0241 | REF | REF | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206507760
|
C | A | 1 | a0008 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.158C>A | p.Ala53Glu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 230/3799 | 158/1257 | 53/418 | chr1 | 206507760 | ||
chr1:206507789
|
C | T | 1 | a0007 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.187C>T | p.Arg63Trp | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 259/3799 | 187/1257 | 63/418 | chr1 | 206507789 | ||
chr1:206507816
|
C | T | 1 | a0006 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.214C>T | p.Pro72Ser | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 286/3799 | 214/1257 | 72/418 | chr1 | 206507816 | ||
chr1:206508050
|
C | T | 1 | a0002 | 8 | HG02451.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.448C>T | p.Arg150Cys | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 520/3799 | 448/1257 | 150/418 | chr1 | 206508050 | ||
chr1:206538279
|
G | A | 1 | a0003 | 4 | HG02056.hp1 NA18986.hp2 NA19004.hp1 others(1): Show |
missense_variant | MODERATE | c.565G>A | p.Val189Met | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/6 | 637/3799 | 565/1257 | 189/418 | chr1 | 206538279 | ||
chr1:206584439
|
G | A | 1 | a0005 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.743G>A | p.Arg248Gln | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/6 | 815/3799 | 743/1257 | 248/418 | chr1 | 206584439 | ||
chr1:206584663
|
C | T | 1 | a0004 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.967C>T | p.Arg323Trp | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/6 | 1039/3799 | 967/1257 | 323/418 | chr1 | 206584663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206507650
|
A | C | 15 | a0001c0001a0001c0002a0001c0004others(12): Show | 333 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(330): Show |
synonymous_variant | LOW | c.48A>C | p.Leu16Leu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 120/3799 | 48/1257 | 16/418 | chr1 | 206507650 | ||
chr1:206507651
|
T | C | 1 | a0001c0010 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.49T>C | p.Leu17Leu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 121/3799 | 49/1257 | 17/418 | chr1 | 206507651 | ||
chr1:206507689
|
C | T | 1 | a0001c0016 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.87C>T | p.Ser29Ser | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 159/3799 | 87/1257 | 29/418 | chr1 | 206507689 | ||
chr1:206507990
|
C | T | 1 | a0001c0004 | 12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.388C>T | p.Leu130Leu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 460/3799 | 388/1257 | 130/418 | chr1 | 206507990 | ||
chr1:206538179
|
A | G | 1 | a0001c0007 | 4 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.465A>G | p.Lys155Lys | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/6 | 537/3799 | 465/1257 | 155/418 | chr1 | 206538179 | ||
chr1:206538281
|
G | A | 1 | a0001c0008 | 2 | HG01952.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.567G>A | p.Val189Val | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/6 | 639/3799 | 567/1257 | 189/418 | chr1 | 206538281 | ||
chr1:206584525
|
C | A | 2 | a0001c0002a0002c0013 | 43 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(40): Show |
synonymous_variant | LOW | c.829C>A | p.Arg277Arg | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/6 | 901/3799 | 829/1257 | 277/418 | chr1 | 206584525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206587021
|
G | GTATTATT others(3): Show |
1 | a0001c0001t0017 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51_*60dupAATTATTA others(2): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 61 | INFO_REALIGN_3_PRIME | chr1 | 206587021 | ||||
chr1:206587142
|
C | T | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0029others(6): Show | 77 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*164C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 164 | chr1 | 206587142 | |||||
chr1:206587144
|
A | G | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(42): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*166A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 166 | chr1 | 206587144 | |||||
chr1:206587162
|
C | T | 1 | a0001c0001t0031 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 184 | chr1 | 206587162 | |||||
chr1:206587304
|
C | G | 1 | a0001c0001t0021 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 326 | chr1 | 206587304 | |||||
chr1:206587354
|
A | T | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(18): Show | 159 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 376 | chr1 | 206587354 | |||||
chr1:206587362
|
C | T | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(33): Show | 206 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*384C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 384 | chr1 | 206587362 | |||||
chr1:206587416
|
T | C | 2 | a0001c0001t0011a0001c0007t0011 | 4 | HG03139.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*438T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 438 | chr1 | 206587416 | |||||
chr1:206587489
|
C | G | 1 | a0001c0002t0027 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 511 | chr1 | 206587489 | |||||
chr1:206587719
|
G | A | 2 | a0001c0002t0015a0001c0002t0022 | 3 | HG02055.hp1 HG02965.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*741G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 741 | chr1 | 206587719 | |||||
chr1:206588034
|
C | T | 1 | a0001c0002t0020 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1056 | chr1 | 206588034 | |||||
chr1:206588099
|
G | A | 4 | a0001c0001t0007a0001c0001t0012a0001c0004t0007others(1): Show | 14 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1121G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1121 | chr1 | 206588099 | |||||
chr1:206588120
|
G | A | 1 | a0001c0007t0023 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1142 | chr1 | 206588120 | |||||
chr1:206588460
|
G | C | 1 | a0002c0005t0028 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1482G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1482 | chr1 | 206588460 | |||||
chr1:206588592
|
A | G | 1 | a0001c0001t0016 | 2 | NA18948.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1614A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1614 | chr1 | 206588592 | |||||
chr1:206588606
|
T | C | 16 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(13): Show | 89 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1628T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1628 | chr1 | 206588606 | |||||
chr1:206588623
|
A | G | 1 | a0001c0001t0012 | 4 | HG02647.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1645A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1645 | chr1 | 206588623 | |||||
chr1:206588709
|
C | T | 1 | a0001c0001t0019 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1731C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1731 | chr1 | 206588709 | |||||
chr1:206588829
|
A | C | 2 | a0001c0001t0025a0001c0004t0024 | 2 | HG02280.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1851A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1851 | chr1 | 206588829 | |||||
chr1:206588863
|
T | G | 1 | a0001c0002t0022 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1885T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1885 | chr1 | 206588863 | |||||
chr1:206588948
|
A | T | 2 | a0001c0004t0024a0001c0004t0030 | 2 | HG02280.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1970A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1970 | chr1 | 206588948 | |||||
chr1:206588993
|
A | G | 1 | a0001c0001t0018 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2015 | chr1 | 206588993 | |||||
chr1:206589123
|
C | T | 5 | a0001c0001t0006a0001c0002t0006a0001c0004t0006others(2): Show | 16 | HG01257.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2145C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2145 | chr1 | 206589123 | |||||
chr1:206589328
|
C | T | 1 | a0001c0001t0008 | 10 | HG00558.hp2 HG02129.hp1 NA18971.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2350C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2350 | chr1 | 206589328 | |||||
chr1:206589343
|
G | A | 4 | a0001c0001t0010a0001c0001t0013a0001c0001t0025others(1): Show | 11 | HG01109.hp2 HG02109.hp1 HG02132.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2365G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2365 | chr1 | 206589343 | |||||
chr1:206589352
|
C | T | 8 | a0001c0001t0004a0001c0001t0029a0001c0002t0004others(5): Show | 29 | HG00099.hp2 HG00323.hp2 HG01070.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2374C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2374 | chr1 | 206589352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206508171
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.457+112G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508171 | ||||||
chr1:206508322
|
C | CCA | 68 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0052others(65): Show | 73 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.457+295_457+296dup others(2): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | |||||
chr1:206508322
|
C | CCACA | 21 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0036others(18): Show | 21 | HG01109.hp1 HG02055.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.457+293_457+296dup others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | |||||
chr1:206508322
|
C | CCACACAC others(3): Show |
2 | a0001c0001t0002g0021a0001c0001t0003g0022 | 2 | HG03139.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.457+287_457+296dup others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | |||||
chr1:206508322
|
C | CCACACAC others(5): Show |
3 | a0001c0004t0005g0018a0001c0004t0006g0019a0001c0004t0024g0020 | 3 | HG02280.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+285_457+296dup others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | |||||
chr1:206508322
|
CCA | C | 14 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0317others(11): Show | 15 | HG00597.hp1 HG00621.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+295_457+296del others(2): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | |||||
chr1:206508322
|
CCACA | C | 7 | a0001c0001t0001g0326a0001c0001t0002g0325a0001c0001t0002g0329others(4): Show | 7 | HG01361.hp2 HG02818.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.457+293_457+296del others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | |||||
chr1:206508383
|
G | T | 1 | a0001c0001t0006g0309 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.457+324G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508383 | ||||||
chr1:206508423
|
C | T | 2 | a0001c0001t0001g0014a0001c0008t0005g0106 | 3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.457+364C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508423 | ||||||
chr1:206508697
|
C | G | 10 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(7): Show | 13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.457+638C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508697 | ||||||
chr1:206508705
|
A | G | 69 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0100others(66): Show | 73 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.457+646A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508705 | ||||||
chr1:206508857
|
G | A | 3 | a0001c0001t0002g0096a0001c0001t0003g0095a0001c0001t0003g0253 | 3 | HG02135.hp2 NA18952.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.457+798G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508857 | ||||||
chr1:206509015
|
T | G | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+956T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509015 | ||||||
chr1:206509625
|
T | C | 84 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0121others(81): Show | 88 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.457+1566T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509625 | ||||||
chr1:206509639
|
A | T | 1 | a0001c0001t0002g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.457+1580A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509639 | ||||||
chr1:206509726
|
CT | C | 155 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+1679delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206509726 | |||||
chr1:206509758
|
G | A | 12 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(9): Show | 15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1699G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509758 | ||||||
chr1:206509762
|
G | T | 115 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(112): Show | 119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.457+1703G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509762 | ||||||
chr1:206509788
|
G | C | 1 | a0001c0004t0030g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.457+1729G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509788 | ||||||
chr1:206509836
|
C | T | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+1777C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509836 | ||||||
chr1:206509893
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.457+1834G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509893 | ||||||
chr1:206510060
|
A | C | 1 | a0001c0001t0003g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.457+2001A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510060 | ||||||
chr1:206510251
|
G | T | 12 | a0001c0001t0002g0248a0001c0001t0003g0245a0001c0001t0003g0246others(9): Show | 12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+2192G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510251 | ||||||
chr1:206510358
|
CTCTG | C | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+2301_457+2304d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206510358 | |||||
chr1:206510390
|
A | G | 159 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(156): Show | 168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.457+2331A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510390 | ||||||
chr1:206510434
|
A | C | 1 | a0001c0004t0007g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.457+2375A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510434 | ||||||
chr1:206510560
|
C | T | 1 | a0001c0002t0001g0307 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.457+2501C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510560 | ||||||
chr1:206510644
|
A | G | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+2585A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510644 | ||||||
chr1:206510768
|
T | C | 4 | a0001c0001t0001g0111a0001c0001t0003g0108a0001c0001t0003g0109others(1): Show | 4 | HG02071.hp1 HG02074.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+2709T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510768 | ||||||
chr1:206510785
|
C | A | 1 | a0001c0001t0005g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.457+2726C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510785 | ||||||
chr1:206511364
|
C | T | 1 | a0001c0001t0003g0306 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.457+3305C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511364 | ||||||
chr1:206511464
|
C | G | 1 | a0001c0004t0030g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.457+3405C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511464 | ||||||
chr1:206511644
|
A | C | 167 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(164): Show | 176 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.457+3585A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511644 | ||||||
chr1:206511645
|
A | T | 167 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(164): Show | 176 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.457+3586A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511645 | ||||||
chr1:206511687
|
C | G | 1 | a0001c0001t0002g0305 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.457+3628C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511687 | ||||||
chr1:206511689
|
A | G | 10 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(7): Show | 13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.457+3630A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511689 | ||||||
chr1:206511794
|
C | T | 2 | a0001c0001t0016g0303a0001c0001t0016g0304 | 2 | NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.457+3735C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511794 | ||||||
chr1:206511815
|
C | CCACTTTC others(2): Show |
2 | a0001c0001t0003g0008a0001c0001t0004g0177 | 3 | NA18939.hp2 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.457+3769_457+3777d others(11): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206511815 | |||||
chr1:206511818
|
C | T | 1 | a0001c0001t0010g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.457+3759C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511818 | ||||||
chr1:206511852
|
C | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+3793C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511852 | ||||||
chr1:206512069
|
G | A | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+4010G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512069 | ||||||
chr1:206512091
|
G | A | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+4032G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512091 | ||||||
chr1:206512294
|
T | C | 328 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(325): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(341): Show |
intron_variant | MODIFIER | c.457+4235T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512294 | ||||||
chr1:206512299
|
C | T | 1 | a0001c0001t0010g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.457+4240C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512299 | ||||||
chr1:206512309
|
C | A | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+4250C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512309 | ||||||
chr1:206512371
|
G | A | 2 | a0001c0003t0005g0181a0001c0003t0005g0220 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.457+4312G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512371 | ||||||
chr1:206512396
|
C | T | 115 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(112): Show | 119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.457+4337C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512396 | ||||||
chr1:206512564
|
C | T | 13 | a0001c0001t0001g0174a0001c0001t0001g0311a0001c0001t0003g0008others(10): Show | 14 | HG00558.hp2 HG00621.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+4505C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512564 | ||||||
chr1:206512819
|
C | A | 3 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0004t0024g0020 | 3 | HG02280.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.457+4760C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512819 | ||||||
chr1:206512978
|
G | A | 4 | a0001c0001t0002g0112a0003c0006t0001g0113a0003c0006t0001g0115others(1): Show | 4 | HG00438.hp1 HG02056.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+4919G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512978 | ||||||
chr1:206513027
|
G | A | 7 | a0001c0001t0001g0121a0001c0001t0002g0118a0001c0001t0006g0122others(4): Show | 7 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+4968G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513027 | ||||||
chr1:206513211
|
C | A | 1 | a0001c0002t0009g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.457+5152C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513211 | ||||||
chr1:206513789
|
G | C | 3 | a0001c0001t0002g0118a0001c0001t0011g0116a0001c0001t0011g0117 | 3 | HG02109.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.457+5730G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513789 | ||||||
chr1:206513910
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.457+5851C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513910 | ||||||
chr1:206513930
|
C | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0052others(40): Show | 45 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.457+5871C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513930 | ||||||
chr1:206514232
|
C | T | 1 | a0001c0004t0006g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.457+6173C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514232 | ||||||
chr1:206514547
|
G | A | 4 | a0001c0001t0005g0039a0001c0001t0007g0251a0001c0001t0007g0252others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+6488G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514547 | ||||||
chr1:206514553
|
T | C | 22 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0002g0308others(19): Show | 27 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.457+6494T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514553 | ||||||
chr1:206514603
|
T | C | 316 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(313): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.457+6544T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514603 | ||||||
chr1:206514720
|
A | T | 1 | a0001c0001t0002g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.457+6661A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514720 | ||||||
chr1:206515032
|
G | A | 12 | a0001c0001t0002g0248a0001c0001t0003g0245a0001c0001t0003g0246others(9): Show | 12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+6973G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515032 | ||||||
chr1:206515083
|
G | T | 1 | a0001c0001t0003g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.457+7024G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515083 | ||||||
chr1:206515235
|
C | T | 4 | a0001c0001t0005g0039a0001c0001t0007g0251a0001c0001t0007g0252others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+7176C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515235 | ||||||
chr1:206515253
|
G | C | 1 | a0001c0002t0002g0323 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.457+7194G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515253 | ||||||
chr1:206515418
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.457+7359G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515418 | ||||||
chr1:206515626
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0003g0090a0001c0001t0003g0091others(1): Show | 4 | HG01993.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+7567C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515626 | ||||||
chr1:206515895
|
C | A | 1 | a0001c0002t0002g0323 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.457+7836C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515895 | ||||||
chr1:206516441
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.457+8382A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516441 | ||||||
chr1:206516462
|
C | CT | 6 | a0001c0001t0001g0014a0001c0001t0002g0118a0001c0001t0005g0045others(3): Show | 7 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+8415dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206516462 | |||||
chr1:206516658
|
C | T | 22 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0002g0308others(19): Show | 27 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.457+8599C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516658 | ||||||
chr1:206516810
|
C | T | 2 | a0001c0001t0001g0014a0001c0008t0005g0106 | 3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.457+8751C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516810 | ||||||
chr1:206516811
|
G | A | 1 | a0001c0002t0004g0183 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.457+8752G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516811 | ||||||
chr1:206516953
|
C | T | 149 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(146): Show | 158 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.457+8894C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516953 | ||||||
chr1:206516994
|
G | A | 2 | a0002c0005t0001g0184a0002c0005t0001g0185 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.457+8935G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516994 | ||||||
chr1:206517293
|
G | A | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.457+9234G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517293 | ||||||
chr1:206517405
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+9346G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517405 | ||||||
chr1:206517413
|
A | C | 12 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(9): Show | 15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+9354A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517413 | ||||||
chr1:206517436
|
C | T | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+9377C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517436 | ||||||
chr1:206517450
|
T | C | 155 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(152): Show | 164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+9391T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517450 | ||||||
chr1:206517524
|
G | A | 12 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(9): Show | 15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+9465G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517524 | ||||||
chr1:206517532
|
T | A | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+9473T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517532 | ||||||
chr1:206517881
|
C | A | 1 | a0001c0001t0021g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.457+9822C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517881 | ||||||
chr1:206517910
|
A | C | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+9851A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517910 | ||||||
chr1:206518019
|
G | A | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+9960G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518019 | ||||||
chr1:206518172
|
C | G | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+10113C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518172 | ||||||
chr1:206518454
|
C | T | 1 | a0001c0002t0015g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.457+10395C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518454 | ||||||
chr1:206518744
|
