geneid | 10056 |
---|---|
ensemblid | ENSG00000116120.11 |
hgncid | 17800 |
symbol | FARSB |
name | phenylalanyl-tRNA synthetase subunit beta |
refseq_nuc | NM_005687.5 |
refseq_prot | NP_005678.3 |
ensembl_nuc | ENST00000281828.8 |
ensembl_prot | ENSP00000281828.6 |
mane_status | MANE Select |
chr | chr2 |
start | 222566899 |
end | 222656092 |
strand | - |
ver | v1.2 |
region | chr2:222566899-222656092 |
region5000 | chr2:222561899-222661092 |
regionname0 | FARSB_chr2_222566899_222656092 |
regionname5000 | FARSB_chr2_222561899_222661092 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 589 | 285 | 46 | 50 | 138 | 12 | 38 | 112 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002 | 1/0 | 589 | 56 | 37 | 9 | 4 | 0 | 5 | 2 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0003 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0004 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0005 | 0/0 | 589 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1770 | 283 | 46 | 50 | 137 | 12 | 37 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
c0002 | 1/0 | 1770 | 56 | 37 | 9 | 4 | 0 | 5 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
c0003 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
c0004 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
c0005 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
c0006 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
c0007 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4992 | 84 | 9 | 13 | 49 | 3 | 10 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0002 | 0/0 | 4992 | 76 | 0 | 10 | 56 | 1 | 9 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0003 | 0/1 | 5000 | 57 | 8 | 13 | 20 | 4 | 11 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0004 | 1/0 | 4992 | 36 | 18 | 8 | 4 | 0 | 5 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0005 | 0/0 | 4991 | 15 | 10 | 2 | 2 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0006 | 0/0 | 4992 | 14 | 14 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0007 | 0/0 | 4992 | 8 | 0 | 4 | 0 | 1 | 3 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0008 | 0/0 | 5001 | 7 | 6 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0009 | 0/0 | 4991 | 5 | 5 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0010 | 0/0 | 4991 | 4 | 3 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0011 | 0/0 | 4992 | 4 | 3 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0012 | 0/0 | 5000 | 3 | 3 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0013 | 0/0 | 5001 | 2 | 0 | 0 | 0 | 2 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0014 | 0/0 | 5001 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0015 | 0/0 | 5000 | 2 | 0 | 2 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0016 | 0/0 | 4992 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0017 | 0/0 | 4993 | 2 | 0 | 0 | 1 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0018 | 0/0 | 4992 | 2 | 0 | 0 | 0 | 0 | 2 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0019 | 0/0 | 4992 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0020 | 0/0 | 4992 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0021 | 0/0 | 5000 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0022 | 0/0 | 5000 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0023 | 0/0 | 5000 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0024 | 0/0 | 4992 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0025 | 0/0 | 4992 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0026 | 0/0 | 4992 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0027 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0028 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0029 | 0/0 | 4992 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0030 | 0/0 | 4992 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0031 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0032 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0033 | 0/0 | 4992 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0034 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
t0035 | 0/0 | 4993 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1770 | 283 | 46 | 50 | 137 | 12 | 37 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0004 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0007 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002c0002 | 1/0 | 1770 | 56 | 37 | 9 | 4 | 0 | 5 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0003c0003 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0004c0005 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0005c0006 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6761 | 83 | 9 | 13 | 49 | 3 | 9 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0002 | 0/0 | 6761 | 74 | 0 | 10 | 55 | 1 | 8 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0003 | 0/1 | 6769 | 57 | 8 | 13 | 20 | 4 | 11 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0005 | 0/0 | 6760 | 15 | 10 | 2 | 2 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0007 | 0/0 | 6761 | 8 | 0 | 4 | 0 | 1 | 3 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0008 | 0/0 | 6770 | 7 | 6 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0010 | 0/0 | 6760 | 4 | 3 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0011 | 0/0 | 6761 | 4 | 3 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0012 | 0/0 | 6769 | 3 | 3 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0013 | 0/0 | 6770 | 2 | 0 | 0 | 0 | 2 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0014 | 0/0 | 6770 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0015 | 0/0 | 6769 | 2 | 0 | 2 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0016 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0017 | 0/0 | 6762 | 2 | 0 | 0 | 1 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0018 | 0/0 | 6761 | 2 | 0 | 0 | 0 | 0 | 2 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0019 | 0/0 | 6761 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0020 | 0/0 | 6761 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0021 | 0/0 | 6769 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0022 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0023 | 0/0 | 6769 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0025 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0026 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0027 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0029 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0030 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0031 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0032 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0033 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0001t0034 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0004t0002 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0001c0007t0002 | 0/0 | 6761 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002c0002t0004 | 1/0 | 6761 | 35 | 17 | 8 | 4 | 0 | 5 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002c0002t0006 | 0/0 | 6761 | 14 | 14 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002c0002t0009 | 0/0 | 6760 | 5 | 5 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002c0002t0024 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0002c0002t0028 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0003c0003t0004 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0004c0005t0001 | 0/0 | 6761 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
a0005c0006t0035 | 0/0 | 6762 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | copy fasta | chr2 | 222561899 | 222661092 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0010g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0010g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0011g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0011g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0013g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0013g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0014g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0014g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0015g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0015g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0017g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0017g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0018g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0018g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0019g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0019g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0020g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0021g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0022g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0023g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0025g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0026g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0029g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0030g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0031g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0032g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0033g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0001t0034g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0001c0007t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0009g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0024g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0002c0002t0028g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0003c0003t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0004c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
a0005c0006t0035g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0013 | g0292 | EUR | GBR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0038 | EUR | GBR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00280 | hp1 | a0001 | c0001 | t0013 | g0285 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0037 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0023 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0215 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00597 | hp2 | a0001 | c0001 | t0033 | g0137 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0304 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00642 | hp1 | a0002 | c0002 | t0004 | g0190 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0138 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00735 | hp2 | a0001 | c0001 | t0034 | g0163 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00741 | hp1 | a0002 | c0002 | t0004 | g0196 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0042 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0134 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01106 | hp2 | a0001 | c0001 | t0031 | g0136 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0303 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01175 | hp1 | a0001 | c0001 | t0022 | g0040 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01192 | hp2 | a0002 | c0002 | t0004 | g0207 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01243 | hp1 | a0002 | c0002 | t0004 | g0197 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01255 | hp2 | a0001 | c0001 | t0015 | g0066 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0087 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01257 | hp1 | a0002 | c0002 | t0028 | g0208 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01261 | hp1 | a0002 | c0002 | t0004 | g0205 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01346 | hp2 | a0002 | c0002 | t0004 | g0201 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01358 | hp1 | a0002 | c0002 | t0004 | g0206 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0320 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01433 | hp2 | a0001 | c0001 | t0032 | g0142 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01515 | hp1 | a0001 | c0001 | t0017 | g0255 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0047 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01884 | hp1 | a0001 | c0001 | t0014 | g0289 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0307 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01891 | hp1 | a0002 | c0002 | t0006 | g0213 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01928 | hp1 | a0005 | c0006 | t0035 | g0299 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0314 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02015 | hp1 | a0001 | c0001 | t0020 | g0020 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02040 | hp2 | a0001 | c0001 | t0020 | g0020 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02055 | hp1 | a0002 | c0002 | t0004 | g0161 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02074 | hp2 | a0002 | c0002 | t0004 | g0187 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02132 | hp2 | a0002 | c0002 | t0004 | g0012 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02145 | hp1 | a0002 | c0002 | t0006 | g0170 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02145 | hp2 | a0002 | c0002 | t0004 | g0210 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CDX | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02155 | hp2 | a0001 | c0001 | t0026 | g0244 | EAS | CDX | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0286 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0185 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02258 | hp1 | a0002 | c0002 | t0009 | g0176 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0301 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02280 | hp2 | a0002 | c0002 | t0006 | g0186 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02293 | hp1 | a0002 | c0002 | t0004 | g0012 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02451 | hp1 | a0002 | c0002 | t0006 | g0174 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0311 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02602 | hp1 | a0001 | c0001 | t0023 | g0071 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02622 | hp1 | a0002 | c0002 | t0004 | g0202 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02622 | hp2 | a0002 | c0002 | t0006 | g0298 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02630 | hp1 | a0002 | c0002 | t0009 | g0011 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0291 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02647 | hp1 | a0003 | c0003 | t0004 | g0160 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02647 | hp2 | a0002 | c0002 | t0006 | g0175 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0135 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02698 | hp1 | a0001 | c0001 | t0007 | g0139 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02698 | hp2 | a0002 | c0002 | t0004 | g0193 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02717 | hp1 | a0002 | c0002 | t0004 | g0014 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0308 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02723 | hp1 | a0002 | c0002 | t0004 | g0162 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0302 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02735 | hp2 | a0002 | c0002 | t0004 | g0211 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02738 | hp2 | a0002 | c0002 | t0004 | g0195 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02809 | hp2 | a0002 | c0002 | t0006 | g0212 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02886 | hp1 | a0002 | c0002 | t0006 | g0297 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02886 | hp2 | a0002 | c0002 | t0024 | g0180 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02922 | hp1 | a0002 | c0002 | t0009 | g0171 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02922 | hp2 | a0002 | c0002 | t0004 | g0199 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0191 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02970 | hp2 | a0002 | c0002 | t0006 | g0173 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0283 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0312 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0288 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0317 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0305 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0293 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03139 | hp2 | a0002 | c0002 | t0004 | g0192 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03195 | hp2 | a0002 | c0002 | t0004 | g0013 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03209 | hp1 | a0002 | c0002 | t0004 | g0204 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03225 | hp1 | a0002 | c0002 | t0006 | g0010 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0316 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0306 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03491 | hp1 | a0001 | c0001 | t0018 | g0281 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03492 | hp1 | a0001 | c0001 | t0018 | g0282 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0313 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03540 | hp2 | a0002 | c0002 | t0004 | g0013 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03579 | hp1 | a0002 | c0002 | t0006 | g0181 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03579 | hp2 | a0002 | c0002 | t0009 | g0178 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03710 | hp1 | a0002 | c0002 | t0004 | g0198 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03831 | hp1 | a0001 | c0001 | t0008 | g0072 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03834 | hp1 | a0001 | c0001 | t0007 | g0153 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03927 | hp2 | a0002 | c0002 | t0004 | g0194 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04199 | hp1 | a0004 | c0005 | t0001 | g0133 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04199 | hp2 | a0001 | c0007 | t0002 | g0144 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0300 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18522 | hp2 | a0002 | c0002 | t0004 | g0200 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18906 | hp1 | a0002 | c0002 | t0006 | g0179 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18942 | hp2 | a0001 | c0001 | t0019 | g0169 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18967 | hp1 | a0001 | c0001 | t0017 | g0182 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18968 | hp2 | a0001 | c0001 | t0019 | g0249 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18974 | hp2 | a0001 | c0001 | t0027 | g0232 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18987 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18999 | hp1 | a0001 | c0001 | t0029 | g0272 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19011 | hp1 | a0001 | c0001 | t0030 | g0131 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0203 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0310 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19043 | hp1 | a0002 | c0002 | t0004 | g0172 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19043 | hp2 | a0002 | c0002 | t0004 | g0014 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19054 | hp1 | a0001 | c0001 | t0025 | g0217 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19070 | hp2 | a0002 | c0002 | t0004 | g0189 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19074 | hp1 | a0001 | c0004 | t0002 | g0100 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA19240 | hp2 | a0002 | c0002 | t0004 | g0209 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ASW | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0290 | AFR | ASW | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0081 | EUR | TSI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | GIH | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA20905 | hp2 | a0001 | c0001 | t0021 | g0039 | SAS | GIH | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02109 | hp1 | a0002 | c0002 | t0006 | g0177 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0309 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02486 | hp1 | a0002 | c0002 | t0009 | g0011 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03471 | hp1 | a0002 | c0002 | t0006 | g0010 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | USA | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
HG06807 | hp2 | a0001 | c0001 | t0016 | g0184 | AFR | USA | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA18955 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0063 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0043 | REF | REF | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0004 | g0222 | REF | REF | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222571888
|
C | T | 3 | a0001a0004a0005 | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
missense_variant | MODERATE | c.1753G>A | p.Val585Ile | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1772/6761 | 1753/1770 | 585/589 | chr2 | 222571888 | ||
chr2:222613814
|
T | C | 1 | a0004 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1459A>G | p.Thr487Ala | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/17 | 1478/6761 | 1459/1770 | 487/589 | chr2 | 222613814 | ||
chr2:222639607
|
T | C | 1 | a0005 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.428A>G | p.Gln143Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/17 | 447/6761 | 428/1770 | 143/589 | chr2 | 222639607 | ||
chr2:222639655
|
C | T | 1 | a0003 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.380G>A | p.Arg127His | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/17 | 399/6761 | 380/1770 | 127/589 | chr2 | 222639655 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222572000
|
T | G | 1 | a0001c0004 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.1641A>C | p.Arg547Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1660/6761 | 1641/1770 | 547/589 | chr2 | 222572000 | ||
chr2:222623700
|
G | T | 1 | a0005c0006 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.1201C>A | p.Arg401Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/17 | 1220/6761 | 1201/1770 | 401/589 | chr2 | 222623700 | ||
chr2:222642852
|
T | G | 1 | a0001c0007 | 1 | HG04199.hp2 | splice_region_variant&synonymous_variant | LOW | c.268A>C | p.Arg90Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/17 | 287/6761 | 268/1770 | 90/589 | chr2 | 222642852 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222567060
|
T | A | 1 | a0001c0001t0032 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4811A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4811 | chr2 | 222567060 | |||||
chr2:222567181
|
A | G | 1 | a0001c0001t0026 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4690T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4690 | chr2 | 222567181 | |||||
chr2:222567303
|
A | C | 1 | a0001c0001t0015 | 2 | HG01081.hp1 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4568T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4568 | chr2 | 222567303 | |||||
