geneid | 94081 |
---|---|
ensemblid | ENSG00000164466.13 |
hgncid | 16085 |
symbol | SFXN1 |
name | sideroflexin 1 |
refseq_nuc | NM_022754.7 |
refseq_prot | NP_073591.2 |
ensembl_nuc | ENST00000321442.10 |
ensembl_prot | ENSP00000316905.5 |
mane_status | MANE Select |
chr | chr5 |
start | 175478560 |
end | 175529742 |
strand | + |
ver | v1.2 |
region | chr5:175478560-175529742 |
region5000 | chr5:175473560-175534742 |
regionname0 | SFXN1_chr5_175478560_175529742 |
regionname5000 | SFXN1_chr5_175473560_175534742 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 322 | 366 | 89 | 69 | 146 | 14 | 46 | 110 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0002 | 0/0 | 322 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0003 | 0/0 | 322 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0004 | 0/0 | 322 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0005 | 0/0 | 322 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0006 | 0/0 | 322 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 969 | 244 | 47 | 52 | 109 | 11 | 23 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0002 | 0/0 | 969 | 105 | 39 | 12 | 33 | 3 | 18 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0003 | 0/0 | 969 | 12 | 0 | 5 | 3 | 0 | 4 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0004 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0005 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0006 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0007 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0008 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0009 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0010 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0011 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
c0012 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3098 | 69 | 7 | 20 | 27 | 8 | 6 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0002 | 0/0 | 3102 | 67 | 23 | 11 | 19 | 3 | 11 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0003 | 0/0 | 3097 | 66 | 2 | 16 | 36 | 2 | 10 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0004 | 0/0 | 3098 | 31 | 0 | 6 | 24 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0005 | 0/0 | 3102 | 13 | 10 | 3 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0006 | 0/0 | 3103 | 8 | 4 | 0 | 1 | 0 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0007 | 0/0 | 3102 | 8 | 0 | 2 | 3 | 0 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0008 | 0/0 | 3099 | 7 | 0 | 2 | 4 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0009 | 0/0 | 3097 | 6 | 3 | 2 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0010 | 0/0 | 3099 | 6 | 0 | 2 | 3 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0011 | 0/0 | 3098 | 5 | 0 | 0 | 5 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0012 | 0/0 | 3101 | 5 | 1 | 0 | 3 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0013 | 0/0 | 3102 | 5 | 5 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0014 | 0/0 | 3102 | 5 | 0 | 0 | 5 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0015 | 0/0 | 3102 | 4 | 4 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0016 | 0/0 | 3098 | 4 | 4 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0017 | 0/0 | 3098 | 4 | 1 | 0 | 3 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0018 | 0/0 | 3101 | 4 | 3 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0019 | 0/0 | 3102 | 3 | 3 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0020 | 0/0 | 3101 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0021 | 0/0 | 3102 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0022 | 0/0 | 3102 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0023 | 0/0 | 3102 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0024 | 0/0 | 3097 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0025 | 0/0 | 3102 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0026 | 0/0 | 3098 | 2 | 1 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0027 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0028 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0029 | 0/0 | 3102 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0030 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0031 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0032 | 0/0 | 3102 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0033 | 0/0 | 3102 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0034 | 0/0 | 3102 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0035 | 0/0 | 3104 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0036 | 0/0 | 3099 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0037 | 0/0 | 3103 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0038 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0039 | 0/0 | 3101 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0040 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0041 | 0/0 | 3103 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0042 | 0/0 | 3103 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0043 | 0/0 | 3101 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0044 | 0/0 | 3097 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0045 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0046 | 0/0 | 3097 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0047 | 0/0 | 3103 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0048 | 0/0 | 3099 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0049 | 0/0 | 3102 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0050 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0051 | 1/0 | 3098 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0052 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0053 | 0/0 | 3097 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0054 | 0/0 | 3097 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0055 | 0/0 | 3097 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0056 | 0/0 | 3098 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0057 | 0/0 | 3101 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0058 | 0/0 | 3098 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0059 | 0/0 | 3099 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0060 | 0/0 | 3099 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0061 | 0/0 | 3097 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0062 | 0/0 | 3098 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0063 | 0/0 | 3103 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
t0064 | 0/0 | 3103 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0004 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0340 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 969 | 244 | 47 | 52 | 109 | 11 | 23 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002 | 0/0 | 969 | 105 | 39 | 12 | 33 | 3 | 18 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0003 | 0/0 | 969 | 12 | 0 | 5 | 3 | 0 | 4 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0004 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0007 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0010 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0012 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0002c0005 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0003c0008 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0004c0011 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0005c0009 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0006c0006 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4066 | 68 | 7 | 20 | 27 | 8 | 5 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0002 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0003 | 0/0 | 4065 | 64 | 1 | 16 | 36 | 2 | 9 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0004 | 0/0 | 4066 | 28 | 0 | 4 | 23 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0005 | 0/0 | 4070 | 13 | 10 | 3 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0008 | 0/0 | 4067 | 6 | 0 | 1 | 4 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0009 | 0/0 | 4065 | 6 | 3 | 2 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0010 | 0/0 | 4067 | 6 | 0 | 2 | 3 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0013 | 0/0 | 4070 | 5 | 5 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0014 | 0/0 | 4070 | 5 | 0 | 0 | 5 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0016 | 0/0 | 4066 | 4 | 4 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0017 | 0/0 | 4066 | 4 | 1 | 0 | 3 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0018 | 0/0 | 4069 | 4 | 3 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0019 | 0/0 | 4070 | 3 | 3 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0020 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0024 | 0/0 | 4065 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0025 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0026 | 0/0 | 4066 | 2 | 1 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0044 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0045 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0046 