G | T | 115 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(112): Show | 119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.457+10685G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518744 | ||||||
chr1:206518834
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.457+10775G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518834 | ||||||
chr1:206518950
|
T | G | 1 | a0001c0002t0015g0244 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.457+10891T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518950 | ||||||
chr1:206519135
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0019g0089 | 2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.457+11076C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519135 | ||||||
chr1:206519169
|
G | A | 12 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(9): Show | 15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+11110G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519169 | ||||||
chr1:206519201
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0004g0177 | 3 | NA18939.hp2 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.457+11142T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519201 | ||||||
chr1:206519258
|
T | C | 4 | a0001c0001t0005g0039a0001c0001t0007g0251a0001c0001t0007g0252others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+11199T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519258 | ||||||
chr1:206519300
|
T | G | 178 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(175): Show | 187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.457+11241T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519300 | ||||||
chr1:206519440
|
C | T | 3 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130 | 3 | NA18984.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.457+11381C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519440 | ||||||
chr1:206519493
|
G | C | 1 | a0001c0002t0009g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+11434G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519493 | ||||||
chr1:206519568
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.457+11509C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519568 | ||||||
chr1:206519826
|
C | G | 175 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(172): Show | 184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.457+11767C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519826 | ||||||
chr1:206520333
|
G | C | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+12274G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520333 | ||||||
chr1:206520337
|
T | C | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+12278T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520337 | ||||||
chr1:206520410
|
A | C | 197 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(194): Show | 207 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.457+12351A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520410 | ||||||
chr1:206520435
|
C | T | 5 | a0001c0001t0001g0302a0001c0001t0002g0325a0001c0001t0003g0312others(2): Show | 5 | HG01361.hp2 HG01993.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+12376C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520435 | ||||||
chr1:206520452
|
G | T | 1 | a0001c0002t0004g0218 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.457+12393G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520452 | ||||||
chr1:206520481
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.457+12422C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520481 | ||||||
chr1:206520531
|
C | G | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.457+12472C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520531 | ||||||
chr1:206520545
|
T | C | 178 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(175): Show | 187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.457+12486T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520545 | ||||||
chr1:206520563
|
C | T | 1 | a0001c0001t0003g0005 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.457+12504C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520563 | ||||||
chr1:206520564
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.457+12505G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520564 | ||||||
chr1:206520594
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(322): Show | 341 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(338): Show |
intron_variant | MODIFIER | c.457+12535A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520594 | ||||||
chr1:206520606
|
C | CA | 150 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(147): Show | 155 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.457+12563dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206520606 | |||||
chr1:206520606
|
C | CAAAA | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+12560_457+1256 others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206520606 | |||||
chr1:206520642
|
G | A | 116 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(113): Show | 120 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.457+12583G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520642 | ||||||
chr1:206520838
|
A | C | 159 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(156): Show | 164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+12779A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520838 | ||||||
chr1:206521056
|
T | A | 1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.457+12997T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521056 | ||||||
chr1:206521178
|
G | A | 8 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.457+13119G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521178 | ||||||
chr1:206521337
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182others(1): Show | 4 | HG02145.hp2 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+13278G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521337 | ||||||
chr1:206521346
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.457+13287T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521346 | ||||||
chr1:206521366
|
A | T | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+13307A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521366 | ||||||
chr1:206521567
|
T | C | 3 | a0001c0001t0002g0118a0001c0001t0011g0116a0001c0001t0011g0117 | 3 | HG02109.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.457+13508T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521567 | ||||||
chr1:206521576
|
A | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | NA18953.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.457+13517A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521576 | ||||||
chr1:206521847
|
G | T | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.457+13788G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521847 | ||||||
chr1:206521902
|
G | A | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0016t0002g0133 | 3 | NA18960.hp2 NA18982.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.457+13843G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521902 | ||||||
chr1:206521927
|
G | A | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+13868G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521927 | ||||||
chr1:206522184
|
T | A | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+14125T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522184 | ||||||
chr1:206522251
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14192G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522251 | ||||||
chr1:206522254
|
CAAATGAA others(60): Show |
C | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14196_457+1426 others(71): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522254 | ||||||
chr1:206522325
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14266T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522325 | ||||||
chr1:206522331
|
C | G | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14272C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522331 | ||||||
chr1:206522333
|
C | A | 51 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0143others(48): Show | 54 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.457+14274C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522333 | ||||||
chr1:206522333
|
C | G | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14274C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522333 | ||||||
chr1:206522337
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14278G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522337 | ||||||
chr1:206522398
|
G | A | 21 | a0001c0001t0001g0014a0001c0001t0002g0308a0001c0001t0003g0022others(18): Show | 25 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.457+14339G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522398 | ||||||
chr1:206522433
|
A | C | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.457+14374A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522433 | ||||||
chr1:206522482
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+14423G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522482 | ||||||
chr1:206522608
|
A | T | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.457+14549A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522608 | ||||||
chr1:206522614
|
G | A | 2 | a0001c0001t0001g0254a0001c0002t0004g0255 | 2 | HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.457+14555G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522614 | ||||||
chr1:206522800
|
T | A | 1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.457+14741T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522800 | ||||||
chr1:206522857
|
AAAAATGA others(10): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14803_457+1481 others(21): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206522857 | |||||
chr1:206522879
|
A | C | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14820A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522879 | ||||||
chr1:206522881
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14822T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522881 | ||||||
chr1:206522886
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14827A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522886 | ||||||
chr1:206522889
|
G | C | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14830G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522889 | ||||||
chr1:206522891
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14832T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522891 | ||||||
chr1:206522892
|
T | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14833T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522892 | ||||||
chr1:206522894
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14835A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522894 | ||||||
chr1:206522896
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14837C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522896 | ||||||
chr1:206522897
|
T | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14838T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522897 | ||||||
chr1:206522898
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14839A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522898 | ||||||
chr1:206522903
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14844A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522903 | ||||||
chr1:206522904
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14845A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522904 | ||||||
chr1:206522906
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14847A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522906 | ||||||
chr1:206522910
|
C | T | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+14851C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522910 | ||||||
chr1:206523102
|
C | G | 2 | a0004c0009t0001g0042a0004c0009t0001g0294 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.457+15043C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523102 | ||||||
chr1:206523405
|
AATATTAT | A | 119 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(116): Show | 123 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.458-14749_458-1474 others(11): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523405 | |||||
chr1:206523423
|
T | A | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-14749T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523423 | ||||||
chr1:206523430
|
A | T | 4 | a0001c0001t0003g0327a0001c0001t0003g0328a0001c0001t0006g0015others(1): Show | 5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-14742A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523430 | ||||||
chr1:206523441
|
A | G | 2 | a0001c0003t0005g0181a0001c0003t0005g0220 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.458-14731A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523441 | ||||||
chr1:206523461
|
A | AATATATT others(28): Show |
1 | a0001c0001t0001g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.458-14696_458-1466 others(39): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523461 | |||||
chr1:206523480
|
ATATAATA others(9): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-14691_458-1467 others(20): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523480 | ||||||
chr1:206523481
|
TATA | T | 8 | a0001c0001t0001g0009a0001c0001t0002g0226a0001c0001t0002g0227others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-14687_458-1468 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523481 | |||||
chr1:206523482
|
ATAATATT others(13): Show |
A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14688_458-1466 others(24): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523482 | |||||
chr1:206523484
|
AATATTAT others(16): Show |
A | 231 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(228): Show | 240 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.458-14653_458-1463 others(27): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523484 | |||||
chr1:206523485
|
ATATTATA others(19): Show |
A | 8 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-14683_458-1465 others(30): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523485 | |||||
chr1:206523505
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14667T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523505 | ||||||
chr1:206523513
|
ATATATTA others(14): Show |
A | 1 | a0001c0016t0002g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14653_458-1463 others(25): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523513 | |||||
chr1:206523527
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14645T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523527 | ||||||
chr1:206523543
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14629T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523543 | ||||||
chr1:206523600
|
T | G | 1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-14572T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523600 | ||||||
chr1:206523612
|
A | ATATATAA others(31): Show |
23 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0121others(20): Show | 24 | HG00597.hp2 HG00609.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.458-14527_458-1449 others(42): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523612 | |||||
chr1:206523612
|
ATATATAA others(31): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.458-14527_458-1449 others(42): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523612 | |||||
chr1:206523634
|
A | ATTATATA others(30): Show |
1 | a0001c0001t0010g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.458-14537_458-1450 others(41): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523634 | |||||
chr1:206523635
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14537T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523635 | ||||||
chr1:206523649
|
T | TTTATATA others(30): Show |
5 | a0001c0001t0002g0112a0003c0006t0001g0113a0003c0006t0001g0115others(2): Show | 5 | HG00438.hp1 HG02056.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-14490_458-1448 others(41): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523649 | |||||
chr1:206523657
|
A | AAATATAT others(31): Show |
5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-14490_458-1448 others(42): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523657 | |||||
chr1:206523657
|
A | AAATATAT others(121): Show |
4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14490_458-1448 others(132): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523657 | |||||
chr1:206523657
|
A | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0086 | 2 | HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.458-14515A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523657 | ||||||
chr1:206523680
|
TA | T | 4 | a0001c0001t0001g0055a0001c0001t0004g0250a0001c0001t0009g0054others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14489delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523680 | |||||
chr1:206523705
|
A | C | 1 | a0001c0001t0003g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.458-14467A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523705 | ||||||
chr1:206523723
|
T | TTA | 231 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(228): Show | 240 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.458-14443_458-1444 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523723 | |||||
chr1:206523729
|
A | ATTATATA others(8): Show |
18 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0059others(15): Show | 19 | HG00423.hp2 HG00558.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.458-14440_458-1442 others(19): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523729 | |||||
chr1:206523735
|
T | C | 26 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0002g0308others(23): Show | 31 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.458-14437T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523735 | ||||||
chr1:206523806
|
CAATATAT others(16): Show |
C | 1 | a0001c0003t0005g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.458-14349_458-1432 others(27): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523806 | |||||
chr1:206523821
|
A | ATTATATA others(32): Show |
9 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0166others(6): Show | 9 | HG02074.hp2 HG02083.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-14342_458-1430 others(43): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523821 | |||||
chr1:206523839
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-14333T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523839 | ||||||
chr1:206523849
|
A | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.458-14323A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523849 | ||||||
chr1:206523878
|
T | A | 1 | a0001c0001t0003g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.458-14294T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523878 | ||||||
chr1:206523893
|
T | C | 1 | a0001c0002t0020g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.458-14279T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523893 | ||||||
chr1:206523900
|
T | TATATATT others(27): Show |
2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-14217_458-1418 others(38): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523900 | |||||
chr1:206523918
|
T | G | 1 | a0001c0001t0001g0326 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.458-14254T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523918 | ||||||
chr1:206523925
|
A | G | 1 | a0001c0001t0010g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.458-14247A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523925 | ||||||
chr1:206523949
|
TAA | T | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-14222_458-1422 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523949 | ||||||
chr1:206523951
|
A | T | 1 | a0001c0016t0002g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14221A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523951 | ||||||
chr1:206523952
|
T | A | 1 | a0001c0016t0002g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14220T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523952 | ||||||
chr1:206523953
|
A | T | 1 | a0001c0016t0002g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14219A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523953 | ||||||
chr1:206523955
|
A | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14217A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523955 | ||||||
chr1:206523960
|
C | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14212C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523960 | ||||||
chr1:206523969
|
A | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14203A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523969 | ||||||
chr1:206523972
|
T | C | 5 | a0002c0005t0001g0184a0002c0005t0001g0185a0002c0005t0001g0189others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-14200T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523972 | ||||||
chr1:206523985
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-14187A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523985 | ||||||
chr1:206523988
|
T | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14184T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523988 | ||||||
chr1:206523988
|
T | TATATACC others(61): Show |
2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14184_458-1418 others(72): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523988 | ||||||
chr1:206523988
|
T | TGTATACC others(27): Show |
1 | a0001c0001t0003g0108 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.458-14179_458-1417 others(38): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523988 | |||||
chr1:206523993
|
AT | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14178delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523993 | ||||||
chr1:206523994
|
T | C | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14178T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523994 | ||||||
chr1:206524003
|
G | A | 6 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-14169G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524003 | ||||||
chr1:206524016
|
A | C | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14156A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524016 | ||||||
chr1:206524028
|
C | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14144C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524028 | ||||||
chr1:206524050
|
A | C | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14122A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524050 | ||||||
chr1:206524056
|
G | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14116G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524056 | ||||||
chr1:206524062
|
A | C | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14110A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524062 | ||||||
chr1:206524065
|
TATATA | T | 71 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0100others(68): Show | 75 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.458-14101_458-1409 others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524065 | |||||
chr1:206524085
|
TAA | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14086_458-1408 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524085 | ||||||
chr1:206524091
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14081G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524091 | ||||||
chr1:206524092
|
T | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14080T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524092 | ||||||
chr1:206524099
|
TATATA | T | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-14067_458-1406 others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524099 | |||||
chr1:206524102
|
A | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14070A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524102 | ||||||
chr1:206524110
|
T | C | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14062T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524110 | ||||||
chr1:206524112
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14060T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524112 | ||||||
chr1:206524119
|
T | TAA | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14053_458-1405 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524119 | ||||||
chr1:206524140
|
T | A | 1 | a0002c0005t0007g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.458-14032T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524140 | ||||||
chr1:206524208
|
T | C | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13964T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524208 | ||||||
chr1:206524210
|
C | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13962C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524210 | ||||||
chr1:206524221
|
A | ATATAGAT others(27): Show |
9 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(6): Show | 10 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-13889_458-1385 others(38): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524221 | |||||
chr1:206524221
|
A | ATATAGAT others(61): Show |
7 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(4): Show | 10 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-13931_458-1393 others(72): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524221 | |||||
chr1:206524221
|
A | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13951A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524221 | ||||||
chr1:206524242
|
C | T | 1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-13930C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524242 | ||||||
chr1:206524244
|
T | C | 1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-13928T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524244 | ||||||
chr1:206524246
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13926T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524246 | ||||||
chr1:206524250
|
A | ATATAATA others(59): Show |
1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-13918_458-1391 others(70): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524250 | |||||