chr2:222567378
|
T | C | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(7): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*4493A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4493 | chr2 | 222567378 | |||||
chr2:222567785
|
T | C | 1 | a0001c0001t0023 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4086A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4086 | chr2 | 222567785 | |||||
chr2:222567899
|
A | G | 1 | a0005c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3972 | chr2 | 222567899 | |||||
chr2:222567957
|
A | C | 1 | a0005c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3914T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3914 | chr2 | 222567957 | |||||
chr2:222568110
|
AC | A | 2 | a0001c0001t0005a0001c0001t0010 | 19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3760delG | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3760 | chr2 | 222568110 | |||||
chr2:222568160
|
A | T | 1 | a0001c0001t0018 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3711T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3711 | chr2 | 222568160 | |||||
chr2:222568233
|
GT | G | 2 | a0001c0001t0027a0002c0002t0009 | 6 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3637delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3637 | chr2 | 222568233 | |||||
chr2:222568248
|
T | C | 5 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(2): Show | 64 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3623A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3623 | chr2 | 222568248 | |||||
chr2:222568277
|
C | T | 1 | a0005c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3594G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3594 | chr2 | 222568277 | |||||
chr2:222568325
|
T | C | 1 | a0005c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3546A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3546 | chr2 | 222568325 | |||||
chr2:222568329
|
G | A | 1 | a0001c0001t0020 | 2 | HG02015.hp1 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3542C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3542 | chr2 | 222568329 | |||||
chr2:222568442
|
C | T | 10 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(7): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3429G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3429 | chr2 | 222568442 | |||||
chr2:222568843
|
A | C | 1 | a0001c0001t0010 | 4 | HG00639.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3028T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3028 | chr2 | 222568843 | |||||
chr2:222568986
|
G | T | 1 | a0001c0001t0021 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2885C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2885 | chr2 | 222568986 | |||||
chr2:222568989
|
G | T | 1 | a0005c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2882C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2882 | chr2 | 222568989 | |||||
chr2:222569096
|
G | C | 1 | a0001c0001t0012 | 3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2775C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2775 | chr2 | 222569096 | |||||
chr2:222569639
|
A | G | 1 | a0001c0001t0025 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2232T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2232 | chr2 | 222569639 | |||||
chr2:222569871
|
G | A | 1 | a0002c0002t0028 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2000 | chr2 | 222569871 | |||||
chr2:222569932
|
G | A | 1 | a0001c0001t0019 | 2 | NA18942.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1939C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1939 | chr2 | 222569932 | |||||
chr2:222570049
|
T | C | 3 | a0001c0001t0007a0001c0001t0031a0001c0001t0033 | 10 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1822A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1822 | chr2 | 222570049 | |||||
chr2:222570101
|
T | C | 1 | a0005c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1770 | chr2 | 222570101 | |||||
chr2:222570296
|
G | A | 1 | a0001c0001t0033 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1575C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1575 | chr2 | 222570296 | |||||
chr2:222570328
|
T | G | 4 | a0001c0001t0008a0001c0001t0013a0001c0001t0014others(1): Show | 12 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1543 | chr2 | 222570328 | |||||
chr2:222570337
|
G | A | 10 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(7): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1534C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1534 | chr2 | 222570337 | |||||
chr2:222570354
|
A | C | 9 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(6): Show | 99 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1517T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1517 | chr2 | 222570354 | |||||
chr2:222570528
|
C | CT | 5 | a0001c0001t0008a0001c0001t0013a0001c0001t0014others(2): Show | 14 | HG00140.hp1 HG00280.hp1 HG01515.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1342dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1342 | chr2 | 222570528 | |||||
chr2:222570721
|
C | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*1150G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1150 | chr2 | 222570721 | |||||
chr2:222570723
|
A | T | 1 | a0001c0001t0014 | 2 | HG01884.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1148T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1148 | chr2 | 222570723 | |||||
chr2:222570799
|
A | T | 1 | a0001c0001t0031 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1072T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1072 | chr2 | 222570799 | |||||
chr2:222570932
|
C | T | 8 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(5): Show | 98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 939 | chr2 | 222570932 | |||||
chr2:222571153
|
A | G | 1 | a0002c0002t0024 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*718T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 718 | chr2 | 222571153 | |||||
chr2:222571222
|
T | A | 1 | a0001c0001t0029 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 649 | chr2 | 222571222 | |||||
chr2:222571465
|
C | CGAACTCA others(1): Show |
9 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(6): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*398_*405dupATGAGT others(2): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 405 | chr2 | 222571465 | |||||
chr2:222571639
|
C | T | 1 | a0001c0001t0030 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 232 | chr2 | 222571639 | |||||
chr2:222571683
|
C | T | 23 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(20): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*188G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 188 | chr2 | 222571683 | |||||
chr2:222571709
|
T | C | 9 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(6): Show | 99 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 162 | chr2 | 222571709 | |||||
chr2:222571867
|
A | G | 1 | a0001c0001t0013 | 2 | HG00140.hp1 HG00280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4 | chr2 | 222571867 | |||||
chr2:222656078
|
T | G | 4 | a0001c0001t0005a0001c0001t0010a0001c0001t0011others(1): Show | 24 | HG00639.hp2 HG01109.hp2 HG01361.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-5A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/17 | 5 | chr2 | 222656078 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:222572141
|
A | G | 70 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(67): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1619-119T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572141 | ||||||
chr2:222572153
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-131G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572153 | ||||||
chr2:222572437
|
A | T | 1 | a0001c0001t0017g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1619-415T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572437 | ||||||
chr2:222572461
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1619-439T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572461 | ||||||
chr2:222572625
|
A | G | 2 | a0002c0002t0004g0161a0003c0003t0004g0160 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1619-603T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572625 | ||||||
chr2:222572644
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1619-622T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572644 | ||||||
chr2:222573235
|
T | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-1213A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222573235 | ||||||
chr2:222573460
|
C | A | 2 | a0002c0002t0006g0010a0002c0002t0006g0177 | 3 | HG02109.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1619-1438G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222573460 | ||||||
chr2:222573789
|
C | T | 1 | a0001c0001t0005g0320 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1619-1767G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222573789 | ||||||
chr2:222574136
|
A | G | 1 | a0001c0001t0003g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1619-2114T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574136 | ||||||
chr2:222574160
|
C | CT | 75 | a0001c0001t0001g0140a0001c0001t0003g0001a0001c0001t0003g0003others(72): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1619-2139dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574160 | ||||||
chr2:222574160
|
CT | C | 7 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1619-2139delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574160 | ||||||
chr2:222574227
|
G | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-2205C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574227 | ||||||
chr2:222574237
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1619-2215A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574237 | ||||||
chr2:222574952
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1619-2930C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574952 | ||||||
chr2:222574980
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-2958G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574980 | ||||||
chr2:222575042
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-3020A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575042 | ||||||
chr2:222575182
|
G | C | 2 | a0002c0002t0006g0297a0002c0002t0006g0298 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1619-3160C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575182 | ||||||
chr2:222575222
|
T | C | 71 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(68): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1619-3200A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575222 | ||||||
chr2:222575454
|
A | T | 1 | a0001c0001t0003g0044 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1619-3432T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575454 | ||||||
chr2:222575561
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-3539C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575561 | ||||||
chr2:222575621
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-3599G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575621 | ||||||
chr2:222575735
|
C | T | 1 | a0002c0002t0004g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1619-3713G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575735 | ||||||
chr2:222575871
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0147 | 3 | HG01070.hp1 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1619-3849C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575871 | ||||||
chr2:222575977
|
CT | C | 74 | a0001c0001t0001g0141a0001c0001t0002g0233a0001c0001t0002g0245others(71): Show | 80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1619-3956delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575977 | ||||||
chr2:222575984
|
T | C | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1619-3962A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575984 | ||||||
chr2:222576001
|
A | G | 1 | a0001c0001t0005g0312 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-3979T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576001 | ||||||
chr2:222576171
|
C | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-4149G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576171 | ||||||
chr2:222576454
|
A | G | 2 | a0001c0001t0005g0320a0001c0001t0034g0163 | 2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1619-4432T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576454 | ||||||
chr2:222576519
|
T | A | 11 | a0001c0001t0008g0072a0001c0001t0008g0284a0001c0001t0008g0286others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1619-4497A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576519 | ||||||
chr2:222576854
|
C | T | 1 | a0002c0002t0006g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1619-4832G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576854 | ||||||
chr2:222577324
|
T | C | 5 | a0002c0002t0006g0170a0002c0002t0006g0181a0002c0002t0006g0186others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-5302A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577324 | ||||||
chr2:222577339
|
C | T | 3 | a0001c0001t0003g0041a0001c0001t0003g0070a0001c0001t0023g0071 | 3 | HG02602.hp1 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1619-5317G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577339 | ||||||
chr2:222577581
|
G | A | 59 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(56): Show | 65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1619-5559C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577581 | ||||||
chr2:222577587
|
G | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1619-5565C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577587 | ||||||
chr2:222577656
|
A | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-5634T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577656 | ||||||
chr2:222577677
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1619-5655G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577677 | ||||||
chr2:222577807
|
A | T | 81 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(78): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1619-5785T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577807 | ||||||
chr2:222577896
|
T | C | 59 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(56): Show | 65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1619-5874A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577896 | ||||||
chr2:222578071
|
T | G | 1 | a0002c0002t0004g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1619-6049A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578071 | ||||||
chr2:222578180
|
G | T | 16 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(13): Show | 18 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1619-6158C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578180 | ||||||
chr2:222578239
|
A | G | 1 | a0001c0001t0015g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1619-6217T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578239 | ||||||
chr2:222578299
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-6277T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578299 | ||||||
chr2:222578336
|
C | G | 1 | a0001c0001t0001g0008 | 2 | NA18982.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1619-6314G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578336 | ||||||
chr2:222578470
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1619-6448T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578470 | ||||||
chr2:222578795
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1619-6773A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578795 | ||||||
chr2:222578842
|
CG | C | 81 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(78): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1619-6821delC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578842 | ||||||
chr2:222578883
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-6861T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578883 | ||||||
chr2:222579042
|
T | C | 81 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(78): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1619-7020A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579042 | ||||||
chr2:222579104
|
T | TG | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-7083dupC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579104 | ||||||
chr2:222579120
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 5 | HG01496.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-7098T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579120 | ||||||
chr2:222579134
|
A | G | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1619-7112T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579134 | ||||||
chr2:222579141
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1619-7119G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579141 | ||||||
chr2:222579391
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1619-7369C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579391 | ||||||
chr2:222579649
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-7627T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579649 | ||||||
chr2:222579926
|
G | A | 5 | a0002c0002t0004g0172a0002c0002t0004g0192a0002c0002t0004g0203others(2): Show | 5 | HG02976.hp1 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-7904C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579926 | ||||||
chr2:222579941
|
A | G | 2 | a0001c0001t0002g0215a0001c0001t0002g0236 | 2 | HG00323.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1619-7919T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579941 | ||||||
chr2:222580031
|
A | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1619-8009T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580031 | ||||||
chr2:222580096
|
A | G | 64 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(61): Show | 70 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1619-8074T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580096 | ||||||
chr2:222580146
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1619-8124T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580146 | ||||||
chr2:222580201
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-8179G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580201 | ||||||
chr2:222580297
|
A | C | 1 | a0001c0001t0003g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1619-8275T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580297 | ||||||
chr2:222580494
|
C | CA | 12 | a0001c0001t0005g0312a0001c0001t0005g0313a0001c0001t0005g0314others(9): Show | 12 | HG00735.hp2 HG01361.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1619-8473dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580494 | ||||||
chr2:222580494
|
CA | C | 152 | a0001c0001t0001g0101a0001c0001t0001g0113a0001c0001t0001g0126others(149): Show | 164 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1619-8473delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580494 | ||||||
chr2:222580514
|
T | C | 3 | a0001c0001t0010g0021a0001c0001t0010g0304a0001c0001t0010g0305 | 4 | HG00639.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1619-8492A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580514 | ||||||
chr2:222580523
|
A | G | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1619-8501T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580523 | ||||||
chr2:222580663
|
C | A | 20 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(17): Show | 21 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1619-8641G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580663 | ||||||
chr2:222580676
|
C | T | 3 | a0002c0002t0006g0010a0002c0002t0006g0177a0002c0002t0024g0180 | 4 | HG02109.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1619-8654G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580676 | ||||||
chr2:222580697
|
A | G | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-8675T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580697 | ||||||
chr2:222580859
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1619-8837C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580859 | ||||||
chr2:222580902
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1619-8880A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580902 | ||||||
chr2:222580953
|
A | T | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1619-8931T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580953 | ||||||
chr2:222580957
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-8935C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580957 | ||||||
chr2:222580995
|
G | A | 14 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1619-8973C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580995 | ||||||
chr2:222581020
|
C | T | 22 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(19): Show | 23 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1619-8998G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581020 | ||||||
chr2:222581184
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-9162A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581184 | ||||||
chr2:222581243
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-9221C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581243 | ||||||
chr2:222581265
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-9243A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581265 | ||||||
chr2:222581383
|
A | G | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1619-9361T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581383 | ||||||
chr2:222581591
|
C | G | 1 | a0002c0002t0006g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1619-9569G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581591 | ||||||
chr2:222581609
|
C | T | 1 | a0001c0001t0011g0303 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1619-9587G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581609 | ||||||
chr2:222581700
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-9678G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581700 | ||||||
chr2:222581858
|
T | C | 6 | a0001c0001t0002g0219a0001c0001t0002g0225a0001c0001t0002g0226others(3): Show | 6 | HG01069.hp1 NA18973.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1619-9836A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581858 | ||||||
chr2:222582124
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1619-10102T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582124 | ||||||
chr2:222582193
|
T | G | 1 | a0001c0001t0003g0026 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1619-10171A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582193 | ||||||
chr2:222582437
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1619-10415T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582437 | ||||||