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0047 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0048 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0049 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0050 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0051 | 1/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0052 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0053 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0054 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0055 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0056 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0057 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0058 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0059 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0061 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0062 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0001t0063 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0002 | 0/0 | 4070 | 66 | 23 | 11 | 18 | 3 | 11 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0003 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0006 | 0/0 | 4071 | 7 | 3 | 0 | 1 | 0 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0011 | 0/0 | 4066 | 5 | 0 | 0 | 5 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0012 | 0/0 | 4069 | 5 | 1 | 0 | 3 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0015 | 0/0 | 4070 | 4 | 4 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0021 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0022 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0027 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0028 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0029 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0030 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0031 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0032 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0034 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0035 | 0/0 | 4072 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0036 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0037 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0039 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0041 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0042 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0002t0064 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0003t0004 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0003t0007 | 0/0 | 4070 | 8 | 0 | 2 | 3 | 0 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0003t0008 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0003t0043 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0003t0060 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0004t0006 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0004t0038 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0007t0040 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0010t0001 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0001c0012t0004 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0002c0005t0023 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0003c0008t0022 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0004c0011t0004 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0005c0009t0033 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
a0006c0006t0003 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | copy fasta | chr5 | 175473560 | 175534742 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0009g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0009g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0010g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0010g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0010g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0013g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0013g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0014g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0014g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0014g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0014g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0014g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0017g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0017g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0017g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0018g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0018g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0018g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0018g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0019g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0019g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0020g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0024g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0024g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0025g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0025g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0026g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0044g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0045g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0046g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0047g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0048g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0049g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0050g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0051g0340 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0052g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0053g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0054g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0055g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0056g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0057g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0058g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0059g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0061g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0062g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0001t0063g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0011g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0012g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0012g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0012g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0012g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0012g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0015g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0015g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0021g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0021g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0022g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0027g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0029g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0030g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0031g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0032g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0034g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0035g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0036g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0037g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0039g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0041g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0042g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0002t0064g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0008g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0043g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0003t0060g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0004t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0004t0038g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0007t0040g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0010t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0001c0012t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0002c0005t0023g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0002c0005t0023g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0003c0008t0022g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0004c0011t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0005c0009t0033g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