chr1:206524260
|
G | T | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13912G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524260 | ||||||
chr1:206524283
|
T | C | 2 | a0001c0001t0002g0051a0005c0012t0002g0191 | 2 | NA18951.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.458-13889T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524283 | ||||||
chr1:206524317
|
C | T | 3 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0003g0216 | 3 | NA18979.hp1 NA18985.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.458-13855C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524317 | ||||||
chr1:206524404
|
A | G | 1 | a0001c0001t0008g0157 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.458-13768A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524404 | ||||||
chr1:206524443
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13729A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524443 | ||||||
chr1:206524456
|
A | ATT | 7 | a0001c0001t0002g0158a0001c0001t0005g0165a0001c0001t0012g0160others(4): Show | 8 | HG02622.hp1 HG02647.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-13715_458-1371 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524456 | |||||
chr1:206524457
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13715T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524457 | ||||||
chr1:206524466
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13706T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524466 | ||||||
chr1:206524551
|
C | CATAAATA others(52): Show |
1 | a0001c0001t0002g0134 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13618_458-1361 others(63): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524551 | |||||
chr1:206524558
|
A | AATATATT others(18): Show |
1 | a0001c0001t0001g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.458-13604_458-1358 others(29): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(52): Show |
5 | a0001c0001t0001g0011a0001c0001t0001g0258a0001c0001t0001g0297others(2): Show | 6 | HG00438.hp2 NA18947.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-13588_458-1358 others(63): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(77): Show |
1 | a0001c0001t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.458-13588_458-1358 others(88): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(25): Show |
3 | a0001c0001t0001g0055a0001c0001t0002g0261a0001c0001t0009g0054 | 3 | HG02630.hp1 HG02886.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.458-13579_458-1354 others(36): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(50): Show |
181 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0028others(178): Show | 187 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.458-13560_458-1350 others(61): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(75): Show |
3 | a0001c0001t0001g0100a0001c0001t0002g0292a0001c0001t0003g0099 | 3 | NA18956.hp1 NA18960.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.458-13604_458-1352 others(86): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(107): Show |
5 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-13504_458-1350 others(118): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(43): Show |
1 | a0001c0001t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.458-13580_458-1357 others(54): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524558
|
A | AATATATT others(48): Show |
1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13598_458-1359 others(59): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | |||||
chr1:206524587
|
T | A | 4 | a0001c0007t0002g0222a0001c0007t0002g0223a0001c0007t0011g0221others(1): Show | 4 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13585T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524587 | ||||||
chr1:206524589
|
T | A | 4 | a0001c0007t0002g0222a0001c0007t0002g0223a0001c0007t0011g0221others(1): Show | 4 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13583T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524589 | ||||||
chr1:206524589
|
T | TTATATAT others(50): Show |
3 | a0001c0001t0012g0322a0001c0004t0007g0001a0001c0004t0013g0104 | 4 | HG02258.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-13548_458-1354 others(61): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | |||||
chr1:206524589
|
T | TTATATAT others(114): Show |
2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-13548_458-1354 others(125): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | |||||
chr1:206524589
|
T | TTATATAT others(75): Show |
2 | a0004c0009t0001g0042a0004c0009t0001g0294 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.458-13504_458-1350 others(86): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | |||||
chr1:206524589
|
T | TTATGTAT others(68): Show |
4 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(1): Show | 5 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13580_458-1357 others(79): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | |||||
chr1:206524614
|
A | ATATATAT | 7 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0004t0003g0102others(4): Show | 8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-13554_458-1354 others(11): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524614 | |||||
chr1:206524614
|
A | ATATATAT others(82): Show |
1 | a0001c0002t0004g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.458-13504_458-1350 others(93): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524614 | |||||
chr1:206524615
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(1): Show | 5 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13557T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524615 | ||||||
chr1:206524637
|
A | AAATATAT others(16): Show |
3 | a0001c0001t0012g0322a0001c0004t0007g0001a0001c0004t0013g0104 | 4 | HG02258.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-13518_458-1349 others(27): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | |||||
chr1:206524637
|
A | AAATATAT others(98): Show |
1 | a0001c0004t0007g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.458-13504_458-1350 others(109): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | |||||
chr1:206524637
|
A | AAATATAT others(66): Show |
2 | a0001c0004t0007g0001a0001c0004t0007g0103 | 3 | HG01884.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.458-13523_458-1352 others(77): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | |||||
chr1:206524637
|
A | AAATATAT others(114): Show |
2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-13523_458-1352 others(125): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | |||||
chr1:206524637
|
A | AAATATAT others(116): Show |
3 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0004t0024g0020 | 3 | HG02280.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.458-13523_458-1352 others(127): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | |||||
chr1:206524640
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(1): Show | 5 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13532T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524640 | ||||||
chr1:206524650
|
A | G | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13522A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524650 | ||||||
chr1:206524654
|
T | A | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13518T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524654 | ||||||
chr1:206524657
|
G | A | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13515G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524657 | ||||||
chr1:206524662
|
A | AAAGATAT others(82): Show |
1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13510_458-1350 others(93): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524662 | ||||||
chr1:206524662
|
A | ATATATAT others(57): Show |
2 | a0001c0001t0005g0045a0001c0001t0017g0044 | 2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.458-13478_458-1347 others(68): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524662 | |||||
chr1:206524662
|
A | ATATATAT others(89): Show |
2 | a0001c0001t0001g0014a0001c0008t0005g0106 | 3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.458-13478_458-1347 others(100): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524662 | |||||
chr1:206524662
|
A | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13510A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524662 | ||||||
chr1:206524675
|
A | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13497A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524675 | ||||||
chr1:206524850
|
C | T | 2 | a0001c0001t0003g0212a0001c0001t0005g0211 | 2 | HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.458-13322C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524850 | ||||||
chr1:206524916
|
G | A | 21 | a0001c0001t0001g0014a0001c0001t0002g0308a0001c0001t0003g0022others(18): Show | 25 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.458-13256G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524916 | ||||||
chr1:206524964
|
A | T | 2 | a0001c0001t0001g0014a0001c0008t0005g0106 | 3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.458-13208A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524964 | ||||||
chr1:206524990
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13182T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524990 | ||||||
chr1:206524991
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13181C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524991 | ||||||
chr1:206524993
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13179T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524993 | ||||||
chr1:206525015
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0002g0156 | 3 | NA18942.hp2 NA18947.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.458-13157C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525015 | ||||||
chr1:206525016
|
A | G | 243 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(240): Show | 255 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.458-13156A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525016 | ||||||
chr1:206525106
|
C | T | 5 | a0001c0001t0002g0053a0001c0007t0002g0222a0001c0007t0002g0223others(2): Show | 5 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13066C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525106 | ||||||
chr1:206525156
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0013g0002others(6): Show | 10 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-13016T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525156 | ||||||
chr1:206525220
|
C | T | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-12952C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525220 | ||||||
chr1:206525278
|
G | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0003g0197others(2): Show | 5 | HG01433.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-12894G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525278 | ||||||
chr1:206525386
|
C | A | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-12786C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525386 | ||||||
chr1:206525404
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.458-12768G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525404 | ||||||
chr1:206525408
|
G | T | 21 | a0001c0001t0001g0014a0001c0001t0002g0308a0001c0001t0003g0022others(18): Show | 25 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.458-12764G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525408 | ||||||
chr1:206525608
|
AAAAACAA others(3): Show |
A | 3 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182 | 3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.458-12549_458-1254 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206525608 | |||||
chr1:206525758
|
G | T | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-12414G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525758 | ||||||
chr1:206525936
|
C | G | 1 | a0001c0002t0009g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.458-12236C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525936 | ||||||
chr1:206526136
|
C | G | 10 | a0001c0001t0005g0208a0001c0002t0003g0032a0002c0005t0001g0184others(7): Show | 10 | HG01109.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-12036C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526136 | ||||||
chr1:206526140
|
C | T | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-12032C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526140 | ||||||
chr1:206526269
|
A | AGTGTGTG others(1): Show |
5 | a0001c0001t0002g0053a0001c0007t0002g0222a0001c0007t0002g0223others(2): Show | 5 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-11886_458-1187 others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(3): Show |
44 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0052others(41): Show | 46 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.458-11888_458-1187 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0003g0038a0001c0001t0006g0015a0001c0001t0006g0314 | 4 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-11890_458-1187 others(16): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(7): Show |
14 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0198others(11): Show | 17 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.458-11892_458-1187 others(18): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(9): Show |
59 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0152others(56): Show | 61 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.458-11894_458-1187 others(20): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(11): Show |
105 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(102): Show | 110 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-11896_458-1187 others(22): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(13): Show |
29 | a0001c0001t0001g0028a0001c0001t0001g0143a0001c0001t0001g0265others(26): Show | 29 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.458-11898_458-1187 others(24): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(15): Show |
14 | a0001c0001t0001g0126a0001c0001t0002g0125a0001c0001t0003g0099others(11): Show | 14 | HG01952.hp2 HG02056.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.458-11900_458-1187 others(26): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(17): Show |
7 | a0001c0001t0001g0111a0001c0001t0001g0121a0001c0001t0001g0299others(4): Show | 7 | HG00609.hp1 HG01175.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-11902_458-1187 others(28): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(19): Show |
10 | a0001c0001t0002g0112a0001c0001t0002g0128a0001c0001t0002g0129others(7): Show | 11 | HG00438.hp1 HG02071.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.458-11879_458-1187 others(30): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(21): Show |
1 | a0001c0001t0006g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458-11879_458-1187 others(32): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526269
|
A | AGTGTGTG others(23): Show |
2 | a0001c0001t0001g0024a0001c0001t0006g0023 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.458-11879_458-1187 others(34): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | |||||
chr1:206526293
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-11879_458-1187 others(23): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526293 | ||||||
chr1:206526295
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-11877G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526295 | ||||||
chr1:206526303
|
G | A | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-11869G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526303 | ||||||
chr1:206526352
|
C | T | 3 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130 | 3 | NA18984.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.458-11820C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526352 | ||||||
chr1:206526438
|
A | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0002g0308others(24): Show | 32 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.458-11734A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526438 | ||||||
chr1:206526744
|
G | A | 1 | a0001c0002t0004g0199 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.458-11428G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526744 | ||||||
chr1:206526834
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.458-11338C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526834 | ||||||
chr1:206526870
|
G | A | 2 | a0001c0002t0001g0120a0001c0002t0020g0119 | 2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.458-11302G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526870 | ||||||
chr1:206526933
|
G | A | 13 | a0001c0001t0001g0256a0001c0001t0001g0269a0001c0001t0001g0270others(10): Show | 13 | NA18612.hp2 NA18747.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-11239G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526933 | ||||||
chr1:206527127
|
T | C | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-11045T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527127 | ||||||
chr1:206527131
|
A | C | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-11041A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527131 | ||||||
chr1:206527267
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0006g0122 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.458-10905C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527267 | ||||||
chr1:206527284
|
C | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-10888C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527284 | ||||||
chr1:206527366
|
G | T | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-10806G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527366 | ||||||
chr1:206527456
|
G | A | 45 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0143others(42): Show | 47 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.458-10716G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527456 | ||||||
chr1:206527491
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.458-10681C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527491 | ||||||
chr1:206527610
|
C | T | 2 | a0001c0002t0001g0120a0001c0002t0020g0119 | 2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.458-10562C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527610 | ||||||
chr1:206527678
|
T | C | 7 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(4): Show | 8 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-10494T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527678 | ||||||
chr1:206527833
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0006g0023a0001c0001t0006g0025 | 3 | HG02572.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.458-10339C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527833 | ||||||
chr1:206528139
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.458-10033G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528139 | ||||||
chr1:206528196
|
C | A | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.458-9976C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528196 | ||||||
chr1:206528248
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.458-9924A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528248 | ||||||
chr1:206528402
|
G | T | 5 | a0002c0005t0001g0184a0002c0005t0001g0185a0002c0005t0001g0189others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-9770G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528402 | ||||||
chr1:206528580
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0006g0030a0001c0001t0006g0031others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-9592G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528580 | ||||||
chr1:206528669
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.458-9503G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528669 | ||||||
chr1:206528715
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.458-9457G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528715 | ||||||
chr1:206528866
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0002g0155a0001c0001t0008g0157 | 3 | NA18959.hp2 NA18967.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.458-9306C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528866 | ||||||
chr1:206528905
|
A | G | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.458-9267A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528905 | ||||||
chr1:206528960
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-9212G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528960 | ||||||
chr1:206529122
|
T | C | 27 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0002g0308others(24): Show | 32 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.458-9050T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529122 | ||||||
chr1:206529275
|
G | A | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-8897G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529275 | ||||||
chr1:206529294
|
C | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-8878C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529294 | ||||||
chr1:206529323
|
G | A | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-8849G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529323 | ||||||
chr1:206529334
|
C | T | 1 | a0001c0002t0004g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.458-8838C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529334 | ||||||
chr1:206529336
|
C | T | 1 | a0001c0002t0003g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-8836C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529336 | ||||||
chr1:206529386
|
G | A | 46 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0143others(43): Show | 48 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.458-8786G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529386 | ||||||
chr1:206529424
|
G | T | 8 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-8748G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529424 | ||||||
chr1:206529444
|
C | G | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-8728C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529444 | ||||||
chr1:206529479
|
C | T | 1 | a0001c0001t0004g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.458-8693C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529479 | ||||||
chr1:206529544
|
C | T | 12 | a0001c0001t0002g0248a0001c0001t0003g0245a0001c0001t0003g0246others(9): Show | 12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-8628C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529544 | ||||||
chr1:206529578
|
G | A | 1 | a0001c0003t0005g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.458-8594G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529578 | ||||||
chr1:206529677
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-8495G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529677 | ||||||
chr1:206529699
|
C | T | 1 | a0001c0004t0003g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.458-8473C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529699 | ||||||
chr1:206529765
|
C | CA | 216 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(213): Show | 227 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.458-8397dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206529765 | |||||
chr1:206529765
|
C | CAA | 6 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(3): Show | 7 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-8398_458-8397d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206529765 | |||||
chr1:206529786
|
G | A | 4 | a0001c0001t0001g0093a0001c0001t0003g0090a0001c0001t0003g0091others(1): Show | 4 | HG01993.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-8386G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529786 | ||||||
chr1:206529840
|
G | T | 1 | a0001c0002t0003g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-8332G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529840 | ||||||
chr1:206530069
|
C | T | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-8103C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530069 | ||||||
chr1:206530070
|
G | A | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.458-8102G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530070 | ||||||
chr1:206530152
|
T | A | 243 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(240): Show | 255 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.458-8020T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530152 | ||||||
chr1:206530155
|
CT | C | 10 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(7): Show | 13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-8016delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530155 | ||||||
chr1:206530203
|
T | G | 1 | a0002c0005t0007g0190 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.458-7969T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530203 | ||||||
chr1:206530344
|
C | T | 1 | a0001c0001t0003g0099 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.458-7828C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530344 | ||||||
chr1:206530440
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-7732T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530440 | ||||||
chr1:206530627
|
A | G | 114 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0036others(111): Show | 118 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.458-7545A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530627 | ||||||
chr1:206530780
|
C | G | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-7392C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530780 | ||||||
chr1:206530796
|
G | A | 6 | a0001c0001t0001g0111a0001c0001t0003g0108a0001c0001t0003g0109others(3): Show | 6 | HG00597.hp2 HG00609.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-7376G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530796 | ||||||
chr1:206530949
|
C | G | 1 | a0001c0001t0009g0048 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.458-7223C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530949 | ||||||
chr1:206531169
|
G | A | 12 | a0001c0001t0002g0248a0001c0001t0003g0245a0001c0001t0003g0246others(9): Show | 12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-7003G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531169 | ||||||