chr2:222582488
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1619-10466G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582488 | ||||||
chr2:222582562
|
T | C | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1619-10540A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582562 | ||||||
chr2:222582650
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1619-10628G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582650 | ||||||
chr2:222582651
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1619-10629C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582651 | ||||||
chr2:222582732
|
T | C | 1 | a0001c0001t0015g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1619-10710A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582732 | ||||||
chr2:222582835
|
G | A | 2 | a0001c0001t0002g0215a0001c0001t0002g0236 | 2 | HG00323.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1619-10813C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582835 | ||||||
chr2:222582874
|
G | A | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1619-10852C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582874 | ||||||
chr2:222582930
|
G | GA | 5 | a0001c0001t0002g0017a0001c0001t0002g0214a0001c0001t0002g0233others(2): Show | 6 | NA18942.hp2 NA18946.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1619-10909dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582930 | ||||||
chr2:222583556
|
C | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1619-11534G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583556 | ||||||
chr2:222583672
|
C | G | 2 | a0001c0001t0002g0253a0001c0001t0002g0258 | 2 | HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1619-11650G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583672 | ||||||
chr2:222583729
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-11707C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583729 | ||||||
chr2:222583733
|
G | C | 14 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1619-11711C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583733 | ||||||
chr2:222583780
|
T | C | 71 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(68): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1619-11758A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583780 | ||||||
chr2:222583874
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-11852G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583874 | ||||||
chr2:222584013
|
G | A | 4 | a0001c0001t0005g0312a0001c0001t0010g0021a0001c0001t0010g0304others(1): Show | 5 | HG00639.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-11991C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584013 | ||||||
chr2:222584231
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1619-12209A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584231 | ||||||
chr2:222584390
|
G | A | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1619-12368C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584390 | ||||||
chr2:222584423
|
G | A | 79 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(76): Show | 84 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1619-12401C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584423 | ||||||
chr2:222584431
|
T | C | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-12409A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584431 | ||||||
chr2:222584467
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0114 | 2 | NA18942.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1619-12445C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584467 | ||||||
chr2:222584526
|
C | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1619-12504G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584526 | ||||||
chr2:222584619
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-12597C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584619 | ||||||
chr2:222584726
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-12704G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584726 | ||||||
chr2:222584786
|
C | T | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1619-12764G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584786 | ||||||
chr2:222584819
|
G | A | 2 | a0001c0001t0003g0004a0001c0001t0003g0027 | 3 | HG00609.hp1 HG02155.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1619-12797C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584819 | ||||||
chr2:222584855
|
C | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-12833G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584855 | ||||||
chr2:222584977
|
G | A | 1 | a0001c0001t0005g0312 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-12955C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584977 | ||||||
chr2:222585083
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1619-13061A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585083 | ||||||
chr2:222585101
|
G | A | 1 | a0001c0001t0005g0312 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-13079C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585101 | ||||||
chr2:222585112
|
C | T | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1619-13090G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585112 | ||||||
chr2:222585137
|
C | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-13115G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585137 | ||||||
chr2:222585218
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1619-13196G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585218 | ||||||
chr2:222585225
|
A | G | 1 | a0002c0002t0004g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-13203T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585225 | ||||||
chr2:222585349
|
C | A | 1 | a0001c0001t0002g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1619-13327G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585349 | ||||||
chr2:222585487
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1619-13465G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585487 | ||||||
chr2:222585488
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-13466C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585488 | ||||||
chr2:222585624
|
G | C | 1 | a0002c0002t0004g0207 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1619-13602C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585624 | ||||||
chr2:222585754
|
G | T | 280 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1619-13732C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585754 | ||||||
chr2:222585772
|
A | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1619-13750T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585772 | ||||||
chr2:222585882
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1619-13860C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585882 | ||||||
chr2:222585925
|
G | C | 18 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(15): Show | 19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1619-13903C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585925 | ||||||
chr2:222585963
|
T | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1619-13941A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585963 | ||||||
chr2:222585994
|
A | T | 22 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(19): Show | 23 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1618+13934T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585994 | ||||||
chr2:222586146
|
A | T | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+13782T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586146 | ||||||
chr2:222586264
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+13664A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586264 | ||||||
chr2:222586369
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1618+13559T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586369 | ||||||
chr2:222586369
|
A | T | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+13559T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586369 | ||||||
chr2:222586384
|
C | T | 2 | a0001c0001t0011g0302a0001c0001t0011g0303 | 2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1618+13544G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586384 | ||||||
chr2:222586510
|
A | C | 1 | a0001c0001t0008g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1618+13418T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586510 | ||||||
chr2:222586611
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1618+13317G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586611 | ||||||
chr2:222586696
|
A | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+13232T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586696 | ||||||
chr2:222586806
|
A | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1618+13122T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586806 | ||||||
chr2:222587293
|
T | C | 3 | a0001c0001t0012g0036a0001c0001t0012g0062a0001c0001t0012g0063 | 3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1618+12635A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587293 | ||||||
chr2:222587312
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+12616C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587312 | ||||||
chr2:222587396
|
G | C | 1 | a0002c0002t0004g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+12532C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587396 | ||||||
chr2:222587579
|
T | C | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1618+12349A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587579 | ||||||
chr2:222587600
|
T | C | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+12328A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587600 | ||||||
chr2:222587727
|
T | C | 280 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1618+12201A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587727 | ||||||
chr2:222587765
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+12163C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587765 | ||||||
chr2:222587842
|
G | T | 1 | a0001c0001t0001g0110 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1618+12086C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587842 | ||||||
chr2:222588055
|
A | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1618+11873T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588055 | ||||||
chr2:222588171
|
T | C | 1 | a0002c0002t0006g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1618+11757A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588171 | ||||||
chr2:222588459
|
G | C | 4 | a0001c0001t0002g0247a0001c0001t0002g0261a0001c0001t0002g0262others(1): Show | 4 | HG00597.hp1 NA18957.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+11469C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588459 | ||||||
chr2:222588550
|
A | T | 1 | a0001c0001t0015g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1618+11378T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588550 | ||||||
chr2:222588630
|
C | T | 17 | a0001c0001t0003g0023a0001c0001t0003g0038a0001c0001t0003g0047others(14): Show | 17 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1618+11298G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588630 | ||||||
chr2:222588710
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1618+11218G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588710 | ||||||
chr2:222588915
|
C | T | 4 | a0002c0002t0009g0011a0002c0002t0009g0171a0002c0002t0009g0176others(1): Show | 5 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+11013G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588915 | ||||||
chr2:222588926
|
C | T | 10 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0024others(7): Show | 12 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1618+11002G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588926 | ||||||
chr2:222588980
|
T | G | 71 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(68): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1618+10948A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588980 | ||||||
chr2:222588993
|
G | A | 3 | a0001c0001t0012g0036a0001c0001t0012g0062a0001c0001t0012g0063 | 3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1618+10935C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588993 | ||||||
chr2:222589080
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0126 | 2 | HG02027.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1618+10848A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589080 | ||||||
chr2:222589528
|
T | TAAAGAGC others(312): Show |
2 | a0002c0002t0006g0297a0002c0002t0006g0298 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1618+10399_1618+10 others(325): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | ||||||
chr2:222589528
|
T | TAAAGAGC others(313): Show |
8 | a0002c0002t0006g0170a0002c0002t0006g0173a0002c0002t0006g0174others(5): Show | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618+10399_1618+10 others(326): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | ||||||
chr2:222589528
|
T | TAAAGAGC others(314): Show |
3 | a0002c0002t0006g0010a0002c0002t0006g0175a0002c0002t0006g0177 | 4 | HG02109.hp1 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618+10399_1618+10 others(327): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | ||||||
chr2:222589528
|
T | TAAAGAGC others(316): Show |
1 | a0002c0002t0024g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+10399_1618+10 others(329): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | ||||||
chr2:222589656
|
C | G | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+10272G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589656 | ||||||
chr2:222589733
|
C | T | 2 | a0001c0001t0005g0316a0001c0001t0005g0317 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1618+10195G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589733 | ||||||
chr2:222590066
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0122others(1): Show | 6 | NA18945.hp1 NA18955.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618+9862C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590066 | ||||||
chr2:222590085
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+9843T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590085 | ||||||
chr2:222590168
|
C | T | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(3): Show | 6 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618+9760G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590168 | ||||||
chr2:222590324
|
T | C | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1618+9604A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590324 | ||||||
chr2:222590363
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+9565G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590363 | ||||||
chr2:222590369
|
G | A | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1618+9559C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590369 | ||||||
chr2:222590380
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1618+9548C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590380 | ||||||
chr2:222590513
|
T | TA | 18 | a0001c0001t0002g0254a0001c0001t0005g0306a0001c0001t0005g0307others(15): Show | 19 | HG00639.hp2 HG01361.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1618+9414dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590513 | ||||||
chr2:222590548
|
C | CA | 8 | a0001c0001t0003g0025a0001c0001t0022g0040a0002c0002t0006g0181others(5): Show | 9 | HG01175.hp1 HG01928.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618+9379dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590548 | ||||||
chr2:222590548
|
CA | C | 18 | a0001c0001t0001g0141a0001c0001t0002g0216a0001c0001t0008g0284others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1618+9379delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590548 | ||||||
chr2:222590548
|
CAA | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1618+9378_1618+937 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590548 | ||||||
chr2:222590628
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+9300A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590628 | ||||||
chr2:222590645
|
G | A | 1 | a0001c0001t0002g0278 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1618+9283C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590645 | ||||||
chr2:222591049
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+8879A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591049 | ||||||
chr2:222591122
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1618+8806T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591122 | ||||||
chr2:222591158
|
G | A | 1 | a0002c0002t0004g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1618+8770C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591158 | ||||||
chr2:222591211
|
T | TA | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 113 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1618+8716dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591211 | ||||||
chr2:222591252
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+8676C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591252 | ||||||
chr2:222591269
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1618+8659A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591269 | ||||||
chr2:222591454
|
A | G | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+8474T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591454 | ||||||
chr2:222591461
|
A | G | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+8467T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591461 | ||||||
chr2:222591629
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+8299C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591629 | ||||||
chr2:222591839
|
A | T | 1 | a0001c0001t0029g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1618+8089T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591839 | ||||||
chr2:222592017
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+7911C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592017 | ||||||
chr2:222592133
|
T | C | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+7795A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592133 | ||||||
chr2:222592279
|
G | A | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+7649C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592279 | ||||||
chr2:222592356
|
C | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230 | 3 | HG01169.hp1 HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1618+7572G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592356 | ||||||
chr2:222592357
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+7571C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592357 | ||||||
chr2:222592415
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+7513G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592415 | ||||||
chr2:222592474
|
C | T | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1618+7454G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592474 | ||||||
chr2:222592505
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+7423A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592505 | ||||||
chr2:222592573
|
G | A | 1 | a0002c0002t0004g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1618+7355C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592573 | ||||||
chr2:222592618
|
A | G | 4 | a0001c0001t0008g0284a0001c0001t0008g0287a0001c0001t0014g0288others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618+7310T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592618 | ||||||
chr2:222592664
|
G | A | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+7264C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592664 | ||||||
chr2:222592682
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1618+7246A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592682 | ||||||
chr2:222592865
|
T | G | 4 | a0001c0001t0005g0312a0001c0001t0010g0021a0001c0001t0010g0304others(1): Show | 5 | HG00639.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+7063A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592865 | ||||||
chr2:222593044
|
G | A | 6 | a0001c0001t0005g0313a0001c0001t0005g0314a0001c0001t0005g0315others(3): Show | 6 | HG01361.hp1 HG01975.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618+6884C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593044 | ||||||
chr2:222593154
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+6774C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593154 | ||||||
chr2:222593197
|
C | T | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1618+6731G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593197 | ||||||
chr2:222593227
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1618+6701T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593227 | ||||||
chr2:222593309
|
T | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+6619A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593309 | ||||||
chr2:222593470
|
T | C | 11 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1618+6458A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593470 | ||||||
chr2:222593493
|
G | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0168a0001c0001t0002g0279 | 4 | NA18956.hp1 NA18966.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+6435C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593493 | ||||||
chr2:222593495
|
G | A | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+6433C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593495 | ||||||
chr2:222593511
|
G | A | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+6417C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593511 | ||||||
chr2:222593537
|
G | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1618+6391C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593537 | ||||||
chr2:222593721
|
A | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+6207T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593721 | ||||||
chr2:222593806
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1618+6122C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593806 | ||||||
chr2:222593846
|
T | G | 21 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(18): Show | 22 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1618+6082A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593846 | ||||||
chr2:222593853
|
C | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+6075G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593853 | ||||||
chr2:222593988
|
G | A | 1 | a0002c0002t0024g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+5940C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593988 | ||||||
chr2:222594014
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+5914G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594014 | ||||||
chr2:222594088
|