chr1:206531354
|
C | T | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-6818C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531354 | ||||||
chr1:206531364
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.458-6808G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531364 | ||||||
chr1:206531369
|
G | A | 1 | a0001c0001t0010g0324 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.458-6803G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531369 | ||||||
chr1:206531477
|
A | G | 12 | a0001c0001t0002g0248a0001c0001t0003g0245a0001c0001t0003g0246others(9): Show | 12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-6695A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531477 | ||||||
chr1:206531539
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.458-6633G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531539 | ||||||
chr1:206531606
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0005g0045a0001c0001t0017g0044others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-6566C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531606 | ||||||
chr1:206531715
|
T | C | 46 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0143others(43): Show | 48 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.458-6457T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531715 | ||||||
chr1:206531813
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-6359G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531813 | ||||||
chr1:206531872
|
C | T | 1 | a0001c0002t0015g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.458-6300C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531872 | ||||||
chr1:206531873
|
T | TAA | 8 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0322others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-6291_458-6290d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206531873 | |||||
chr1:206531883
|
T | A | 286 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(283): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.458-6289T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531883 | ||||||
chr1:206531883
|
T | TA | 18 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0003g0327others(15): Show | 20 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.458-6286dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206531883 | |||||
chr1:206531907
|
C | T | 2 | a0001c0001t0011g0116a0001c0001t0011g0117 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.458-6265C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531907 | ||||||
chr1:206531913
|
A | G | 5 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328others(2): Show | 6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-6259A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531913 | ||||||
chr1:206531922
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.458-6250G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531922 | ||||||
chr1:206532058
|
G | GA | 195 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(192): Show | 206 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.458-6104dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206532058 | |||||
chr1:206532058
|
G | GAA | 9 | a0001c0001t0001g0014a0001c0001t0002g0226a0001c0001t0005g0045others(6): Show | 10 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-6105_458-6104d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206532058 | |||||
chr1:206532276
|
A | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(287): Show | 304 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.458-5896A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532276 | ||||||
chr1:206532298
|
A | G | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-5874A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532298 | ||||||
chr1:206532343
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0002g0325a0001c0001t0003g0312others(7): Show | 11 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.458-5829C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532343 | ||||||
chr1:206532611
|
C | T | 5 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0001t0012g0161others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-5561C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532611 | ||||||
chr1:206532758
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.458-5414G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532758 | ||||||
chr1:206532906
|
A | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0003g0327others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.458-5266A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532906 | ||||||
chr1:206533086
|
A | G | 192 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0024others(189): Show | 201 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.458-5086A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533086 | ||||||
chr1:206533256
|
G | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0326a0001c0001t0003g0327others(7): Show | 11 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.458-4916G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533256 | ||||||
chr1:206533278
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0003g0035a0001c0002t0003g0034others(3): Show | 6 | HG02055.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-4894G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533278 | ||||||
chr1:206533332
|
A | C | 3 | a0001c0001t0003g0153a0001c0001t0008g0144a0001c0001t0008g0154 | 3 | HG02129.hp1 HG02523.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.458-4840A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533332 | ||||||
chr1:206533728
|
C | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182others(1): Show | 4 | HG02145.hp2 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-4444C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533728 | ||||||
chr1:206534049
|
C | T | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-4123C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534049 | ||||||
chr1:206534336
|
T | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(326): Show | 345 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.458-3836T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534336 | ||||||
chr1:206534425
|
G | C | 1 | a0001c0001t0002g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.458-3747G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534425 | ||||||
chr1:206534560
|
C | T | 1 | a0001c0001t0019g0089 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.458-3612C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534560 | ||||||
chr1:206534721
|
T | A | 8 | a0001c0001t0001g0036a0001c0001t0003g0035a0001c0001t0011g0217others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-3451T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534721 | ||||||
chr1:206534787
|
G | C | 2 | a0001c0007t0002g0222a0001c0007t0011g0221 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.458-3385G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534787 | ||||||
chr1:206534855
|
G | T | 1 | a0001c0002t0026g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458-3317G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534855 | ||||||
chr1:206535154
|
G | A | 3 | a0001c0001t0001g0278a0004c0009t0001g0042a0004c0009t0001g0294 | 3 | HG00741.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.458-3018G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535154 | ||||||
chr1:206535382
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.458-2790T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535382 | ||||||
chr1:206535392
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 89 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.458-2780T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535392 | ||||||
chr1:206535530
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.458-2642G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535530 | ||||||
chr1:206535582
|
A | G | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2590A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535582 | ||||||
chr1:206535686
|
T | G | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-2486T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535686 | ||||||
chr1:206535703
|
C | CTG | 3 | a0001c0001t0003g0312a0001c0004t0003g0102a0001c0004t0030g0043 | 3 | HG02965.hp2 HG03209.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.458-2458_458-2457d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535703 | |||||
chr1:206535703
|
C | G | 1 | a0001c0001t0017g0044 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.458-2469C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535703 | ||||||
chr1:206535705
|
G | C | 1 | a0001c0001t0017g0044 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.458-2467G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535705 | ||||||
chr1:206535712
|
TGTG | T | 122 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(119): Show | 126 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.458-2456_458-2454d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535712 | |||||
chr1:206535714
|
TG | T | 61 | a0001c0001t0001g0055a0001c0001t0001g0139a0001c0001t0001g0141others(58): Show | 66 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.458-2456delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535714 | |||||
chr1:206535715
|
G | GT | 50 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0047others(47): Show | 52 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.458-2457_458-2456i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535715 | ||||||
chr1:206535715
|
GGT | G | 7 | a0001c0001t0002g0053a0001c0003t0001g0238a0001c0003t0005g0057others(4): Show | 7 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-2429_458-2428d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535715 | |||||
chr1:206535715
|
GGTGT | G | 70 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0121others(67): Show | 72 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.458-2431_458-2428d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535715 | |||||
chr1:206535716
|
G | T | 13 | a0001c0001t0001g0028a0001c0001t0001g0326a0001c0001t0003g0327others(10): Show | 15 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-2456G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535716 | ||||||
chr1:206535717
|
T | G | 13 | a0001c0001t0001g0028a0001c0001t0001g0326a0001c0001t0003g0327others(10): Show | 15 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-2455T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535717 | ||||||
chr1:206535718
|
GT | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0047others(104): Show | 114 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.458-2453delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535718 | ||||||
chr1:206535720
|
GT | G | 122 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(119): Show | 126 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.458-2451delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535720 | ||||||
chr1:206535743
|
T | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0265a0001c0001t0003g0005others(6): Show | 11 | HG00642.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-2429T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535743 | ||||||
chr1:206535745
|
A | T | 7 | a0001c0001t0001g0028a0001c0001t0006g0015a0001c0001t0006g0030others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-2427A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535745 | ||||||
chr1:206535747
|
A | T | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2425A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535747 | ||||||
chr1:206535749
|
A | T | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2423A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535749 | ||||||
chr1:206535751
|
A | T | 2 | a0001c0004t0005g0018a0001c0004t0006g0019 | 2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2421A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535751 | ||||||
chr1:206535779
|
A | G | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-2393A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535779 | ||||||
chr1:206535979
|
C | T | 3 | a0001c0001t0002g0308a0001c0001t0003g0022a0001c0004t0024g0020 | 3 | HG02280.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.458-2193C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535979 | ||||||
chr1:206536063
|
G | A | 1 | a0001c0001t0003g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.458-2109G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536063 | ||||||
chr1:206536100
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0003g0035a0001c0002t0003g0034others(3): Show | 6 | HG02055.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-2072G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536100 | ||||||
chr1:206536144
|
C | G | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.458-2028C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536144 | ||||||
chr1:206536206
|
T | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0047others(115): Show | 122 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.458-1966T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536206 | ||||||
chr1:206536238
|
A | G | 1 | a0001c0001t0003g0328 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.458-1934A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536238 | ||||||
chr1:206536333
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.458-1839A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536333 | ||||||
chr1:206536549
|
AG | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0005g0045others(3): Show | 8 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-1617delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206536549 | |||||
chr1:206536694
|
A | G | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.458-1478A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536694 | ||||||
chr1:206536783
|
C | A | 1 | a0001c0002t0009g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.458-1389C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536783 | ||||||
chr1:206536901
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0003g0206 | 2 | NA18983.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.458-1271A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536901 | ||||||
chr1:206537012
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0006g0015a0001c0001t0006g0030others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-1160A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537012 | ||||||
chr1:206537024
|
C | T | 1 | a0001c0002t0015g0244 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.458-1148C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537024 | ||||||
chr1:206537062
|
C | T | 1 | a0001c0002t0022g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.458-1110C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537062 | ||||||
chr1:206537285
|
C | G | 1 | a0001c0001t0031g0229 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.458-887C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537285 | ||||||
chr1:206537547
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.458-625G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537547 | ||||||
chr1:206537696
|
G | A | 7 | a0001c0001t0005g0208a0001c0001t0013g0002a0001c0001t0013g0049others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-476G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537696 | ||||||
chr1:206537771
|
T | G | 7 | a0001c0001t0005g0208a0001c0001t0013g0002a0001c0001t0013g0049others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-401T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537771 | ||||||
chr1:206537807
|
T | G | 7 | a0001c0001t0001g0028a0001c0001t0006g0015a0001c0001t0006g0030others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-365T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537807 | ||||||
chr1:206537817
|
T | C | 21 | a0001c0001t0002g0158a0001c0001t0002g0329a0001c0001t0003g0245others(18): Show | 24 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.458-355T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537817 | ||||||
chr1:206537893
|
T | C | 10 | a0001c0001t0005g0208a0001c0001t0009g0027a0001c0001t0009g0048others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-279T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537893 | ||||||
chr1:206537960
|
CA | C | 7 | a0001c0001t0005g0208a0001c0001t0013g0002a0001c0001t0013g0049others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-211delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537960 | ||||||
chr1:206537974
|
G | C | 1 | a0001c0001t0003g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.458-198G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537974 | ||||||
chr1:206538069
|
C | G | 7 | a0001c0001t0005g0208a0001c0001t0013g0002a0001c0001t0013g0049others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-103C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206538069 | ||||||
chr1:206538583
|
A | G | 17 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(14): Show | 20 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+290A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538583 | ||||||
chr1:206538649
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0062others(3): Show | 7 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+356G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538649 | ||||||
chr1:206538710
|
C | G | 2 | a0001c0001t0011g0116a0001c0001t0011g0117 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+417C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538710 | ||||||
chr1:206538750
|
C | T | 3 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182 | 3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+457C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538750 | ||||||
chr1:206538784
|
A | G | 17 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(14): Show | 20 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+491A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538784 | ||||||
chr1:206538793
|
G | A | 1 | a0001c0002t0004g0169 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.579+500G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538793 | ||||||
chr1:206538795
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0006g0015a0001c0001t0006g0030others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+502A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538795 | ||||||
chr1:206538989
|
G | A | 17 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(14): Show | 20 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+696G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538989 | ||||||
chr1:206539214
|
A | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 198 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.579+921A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539214 | ||||||
chr1:206539275
|
T | C | 1 | a0001c0001t0019g0089 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.579+982T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539275 | ||||||
chr1:206539501
|
C | T | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.579+1208C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539501 | ||||||
chr1:206539549
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+1256A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539549 | ||||||
chr1:206539623
|
C | T | 3 | a0001c0002t0003g0034a0001c0002t0006g0033a0001c0002t0009g0186 | 3 | HG02723.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.579+1330C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539623 | ||||||
chr1:206539896
|
G | A | 1 | a0001c0001t0001g0086 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.579+1603G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539896 | ||||||
chr1:206540171
|
G | T | 1 | a0001c0001t0003g0108 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.579+1878G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540171 | ||||||
chr1:206540226
|
G | C | 2 | a0001c0001t0003g0127a0001c0001t0003g0180 | 2 | HG00597.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.579+1933G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540226 | ||||||
chr1:206540361
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.579+2068A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540361 | ||||||
chr1:206540479
|
C | T | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+2186C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540479 | ||||||
chr1:206540588
|
A | G | 2 | a0001c0001t0005g0208a0001c0004t0005g0018 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.579+2295A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540588 | ||||||
chr1:206540635
|
C | G | 1 | a0001c0001t0003g0327 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+2342C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540635 | ||||||
chr1:206540759
|
G | C | 27 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(24): Show | 30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2466G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540759 | ||||||
chr1:206540898
|
T | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 198 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.579+2605T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540898 | ||||||
chr1:206540901
|
T | A | 27 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(24): Show | 30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2608T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540901 | ||||||
chr1:206540938
|
A | G | 27 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(24): Show | 30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2645A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540938 | ||||||
chr1:206541082
|
T | A | 27 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(24): Show | 30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2789T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541082 | ||||||
chr1:206541183
|
C | T | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+2890C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541183 | ||||||
chr1:206541191
|
G | A | 204 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 214 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.579+2898G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541191 | ||||||
chr1:206541462
|
G | A | 1 | a0001c0004t0003g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.579+3169G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541462 | ||||||
chr1:206541489
|
C | T | 203 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 213 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.579+3196C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541489 | ||||||
chr1:206541513
|
C | T | 24 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(21): Show | 27 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.579+3220C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541513 | ||||||
chr1:206541516
|
T | A | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+3223T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541516 | ||||||
chr1:206541679
|
A | G | 3 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182 | 3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+3386A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541679 | ||||||
chr1:206541708
|
T | C | 3 | a0001c0001t0002g0329a0001c0002t0015g0244a0001c0002t0022g0315 | 3 | HG02055.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.579+3415T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541708 | ||||||
chr1:206541806
|
C | T | 2 | a0002c0005t0007g0190a0002c0005t0028g0209 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+3513C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541806 | ||||||
chr1:206541857
|
G | A | 15 | a0001c0001t0003g0085a0001c0001t0003g0192a0001c0001t0003g0193others(12): Show | 16 | HG00558.hp2 HG00642.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.579+3564G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541857 | ||||||
chr1:206541895
|
C | T | 3 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182 | 3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+3602C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541895 | ||||||
chr1:206541928
|
A | G | 3 | a0001c0001t0001g0293a0001c0002t0001g0286a0001c0002t0001g0307 | 3 | HG01952.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.579+3635A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541928 | ||||||
chr1:206541949
|
A | C | 3 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182 | 3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+3656A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541949 | ||||||
chr1:206542021
|
G | A | 14 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(11): Show | 17 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.579+3728G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542021 | ||||||
chr1:206542298
|
A | G | 1 | a0001c0007t0002g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.579+4005A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542298 | ||||||
chr1:206542387
|
G | A | 233 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(230): Show | 246 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.579+4094G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542387 | ||||||
chr1:206542401
|
C | T | 8 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0001t0007g0251others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+4108C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542401 | ||||||
chr1:206542463
|
T | C | 2 | a0002c0005t0007g0190a0002c0005t0028g0209 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+4170T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542463 | ||||||
chr1:206542465
|
C | G | 3 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0182 | 3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+4172C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542465 | ||||||
chr1:206542470
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.579+4177G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542470 | ||||||