C | A | 2 | a0002c0002t0006g0212a0002c0002t0006g0213 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1618+5840G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594088 | ||||||
chr2:222594093
|
C | CA | 156 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 169 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1618+5834dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | ||||||
chr2:222594093
|
C | CAA | 85 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0097others(82): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1618+5833_1618+583 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | ||||||
chr2:222594093
|
C | CAAA | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0046others(9): Show | 12 | HG01175.hp1 HG01891.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1618+5832_1618+583 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | ||||||
chr2:222594093
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0227 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1618+5824_1618+583 others(15): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | ||||||
chr2:222594120
|
G | A | 2 | a0001c0001t0003g0074a0001c0001t0003g0080 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1618+5808C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594120 | ||||||
chr2:222594157
|
C | T | 7 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+5771G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594157 | ||||||
chr2:222594367
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+5561C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594367 | ||||||
chr2:222594447
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1618+5481A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594447 | ||||||
chr2:222594451
|
C | T | 1 | a0002c0002t0004g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1618+5477G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594451 | ||||||
chr2:222594771
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1618+5157G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594771 | ||||||
chr2:222594963
|
T | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 95 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1618+4965A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594963 | ||||||
chr2:222594987
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 8 | HG01496.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618+4941G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594987 | ||||||
chr2:222595086
|
T | C | 2 | a0002c0002t0004g0203a0002c0002t0004g0283 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1618+4842A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595086 | ||||||
chr2:222595322
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+4606T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595322 | ||||||
chr2:222595461
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+4467G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595461 | ||||||
chr2:222595579
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+4349G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595579 | ||||||
chr2:222595583
|
T | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1618+4345A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595583 | ||||||
chr2:222595677
|
GA | G | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+4250delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595677 | ||||||
chr2:222595704
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1618+4224C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595704 | ||||||
chr2:222595820
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+4108C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595820 | ||||||
chr2:222595921
|
C | CAT | 31 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0097others(28): Show | 34 | HG00423.hp2 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1618+4005_1618+400 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | ||||||
chr2:222595921
|
C | CATAT | 65 | a0001c0001t0001g0149a0001c0001t0002g0015a0001c0001t0002g0016others(62): Show | 70 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1618+4003_1618+400 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | ||||||
chr2:222595921
|
C | CATATAT | 11 | a0001c0001t0002g0215a0001c0001t0002g0218a0001c0001t0002g0231others(8): Show | 11 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1618+4001_1618+400 others(10): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | ||||||
chr2:222595921
|
C | CATATATA others(3): Show |
1 | a0001c0001t0002g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1618+3997_1618+400 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | ||||||
chr2:222596183
|
C | G | 2 | a0001c0001t0010g0304a0001c0001t0010g0305 | 2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1618+3745G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596183 | ||||||
chr2:222596283
|
G | A | 1 | a0001c0001t0003g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1618+3645C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596283 | ||||||
chr2:222596311
|
T | A | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1618+3617A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596311 | ||||||
chr2:222596392
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+3536T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596392 | ||||||
chr2:222596423
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+3505T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596423 | ||||||
chr2:222596499
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0107others(3): Show | 7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+3429A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596499 | ||||||
chr2:222596505
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+3423G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596505 | ||||||
chr2:222596695
|
T | C | 1 | a0002c0002t0024g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+3233A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596695 | ||||||
chr2:222596839
|
T | C | 1 | a0002c0002t0024g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+3089A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596839 | ||||||
chr2:222596854
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1618+3074T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596854 | ||||||
chr2:222596855
|
C | T | 2 | a0001c0001t0005g0316a0001c0001t0005g0317 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1618+3073G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596855 | ||||||
chr2:222597006
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+2922C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597006 | ||||||
chr2:222597124
|
G | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+2804C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597124 | ||||||
chr2:222597165
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1618+2763C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597165 | ||||||
chr2:222597341
|
T | C | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1618+2587A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597341 | ||||||
chr2:222597557
|
A | G | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+2371T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597557 | ||||||
chr2:222597679
|
A | G | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+2249T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597679 | ||||||
chr2:222597754
|
C | T | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+2174G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597754 | ||||||
chr2:222597794
|
T | A | 1 | a0001c0001t0002g0248 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1618+2134A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597794 | ||||||
chr2:222598163
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0123 | 2 | NA18963.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1618+1765G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598163 | ||||||
chr2:222598255
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1618+1673A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598255 | ||||||
chr2:222598420
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1618+1508A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598420 | ||||||
chr2:222598504
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1618+1424G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598504 | ||||||
chr2:222598674
|
T | C | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+1254A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598674 | ||||||
chr2:222598753
|
G | A | 1 | a0002c0002t0004g0210 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1618+1175C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598753 | ||||||
chr2:222598812
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1618+1116C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598812 | ||||||
chr2:222598918
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1618+1010C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598918 | ||||||
chr2:222598941
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1618+987A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598941 | ||||||
chr2:222598941
|
TAA | T | 76 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(73): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1618+985_1618+986d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598941 | ||||||
chr2:222599072
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+856C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599072 | ||||||
chr2:222599088
|
G | GA | 79 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(76): Show | 83 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1618+839dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599088 | ||||||
chr2:222599096
|
C | A | 315 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(312): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1618+832G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599096 | ||||||
chr2:222599136
|
C | T | 6 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0003g0058others(3): Show | 6 | HG01070.hp2 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618+792G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599136 | ||||||
chr2:222599198
|
G | A | 4 | a0001c0001t0005g0312a0001c0001t0010g0021a0001c0001t0010g0304others(1): Show | 5 | HG00639.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+730C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599198 | ||||||
chr2:222599322
|
G | C | 1 | a0001c0001t0003g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1618+606C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599322 | ||||||
chr2:222599369
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+559A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599369 | ||||||
chr2:222599522
|
C | A | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1618+406G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599522 | ||||||
chr2:222599732
|
C | T | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1618+196G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599732 | ||||||
chr2:222599795
|
T | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+133A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599795 | ||||||
chr2:222600112
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-29C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600112 | ||||||
chr2:222600226
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-143G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600226 | ||||||
chr2:222600262
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1463-179T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600262 | ||||||
chr2:222600291
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1463-208T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600291 | ||||||
chr2:222600673
|
A | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-590T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600673 | ||||||
chr2:222600679
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1463-596G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600679 | ||||||
chr2:222600712
|
T | C | 4 | a0001c0001t0003g0023a0001c0001t0003g0047a0001c0001t0003g0077others(1): Show | 4 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-629A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600712 | ||||||
chr2:222600942
|
G | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-859C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600942 | ||||||
chr2:222601000
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-917A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601000 | ||||||
chr2:222601061
|
C | CT | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1463-979dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601061 | ||||||
chr2:222601186
|
A | C | 1 | a0002c0002t0006g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1463-1103T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601186 | ||||||
chr2:222601225
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1463-1142G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601225 | ||||||
chr2:222601360
|
C | T | 1 | a0001c0001t0007g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1463-1277G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601360 | ||||||
chr2:222601413
|
C | CAAT | 3 | a0001c0001t0001g0149a0001c0001t0002g0264a0001c0001t0003g0047 | 3 | HG00673.hp1 HG01516.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1463-1333_1463-133 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601413 | ||||||
chr2:222601437
|
A | T | 1 | a0001c0001t0002g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1463-1354T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601437 | ||||||
chr2:222601489
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 91 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1463-1406G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601489 | ||||||
chr2:222601675
|
T | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1463-1592A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601675 | ||||||
chr2:222602009
|
A | C | 1 | a0001c0001t0002g0270 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1463-1926T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602009 | ||||||
chr2:222602042
|
C | T | 1 | a0002c0002t0024g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1463-1959G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602042 | ||||||
chr2:222602140
|
C | T | 6 | a0001c0001t0005g0313a0001c0001t0005g0314a0001c0001t0005g0315others(3): Show | 6 | HG01361.hp1 HG01975.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1463-2057G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602140 | ||||||
chr2:222602192
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1463-2109C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602192 | ||||||
chr2:222602256
|
C | T | 1 | a0001c0001t0008g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1463-2173G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602256 | ||||||
chr2:222602329
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1463-2246T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602329 | ||||||
chr2:222602574
|
C | A | 2 | a0001c0001t0011g0300a0001c0001t0011g0301 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1463-2491G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602574 | ||||||
chr2:222602574
|
C | T | 2 | a0001c0001t0011g0302a0001c0001t0011g0303 | 2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1463-2491G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602574 | ||||||
chr2:222602574
|
CT | C | 15 | a0001c0001t0002g0238a0002c0002t0006g0010a0002c0002t0006g0170others(12): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1463-2492delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602574 | ||||||
chr2:222602614
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-2531A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602614 | ||||||
chr2:222602632
|
T | G | 4 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0045others(1): Show | 5 | NA18945.hp2 NA18964.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-2549A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602632 | ||||||
chr2:222602670
|
C | T | 1 | a0001c0001t0031g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1463-2587G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602670 | ||||||
chr2:222602823
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1463-2740G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602823 | ||||||
chr2:222602862
|
C | A | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-2779G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602862 | ||||||
chr2:222602864
|
T | C | 1 | a0001c0001t0002g0279 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1463-2781A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602864 | ||||||
chr2:222602892
|
T | A | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0004g0199others(3): Show | 8 | HG02622.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1463-2809A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602892 | ||||||
chr2:222603261
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1463-3178A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603261 | ||||||
chr2:222603367
|
T | C | 1 | a0001c0001t0005g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1463-3284A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603367 | ||||||
chr2:222603665
|
A | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-3582T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603665 | ||||||
chr2:222603679
|
ATATTATA others(3): Show |
A | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1463-3606_1463-359 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603679 | ||||||
chr2:222603680
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-3597A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603680 | ||||||
chr2:222603692
|
TTA | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-3611_1463-361 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603692 | ||||||
chr2:222603704
|
G | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-3621C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603704 | ||||||
chr2:222603719
|
T | C | 2 | a0001c0001t0002g0238a0005c0006t0035g0299 | 2 | HG01928.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1463-3636A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603719 | ||||||
chr2:222603801
|
A | G | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-3718T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603801 | ||||||
chr2:222603833
|
T | C | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1463-3750A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603833 | ||||||
chr2:222603906
|
T | C | 1 | a0001c0001t0005g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1463-3823A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603906 | ||||||
chr2:222603998
|
C | A | 1 | a0002c0002t0004g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1463-3915G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603998 | ||||||
chr2:222604210
|
T | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0073 | 2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1463-4127A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604210 | ||||||
chr2:222604217
|
T | TA | 8 | a0001c0001t0001g0035a0001c0001t0002g0224a0001c0001t0003g0058others(5): Show | 8 | HG00642.hp1 HG01109.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1463-4135dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604217 | ||||||
chr2:222604348
|
C | CAGTG | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-4269_1463-426 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604348 | ||||||
chr2:222604495
|
T | C | 1 | a0001c0001t0002g0240 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1463-4412A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604495 | ||||||
chr2:222604672
|
C | A | 1 | a0001c0001t0020g0020 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1463-4589G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604672 | ||||||
chr2:222604722
|
A | AT | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 181 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1463-4640dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | ||||||
chr2:222604722
|
A | ATT | 32 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0097others(29): Show | 33 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1463-4641_1463-464 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | ||||||
chr2:222604722
|
A | ATTT | 50 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(47): Show | 55 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1463-4642_1463-464 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | ||||||
chr2:222604722
|
ATTTTTT | A | 17 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(14): Show | 18 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-4645_1463-464 others(10): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | ||||||
chr2:222604836
|
G | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-4753C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604836 | ||||||
chr2:222604975
|
T | TG | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1463-4893dupC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604975 | ||||||
chr2:222605125
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1463-5042T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605125 | ||||||
chr2:222605158
|
A | ACTCTCTC others(7): Show |
1 | a0001c0001t0003g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-5076_1463-507 others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605158 | ||||||
chr2:222605161
|
T | C | 1 | a0001c0001t0003g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-5078A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TACTTTCT others(13): Show |
1 | a0001c0001t0005g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1463-5079_1463-507 others(24): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TCTCTCTC others(8): Show |
6 | a0001c0001t0001g0035a0001c0001t0001g0120a0001c0001t0001g0141others(3): Show | 6 | HG00673.hp1 HG02027.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-5079_1463-507 others(19): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TCTCTCTC others(10): Show |
2 | a0001c0001t0011g0303a0002c0002t0006g0186 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1463-5079_1463-507 others(21): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TCTCTCTC others(12): Show |
1 | a0001c0001t0001g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1463-5079_1463-507 others(23): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TCTCTCTC others(14): Show |
2 | a0001c0001t0001g0105a0001c0001t0005g0320 | 2 | HG01361.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1463-5079_1463-507 others(25): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTC | 5 | a0001c0001t0002g0268a0001c0001t0002g0274a0001c0001t0007g0154others(2): Show | 5 | HG00642.hp2 HG01891.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1463-5080_1463-507 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTC | 48 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(45): Show | 53 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1463-5082_1463-507 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTC | 9 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0003g0074others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463-5084_1463-507 others(10): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(1): Show |
10 | a0001c0001t0001g0126a0001c0001t0001g0183a0001c0001t0001g0295others(7): Show | 11 | HG01261.hp2 HG01928.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1463-5086_1463-507 others(12): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(3): Show |
53 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0108others(50): Show | 59 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1463-5088_1463-507 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(5): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0097others(13): Show | 17 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1463-5090_1463-507 others(16): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(7): Show |
45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(42): Show | 50 | HG00741.hp2 HG01070.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.1463-5092_1463-507 others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(9): Show |
12 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0104others(9): Show | 12 | HG00280.hp2 HG01192.hp1 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.1463-5094_1463-507 others(20): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(11): Show |
14 | a0001c0001t0001g0099a0001c0001t0001g0121a0001c0001t0001g0143others(11): Show | 15 | HG00735.hp1 HG01106.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1463-5096_1463-507 others(22): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(13): Show |
6 | a0001c0001t0005g0309a0001c0001t0005g0318a0001c0001t0010g0021others(3): Show | 7 | HG02109.hp2 HG02257.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1463-5098_1463-507 others(24): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(15): Show |
6 | a0001c0001t0001g0123a0001c0001t0005g0312a0001c0001t0005g0319others(3): Show | 6 | HG00639.hp2 HG00735.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-5100_1463-507 others(26): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(17): Show |
3 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0311 | 3 | HG01884.hp2 HG02572.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1463-5102_1463-507 others(28): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(25): Show |
1 | a0001c0001t0005g0315 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1463-5110_1463-507 others(36): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605161
|
T | TTCTCTCT others(29): Show |
1 | a0001c0001t0005g0313 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1463-5079_1463-507 others(40): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | ||||||
chr2:222605195
|
G | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0130others(2): Show | 6 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-5112C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605195 | ||||||
chr2:222605264
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-5181G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605264 | ||||||
chr2:222605384
|
T | A | 1 | a0002c0002t0006g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1463-5301A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605384 | ||||||
chr2:222605547
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-5464A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605547 | ||||||
chr2:222605683
|
C | T | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-5600G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605683 | ||||||
chr2:222605754
|
C | CA | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1463-5672dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605754 | ||||||
chr2:222605808
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-5725T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605808 | ||||||
chr2:222605928
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1463-5845T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605928 | ||||||
chr2:222606069
|
A | ATTTCTAG others(3): Show |
1 | a0001c0001t0003g0025 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1463-5996_1463-598 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606069 | ||||||
chr2:222606128
|
G | A | 1 | a0001c0001t0019g0249 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1463-6045C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606128 | ||||||
chr2:222606193
|
G | A | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1463-6110C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606193 | ||||||
chr2:222606287
|
C | T | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1463-6204G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606287 | ||||||
chr2:222606361
|
AG | A | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1463-6279delC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606361 | ||||||
chr2:222606549
|
C | G | 80 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0017others(77): Show | 85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1463-6466G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606549 | ||||||
chr2:222606651
|
T | G | 1 | a0001c0001t0016g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1463-6568A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606651 | ||||||
chr2:222606685
|
C | A | 1 | a0001c0001t0002g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1463-6602G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606685 | ||||||
chr2:222606717
|
T | A | 1 | a0001c0007t0002g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1463-6634A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606717 | ||||||
chr2:222606735
|
G | A | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-6652C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606735 | ||||||
chr2:222606740
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-6657C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606740 | ||||||
chr2:222606896
|
G | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-6813C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606896 | ||||||
chr2:222607225
|
T | C | 2 | a0001c0001t0005g0313a0001c0001t0005g0315 | 2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1462+6586A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607225 | ||||||
chr2:222607259
|
T | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0132others(2): Show | 5 | HG00735.hp2 HG01257.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462+6552A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607259 | ||||||
chr2:222607591
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1462+6220C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607591 | ||||||
chr2:222607605
|
C | T | 15 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1462+6206G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607605 | ||||||
chr2:222607649
|
A | T | 278 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1462+6162T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607649 | ||||||
chr2:222607650
|
A | T | 1 | a0001c0001t0003g0025 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1462+6161T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607650 | ||||||
chr2:222607742
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+6069A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607742 | ||||||
chr2:222607747
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+6064A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607747 | ||||||
chr2:222607748
|
A | T | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1462+6063T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607748 | ||||||
chr2:222607753
|
G | A | 74 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1462+6058C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607753 | ||||||
chr2:222607974
|
C | A | 1 | a0001c0001t0002g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1462+5837G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607974 | ||||||
chr2:222608138
|
G | A | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1462+5673C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608138 | ||||||
chr2:222608264
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1462+5547T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608264 | ||||||
chr2:222608280
|
A | G | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+5531T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608280 | ||||||
chr2:222608482
|
T | C | 5 | a0001c0001t0005g0312a0001c0001t0010g0021a0001c0001t0010g0304others(2): Show | 6 | HG00639.hp2 HG01928.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1462+5329A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608482 | ||||||
chr2:222608498
|
C | T | 14 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(11): Show | 14 | HG01361.hp1 HG01884.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1462+5313G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608498 | ||||||
chr2:222608589
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1462+5222T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608589 | ||||||
chr2:222608614
|
A | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0025a0001c0001t0003g0030 | 4 | HG01952.hp2 NA19010.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462+5197T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608614 | ||||||
chr2:222608675
|
G | C | 2 | a0001c0001t0002g0254a0001c0001t0002g0256 | 2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1462+5136C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608675 | ||||||
chr2:222608794
|
T | G | 3 | a0001c0001t0003g0038a0001c0001t0021g0039a0001c0001t0022g0040 | 3 | HG00140.hp2 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1462+5017A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608794 | ||||||
chr2:222609622
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+4189G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609622 | ||||||
chr2:222609671
|
G | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+4140C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609671 | ||||||
chr2:222609715
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1462+4096A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609715 | ||||||
chr2:222609767
|
T | A | 4 | a0001c0001t0003g0023a0001c0001t0003g0047a0001c0001t0003g0077others(1): Show | 4 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+4044A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609767 | ||||||
chr2:222609768
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1462+4043A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609768 | ||||||
chr2:222609911
|
A | G | 11 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462+3900T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609911 | ||||||
chr2:222609913
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1462+3898C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609913 | ||||||
chr2:222609978
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1462+3833C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609978 | ||||||
chr2:222610028
|
A | T | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1462+3783T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610028 | ||||||
chr2:222610048
|
A | G | 1 | a0001c0001t0008g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1462+3763T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610048 | ||||||
chr2:222610060
|
A | G | 1 | a0001c0001t0008g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1462+3751T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610060 | ||||||
chr2:222610475
|
A | G | 76 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(73): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1462+3336T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610475 | ||||||
chr2:222610493
|
AT | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1462+3317delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610493 | ||||||
chr2:222610503
|
G | A | 76 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(73): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1462+3308C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610503 | ||||||
chr2:222610525
|
A | T | 6 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0010g0021others(3): Show | 7 | HG00639.hp2 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1462+3286T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610525 | ||||||
chr2:222610602
|
T | A | 1 | a0001c0001t0002g0251 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1462+3209A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610602 | ||||||
chr2:222610691
|
T | C | 1 | a0002c0002t0006g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1462+3120A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610691 | ||||||
chr2:222610804
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0034 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1462+3007A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610804 | ||||||
chr2:222610926
|
C | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+2885G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610926 | ||||||
chr2:222611053
|
A | G | 2 | a0002c0002t0006g0010a0002c0002t0006g0177 | 3 | HG02109.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1462+2758T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611053 | ||||||
chr2:222611448
|
C | CG | 21 | a0001c0001t0001g0032a0001c0001t0002g0240a0001c0001t0005g0306others(18): Show | 22 | HG00639.hp2 HG00735.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1462+2362dupC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611448 | ||||||
chr2:222611457
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1462+2354C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611457 | ||||||
chr2:222611459
|
G | A | 7 | a0001c0001t0007g0037a0001c0001t0007g0087a0001c0001t0007g0134others(4): Show | 7 | HG00280.hp2 HG00735.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1462+2352C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611459 | ||||||
chr2:222611552
|
G | A | 280 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1462+2259C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611552 | ||||||
chr2:222611590
|
G | A | 1 | a0001c0001t0005g0314 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1462+2221C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611590 | ||||||
chr2:222611661
|
C | G | 14 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1462+2150G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611661 | ||||||
chr2:222611815
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+1996G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611815 | ||||||
chr2:222611971
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1462+1840C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611971 | ||||||
chr2:222611981
|
C | T | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1462+1830G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611981 | ||||||
chr2:222612235
|
T | C | 7 | a0002c0002t0004g0172a0002c0002t0004g0192a0002c0002t0004g0203others(4): Show | 7 | HG01257.hp1 HG02145.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1462+1576A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612235 | ||||||
chr2:222612259
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+1552A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612259 | ||||||
chr2:222612441
|
A | G | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1462+1370T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612441 | ||||||
chr2:222612448
|
G | A | 1 | a0001c0001t0007g0037 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1462+1363C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612448 | ||||||
chr2:222612459
|
G | T | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1462+1352C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612459 | ||||||
chr2:222612466
|
C | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+1345G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612466 | ||||||
chr2:222612512
|
C | A | 3 | a0001c0001t0010g0021a0001c0001t0010g0304a0001c0001t0010g0305 | 4 | HG00639.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462+1299G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612512 | ||||||
chr2:222612561
|
G | A | 1 | a0001c0004t0002g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1462+1250C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612561 | ||||||
chr2:222612718
|
T | C | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1462+1093A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612718 | ||||||
chr2:222612729
|
C | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+1082G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612729 | ||||||
chr2:222612730
|
C | CAATGCAC others(11): Show |
1 | a0001c0001t0002g0294 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1462+1063_1462+108 others(22): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612730 | ||||||
chr2:222612743
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1462+1068C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612743 | ||||||
chr2:222612910
|
A | G | 3 | a0001c0001t0012g0036a0001c0001t0012g0062a0001c0001t0012g0063 | 3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1462+901T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612910 | ||||||
chr2:222613013
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1462+798T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613013 | ||||||
chr2:222613044
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | NA18984.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1462+767C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613044 | ||||||
chr2:222613049
|
A | G | 1 | a0001c0001t0003g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1462+762T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613049 | ||||||
chr2:222613239
|
G | T | 2 | a0001c0001t0002g0239a0001c0001t0002g0260 | 2 | NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1462+572C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613239 | ||||||
chr2:222613374
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1462+437C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613374 | ||||||
chr2:222613435
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1462+376G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613435 | ||||||
chr2:222613727
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1462+84A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613727 | ||||||
chr2:222613780
|
A | C | 1 | a0002c0002t0004g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1462+31T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613780 | ||||||
chr2:222614146
|
A | C | 3 | a0001c0001t0003g0038a0001c0001t0021g0039a0001c0001t0022g0040 | 3 | HG00140.hp2 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1345-218T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614146 | ||||||
chr2:222614286
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1345-358T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614286 | ||||||
chr2:222614494
|
C | A | 1 | a0001c0001t0005g0314 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1345-566G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614494 | ||||||
chr2:222614561
|
T | C | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1345-633A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614561 | ||||||
chr2:222615210
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1345-1282C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615210 | ||||||
chr2:222615237
|
T | C | 3 | a0001c0001t0003g0053a0001c0001t0003g0060a0001c0001t0003g0061 | 3 | HG02615.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1345-1309A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615237 | ||||||
chr2:222615276
|
T | A | 4 | a0002c0002t0009g0011a0002c0002t0009g0171a0002c0002t0009g0176others(1): Show | 5 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-1348A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615276 | ||||||
chr2:222615412
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-1484G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615412 | ||||||
chr2:222615984
|
A | C | 2 | a0002c0002t0004g0161a0003c0003t0004g0160 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1345-2056T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615984 | ||||||
chr2:222615996
|
T | A | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1345-2068A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615996 | ||||||
chr2:222616254
|
A | G | 11 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1345-2326T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616254 | ||||||
chr2:222616398
|
T | G | 1 | a0001c0001t0002g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1345-2470A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616398 | ||||||
chr2:222616407
|
C | T | 7 | a0002c0002t0004g0172a0002c0002t0004g0192a0002c0002t0004g0203others(4): Show | 7 | HG01257.hp1 HG02145.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-2479G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616407 | ||||||
chr2:222616454
|
G | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1345-2526C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616454 | ||||||
chr2:222616455
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1345-2527C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616455 | ||||||
chr2:222616528
|
A | G | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345-2600T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616528 | ||||||
chr2:222616545
|
C | CA | 61 | a0001c0001t0002g0225a0001c0001t0003g0001a0001c0001t0003g0003others(58): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1345-2618dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | ||||||
chr2:222616545
|
C | CAA | 76 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(73): Show | 83 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1345-2619_1345-261 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | ||||||
chr2:222616545
|
C | CAAA | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1345-2620_1345-261 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | ||||||
chr2:222616545
|