chr1:206542518
|
C | G | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+4225C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542518 | ||||||
chr1:206542522
|
A | G | 206 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(203): Show | 216 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.579+4229A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542522 | ||||||
chr1:206542648
|
G | A | 7 | a0001c0001t0005g0208a0001c0001t0013g0002a0001c0001t0013g0049others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+4355G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542648 | ||||||
chr1:206542875
|
T | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+4582T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542875 | ||||||
chr1:206542986
|
A | G | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+4693A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542986 | ||||||
chr1:206543138
|
C | T | 1 | a0001c0001t0001g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.579+4845C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543138 | ||||||
chr1:206543221
|
T | TAAA | 12 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0179others(9): Show | 13 | HG01256.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+4942_579+4944d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | |||||
chr1:206543221
|
T | TAAAA | 185 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 194 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.579+4941_579+4944d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | |||||
chr1:206543221
|
T | TAAAAA | 9 | a0001c0001t0001g0062a0001c0001t0001g0317a0001c0001t0002g0021others(6): Show | 9 | HG01175.hp2 HG01981.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+4940_579+4944d others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | |||||
chr1:206543221
|
T | TAAAAAA | 21 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0249others(18): Show | 24 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.579+4939_579+4944d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | |||||
chr1:206543221
|
TA | T | 6 | a0001c0001t0002g0017a0001c0001t0002g0325a0001c0001t0003g0056others(3): Show | 6 | HG00099.hp1 HG01069.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+4944delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | |||||
chr1:206543450
|
C | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(227): Show | 243 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.579+5157C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543450 | ||||||
chr1:206543565
|
A | ATG | 7 | a0001c0001t0001g0265a0001c0001t0002g0292a0001c0001t0009g0027others(4): Show | 7 | HG00642.hp1 HG00741.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+5298_579+5299d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | |||||
chr1:206543565
|
ATG | A | 3 | a0001c0001t0002g0279a0001c0001t0005g0045a0001c0001t0017g0044 | 3 | HG00423.hp1 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.579+5298_579+5299d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | |||||
chr1:206543565
|
ATGTG | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(206): Show | 222 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.579+5296_579+5299d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | |||||
chr1:206543565
|
ATGTGTG | A | 18 | a0001c0001t0002g0329a0001c0001t0003g0245a0001c0001t0003g0246others(15): Show | 18 | HG01952.hp2 HG01978.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+5294_579+5299d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | |||||
chr1:206543565
|
ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0010g0213a0001c0002t0003g0034a0001c0002t0006g0033others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5292_579+5299d others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | |||||
chr1:206543565
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0002t0022g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+5290_579+5299d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | |||||
chr1:206543572
|
T | C | 2 | a0002c0005t0007g0190a0002c0005t0028g0209 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+5279T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543572 | ||||||
chr1:206543658
|
G | T | 4 | a0001c0001t0002g0325a0001c0001t0003g0056a0001c0001t0005g0225others(1): Show | 4 | HG00099.hp1 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5365G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543658 | ||||||
chr1:206543663
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0002g0163 | 2 | NA18747.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.579+5370C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543663 | ||||||
chr1:206543739
|
T | C | 1 | a0002c0005t0001g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.579+5446T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543739 | ||||||
chr1:206543806
|
T | G | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+5513T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543806 | ||||||
chr1:206543884
|
G | T | 1 | a0001c0004t0006g0019 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.579+5591G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543884 | ||||||
chr1:206543968
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0006g0023 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.579+5675G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543968 | ||||||
chr1:206544039
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.579+5746A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544039 | ||||||
chr1:206544232
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0002g0112a0001c0001t0002g0305others(1): Show | 4 | HG00438.hp1 NA18959.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5939G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544232 | ||||||
chr1:206544234
|
GGCTC | G | 3 | a0001c0002t0003g0034a0001c0002t0006g0033a0001c0002t0009g0186 | 3 | HG02723.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.579+5942_579+5945d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544234 | ||||||
chr1:206544318
|
C | G | 19 | a0001c0001t0001g0028a0001c0001t0005g0208a0001c0001t0006g0015others(16): Show | 20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+6025C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544318 | ||||||
chr1:206544330
|
T | G | 40 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0174others(37): Show | 44 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.579+6037T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544330 | ||||||
chr1:206544385
|
C | T | 15 | a0001c0001t0003g0022a0001c0001t0003g0245a0001c0001t0003g0246others(12): Show | 18 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+6092C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544385 | ||||||
chr1:206544432
|
A | G | 1 | a0001c0001t0010g0213 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579+6139A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544432 | ||||||
chr1:206544656
|
G | GC | 41 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0060others(38): Show | 43 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.579+6365dupC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206544656 | |||||
chr1:206544670
|
A | T | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+6377A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544670 | ||||||
chr1:206544791
|
G | A | 12 | a0001c0001t0002g0329a0001c0001t0006g0015a0001c0001t0006g0030others(9): Show | 13 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+6498G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544791 | ||||||
chr1:206544813
|
C | T | 8 | a0001c0001t0005g0045a0001c0001t0009g0027a0001c0001t0009g0048others(5): Show | 8 | HG01952.hp2 HG01978.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+6520C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544813 | ||||||
chr1:206544815
|
T | C | 14 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0005g0208others(11): Show | 14 | HG01109.hp1 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+6522T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544815 | ||||||
chr1:206544850
|
C | A | 2 | a0001c0001t0012g0161a0001c0001t0012g0162 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.579+6557C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544850 | ||||||
chr1:206544894
|
G | GA | 8 | a0001c0001t0001g0293a0001c0001t0009g0027a0001c0001t0009g0048others(5): Show | 8 | HG01109.hp2 HG01952.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+6613dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206544894 | |||||
chr1:206544895
|
A | G | 1 | a0001c0002t0022g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+6602A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544895 | ||||||
chr1:206545024
|
G | A | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.579+6731G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545024 | ||||||
chr1:206545344
|
TG | T | 4 | a0001c0004t0003g0102a0001c0004t0030g0043a0002c0005t0003g0187others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+7052delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545344 | ||||||
chr1:206545345
|
GT | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(152): Show | 167 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.579+7072delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545345 | |||||
chr1:206545345
|
GTT | G | 133 | a0001c0001t0001g0024a0001c0001t0001g0070a0001c0001t0001g0087others(130): Show | 135 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.579+7071_579+7072d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545345 | |||||
chr1:206545345
|
GTTT | G | 17 | a0001c0001t0002g0118a0001c0001t0003g0246a0001c0001t0003g0249others(14): Show | 18 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+7070_579+7072d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545345 | |||||
chr1:206545348
|
T | G | 4 | a0001c0001t0002g0016a0001c0001t0002g0017a0002c0005t0007g0190others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+7055T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545348 | ||||||
chr1:206545352
|
T | G | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.579+7059T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545352 | ||||||
chr1:206545356
|
T | G | 4 | a0001c0004t0003g0102a0001c0004t0030g0043a0002c0005t0003g0187others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+7063T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545356 | ||||||
chr1:206545487
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0007g0029 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.579+7194G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545487 | ||||||
chr1:206545516
|
GT | G | 228 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(225): Show | 238 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(235): Show |
intron_variant | MODIFIER | c.579+7230delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545516 | |||||
chr1:206545524
|
A | G | 33 | a0001c0001t0002g0118a0001c0001t0003g0246a0001c0001t0003g0249others(30): Show | 34 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.579+7231A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545524 | ||||||
chr1:206545687
|
C | A | 2 | a0002c0005t0007g0190a0002c0005t0028g0209 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+7394C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545687 | ||||||
chr1:206545693
|
T | C | 6 | a0001c0001t0001g0073a0001c0001t0001g0299a0001c0001t0002g0136others(3): Show | 6 | HG01358.hp2 HG02083.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+7400T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545693 | ||||||
chr1:206545953
|
A | AT | 10 | a0001c0001t0002g0118a0001c0001t0002g0292a0001c0001t0003g0214others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+7677dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545953 | |||||
chr1:206545953
|
AT | A | 27 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0078others(24): Show | 28 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.579+7677delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545953 | |||||
chr1:206545979
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0003g0263 | 2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.579+7686C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545979 | ||||||
chr1:206546089
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0005g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.579+7824_579+7833d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT | A | 4 | a0001c0001t0001g0028a0001c0001t0007g0029a0001c0004t0007g0001others(1): Show | 7 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+7827_579+7833d others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(3): Show |
A | 32 | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0079others(29): Show | 33 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.579+7824_579+7833d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(4): Show |
A | 147 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 154 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.579+7823_579+7833d others(13): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(5): Show |
A | 19 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0254others(16): Show | 19 | HG00099.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.579+7822_579+7833d others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+7821_579+7833d others(15): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0029g0247 | 3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+7820_579+7833d others(16): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(8): Show |
A | 5 | a0001c0001t0003g0273a0001c0001t0009g0027a0001c0001t0009g0048others(2): Show | 5 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+7819_579+7833d others(17): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(9): Show |
A | 15 | a0001c0001t0001g0293a0001c0001t0002g0051a0001c0001t0002g0131others(12): Show | 15 | HG00323.hp2 HG01070.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.579+7818_579+7833d others(18): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(10): Show |
A | 46 | a0001c0001t0001g0073a0001c0001t0001g0269a0001c0001t0001g0282others(43): Show | 48 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.579+7817_579+7833d others(19): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(11): Show |
A | 5 | a0001c0001t0001g0059a0001c0001t0002g0118a0001c0001t0006g0015others(2): Show | 6 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+7816_579+7833d others(20): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546089
|
ATTTTTTT others(12): Show |
A | 15 | a0001c0001t0002g0053a0001c0001t0006g0030a0001c0001t0006g0031others(12): Show | 16 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.579+7815_579+7833d others(21): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | |||||
chr1:206546124
|
T | G | 19 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+7831T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546124 | ||||||
chr1:206546125
|
T | G | 19 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+7832T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546125 | ||||||
chr1:206546126
|
T | G | 23 | a0001c0001t0001g0024a0001c0001t0002g0016a0001c0001t0002g0017others(20): Show | 24 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.579+7833T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546126 | ||||||
chr1:206546222
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+7929C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546222 | ||||||
chr1:206546223
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 230 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.579+7930T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546223 | ||||||
chr1:206546490
|
C | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(300): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.579+8197C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546490 | ||||||
chr1:206546585
|
G | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.579+8292G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546585 | ||||||
chr1:206546648
|
C | T | 223 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.579+8355C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546648 | ||||||
chr1:206546689
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0003g0263 | 2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.579+8396C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546689 | ||||||
chr1:206546690
|
A | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+8397A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546690 | ||||||
chr1:206546795
|
A | C | 3 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0002g0295 | 3 | HG01515.hp2 HG01517.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.579+8502A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546795 | ||||||
chr1:206546856
|
C | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(197): Show | 209 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.579+8563C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546856 | ||||||
chr1:206546879
|
G | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(300): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.579+8586G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546879 | ||||||
chr1:206546897
|
G | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.579+8604G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546897 | ||||||
chr1:206547216
|
C | T | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+8923C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547216 | ||||||
chr1:206547224
|
C | T | 63 | a0001c0001t0001g0073a0001c0001t0001g0179a0001c0001t0001g0269others(60): Show | 65 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.579+8931C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547224 | ||||||
chr1:206547264
|
G | A | 1 | a0001c0001t0002g0271 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.579+8971G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547264 | ||||||
chr1:206547286
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 229 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.579+8993T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547286 | ||||||
chr1:206547437
|
G | A | 217 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(214): Show | 227 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.579+9144G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547437 | ||||||
chr1:206547458
|
C | T | 11 | a0001c0001t0005g0208a0001c0001t0011g0217a0001c0001t0012g0161others(8): Show | 11 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+9165C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547458 | ||||||
chr1:206547547
|
T | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+9254T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547547 | ||||||
chr1:206547891
|
C | T | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.579+9598C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547891 | ||||||
chr1:206548037
|
T | G | 5 | a0001c0001t0002g0053a0001c0004t0003g0102a0001c0004t0030g0043others(2): Show | 5 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+9744T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548037 | ||||||
chr1:206548051
|
T | G | 32 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0139others(29): Show | 32 | HG01261.hp1 HG02055.hp1 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.579+9758T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548051 | ||||||
chr1:206548164
|
T | A | 3 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0029g0247 | 3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+9871T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548164 | ||||||
chr1:206548404
|
C | G | 1 | a0001c0001t0006g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.579+10111C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548404 | ||||||
chr1:206548502
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(198): Show | 210 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.579+10209G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548502 | ||||||
chr1:206548522
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+10229C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548522 | ||||||
chr1:206548647
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.579+10354A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548647 | ||||||
chr1:206548706
|
G | A | 3 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0029g0247 | 3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+10413G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548706 | ||||||
chr1:206548738
|
C | G | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.579+10445C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548738 | ||||||
chr1:206548803
|
G | A | 7 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0009g0027others(4): Show | 7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+10510G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548803 | ||||||
chr1:206548846
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.579+10553C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548846 | ||||||
chr1:206548874
|
ATTTTGTT others(3): Show |
A | 1 | a0001c0001t0001g0009 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.579+10582_579+1059 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548874 | ||||||
chr1:206548884
|
G | A | 7 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0009g0027others(4): Show | 7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+10591G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548884 | ||||||
chr1:206548904
|
T | C | 28 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053others(25): Show | 29 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.579+10611T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548904 | ||||||
chr1:206548908
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.579+10615C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548908 | ||||||
chr1:206548928
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0005g0039a0001c0001t0005g0165others(4): Show | 10 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+10635C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548928 | ||||||
chr1:206548958
|
TG | T | 7 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0009g0027others(4): Show | 7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+10668delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206548958 | |||||
chr1:206549020
|
C | T | 4 | a0001c0001t0003g0056a0001c0001t0003g0146a0001c0001t0003g0147others(1): Show | 4 | HG02735.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+10727C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549020 | ||||||
chr1:206549117
|
T | C | 21 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053others(18): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+10824T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549117 | ||||||
chr1:206549122
|
TC | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.579+10830delC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549122 | ||||||
chr1:206549125
|
C | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.579+10832C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549125 | ||||||
chr1:206549164
|
C | G | 2 | a0001c0001t0003g0197a0001c0001t0003g0212 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.579+10871C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549164 | ||||||
chr1:206549200
|
C | G | 3 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0029g0247 | 3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+10907C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549200 | ||||||
chr1:206549209
|
T | C | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053 | 3 | HG01069.hp1 HG01071.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.579+10916T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549209 | ||||||
chr1:206549210
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.579+10917G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549210 | ||||||
chr1:206549410
|
T | C | 18 | a0001c0001t0002g0118a0001c0001t0006g0015a0001c0001t0006g0030others(15): Show | 19 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+11117T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549410 | ||||||
chr1:206549462
|
A | G | 1 | a0001c0001t0006g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.579+11169A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549462 | ||||||
chr1:206549797
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+11504A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549797 | ||||||
chr1:206549928
|
G | T | 7 | a0001c0001t0001g0139a0001c0001t0002g0325a0001c0001t0005g0225others(4): Show | 7 | HG00099.hp1 HG01361.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+11635G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549928 | ||||||
chr1:206550475
|
G | A | 2 | a0001c0001t0007g0251a0001c0001t0007g0252 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.579+12182G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550475 | ||||||
chr1:206550586
|
A | C | 4 | a0001c0004t0003g0102a0001c0004t0030g0043a0002c0005t0003g0187others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+12293A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550586 | ||||||
chr1:206550833
|
A | G | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053 | 3 | HG01069.hp1 HG01071.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.579+12540A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550833 | ||||||
chr1:206550909
|
C | G | 231 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(228): Show | 241 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.579+12616C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550909 | ||||||
chr1:206550918
|
C | T | 2 | a0001c0002t0004g0316a0001c0002t0015g0321 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.579+12625C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550918 | ||||||
chr1:206551038
|
A | C | 303 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(300): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.579+12745A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551038 | ||||||
chr1:206551326
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0053 | 3 | HG01069.hp1 HG01071.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.579+13033C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551326 | ||||||
chr1:206551331
|
C | G | 9 | a0001c0001t0005g0208a0001c0001t0011g0217a0001c0002t0003g0032others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+13038C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551331 | ||||||
chr1:206551409
|
G | A | 103 | a0001c0001t0001g0028a0001c0001t0001g0055a0001c0001t0001g0073others(100): Show | 109 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(106): Show |
intron_variant | MODIFIER | c.579+13116G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551409 | ||||||
chr1:206551495
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0005g0039a0001c0001t0005g0165others(7): Show | 13 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+13202G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551495 | ||||||
chr1:206551566
|
C | T | 1 | a0001c0001t0010g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.579+13273C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551566 | ||||||
chr1:206551583
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.579+13290C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551583 | ||||||
chr1:206551834
|
A | C | 1 | a0008c0011t0006g0313 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.579+13541A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551834 | ||||||
chr1:206551911
|
G | A | 4 | a0001c0004t0003g0102a0001c0004t0030g0043a0002c0005t0003g0187others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+13618G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551911 | ||||||
chr1:206551944
|
A | G | 12 | a0001c0001t0006g0015a0001c0001t0006g0030a0001c0001t0006g0031others(9): Show | 13 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+13651A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551944 | ||||||
chr1:206552164
|
G | A | 3 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0029g0247 | 3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+13871G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552164 | ||||||
chr1:206552560
|
C | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(203): Show | 215 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.579+14267C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552560 | ||||||
chr1:206552606
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+14313G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552606 | ||||||
chr1:206552816
|
G | A | 7 | a0001c0001t0003g0246a0001c0001t0003g0249a0001c0001t0009g0027others(4): Show | 7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+14523G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552816 | ||||||
chr1:206553119
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+14826G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553119 | ||||||
chr1:206553255
|
G | A | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.579+14962G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553255 | ||||||
chr1:206553401
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.579+15108G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553401 | ||||||
chr1:206553440
|
A | G | 1 | a0001c0001t0002g0267 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.579+15147A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553440 | ||||||
chr1:206553541
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 93 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.579+15248T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553541 | ||||||
chr1:206553660
|
T | A | 137 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0060others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.579+15367T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553660 | ||||||
chr1:206553665
|
G | C | 2 | a0001c0001t0012g0161a0001c0001t0012g0162 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.579+15372G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553665 | ||||||
chr1:206553736
|
C | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+15443C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553736 | ||||||
chr1:206553812
|
A | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.579+15519A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553812 | ||||||
chr1:206553932
|
A | G | 63 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(60): Show | 65 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.579+15639A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553932 | ||||||
chr1:206554054
|
A | G | 8 | a0001c0001t0007g0029a0001c0001t0007g0251a0001c0001t0007g0252others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+15761A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554054 | ||||||
chr1:206554076
|
C | T | 65 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(62): Show | 67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+15783C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554076 | ||||||
chr1:206554107
|
C | T | 65 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(62): Show | 67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+15814C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554107 | ||||||
chr1:206554117
|
C | T | 143 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0060others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.579+15824C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554117 | ||||||
chr1:206554159
|
TACA | T | 3 | a0001c0001t0001g0293a0001c0002t0001g0286a0001c0002t0001g0307 | 3 | HG01952.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.579+15867_579+1586 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554159 | ||||||
chr1:206554189
|
A | T | 6 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+15896A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554189 | ||||||
chr1:206554306
|
T | A | 1 | a0001c0001t0002g0283 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.579+16013T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554306 | ||||||
chr1:206554307
|
G | T | 1 | a0001c0001t0002g0283 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.579+16014G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554307 | ||||||
chr1:206554472
|
C | T | 1 | a0001c0002t0009g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.579+16179C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554472 | ||||||
chr1:206554506
|
G | A | 1 | a0001c0010t0003g0268 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.579+16213G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554506 | ||||||
chr1:206554646
|
C | T | 65 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(62): Show | 67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+16353C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554646 | ||||||
chr1:206554706
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(151): Show | 162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.579+16413C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554706 | ||||||
chr1:206555055
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0004g0177 | 3 | NA18939.hp2 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.579+16762T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555055 | ||||||
chr1:206555366
|
TG | T | 65 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(62): Show | 67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+17074delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555366 | ||||||
chr1:206555428
|
G | A | 1 | a0001c0001t0011g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.579+17135G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555428 | ||||||
chr1:206555508
|
G | GA | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+17218dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206555508 | |||||
chr1:206555511
|
A | AT | 65 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(62): Show | 67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+17218_579+1721 others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555511 | ||||||
chr1:206555643
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.579+17350G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555643 | ||||||
chr1:206555654
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 75 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.579+17361C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555654 | ||||||
chr1:206555713
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+17420G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555713 | ||||||
chr1:206555776
|
G | C | 2 | a0001c0004t0003g0102a0001c0004t0030g0043 | 2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.579+17483G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555776 | ||||||
chr1:206555776
|
G | T | 1 | a0001c0002t0002g0150 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.579+17483G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555776 | ||||||
chr1:206555997
|
G | A | 1 | a0001c0002t0009g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.579+17704G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555997 | ||||||
chr1:206556234
|
C | G | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+17941C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556234 | ||||||
chr1:206556265
|
G | A | 83 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0139others(80): Show | 86 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.579+17972G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556265 | ||||||
chr1:206556294
|
C | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.579+18001C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556294 | ||||||
chr1:206556334
|
G | A | 1 | a0001c0001t0010g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.579+18041G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556334 | ||||||
chr1:206556372
|
C | T | 4 | a0001c0001t0007g0251a0001c0001t0007g0252a0001c0001t0012g0161others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+18079C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556372 | ||||||
chr1:206556652
|
G | A | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+18359G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556652 | ||||||
chr1:206556800
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.579+18507C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556800 | ||||||
chr1:206556810
|
C | T | 1 | a0001c0001t0007g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.579+18517C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556810 | ||||||
chr1:206556818
|
G | C | 2 | a0001c0001t0011g0116a0001c0001t0011g0117 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+18525G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556818 | ||||||
chr1:206556980
|
CA | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.579+18688delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556980 | ||||||
chr1:206557278
|
G | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0318 | 2 | HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.579+18985G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557278 | ||||||
chr1:206557313
|
C | A | 76 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0139others(73): Show | 79 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.579+19020C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557313 | ||||||
chr1:206557363
|
G | C | 78 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0139others(75): Show | 81 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.579+19070G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557363 | ||||||
chr1:206557420
|
C | T | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+19127C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557420 | ||||||
chr1:206557732
|
G | A | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+19439G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557732 | ||||||
chr1:206557763
|
A | C | 1 | a0001c0004t0003g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.579+19470A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557763 | ||||||
chr1:206558116
|
A | G | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+19823A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558116 | ||||||
chr1:206558119
|
G | T | 1 | a0001c0002t0003g0034 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.579+19826G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558119 | ||||||
chr1:206558288
|
C | T | 20 | a0001c0001t0001g0024a0001c0001t0002g0016a0001c0001t0002g0017others(17): Show | 21 | HG01069.hp1 HG01071.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.579+19995C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558288 | ||||||
chr1:206558294
|
T | C | 8 | a0001c0001t0001g0088a0001c0001t0001g0141a0001c0001t0001g0258others(5): Show | 8 | HG01261.hp1 NA18747.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+20001T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558294 | ||||||
chr1:206558332
|
G | A | 1 | a0001c0001t0005g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.579+20039G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558332 | ||||||
chr1:206558539
|
C | T | 1 | a0001c0002t0026g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.579+20246C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558539 | ||||||
chr1:206558669
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+20376C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558669 | ||||||
chr1:206558700
|
A | G | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+20407A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558700 | ||||||
chr1:206558762
|
G | A | 1 | a0006c0014t0001g0080 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.579+20469G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558762 | ||||||
chr1:206559098
|
C | T | 27 | a0001c0001t0001g0024a0001c0001t0002g0016a0001c0001t0002g0017others(24): Show | 28 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.579+20805C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559098 | ||||||
chr1:206559319
|
G | A | 132 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.579+21026G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559319 | ||||||
chr1:206559507
|
C | G | 9 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0045others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+21214C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559507 | ||||||
chr1:206559516
|
C | A | 2 | a0001c0001t0002g0308a0001c0007t0002g0222 | 2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.579+21223C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559516 | ||||||
chr1:206559603
|
T | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 183 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.579+21310T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559603 | ||||||
chr1:206559611
|
C | T | 6 | a0001c0001t0003g0085a0001c0001t0003g0135a0001c0001t0003g0192others(3): Show | 6 | HG00642.hp2 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+21318C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559611 | ||||||
chr1:206559950
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+21657C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559950 | ||||||
chr1:206560089
|
C | T | 132 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.579+21796C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560089 | ||||||
chr1:206560368
|
G | A | 6 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0004t0003g0102others(3): Show | 6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+22075G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560368 | ||||||
chr1:206560382
|
G | A | 2 | a0001c0008t0005g0106a0001c0008t0005g0107 | 2 | HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.579+22089G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560382 | ||||||
chr1:206560386
|
T | A | 1 | a0001c0001t0005g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.579+22093T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560386 | ||||||
chr1:206560443
|
G | A | 7 | a0001c0001t0006g0015a0001c0001t0006g0030a0001c0001t0006g0031others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+22150G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560443 | ||||||
chr1:206560527
|
G | A | 2 | a0001c0001t0016g0303a0001c0001t0016g0304 | 2 | NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.579+22234G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560527 | ||||||
chr1:206560716
|
T | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(63): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.579+22423T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560716 | ||||||
chr1:206561064
|
T | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-22205T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561064 | ||||||
chr1:206561175
|
C | T | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-22094C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561175 | ||||||
chr1:206561310
|
C | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-21959C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561310 | ||||||
chr1:206561502
|
T | C | 57 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0179others(54): Show | 59 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(56): Show |
intron_variant | MODIFIER | c.580-21767T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561502 | ||||||
chr1:206561579
|
G | A | 57 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0179others(54): Show | 59 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(56): Show |
intron_variant | MODIFIER | c.580-21690G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561579 | ||||||
chr1:206561663
|
C | CT | 13 | a0001c0001t0002g0226a0001c0001t0005g0039a0001c0001t0005g0165others(10): Show | 13 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-21587dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561663 | |||||
chr1:206561663
|
CT | C | 141 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0060others(138): Show | 144 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.580-21587delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561663 | |||||
chr1:206561663
|
CTT | C | 12 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0128others(9): Show | 12 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-21588_580-2158 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561663 | |||||
chr1:206561729
|
G | A | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-21540G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561729 | ||||||
chr1:206561820
|
C | A | 1 | a0001c0001t0002g0125 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.580-21449C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561820 | ||||||
chr1:206561840
|
G | GTT | 137 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.580-21419_580-2141 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561840 | |||||
chr1:206561840
|
G | GTTT | 10 | a0001c0001t0001g0024a0001c0001t0002g0128a0001c0001t0002g0129others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-21420_580-2141 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561840 | |||||
chr1:206561869
|
C | T | 6 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0004t0003g0102others(3): Show | 6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-21400C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561869 | ||||||
chr1:206561915
|
A | G | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0045others(14): Show | 17 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-21354A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561915 | ||||||
chr1:206562363
|
C | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 180 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.580-20906C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562363 | ||||||
chr1:206562529
|
C | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.580-20740C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562529 | ||||||
chr1:206562532
|
G | A | 6 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0004t0003g0102others(3): Show | 6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-20737G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562532 | ||||||
chr1:206562660
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(168): Show | 181 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.580-20609T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562660 | ||||||
chr1:206562708
|
G | T | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-20561G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562708 | ||||||
chr1:206562714
|
C | T | 1 | a0001c0004t0030g0043 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.580-20555C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562714 | ||||||
chr1:206562760
|
A | G | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0045others(14): Show | 17 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-20509A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562760 | ||||||
chr1:206562814
|
T | C | 313 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(310): Show | 328 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.580-20455T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562814 | ||||||
chr1:206562843
|
A | T | 2 | a0001c0002t0015g0244a0001c0002t0015g0321 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.580-20426A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562843 | ||||||
chr1:206562871
|
A | G | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0045others(14): Show | 17 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-20398A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562871 | ||||||
chr1:206562880
|
C | T | 1 | a0001c0001t0005g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.580-20389C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562880 | ||||||
chr1:206562885
|
G | A | 9 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0045others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-20384G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562885 | ||||||
chr1:206562912
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.580-20357T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562912 | ||||||
chr1:206562921
|
CA | C | 62 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(59): Show | 64 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(61): Show |
intron_variant | MODIFIER | c.580-20337delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206562921 | |||||
chr1:206563245
|
G | A | 132 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(129): Show | 134 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.580-20024G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563245 | ||||||
chr1:206563267
|
G | C | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-20002G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563267 | ||||||
chr1:206563332
|
A | G | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(4): Show | 7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-19937A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563332 | ||||||
chr1:206563346
|
C | A | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-19923C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563346 | ||||||
chr1:206563368
|
T | C | 1 | a0001c0016t0002g0133 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.580-19901T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563368 | ||||||
chr1:206563601
|
C | A | 2 | a0001c0002t0003g0242a0001c0002t0026g0040 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.580-19668C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563601 | ||||||
chr1:206563914
|
C | A | 19 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(16): Show | 19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-19355C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563914 | ||||||
chr1:206563929
|
T | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.580-19340T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563929 | ||||||
chr1:206563948
|
A | C | 30 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(27): Show | 31 | HG00558.hp2 HG00642.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-19321A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563948 | ||||||
chr1:206564308
|
G | T | 4 | a0001c0002t0003g0242a0001c0002t0009g0007a0001c0002t0009g0159others(1): Show | 5 | HG02145.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-18961G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564308 | ||||||
chr1:206564369
|
C | A | 1 | a0001c0001t0008g0157 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.580-18900C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564369 | ||||||
chr1:206564540
|
C | T | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-18729C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564540 | ||||||
chr1:206564823
|
G | C | 10 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0045others(7): Show | 10 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-18446G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564823 | ||||||
chr1:206564952
|
C | G | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-18317C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564952 | ||||||
chr1:206565031
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.580-18238G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565031 | ||||||
chr1:206565135
|
C | T | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-18134C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565135 | ||||||
chr1:206565257
|
C | T | 11 | a0001c0001t0001g0024a0001c0001t0002g0128a0001c0001t0002g0129others(8): Show | 12 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-18012C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565257 | ||||||
chr1:206565258
|
A | G | 313 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(310): Show | 328 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.580-18011A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565258 | ||||||
chr1:206565542
|
G | C | 1 | a0001c0001t0003g0257 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.580-17727G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565542 | ||||||