C | CAAAA | 6 | a0001c0001t0001g0035a0001c0001t0001g0106a0001c0001t0001g0125others(3): Show | 6 | HG02027.hp2 HG04199.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-2621_1345-261 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | ||||||
chr2:222616571
|
C | G | 2 | a0002c0002t0006g0212a0002c0002t0006g0213 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1345-2643G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616571 | ||||||
chr2:222616893
|
G | A | 4 | a0001c0001t0008g0284a0001c0001t0008g0287a0001c0001t0014g0288others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2752C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616893 | ||||||
chr2:222616906
|
G | A | 39 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 43 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1344+2739C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616906 | ||||||
chr2:222616971
|
CAGAAAGA others(282): Show |
C | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1344+2385_1344+267 others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616971 | ||||||
chr2:222616985
|
C | CT | 18 | a0001c0001t0002g0168a0001c0001t0002g0218a0001c0001t0002g0223others(15): Show | 18 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1344+2659dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616985 | ||||||
chr2:222617460
|
A | G | 95 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(92): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1344+2185T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617460 | ||||||
chr2:222617476
|
A | G | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1344+2169T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617476 | ||||||
chr2:222617585
|
A | G | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1344+2060T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617585 | ||||||
chr2:222617613
|
G | A | 1 | a0002c0002t0004g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1344+2032C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617613 | ||||||
chr2:222617630
|
T | C | 1 | a0001c0001t0002g0018 | 2 | NA18952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1344+2015A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617630 | ||||||
chr2:222617657
|
G | A | 1 | a0001c0001t0033g0137 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1344+1988C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617657 | ||||||
chr2:222617694
|
T | G | 25 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(22): Show | 26 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1344+1951A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617694 | ||||||
chr2:222617775
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0130 | 2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1344+1870G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617775 | ||||||
chr2:222617776
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1344+1869C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617776 | ||||||
chr2:222617819
|
G | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 91 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1344+1826C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617819 | ||||||
chr2:222617861
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0106 | 2 | NA18962.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1344+1784G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617861 | ||||||
chr2:222617957
|
G | A | 1 | a0002c0002t0004g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1344+1688C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617957 | ||||||
chr2:222617972
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344+1673C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617972 | ||||||
chr2:222618098
|
T | C | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1344+1547A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618098 | ||||||
chr2:222618175
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344+1470T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618175 | ||||||
chr2:222618226
|
T | A | 14 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1344+1419A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618226 | ||||||
chr2:222618444
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1344+1201T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618444 | ||||||
chr2:222618516
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+1129A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618516 | ||||||
chr2:222618587
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+1058A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618587 | ||||||
chr2:222618592
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1344+1053A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618592 | ||||||
chr2:222618857
|
A | G | 1 | a0001c0001t0005g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1344+788T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618857 | ||||||
chr2:222618876
|
C | A | 1 | a0002c0002t0004g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1344+769G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618876 | ||||||
chr2:222618951
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1344+694C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618951 | ||||||
chr2:222618969
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+676G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618969 | ||||||
chr2:222619156
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344+489A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619156 | ||||||
chr2:222619319
|
TA | T | 111 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0106others(108): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1344+325delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619319 | ||||||
chr2:222619319
|
TAA | T | 42 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(39): Show | 46 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.1344+324_1344+325d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619319 | ||||||
chr2:222619320
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1344+325T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619320 | ||||||
chr2:222619387
|
G | A | 39 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 43 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1344+258C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619387 | ||||||
chr2:222619508
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 43 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1344+137T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619508 | ||||||
chr2:222619606
|
A | C | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+39T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619606 | ||||||
chr2:222619881
|
G | T | 1 | a0001c0001t0002g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1252-144C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222619881 | ||||||
chr2:222619909
|
A | T | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | NA18984.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1252-172T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222619909 | ||||||
chr2:222620072
|
T | G | 3 | a0001c0001t0007g0087a0001c0001t0007g0138a0001c0001t0007g0139 | 3 | HG00735.hp1 HG01256.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1252-335A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620072 | ||||||
chr2:222620291
|
T | C | 1 | a0001c0001t0011g0302 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1252-554A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620291 | ||||||
chr2:222620385
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1252-648A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620385 | ||||||
chr2:222620439
|
T | C | 4 | a0002c0002t0009g0011a0002c0002t0009g0171a0002c0002t0009g0176others(1): Show | 5 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-702A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620439 | ||||||
chr2:222620460
|
A | G | 1 | a0001c0001t0008g0290 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1252-723T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620460 | ||||||
chr2:222620590
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0126 | 2 | HG02027.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1252-853C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620590 | ||||||
chr2:222620653
|
T | C | 88 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(85): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1252-916A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620653 | ||||||
chr2:222620711
|
G | A | 37 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(34): Show | 41 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.1252-974C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620711 | ||||||
chr2:222621038
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1252-1301T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621038 | ||||||
chr2:222621069
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1252-1332A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621069 | ||||||
chr2:222621328
|
G | A | 13 | a0001c0001t0001g0127a0002c0002t0006g0170a0002c0002t0006g0173others(10): Show | 14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1252-1591C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621328 | ||||||
chr2:222621386
|
C | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1252-1649G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621386 | ||||||
chr2:222621470
|
G | T | 3 | a0002c0002t0009g0011a0002c0002t0009g0176a0002c0002t0009g0178 | 4 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1252-1733C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621470 | ||||||
chr2:222621778
|
T | C | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1251+1872A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621778 | ||||||
chr2:222621949
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1251+1701A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621949 | ||||||
chr2:222622068
|
C | T | 1 | a0001c0001t0002g0235 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1251+1582G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622068 | ||||||
chr2:222622113
|
G | C | 2 | a0001c0001t0003g0077a0001c0001t0003g0078 | 2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1251+1537C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622113 | ||||||
chr2:222622208
|
A | G | 1 | a0001c0001t0005g0312 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1251+1442T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622208 | ||||||
chr2:222622235
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1251+1415G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622235 | ||||||
chr2:222622439
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1251+1211T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622439 | ||||||
chr2:222622503
|
G | A | 75 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(72): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1251+1147C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622503 | ||||||
chr2:222622635
|
C | T | 1 | a0001c0004t0002g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1251+1015G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622635 | ||||||
chr2:222622771
|
C | T | 1 | a0001c0001t0003g0043 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1251+879G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622771 | ||||||
chr2:222622772
|
G | A | 2 | a0002c0002t0004g0203a0002c0002t0004g0283 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1251+878C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622772 | ||||||
chr2:222622841
|
T | C | 1 | a0001c0001t0002g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1251+809A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622841 | ||||||
chr2:222622924
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1251+726C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622924 | ||||||
chr2:222623063
|
GAA | G | 14 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1251+585_1251+586d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623063 | ||||||
chr2:222623067
|
T | G | 14 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1251+583A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623067 | ||||||
chr2:222623088
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1251+562C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623088 | ||||||
chr2:222623517
|
C | G | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1251+133G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623517 | ||||||
chr2:222623734
|
A | G | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1171-4T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222623734 | ||||||
chr2:222623868
|
C | T | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1171-138G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222623868 | ||||||
chr2:222623989
|
C | T | 1 | a0002c0002t0004g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1171-259G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222623989 | ||||||
chr2:222624059
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(237): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1170+213A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222624059 | ||||||
chr2:222624207
|
C | G | 1 | a0001c0001t0003g0052 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1170+65G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222624207 | ||||||
chr2:222624260
|
G | A | 4 | a0001c0001t0002g0231a0001c0001t0002g0254a0001c0001t0002g0256others(1): Show | 4 | HG01255.hp1 HG01346.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+12C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222624260 | ||||||
chr2:222624530
|
GT | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.963-52delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 11/16 | chr2 | 222624530 | ||||||
chr2:222624574
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.963-95G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 11/16 | chr2 | 222624574 | ||||||
chr2:222624703
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.962+11A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 11/16 | chr2 | 222624703 | ||||||
chr2:222625071
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.901-296C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625071 | ||||||
chr2:222625094
|
C | T | 2 | a0001c0001t0011g0300a0001c0001t0011g0301 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.901-319G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625094 | ||||||
chr2:222625134
|
G | T | 1 | a0001c0001t0002g0267 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.901-359C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625134 | ||||||
chr2:222625491
|
G | A | 2 | a0002c0002t0006g0174a0002c0002t0006g0175 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.901-716C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625491 | ||||||
chr2:222625708
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901-933G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625708 | ||||||
chr2:222625845
|
T | C | 2 | a0001c0001t0005g0316a0001c0001t0005g0317 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.901-1070A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625845 | ||||||
chr2:222625855
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.901-1080G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625855 | ||||||
chr2:222625890
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-1115A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625890 | ||||||
chr2:222625942
|
T | C | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-1167A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625942 | ||||||
chr2:222626141
|
C | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901-1366G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626141 | ||||||
chr2:222626243
|
C | CA | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.901-1469dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626243 | ||||||
chr2:222626243
|
C | CAA | 13 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0130others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.901-1470_901-1469d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626243 | ||||||
chr2:222626243
|
CA | C | 11 | a0001c0001t0002g0167a0001c0001t0003g0048a0001c0001t0003g0052others(8): Show | 12 | HG02109.hp1 HG02280.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.901-1469delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626243 | ||||||
chr2:222626287
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.901-1512T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626287 | ||||||
chr2:222626402
|
A | G | 18 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(15): Show | 19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.901-1627T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626402 | ||||||
chr2:222626455
|
A | G | 15 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(12): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.901-1680T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626455 | ||||||
chr2:222626549
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.901-1774G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626549 | ||||||
chr2:222626805
|
G | A | 1 | a0002c0002t0004g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.901-2030C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626805 | ||||||
chr2:222626851
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 95 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.900+1986C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626851 | ||||||
chr2:222626904
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+1933G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626904 | ||||||
chr2:222626909
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+1928C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626909 | ||||||
chr2:222626929
|
G | A | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.900+1908C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626929 | ||||||
chr2:222627014
|
C | T | 32 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(29): Show | 35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.900+1823G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627014 | ||||||
chr2:222627203
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.900+1634T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627203 | ||||||
chr2:222627208
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0159a0001c0001t0034g0163 | 3 | HG00735.hp2 HG01516.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.900+1629A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627208 | ||||||
chr2:222627422
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.900+1415C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627422 | ||||||
chr2:222627446
|
C | T | 18 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(15): Show | 19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.900+1391G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627446 | ||||||
chr2:222627464
|
G | A | 2 | a0002c0002t0006g0212a0002c0002t0006g0213 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.900+1373C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627464 | ||||||
chr2:222627568
|
T | G | 5 | a0002c0002t0004g0172a0002c0002t0004g0192a0002c0002t0004g0203others(2): Show | 5 | HG02976.hp1 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+1269A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627568 | ||||||
chr2:222627933
|
C | T | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.900+904G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627933 | ||||||
chr2:222627988
|
T | C | 1 | a0002c0002t0004g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.900+849A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627988 | ||||||
chr2:222628044
|
C | T | 2 | a0001c0001t0011g0300a0001c0001t0011g0301 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.900+793G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628044 | ||||||
chr2:222628083
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.900+754A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628083 | ||||||
chr2:222628145
|
C | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+692G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628145 | ||||||
chr2:222628260
|
C | T | 18 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(15): Show | 19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.900+577G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628260 | ||||||
chr2:222628302
|
C | T | 32 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(29): Show | 35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.900+535G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628302 | ||||||
chr2:222628355
|
A | G | 1 | a0001c0001t0011g0302 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.900+482T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628355 | ||||||
chr2:222628498
|
A | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.900+339T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628498 | ||||||
chr2:222628533
|
T | C | 2 | a0002c0002t0004g0188a0002c0002t0004g0189 | 2 | NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.900+304A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628533 | ||||||
chr2:222628706
|
T | C | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.900+131A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628706 | ||||||
chr2:222628716
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.900+121C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628716 | ||||||
chr2:222628721
|
G | A | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.900+116C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628721 | ||||||
chr2:222628724
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+113A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628724 | ||||||
chr2:222628738
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.900+99C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628738 | ||||||
chr2:222629079
|
C | G | 12 | a0002c0002t0006g0010a0002c0002t0006g0173a0002c0002t0006g0174others(9): Show | 14 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.849-191G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629079 | ||||||
chr2:222629485
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849-597A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629485 | ||||||
chr2:222629490
|
G | A | 1 | a0002c0002t0006g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849-602C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629490 | ||||||
chr2:222629818
|
G | A | 3 | a0001c0001t0003g0043a0001c0001t0003g0074a0001c0001t0003g0080 | 3 | HG01069.hp2 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.848+295C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629818 | ||||||
chr2:222629980
|