chr1:206565545
|
T | C | 19 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(16): Show | 19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-17724T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565545 | ||||||
chr1:206565672
|
A | T | 19 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(16): Show | 19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-17597A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565672 | ||||||
chr1:206565675
|
G | C | 10 | a0001c0001t0005g0208a0001c0001t0007g0029a0001c0001t0007g0251others(7): Show | 13 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-17594G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565675 | ||||||
chr1:206565781
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580-17488C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565781 | ||||||
chr1:206565959
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0006g0309a0001c0001t0006g0319others(1): Show | 4 | HG01257.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-17310C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565959 | ||||||
chr1:206566018
|
A | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(309): Show | 327 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.580-17251A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566018 | ||||||
chr1:206566084
|
C | T | 4 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0008t0005g0106others(1): Show | 4 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-17185C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566084 | ||||||
chr1:206566196
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0003g0273 | 2 | NA18951.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.580-17073G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566196 | ||||||
chr1:206566230
|
C | T | 9 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0002t0003g0032others(6): Show | 9 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-17039C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566230 | ||||||
chr1:206566235
|
A | G | 1 | a0001c0002t0009g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-17034A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566235 | ||||||
chr1:206566276
|
T | G | 1 | a0001c0001t0018g0288 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580-16993T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566276 | ||||||
chr1:206566431
|
C | T | 16 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0208others(13): Show | 19 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-16838C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566431 | ||||||
chr1:206566437
|
T | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(160): Show | 173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.580-16832T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566437 | ||||||
chr1:206566541
|
G | T | 1 | a0001c0001t0001g0326 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580-16728G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566541 | ||||||
chr1:206566677
|
A | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(176): Show | 192 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.580-16592A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566677 | ||||||
chr1:206566691
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0282 | 2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.580-16578C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566691 | ||||||
chr1:206566692
|
G | A | 8 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0001t0009g0027others(5): Show | 8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-16577G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566692 | ||||||
chr1:206566731
|
A | C | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-16538A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566731 | ||||||
chr1:206566763
|
A | T | 1 | a0001c0002t0009g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.580-16506A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566763 | ||||||
chr1:206566794
|
C | T | 1 | a0001c0001t0010g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.580-16475C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566794 | ||||||
chr1:206567232
|
C | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.580-16037C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567232 | ||||||
chr1:206567420
|
T | C | 6 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-15849T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567420 | ||||||
chr1:206567472
|
A | G | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-15797A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567472 | ||||||
chr1:206567473
|
T | C | 2 | a0001c0002t0004g0262a0001c0002t0004g0284 | 2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.580-15796T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567473 | ||||||
chr1:206567712
|
A | G | 2 | a0004c0009t0001g0042a0004c0009t0001g0294 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.580-15557A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567712 | ||||||
chr1:206567714
|
G | A | 8 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0001t0009g0027others(5): Show | 8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-15555G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567714 | ||||||
chr1:206567915
|
C | T | 1 | a0001c0002t0006g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580-15354C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567915 | ||||||
chr1:206568018
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(1): Show | 4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-15251G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568018 | ||||||
chr1:206568218
|
G | C | 1 | a0001c0001t0007g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.580-15051G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568218 | ||||||
chr1:206568246
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.580-15023A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568246 | ||||||
chr1:206568266
|
T | C | 8 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0001t0009g0027others(5): Show | 8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-15003T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568266 | ||||||
chr1:206568324
|
C | T | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-14945C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568324 | ||||||
chr1:206568536
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.580-14733C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568536 | ||||||
chr1:206568589
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(176): Show | 192 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.580-14680A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568589 | ||||||
chr1:206568633
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580-14636G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568633 | ||||||
chr1:206568681
|
A | G | 8 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0001t0009g0027others(5): Show | 8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-14588A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568681 | ||||||
chr1:206568780
|
G | T | 1 | a0001c0002t0002g0150 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.580-14489G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568780 | ||||||
chr1:206568852
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(168): Show | 184 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.580-14417A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568852 | ||||||
chr1:206568856
|
T | C | 1 | a0001c0001t0002g0283 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.580-14413T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568856 | ||||||
chr1:206568889
|
G | A | 2 | a0001c0002t0009g0007a0001c0002t0009g0159 | 3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-14380G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568889 | ||||||
chr1:206568935
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(63): Show | 72 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.580-14334C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568935 | ||||||
chr1:206569074
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(152): Show | 165 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.580-14195C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569074 | ||||||
chr1:206569146
|
T | C | 1 | a0001c0002t0009g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-14123T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569146 | ||||||
chr1:206569371
|
A | C | 4 | a0001c0004t0003g0102a0001c0004t0030g0043a0002c0005t0003g0187others(1): Show | 4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-13898A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569371 | ||||||
chr1:206569431
|
C | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(172): Show | 188 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.580-13838C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569431 | ||||||
chr1:206569612
|
G | A | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.580-13657G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569612 | ||||||
chr1:206569739
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.580-13530T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569739 | ||||||
chr1:206569902
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-13367G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569902 | ||||||
chr1:206569906
|
T | A | 5 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0004t0024g0020others(2): Show | 5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-13363T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569906 | ||||||
chr1:206570061
|
C | G | 5 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0004t0024g0020others(2): Show | 5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-13208C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570061 | ||||||
chr1:206570078
|
CT | C | 25 | a0001c0001t0001g0028a0001c0001t0001g0126a0001c0001t0001g0141others(22): Show | 25 | HG00597.hp2 HG01109.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.580-13165delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | |||||
chr1:206570078
|
CTT | C | 97 | a0001c0001t0001g0060a0001c0001t0001g0078a0001c0001t0001g0088others(94): Show | 98 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.580-13166_580-1316 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | |||||
chr1:206570078
|
CTTT | C | 14 | a0001c0001t0001g0100a0001c0001t0002g0248a0001c0001t0003g0056others(11): Show | 14 | HG02698.hp2 HG02735.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-13167_580-1316 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | |||||
chr1:206570078
|
CTTTTTTT others(1): Show |
C | 77 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 86 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.580-13172_580-1316 others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | |||||
chr1:206570078
|
CTTTTTTT others(2): Show |
C | 89 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0139others(86): Show | 94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.580-13173_580-1316 others(13): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | |||||
chr1:206570078
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580-13174_580-1316 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | |||||
chr1:206570104
|
T | C | 3 | a0001c0001t0003g0214a0001c0001t0003g0215a0001c0001t0003g0216 | 3 | NA18979.hp1 NA18985.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.580-13165T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570104 | ||||||
chr1:206570112
|
A | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-13157A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570112 | ||||||
chr1:206570241
|
A | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-13028A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570241 | ||||||
chr1:206570248
|
C | G | 1 | a0001c0003t0005g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.580-13021C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570248 | ||||||
chr1:206570337
|
T | G | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-12932T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570337 | ||||||
chr1:206570464
|
C | T | 5 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0004t0024g0020others(2): Show | 5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-12805C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570464 | ||||||
chr1:206570498
|
A | G | 1 | a0001c0003t0005g0057 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.580-12771A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570498 | ||||||
chr1:206570710
|
C | T | 2 | a0001c0001t0005g0208a0001c0004t0005g0018 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-12559C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570710 | ||||||
chr1:206570732
|
T | C | 1 | a0001c0002t0004g0183 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.580-12537T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570732 | ||||||
chr1:206570863
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 183 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.580-12406C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570863 | ||||||
chr1:206570890
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.580-12379G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570890 | ||||||
chr1:206570960
|
T | C | 1 | a0001c0001t0011g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.580-12309T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570960 | ||||||
chr1:206571007
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580-12262A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571007 | ||||||
chr1:206571094
|
G | C | 2 | a0001c0001t0003g0289a0001c0001t0018g0288 | 2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.580-12175G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571094 | ||||||
chr1:206571260
|
T | A | 1 | a0001c0001t0002g0129 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.580-12009T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571260 | ||||||
chr1:206571283
|
G | GT | 163 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(160): Show | 173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.580-11975dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206571283 | |||||
chr1:206571283
|
GT | G | 6 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0006g0033others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-11975delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206571283 | |||||
chr1:206571302
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11967G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571302 | ||||||
chr1:206571305
|
A | T | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11964A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571305 | ||||||
chr1:206571306
|
G | C | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11963G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571306 | ||||||
chr1:206571412
|
G | A | 5 | a0001c0001t0006g0015a0001c0001t0006g0030a0001c0001t0006g0031others(2): Show | 6 | HG01891.hp1 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-11857G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571412 | ||||||
chr1:206571446
|
C | T | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11823C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571446 | ||||||
chr1:206571585
|
G | A | 7 | a0001c0001t0006g0015a0001c0001t0006g0030a0001c0001t0006g0031others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-11684G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571585 | ||||||
chr1:206572038
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.580-11231T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572038 | ||||||
chr1:206572185
|
C | A | 46 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(43): Show | 48 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.580-11084C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572185 | ||||||
chr1:206572195
|
CTTCT | C | 54 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(51): Show | 56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.580-11071_580-1106 others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206572195 | |||||
chr1:206572273
|
G | A | 8 | a0001c0001t0007g0029a0001c0001t0007g0251a0001c0001t0007g0252others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-10996G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572273 | ||||||
chr1:206572297
|
C | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-10972C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572297 | ||||||
chr1:206572397
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(166): Show | 182 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.580-10872T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572397 | ||||||
chr1:206572468
|
G | T | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-10801G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572468 | ||||||
chr1:206572469
|
T | A | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-10800T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572469 | ||||||
chr1:206572510
|
C | T | 1 | a0001c0001t0003g0257 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.580-10759C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572510 | ||||||
chr1:206572606
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0317a0001c0001t0005g0039others(4): Show | 7 | HG01952.hp2 HG01978.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-10663C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572606 | ||||||
chr1:206572650
|
C | T | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-10619C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572650 | ||||||
chr1:206572667
|
C | T | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-10602C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572667 | ||||||
chr1:206572673
|
T | C | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-10596T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572673 | ||||||
chr1:206572797
|
A | G | 30 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(27): Show | 31 | HG00558.hp2 HG00642.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-10472A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572797 | ||||||
chr1:206572855
|
A | G | 1 | a0001c0001t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.580-10414A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572855 | ||||||
chr1:206572908
|
C | T | 1 | a0001c0001t0017g0044 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.580-10361C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572908 | ||||||
chr1:206572909
|
G | A | 8 | a0001c0002t0004g0169a0001c0002t0004g0170a0001c0002t0004g0171others(5): Show | 8 | HG02129.hp2 HG02165.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-10360G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572909 | ||||||
chr1:206573024
|
C | G | 1 | a0001c0001t0005g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.580-10245C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573024 | ||||||
chr1:206573042
|
G | A | 1 | a0001c0001t0003g0094 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.580-10227G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573042 | ||||||
chr1:206573062
|
C | T | 5 | a0001c0001t0013g0002a0001c0001t0013g0049a0001c0001t0013g0050others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-10207C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573062 | ||||||
chr1:206573063
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.580-10206G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573063 | ||||||
chr1:206573094
|
T | C | 1 | a0001c0002t0006g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580-10175T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573094 | ||||||
chr1:206573116
|
G | C | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-10153G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573116 | ||||||
chr1:206573261
|
A | C | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.580-10008A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573261 | ||||||
chr1:206573537
|
A | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.580-9732A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573537 | ||||||
chr1:206573713
|
A | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(166): Show | 182 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.580-9556A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573713 | ||||||
chr1:206573721
|
T | C | 1 | a0001c0001t0011g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.580-9548T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573721 | ||||||
chr1:206573923
|
C | G | 5 | a0001c0001t0001g0036a0001c0001t0012g0160a0002c0005t0001g0184others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-9346C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573923 | ||||||
chr1:206574048
|
A | G | 132 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(129): Show | 134 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.580-9221A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574048 | ||||||
chr1:206574130
|
A | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(298): Show | 316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.580-9139A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574130 | ||||||
chr1:206574375
|
C | T | 1 | a0001c0001t0004g0250 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.580-8894C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574375 | ||||||
chr1:206574456
|
C | G | 2 | a0001c0002t0015g0244a0001c0002t0015g0321 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.580-8813C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574456 | ||||||
chr1:206574617
|
G | A | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-8652G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574617 | ||||||
chr1:206574853
|
C | CT | 58 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0077others(55): Show | 60 | HG00423.hp1 HG01175.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.580-8392dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206574853 | |||||
chr1:206574853
|
CT | C | 136 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(133): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.580-8392delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206574853 | |||||
chr1:206574853
|
CTT | C | 7 | a0001c0001t0003g0090a0001c0001t0003g0147a0001c0001t0005g0208others(4): Show | 7 | HG01975.hp1 HG01993.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-8393_580-8392d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206574853 | |||||
chr1:206575008
|
C | T | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-8261C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575008 | ||||||
chr1:206575009
|
G | A | 2 | a0001c0001t0006g0015a0001c0001t0006g0314 | 3 | HG01891.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.580-8260G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575009 | ||||||
chr1:206575027
|
T | C | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-8242T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575027 | ||||||
chr1:206575039
|
T | TG | 148 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 158 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.580-8230_580-8229i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575039 | ||||||
chr1:206575039
|
T | TGTTTTTG | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-8230_580-8229i others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575039 | ||||||
chr1:206575097
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.580-8172C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575097 | ||||||
chr1:206575167
|
C | T | 1 | a0002c0013t0004g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.580-8102C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575167 | ||||||
chr1:206575339
|
CAG | C | 8 | a0001c0001t0007g0029a0001c0001t0007g0251a0001c0001t0007g0252others(5): Show | 11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-7928_580-7927d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206575339 | |||||
chr1:206575453
|
G | C | 2 | a0001c0001t0005g0225a0001c0008t0005g0106 | 2 | HG00099.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.580-7816G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575453 | ||||||
chr1:206575513
|
A | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(150): Show | 163 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.580-7756A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575513 | ||||||
chr1:206575583
|
C | T | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-7686C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575583 | ||||||
chr1:206575707
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.580-7562G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575707 | ||||||
chr1:206575790
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-7479G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575790 | ||||||
chr1:206575854
|
C | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(168): Show | 184 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.580-7415C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575854 | ||||||
chr1:206576009
|
A | T | 7 | a0001c0001t0006g0015a0001c0001t0006g0030a0001c0001t0006g0031others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-7260A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576009 | ||||||
chr1:206576196
|
C | T | 6 | a0001c0001t0002g0325a0001c0001t0010g0074a0001c0001t0010g0138others(3): Show | 6 | HG01361.hp2 HG02132.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-7073C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576196 | ||||||
chr1:206576202
|
C | T | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-7067C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576202 | ||||||
chr1:206576309
|
A | C | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-6960A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576309 | ||||||
chr1:206576360