A | G | 1 | a0001c0001t0005g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.848+133T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629980 | ||||||
chr2:222630066
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.848+47G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222630066 | ||||||
chr2:222630414
|
A | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.787-240T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630414 | ||||||
chr2:222630500
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.787-326C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630500 | ||||||
chr2:222630543
|
T | C | 1 | a0001c0001t0007g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.787-369A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630543 | ||||||
chr2:222630758
|
A | G | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.787-584T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630758 | ||||||
chr2:222630813
|
A | T | 15 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(12): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.787-639T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630813 | ||||||
chr2:222630957
|
T | A | 1 | a0002c0002t0004g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.786+647A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630957 | ||||||
chr2:222631182
|
CT | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 28 | HG00639.hp2 HG01361.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+421delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631182 | ||||||
chr2:222631250
|
A | C | 2 | a0001c0001t0002g0234a0001c0001t0002g0264 | 2 | NA18959.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.786+354T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631250 | ||||||
chr2:222631265
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.786+339A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631265 | ||||||
chr2:222631277
|
G | A | 2 | a0002c0002t0006g0212a0002c0002t0006g0213 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.786+327C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631277 | ||||||
chr2:222631325
|
A | G | 5 | a0002c0002t0004g0172a0002c0002t0004g0192a0002c0002t0004g0203others(2): Show | 5 | HG02976.hp1 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+279T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631325 | ||||||
chr2:222631357
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.786+247C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631357 | ||||||
chr2:222631391
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.786+213T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631391 | ||||||
chr2:222631490
|
A | G | 4 | a0001c0001t0008g0284a0001c0001t0008g0287a0001c0001t0014g0288others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+114T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631490 | ||||||
chr2:222631847
|
C | T | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.716-173G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631847 | ||||||
chr2:222631898
|
C | T | 30 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(27): Show | 33 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.716-224G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631898 | ||||||
chr2:222631932
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.716-258G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631932 | ||||||
chr2:222631980
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-306C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631980 | ||||||
chr2:222632023
|
G | GATGGTGC others(11): Show |
14 | a0001c0001t0001g0093a0001c0001t0005g0306a0001c0001t0005g0307others(11): Show | 14 | HG01257.hp2 HG01361.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.716-367_716-350dup others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632023 | ||||||
chr2:222632023
|
GATGGTGC others(11): Show |
G | 16 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(13): Show | 18 | HG01928.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.716-367_716-350del others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632023 | ||||||
chr2:222632056
|
C | A | 1 | a0001c0001t0002g0230 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.716-382G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632056 | ||||||
chr2:222632069
|
T | C | 32 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(29): Show | 35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.716-395A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632069 | ||||||
chr2:222632076
|
A | AGAGTG | 2 | a0001c0001t0001g0008a0001c0001t0001g0158 | 3 | NA18982.hp2 NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.716-407_716-403dup others(5): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632076 | ||||||
chr2:222632142
|
AT | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-469delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632142 | ||||||
chr2:222632143
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.716-469A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632143 | ||||||
chr2:222632151
|
A | G | 82 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(79): Show | 91 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.716-477T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632151 | ||||||
chr2:222632198
|
C | G | 1 | a0001c0001t0002g0233 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.716-524G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632198 | ||||||
chr2:222632241
|
C | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-567G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632241 | ||||||
chr2:222632248
|
T | C | 1 | a0002c0002t0024g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.716-574A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632248 | ||||||
chr2:222632293
|
G | A | 1 | a0001c0001t0008g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.716-619C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632293 | ||||||
chr2:222632432
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 90 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.716-758G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632432 | ||||||
chr2:222632792
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.715+407G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632792 | ||||||
chr2:222632840
|
C | A | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.715+359G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632840 | ||||||
chr2:222632842
|
A | AC | 4 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050others(1): Show | 4 | HG01243.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+356_715+357ins others(1): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632842 | ||||||
chr2:222632843
|
A | C | 6 | a0001c0001t0001g0098a0002c0002t0004g0203a0002c0002t0004g0283others(3): Show | 6 | HG01891.hp1 HG01928.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.715+356T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632843 | ||||||
chr2:222632914
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(79): Show | 91 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.715+285A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632914 | ||||||
chr2:222632997
|
G | A | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.715+202C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632997 | ||||||
chr2:222633120
|
A | T | 1 | a0002c0002t0006g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.715+79T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222633120 | ||||||
chr2:222633148
|
G | A | 2 | a0001c0001t0011g0302a0001c0001t0011g0303 | 2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.715+51C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222633148 | ||||||
chr2:222633337
|
GT | G | 5 | a0002c0002t0004g0013a0002c0002t0004g0199a0002c0002t0004g0200others(2): Show | 6 | HG01928.hp1 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-31delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633337 | ||||||
chr2:222633355
|
T | C | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.607-48A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633355 | ||||||
chr2:222633448
|
T | C | 97 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(94): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.607-141A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633448 | ||||||
chr2:222633455
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.607-148C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633455 | ||||||
chr2:222633500
|
T | A | 67 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(64): Show | 74 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.607-193A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633500 | ||||||
chr2:222633514
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.607-207G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633514 | ||||||
chr2:222633543
|
G | A | 1 | a0001c0001t0005g0312 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.607-236C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633543 | ||||||
chr2:222633554
|
T | C | 1 | a0001c0001t0007g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.607-247A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633554 | ||||||
chr2:222633579
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.607-272C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633579 | ||||||
chr2:222633645
|
G | A | 18 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(15): Show | 19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.607-338C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633645 | ||||||
chr2:222633670
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.607-363C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633670 | ||||||
chr2:222633682
|
CA | C | 36 | a0001c0001t0002g0221a0001c0001t0003g0075a0001c0001t0003g0076others(33): Show | 39 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.607-376delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633682 | ||||||
chr2:222633682
|
CAA | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(183): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.607-377_607-376del others(2): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633682 | ||||||
chr2:222633908
|
G | A | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.606+483C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633908 | ||||||
chr2:222633944
|
T | C | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.606+447A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633944 | ||||||
chr2:222633957
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.606+434G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633957 | ||||||
chr2:222634119
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.606+272T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222634119 | ||||||
chr2:222634358
|
C | T | 67 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(64): Show | 74 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.606+33G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222634358 | ||||||
chr2:222634934
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-393G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222634934 | ||||||
chr2:222635033
|
T | C | 1 | a0002c0002t0004g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.456-492A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635033 | ||||||
chr2:222635034
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.456-493G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635034 | ||||||
chr2:222635077
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.456-536C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635077 | ||||||
chr2:222635160
|
A | T | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.456-619T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635160 | ||||||
chr2:222635343
|
G | A | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.456-802C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635343 | ||||||
chr2:222635351
|
G | A | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.456-810C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635351 | ||||||
chr2:222635437
|
G | C | 1 | a0004c0005t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.456-896C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635437 | ||||||
chr2:222635559
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.456-1018G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635559 | ||||||
chr2:222635821
|
T | A | 9 | a0001c0001t0007g0037a0001c0001t0007g0087a0001c0001t0007g0134others(6): Show | 9 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.456-1280A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635821 | ||||||
chr2:222635850
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.456-1309G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635850 | ||||||
chr2:222635877
|
C | G | 22 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(19): Show | 23 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-1336G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635877 | ||||||
chr2:222635983
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456-1442T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635983 | ||||||
chr2:222636176
|
G | C | 3 | a0001c0001t0012g0036a0001c0001t0012g0062a0001c0001t0012g0063 | 3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.456-1635C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636176 | ||||||
chr2:222636279
|
C | T | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.456-1738G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636279 | ||||||
chr2:222636331
|
C | T | 1 | a0002c0002t0004g0190 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.456-1790G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636331 | ||||||
chr2:222636373
|
G | A | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.456-1832C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636373 | ||||||
chr2:222636385
|
C | CA | 59 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(56): Show | 62 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.456-1845dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636385 | ||||||
chr2:222636385
|
C | CAA | 38 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(35): Show | 43 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.456-1846_456-1845d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636385 | ||||||
chr2:222636494
|
CTA | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-1955_456-1954d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636494 | ||||||
chr2:222636558
|
G | T | 3 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230 | 3 | HG01169.hp1 HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.456-2017C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636558 | ||||||
chr2:222636601
|
A | G | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG01175.hp2 HG01515.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-2060T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636601 | ||||||
chr2:222636691
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456-2150C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636691 | ||||||
chr2:222636769
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456-2228G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636769 | ||||||
chr2:222636799
|
A | T | 4 | a0001c0001t0008g0284a0001c0001t0008g0287a0001c0001t0014g0288others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-2258T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636799 | ||||||
chr2:222636875
|
T | C | 1 | a0001c0001t0032g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.456-2334A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636875 | ||||||
chr2:222636923
|
C | T | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.456-2382G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636923 | ||||||
chr2:222636968
|
C | T | 1 | a0001c0001t0008g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.456-2427G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636968 | ||||||
chr2:222637109
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.455+2471C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637109 | ||||||
chr2:222637137
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.455+2443C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637137 | ||||||
chr2:222637174
|
G | A | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.455+2406C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637174 | ||||||
chr2:222637220
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+2360T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637220 | ||||||
chr2:222637488
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.455+2092C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637488 | ||||||
chr2:222637510
|
G | A | 2 | a0002c0002t0004g0014a0002c0002t0004g0204 | 3 | HG02717.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.455+2070C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637510 | ||||||
chr2:222637564
|
T | C | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.455+2016A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637564 | ||||||
chr2:222637828
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+1752A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637828 | ||||||
chr2:222637884
|
G | A | 2 | a0002c0002t0006g0174a0002c0002t0006g0175 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.455+1696C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637884 | ||||||
chr2:222637961
|
A | G | 4 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0227others(1): Show | 4 | HG01069.hp1 NA18973.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.455+1619T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637961 | ||||||
chr2:222638127
|
A | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.455+1453T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638127 | ||||||
chr2:222638179
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+1401G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638179 | ||||||
chr2:222638224
|
A | T | 1 | a0001c0001t0007g0037 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.455+1356T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638224 | ||||||
chr2:222638651
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.455+929G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638651 | ||||||
chr2:222638729
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+851T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638729 | ||||||
chr2:222638979
|
G | A | 1 | a0001c0001t0015g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.455+601C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638979 | ||||||
chr2:222639320
|
T | C | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.455+260A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222639320 | ||||||
chr2:222639884
|
A | G | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.340-189T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222639884 | ||||||
chr2:222640108
|
T | C | 11 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-413A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640108 | ||||||
chr2:222640203
|
G | T | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.340-508C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640203 | ||||||
chr2:222640428
|
T | C | 1 | a0001c0001t0005g0320 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.339+434A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640428 | ||||||
chr2:222640498
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.339+364A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640498 | ||||||
chr2:222640508
|
C | G | 2 | a0002c0002t0004g0188a0002c0002t0004g0189 | 2 | NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.339+354G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640508 | ||||||
chr2:222640671
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.339+191T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640671 | ||||||
chr2:222640754
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.339+108A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640754 | ||||||
chr2:222640997
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.270-66A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222640997 | ||||||
chr2:222641010
|
G | A | 3 | a0002c0002t0004g0205a0002c0002t0004g0206a0002c0002t0004g0207 | 3 | HG01192.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.270-79C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641010 | ||||||
chr2:222641088
|
C | A | 1 | a0001c0001t0002g0221 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.270-157G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641088 | ||||||
chr2:222641089
|
A | C | 1 | a0001c0001t0002g0221 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.270-158T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641089 | ||||||
chr2:222641089
|
A | G | 1 | a0001c0001t0005g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270-158T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641089 | ||||||
chr2:222641153
|
T | C | 67 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(64): Show | 74 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.270-222A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641153 | ||||||
chr2:222641214
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0223a0001c0001t0002g0224 | 4 | HG00609.hp2 NA18981.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-283G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641214 | ||||||
chr2:222641532
|
A | T | 1 | a0002c0002t0004g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.270-601T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641532 | ||||||
chr2:222641732
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.270-801A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641732 | ||||||
chr2:222641862
|
C | G | 1 | a0001c0001t0008g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.270-931G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641862 | ||||||
chr2:222641863
|
C | G | 18 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0311others(15): Show | 20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.270-932G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641863 | ||||||
chr2:222641883
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.270-952G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641883 | ||||||
chr2:222641926
|
TGAA | T | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269+922_269+924del others(3): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641926 | ||||||
chr2:222641991
|
G | C | 1 | a0001c0001t0003g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.269+860C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641991 | ||||||
chr2:222642003
|
CT | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(299): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.269+847delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642003 | ||||||
chr2:222642004
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.269+847A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642004 | ||||||
chr2:222642104
|
C | T | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0310others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.269+747G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642104 | ||||||
chr2:222642135
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.269+716C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642135 | ||||||
chr2:222642193
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.269+658C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642193 | ||||||
chr2:222642540
|
C | G | 1 | a0001c0001t0015g0042 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.269+311G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642540 | ||||||
chr2:222642573
|
C | A | 1 | a0002c0002t0004g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.269+278G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642573 | ||||||
chr2:222642742
|
C | T | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269+109G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642742 | ||||||
chr2:222643114
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-109A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643114 | ||||||
chr2:222643199
|
T | C | 2 | a0001c0001t0002g0277a0001c0001t0002g0278 | 2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.115-194A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643199 | ||||||
chr2:222643664
|
ACAGT | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0156a0001c0001t0002g0261others(1): Show | 4 | HG00597.hp1 NA18957.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-663_115-660del others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643664 | ||||||
chr2:222643713
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.115-708T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643713 | ||||||
chr2:222644418
|
G | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-1413C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644418 | ||||||
chr2:222644502
|
T | G | 32 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(29): Show | 35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.115-1497A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644502 | ||||||
chr2:222644594
|
C | T | 8 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1589G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644594 | ||||||
chr2:222644596
|
G | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-1591C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644596 | ||||||
chr2:222644800
|
G | C | 2 | a0001c0001t0016g0184a0001c0001t0016g0185 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-1795C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644800 | ||||||
chr2:222644929
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-1924C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644929 | ||||||
chr2:222644984
|
CA | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(79): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.115-1980delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644984 | ||||||
chr2:222645106
|
T | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.115-2101A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645106 | ||||||
chr2:222645127
|
G | C | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-2122C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645127 | ||||||
chr2:222645252
|
C | A | 1 | a0001c0001t0008g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.115-2247G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645252 | ||||||
chr2:222645423
|
A | G | 67 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(64): Show | 74 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.115-2418T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645423 | ||||||
chr2:222645501
|
T | G | 30 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(27): Show | 33 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-2496A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645501 | ||||||
chr2:222645542
|
T | C | 77 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(74): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.115-2537A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645542 | ||||||
chr2:222645615
|
CT | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(79): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.115-2611delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645615 | ||||||
chr2:222645675
|
T | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-2670A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645675 | ||||||
chr2:222645724
|
A | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.115-2719T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645724 | ||||||
chr2:222645927
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.114+2813G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645927 | ||||||
chr2:222646085
|
C | T | 1 | a0001c0001t0007g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+2655G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646085 | ||||||
chr2:222646180
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG00673.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.114+2560A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646180 | ||||||
chr2:222646208
|
G | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.114+2532C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646208 | ||||||
chr2:222646227
|
A | G | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+2513T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646227 | ||||||
chr2:222646329
|
ATCT | A | 32 | a0002c0002t0004g0012a0002c0002t0004g0013a0002c0002t0004g0014others(29): Show | 35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.114+2408_114+2410d others(5): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646329 | ||||||
chr2:222646377
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+2363G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646377 | ||||||
chr2:222646538
|
T | A | 16 | a0001c0001t0001g0266a0001c0001t0002g0019a0001c0001t0002g0168others(13): Show | 17 | HG00438.hp1 HG02129.hp2 NA18956.hp1 others(14): Show |
intron_variant | MODIFIER | c.114+2202A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646538 | ||||||
chr2:222646731
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+2009G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646731 | ||||||
chr2:222646789
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1951G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646789 | ||||||
chr2:222646949
|
G | A | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.114+1791C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646949 | ||||||
chr2:222647032
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.114+1708A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647032 | ||||||
chr2:222647071
|
T | C | 1 | a0001c0001t0005g0310 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+1669A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647071 | ||||||
chr2:222647081
|
T | C | 2 | a0002c0002t0004g0210a0002c0002t0028g0208 | 2 | HG01257.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.114+1659A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647081 | ||||||
chr2:222647173
|
T | C | 1 | a0002c0002t0004g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+1567A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647173 | ||||||
chr2:222647231
|
G | T | 1 | a0001c0001t0002g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.114+1509C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647231 | ||||||
chr2:222647523
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.114+1217G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647523 | ||||||
chr2:222647589
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0078 | 2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.114+1151C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647589 | ||||||
chr2:222647626
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+1114T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647626 | ||||||
chr2:222647660
|
G | C | 1 | a0001c0001t0002g0279 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.114+1080C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647660 | ||||||
chr2:222647721
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+1019G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647721 | ||||||
chr2:222647726
|
T | C | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.114+1014A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647726 | ||||||
chr2:222647797
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+943C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647797 | ||||||
chr2:222647941
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+799A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647941 | ||||||
chr2:222648008
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.114+732T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648008 | ||||||
chr2:222648127
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.114+613A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648127 | ||||||
chr2:222648247
|
G | A | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+493C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648247 | ||||||
chr2:222648365
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+375C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648365 | ||||||
chr2:222648426
|
C | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+314G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648426 | ||||||
chr2:222648636
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.114+104T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648636 | ||||||
chr2:222648680
|
CCCTGAAA others(6): Show |
C | 1 | a0001c0001t0007g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+47_114+59delCT others(11): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648680 | ||||||
chr2:222648856
|
T | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-61A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222648856 | ||||||
chr2:222649008
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-213A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649008 | ||||||
chr2:222649044
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-249G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649044 | ||||||
chr2:222649170
|
G | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-375C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649170 | ||||||
chr2:222649175
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0158 | 3 | NA18982.hp2 NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.59-380C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649175 | ||||||
chr2:222649234
|
TA | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(147): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.59-440delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649234 | ||||||
chr2:222649234
|
TAA | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.59-441_59-440delTT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649234 | ||||||
chr2:222649247
|
A | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-452T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649247 | ||||||
chr2:222649263
|
G | A | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-468C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649263 | ||||||
chr2:222649491
|
T | C | 5 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(2): Show | 5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-696A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649491 | ||||||
chr2:222649695
|
C | G | 3 | a0001c0001t0003g0038a0001c0001t0021g0039a0001c0001t0022g0040 | 3 | HG00140.hp2 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-900G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649695 | ||||||
chr2:222649796
|
T | G | 1 | a0001c0001t0003g0031 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.59-1001A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649796 | ||||||
chr2:222649920
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-1125A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649920 | ||||||
chr2:222650235
|
G | C | 12 | a0002c0002t0006g0010a0002c0002t0006g0173a0002c0002t0006g0174others(9): Show | 14 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-1440C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650235 | ||||||
chr2:222650313
|
G | C | 1 | a0002c0002t0004g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.59-1518C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650313 | ||||||
chr2:222650417
|
G | A | 1 | a0002c0002t0006g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.59-1622C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650417 | ||||||
chr2:222650530
|
T | C | 2 | a0002c0002t0006g0212a0002c0002t0006g0213 | 2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.59-1735A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650530 | ||||||
chr2:222650578
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-1783A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650578 | ||||||
chr2:222650650
|
C | T | 3 | a0002c0002t0006g0173a0002c0002t0006g0174a0002c0002t0006g0175 | 3 | HG02451.hp1 HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.59-1855G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650650 | ||||||
chr2:222650846
|
T | C | 19 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0308others(16): Show | 20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-2051A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650846 | ||||||
chr2:222650907
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.59-2112T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650907 | ||||||
chr2:222651192
|
C | A | 3 | a0001c0001t0016g0184a0001c0001t0016g0185a0002c0002t0006g0186 | 3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.59-2397G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651192 | ||||||
chr2:222651338
|
A | G | 77 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(74): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.59-2543T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651338 | ||||||
chr2:222651646
|
T | C | 1 | a0002c0002t0006g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.59-2851A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651646 | ||||||
chr2:222651753
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-2958G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651753 | ||||||
chr2:222651755
|
T | C | 1 | a0001c0001t0003g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.59-2960A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651755 | ||||||
chr2:222651891
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.59-3096A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651891 | ||||||
chr2:222652045
|
T | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(79): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.59-3250A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652045 | ||||||
chr2:222652059
|
G | A | 1 | a0002c0002t0006g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.59-3264C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652059 | ||||||
chr2:222652106
|
G | A | 1 | a0001c0001t0003g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3311C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652106 | ||||||
chr2:222652333
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.59-3538C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652333 | ||||||
chr2:222652415
|
T | G | 1 | a0001c0001t0002g0280 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.58+3601A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652415 | ||||||
chr2:222652458
|
T | C | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.58+3558A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652458 | ||||||
chr2:222652540
|
C | T | 60 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 66 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.58+3476G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652540 | ||||||
chr2:222652584
|
G | A | 2 | a0001c0001t0018g0281a0001c0001t0018g0282 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+3432C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652584 | ||||||
chr2:222652619
|
A | C | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3397T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652619 | ||||||
chr2:222652621
|
C | T | 1 | a0001c0001t0007g0037 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.58+3395G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652621 | ||||||
chr2:222652983
|
T | C | 1 | a0002c0002t0004g0283 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+3033A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652983 | ||||||
chr2:222652986
|
C | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(189): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.58+3030G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652986 | ||||||
chr2:222653015
|
A | G | 1 | a0001c0001t0012g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58+3001T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653015 | ||||||
chr2:222653070
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.58+2946G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653070 | ||||||
chr2:222653160
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034 | 3 | HG02258.hp2 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.58+2856T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653160 | ||||||
chr2:222653229
|
A | G | 1 | a0001c0001t0017g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58+2787T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653229 | ||||||
chr2:222653355
|
TAAAG | T | 15 | a0002c0002t0006g0010a0002c0002t0006g0170a0002c0002t0006g0173others(12): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+2657_58+2660del others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653355 | ||||||
chr2:222653431
|
G | GA | 10 | a0001c0001t0008g0284a0001c0001t0008g0286a0001c0001t0008g0287others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+2584dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653431 | ||||||
chr2:222653432
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 187 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.58+2584T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653432 | ||||||
chr2:222653507
|
A | G | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+2509T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653507 | ||||||
chr2:222653630
|
A | AT | 23 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0005g0306others(20): Show | 24 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.58+2385dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653630 | ||||||
chr2:222653691
|
C | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+2325G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653691 | ||||||
chr2:222653733
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.58+2283G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653733 | ||||||
chr2:222653783
|
A | G | 1 | a0001c0001t0019g0169 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.58+2233T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653783 | ||||||
chr2:222654046
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.58+1970C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654046 | ||||||
chr2:222654088
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1928G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654088 | ||||||
chr2:222654172
|
G | A | 2 | a0002c0002t0006g0297a0002c0002t0006g0298 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58+1844C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654172 | ||||||
chr2:222654178
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.58+1838G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654178 | ||||||
chr2:222654249
|
C | T | 10 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0024others(7): Show | 12 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+1767G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654249 | ||||||
chr2:222654509
|
A | G | 3 | a0001c0001t0002g0165a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | HG02074.hp1 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.58+1507T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654509 | ||||||
chr2:222654611
|
T | C | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+1405A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654611 | ||||||
chr2:222654711
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.58+1305A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654711 | ||||||
chr2:222655171
|
G | A | 2 | a0002c0002t0006g0297a0002c0002t0006g0298 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58+845C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655171 | ||||||
chr2:222655235
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.58+781C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655235 | ||||||
chr2:222655410
|
A | G | 1 | a0001c0001t0003g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.58+606T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655410 | ||||||
chr2:222655465
|
C | T | 4 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0011g0302others(1): Show | 4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+551G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655465 | ||||||
chr2:222655496
|
C | A | 7 | a0001c0001t0005g0312a0001c0001t0005g0313a0001c0001t0005g0314others(4): Show | 7 | HG01361.hp1 HG01975.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+520G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655496 | ||||||
chr2:222655500
|
G | A | 2 | a0001c0001t0005g0318a0001c0001t0005g0319 | 2 | NA18960.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.58+516C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655500 | ||||||
chr2:222655565
|
G | T | 1 | a0005c0006t0035g0299 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+451C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655565 | ||||||
chr2:222655568
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 166 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.58+448G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655568 | ||||||
chr2:222655689
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58+327G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655689 | ||||||
chr2:222655755
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.58+261C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655755 | ||||||
chr2:222655800
|
G | C | 1 | a0001c0001t0020g0020 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.58+216C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655800 |