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(298): Show | 317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.580-6909G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576360 | ||||||
chr1:206576839
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-6430T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576839 | ||||||
chr1:206576970
|
A | G | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-6299A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576970 | ||||||
chr1:206576974
|
T | C | 6 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-6295T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576974 | ||||||
chr1:206576978
|
A | AT | 194 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(191): Show | 207 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.580-6278dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206576978 | |||||
chr1:206576978
|
AT | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-6278delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206576978 | |||||
chr1:206577389
|
C | G | 15 | a0001c0002t0001g0066a0001c0002t0001g0120a0001c0002t0002g0150others(12): Show | 15 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.580-5880C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577389 | ||||||
chr1:206577443
|
AT | A | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0003g0242others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-5823delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206577443 | |||||
chr1:206577458
|
T | A | 1 | a0001c0004t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.580-5811T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577458 | ||||||
chr1:206577564
|
T | C | 1 | a0001c0007t0002g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580-5705T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577564 | ||||||
chr1:206577672
|
C | T | 1 | a0001c0001t0003g0257 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.580-5597C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577672 | ||||||
chr1:206577673
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-5596G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577673 | ||||||
chr1:206577776
|
A | G | 2 | a0001c0001t0005g0208a0001c0004t0005g0018 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-5493A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577776 | ||||||
chr1:206577831
|
G | C | 319 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(316): Show | 335 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.580-5438G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577831 | ||||||
chr1:206577980
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(283): Show | 299 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.580-5289C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577980 | ||||||
chr1:206578069
|
T | TA | 142 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.580-5192dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578069 | |||||
chr1:206578073
|
A | AT | 6 | a0001c0001t0002g0325a0001c0001t0010g0074a0001c0001t0010g0138others(3): Show | 6 | HG01361.hp2 HG02132.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-5196_580-5195i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578073 | ||||||
chr1:206578103
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-5166G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578103 | ||||||
chr1:206578115
|
AC | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 74 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.580-5153delC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578115 | ||||||
chr1:206578174
|
T | C | 1 | a0001c0001t0003g0289 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.580-5095T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578174 | ||||||
chr1:206578202
|
G | C | 9 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-5067G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578202 | ||||||
chr1:206578222
|
CA | C | 19 | a0001c0001t0001g0052a0001c0001t0001g0086a0001c0001t0001g0121others(16): Show | 20 | HG01515.hp1 HG01515.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-5036delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578222 | |||||
chr1:206578232
|
A | AG | 36 | a0001c0001t0001g0269a0001c0001t0002g0012a0001c0001t0002g0013others(33): Show | 38 | HG00423.hp1 HG01175.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.580-5037_580-5036i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | ||||||
chr1:206578232
|
A | AGTG | 14 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0299others(11): Show | 14 | HG00438.hp1 HG02647.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-5037_580-5036i others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | ||||||
chr1:206578232
|
A | AGTGTG | 3 | a0001c0001t0006g0030a0001c0001t0006g0031a0002c0005t0028g0209 | 3 | HG02055.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.580-5037_580-5036i others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | ||||||
chr1:206578232
|
A | AGTGTGTG others(4): Show |
1 | a0001c0001t0006g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.580-5037_580-5036i others(13): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | ||||||
chr1:206578232
|
AAGT | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 75 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.580-5036_580-5034d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | ||||||
chr1:206578233
|
A | AGAGT | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-5035_580-5034i others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578233
|
A | AGT | 18 | a0001c0001t0001g0196a0001c0001t0001g0207a0001c0001t0003g0041others(15): Show | 22 | HG00741.hp2 HG01884.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.580-5007_580-5006d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578233
|
A | AGTGT | 20 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0003g0056others(17): Show | 21 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.580-5009_580-5006d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578233
|
A | AGTGTGT | 16 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0317others(13): Show | 16 | HG00642.hp2 HG01358.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.580-5011_580-5006d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578233
|
A | AGTGTGTG others(1): Show |
35 | a0001c0001t0001g0111a0001c0001t0002g0203a0001c0001t0003g0022others(32): Show | 35 | HG00597.hp2 HG00609.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.580-5013_580-5006d others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578233
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0003g0124a0001c0001t0003g0148a0001c0001t0003g0289 | 3 | HG00621.hp1 HG02698.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.580-5015_580-5006d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578233
|
A | T | 57 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(54): Show | 60 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.580-5036A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578233 | ||||||
chr1:206578233
|
AGTGT | A | 4 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0008t0005g0106others(1): Show | 4 | HG00099.hp1 HG01978.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-5009_580-5006d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | |||||
chr1:206578260
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0003g0249a0001c0001t0003g0327 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.580-5006_580-5005i others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578260 | |||||
chr1:206578295
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.580-4974T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578295 | ||||||
chr1:206578477
|
C | T | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(14): Show | 20 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-4792C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578477 | ||||||
chr1:206578559
|
G | A | 1 | a0001c0003t0002g0233 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.580-4710G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578559 | ||||||
chr1:206578794
|
G | A | 1 | a0001c0001t0002g0012 | 2 | HG02300.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.580-4475G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578794 | ||||||
chr1:206578952
|
T | A | 1 | a0001c0001t0012g0322 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.580-4317T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578952 | ||||||
chr1:206579256
|
T | C | 1 | a0001c0002t0004g0316 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.580-4013T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579256 | ||||||
chr1:206579301
|
A | G | 2 | a0001c0002t0009g0007a0001c0002t0009g0159 | 3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-3968A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579301 | ||||||
chr1:206579333
|
C | T | 7 | a0001c0002t0003g0032a0001c0002t0003g0034a0001c0002t0003g0242others(4): Show | 7 | HG01109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-3936C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579333 | ||||||
chr1:206579339
|
C | G | 1 | a0001c0001t0002g0261 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.580-3930C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579339 | ||||||
chr1:206579396
|
G | T | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3873G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579396 | ||||||
chr1:206579400
|
C | T | 2 | a0001c0002t0009g0007a0001c0002t0009g0159 | 3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-3869C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579400 | ||||||
chr1:206579514
|
G | A | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-3755G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579514 | ||||||
chr1:206579515
|
T | G | 1 | a0001c0001t0003g0312 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-3754T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579515 | ||||||
chr1:206579571
|
A | T | 1 | a0002c0013t0004g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.580-3698A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579571 | ||||||
chr1:206579636
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.580-3633G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579636 | ||||||
chr1:206579661
|
A | AT | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(14): Show | 20 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-3603dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206579661 | |||||
chr1:206579679
|
C | T | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-3590C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579679 | ||||||
chr1:206579697
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.580-3572C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579697 | ||||||
chr1:206579763
|
T | C | 1 | a0001c0001t0011g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.580-3506T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579763 | ||||||
chr1:206579804
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-3465A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579804 | ||||||
chr1:206579816
|
T | C | 9 | a0001c0001t0007g0029a0001c0001t0007g0251a0001c0001t0007g0252others(6): Show | 12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-3453T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579816 | ||||||
chr1:206579832
|
T | A | 9 | a0001c0001t0007g0029a0001c0001t0007g0251a0001c0001t0007g0252others(6): Show | 12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-3437T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579832 | ||||||
chr1:206579844
|
C | CGTGGCT | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3417_580-3412d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206579844 | |||||
chr1:206580145
|
G | T | 3 | a0001c0002t0009g0007a0001c0002t0009g0159a0001c0002t0026g0040 | 4 | HG02622.hp1 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3124G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580145 | ||||||
chr1:206580154
|
G | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.580-3115G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580154 | ||||||
chr1:206580418
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580-2851C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580418 | ||||||
chr1:206580443
|
T | C | 54 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(51): Show | 56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.580-2826T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580443 | ||||||
chr1:206580465
|
T | G | 47 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0141others(44): Show | 47 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.580-2804T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580465 | ||||||
chr1:206580631
|
G | A | 15 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0001t0007g0029others(12): Show | 18 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.580-2638G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580631 | ||||||
chr1:206580705
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-2564G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580705 | ||||||
chr1:206580736
|
T | C | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-2533T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580736 | ||||||
chr1:206580849
|
C | T | 2 | a0001c0001t0005g0208a0001c0004t0005g0018 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-2420C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580849 | ||||||
chr1:206580874
|
G | C | 2 | a0001c0001t0005g0208a0001c0004t0005g0018 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-2395G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580874 | ||||||
chr1:206580883
|
C | T | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-2386C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580883 | ||||||
chr1:206580949
|
C | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.580-2320C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580949 | ||||||
chr1:206581014
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.580-2255C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581014 | ||||||
chr1:206581032
|
G | A | 8 | a0001c0001t0003g0245a0001c0001t0006g0015a0001c0001t0006g0030others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-2237G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581032 | ||||||
chr1:206581266
|
G | A | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-2003G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581266 | ||||||
chr1:206581295
|
T | C | 302 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(299): Show | 318 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.580-1974T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581295 | ||||||
chr1:206581427
|
G | A | 54 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(51): Show | 56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.580-1842G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581427 | ||||||
chr1:206581458
|
G | A | 8 | a0001c0001t0003g0245a0001c0001t0006g0015a0001c0001t0006g0030others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-1811G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581458 | ||||||
chr1:206581561
|
T | C | 291 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(288): Show | 307 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(304): Show |
intron_variant | MODIFIER | c.580-1708T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581561 | ||||||
chr1:206581562
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.580-1707G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581562 | ||||||
chr1:206581596
|
A | AAAAG | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0005g0039others(14): Show | 20 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-1659_580-1656d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206581596 | |||||
chr1:206581622
|
CAG | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 74 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.580-1638_580-1637d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206581622 | |||||
chr1:206581638
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-1631A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581638 | ||||||
chr1:206581672
|
G | GAAAAGAA others(5): Show |
2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-1597_580-1596i others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581672 | ||||||
chr1:206581672
|
G | GGAAAGAA others(1): Show |
23 | a0001c0001t0003g0245a0001c0001t0005g0039a0001c0001t0005g0165others(20): Show | 27 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-1591_580-1584d others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206581672 | |||||
chr1:206581676
|
A | G | 1 | a0001c0001t0002g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580-1593A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581676 | ||||||
chr1:206581734
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.580-1535G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581734 | ||||||
chr1:206581797
|
G | A | 4 | a0001c0001t0009g0027a0001c0001t0009g0048a0001c0001t0009g0054others(1): Show | 4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1472G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581797 | ||||||
chr1:206581824
|
G | T | 8 | a0001c0001t0003g0245a0001c0001t0006g0015a0001c0001t0006g0030others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-1445G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581824 | ||||||
chr1:206581883
|
G | C | 5 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0008t0005g0106others(2): Show | 5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-1386G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581883 | ||||||
chr1:206581914
|
A | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.580-1355A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581914 | ||||||
chr1:206581920
|
C | T | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-1349C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581920 | ||||||
chr1:206581921
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.580-1348G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581921 | ||||||
chr1:206581922
|
TC | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0299others(7): Show | 10 | HG01358.hp2 HG02083.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-1346delC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581922 | ||||||
chr1:206581945
|
A | G | 1 | a0001c0001t0021g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.580-1324A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581945 | ||||||
chr1:206582031
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.580-1238G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582031 | ||||||
chr1:206582056
|
T | C | 2 | a0001c0001t0005g0039a0001c0001t0005g0165 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-1213T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582056 | ||||||
chr1:206582515
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.580-754T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582515 | ||||||
chr1:206582535
|
G | A | 127 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0078others(124): Show | 129 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.580-734G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582535 | ||||||
chr1:206582651
|
G | A | 23 | a0001c0001t0003g0245a0001c0001t0005g0039a0001c0001t0005g0165others(20): Show | 27 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-618G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582651 | ||||||
chr1:206582679
|
T | C | 11 | a0001c0001t0001g0024a0001c0001t0002g0128a0001c0001t0002g0129others(8): Show | 12 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-590T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582679 | ||||||
chr1:206582745
|
C | G | 8 | a0001c0001t0003g0245a0001c0001t0006g0015a0001c0001t0006g0030others(5): Show | 9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-524C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582745 | ||||||
chr1:206582870
|
G | A | 16 | a0001c0001t0001g0269a0001c0001t0002g0021a0001c0001t0002g0096others(13): Show | 16 | HG00438.hp1 NA18612.hp2 NA18948.hp1 others(13): Show |
intron_variant | MODIFIER | c.580-399G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582870 | ||||||
chr1:206583062
|
A | G | 1 | a0006c0014t0001g0080 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.580-207A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583062 | ||||||
chr1:206583130
|
C | T | 15 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0001t0007g0029others(12): Show | 18 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.580-139C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583130 | ||||||
chr1:206583181
|
T | C | 1 | a0001c0001t0002g0279 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.580-88T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583181 | ||||||
chr1:206583202
|
C | T | 5 | a0001c0001t0005g0045a0001c0001t0005g0225a0001c0008t0005g0106others(2): Show | 5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-67C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583202 | ||||||
chr1:206583401
|
A | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.690+22A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583401 | ||||||
chr1:206583497
|
C | T | 2 | a0001c0001t0005g0208a0001c0004t0005g0018 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+118C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583497 | ||||||
chr1:206583738
|
C | T | 54 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0269others(51): Show | 56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.690+359C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583738 | ||||||
chr1:206583773
|
G | A | 15 | a0001c0001t0005g0039a0001c0001t0005g0165a0001c0001t0007g0029others(12): Show | 18 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+394G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583773 | ||||||
chr1:206583792
|
C | T | 1 | a0001c0004t0024g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.690+413C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583792 | ||||||
chr1:206584071
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.691-316A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206584071 | ||||||
chr1:206584099
|
C | A | 7 | a0001c0001t0006g0015a0001c0001t0006g0030a0001c0001t0006g0031others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-288C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206584099 | ||||||
chr1:206584116
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.691-271C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206584116 | ||||||
chr1:206584745
|
A | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0047others(81): Show | 85 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.988+61A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206584745 | ||||||
chr1:206584760
|
G | A | 7 | a0001c0001t0002g0325a0001c0001t0005g0219a0001c0001t0010g0074others(4): Show | 7 | HG01361.hp2 HG02132.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+76G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206584760 | ||||||
chr1:206584824
|
A | G | 1 | a0001c0002t0004g0175 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.988+140A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206584824 | ||||||
chr1:206584883
|
CAGGAAAA others(9): Show |
C | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.988+203_988+218del others(16): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 206584883 | |||||
chr1:206585161
|
A | C | 5 | a0001c0001t0009g0048a0001c0001t0009g0054a0001c0001t0009g0182others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-19A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206585161 | ||||||
chr1:206585641
|
C | T | 10 | a0001c0001t0005g0211a0001c0003t0005g0057a0001c0003t0005g0181others(7): Show | 10 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1104+346C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585641 | ||||||
chr1:206585774
|
C | A | 150 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0021others(147): Show | 156 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.1104+479C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585774 | ||||||
chr1:206585843
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1104+548C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585843 | ||||||
chr1:206585994
|
C | T | 1 | a0001c0002t0026g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1104+699C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585994 | ||||||
chr1:206586266
|
A | C | 199 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0016others(196): Show | 209 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1105-560A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586266 | ||||||
chr1:206586290
|
A | G | 199 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0016others(196): Show | 209 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1105-536A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586290 | ||||||
chr1:206586305
|
G | C | 74 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0022others(71): Show | 77 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1105-521G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586305 | ||||||
chr1:206586451
|
G | A | 77 | a0001c0001t0001g0293a0001c0001t0003g0005a0001c0001t0003g0008others(74): Show | 80 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1105-375G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586451 | ||||||
chr1:206586532
|
T | C | 234 | a0001c0001t0001g0179a0001c0001t0002g0012a0001c0001t0002g0013others(231): Show | 244 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1105-294T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586532 | ||||||
chr1:206586643
|
G | A | 74 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0021others(71): Show | 77 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1105-183G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586643 | ||||||
chr1:206586816
|
C | T | 1 | a0001c0008t0005g0107 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1105-10C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586816 |