a0006c0006t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0278 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0320 | EUR | FIN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00423 | hp1 | a0001 | c0002 | t0022 | g0287 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00423 | hp2 | a0001 | c0003 | t0007 | g0066 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00544 | hp2 | a0001 | c0001 | t0025 | g0128 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0347 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00621 | hp1 | a0001 | c0002 | t0006 | g0212 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00738 | hp1 | a0001 | c0002 | t0029 | g0334 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG00741 | hp2 | a0001 | c0003 | t0008 | g0014 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0272 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0271 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01099 | hp2 | a0001 | c0003 | t0007 | g0230 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01109 | hp2 | a0001 | c0001 | t0063 | g0141 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0284 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0155 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01192 | hp2 | a0001 | c0001 | t0044 | g0010 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01256 | hp1 | a0001 | c0001 | t0049 | g0266 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0335 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01257 | hp1 | a0001 | c0003 | t0004 | g0065 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0224 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01261 | hp1 | a0001 | c0003 | t0043 | g0013 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01433 | hp2 | a0001 | c0001 | t0018 | g0239 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0363 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01884 | hp1 | a0001 | c0001 | t0050 | g0196 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01891 | hp1 | a0001 | c0001 | t0018 | g0326 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01928 | hp2 | a0001 | c0001 | t0010 | g0299 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01943 | hp2 | a0004 | c0011 | t0004 | g0067 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01993 | hp2 | a0001 | c0003 | t0007 | g0071 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02055 | hp1 | a0001 | c0001 | t0057 | g0176 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02055 | hp2 | a0001 | c0002 | t0006 | g0330 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02056 | hp2 | a0001 | c0001 | t0008 | g0151 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02071 | hp2 | a0001 | c0001 | t0024 | g0217 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02074 | hp2 | a0001 | c0001 | t0017 | g0306 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02080 | hp1 | a0001 | c0002 | t0037 | g0346 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02080 | hp2 | a0001 | c0001 | t0062 | g0042 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0348 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0365 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0339 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02155 | hp2 | a0001 | c0001 | t0014 | g0197 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02165 | hp1 | a0001 | c0003 | t0007 | g0135 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02257 | hp1 | a0001 | c0002 | t0015 | g0075 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0238 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0056 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0226 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02280 | hp1 | a0001 | c0002 | t0015 | g0078 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0273 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02300 | hp2 | a0001 | c0001 | t0010 | g0117 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02451 | hp1 | a0001 | c0001 | t0019 | g0057 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02451 | hp2 | a0001 | c0001 | t0052 | g0090 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0053 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0145 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02602 | hp1 | a0001 | c0002 | t0012 | g0229 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02615 | hp1 | a0001 | c0002 | t0039 | g0015 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02615 | hp2 | a0001 | c0002 | t0027 | g0051 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02622 | hp1 | a0001 | c0002 | t0042 | g0077 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02622 | hp2 | a0001 | c0002 | t0031 | g0260 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0072 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02647 | hp2 | a0001 | c0004 | t0038 | g0029 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0329 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02717 | hp2 | a0006 | c0006 | t0003 | g0079 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0282 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0310 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02738 | hp1 | a0001 | c0001 | t0059 | g0204 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02738 | hp2 | a0001 | c0010 | t0001 | g0018 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0242 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0241 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02886 | hp1 | a0001 | c0002 | t0015 | g0074 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02886 | hp2 | a0001 | c0002 | t0015 | g0089 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02896 | hp1 | a0002 | c0005 | t0023 | g0181 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02922 | hp1 | a0001 | c0001 | t0020 | g0192 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02965 | hp2 | a0001 | c0001 | t0053 | g0083 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0251 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02976 | hp2 | a0001 | c0001 | t0018 | g0327 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03041 | hp2 | a0001 | c0001 | t0055 | g0080 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0073 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0150 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03130 | hp1 | a0001 | c0002 | t0028 | g0187 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0085 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0188 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0121 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03225 | hp2 | a0001 | c0001 | t0045 | g0195 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03239 | hp2 | a0001 | c0001 | t0009 | g0168 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03453 | hp1 | a0001 | c0001 | t0020 | g0193 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03490 | hp1 | a0001 | c0001 | t0010 | g0054 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03516 | hp2 | a0001 | c0001 | t0047 | g0250 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03540 | hp1 | a0001 | c0001 | t0018 | g0328 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0352 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0177 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03579 | hp2 | a0001 | c0007 | t0040 | g0178 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03654 | hp1 | a0001 | c0002 | t0034 | g0356 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0221 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03669 | hp2 | a0001 | c0003 | t0007 | g0070 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03688 | hp1 | a0001 | c0001 | t0058 | g0027 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0281 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0361 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03710 | hp1 | a0001 | c0001 | t0026 | g0062 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03710 | hp2 | a0001 | c0002 | t0006 | g0286 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03831 | hp1 | a0001 | c0002 | t0006 | g0209 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03927 | hp1 | a0001 | c0001 | t0046 | g0082 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0222 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03942 | hp1 | a0001 | c0003 | t0007 | g0012 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03942 | hp2 | a0001 | c0002 | t0006 | g0288 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04115 | hp1 | a0001 | c0002 | t0032 | g0167 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0163 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04184 | hp1 | a0001 | c0003 | t0060 | g0069 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04184 | hp2 | a0001 | c0001 | t0048 | g0009 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0283 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG04228 | hp2 | a0001 | c0003 | t0007 | g0068 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0191 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18939 | hp1 | a0001 | c0012 | t0004 | g0355 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18939 | hp2 | a0001 | c0001 | t0014 | g0185 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18945 | hp2 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18947 | hp2 | a0003 | c0008 | t0022 | g0205 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18948 | hp2 | a0001 | c0002 | t0012 | g0332 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18949 | hp1 | a0001 | c0002 | t0021 | g0261 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18949 | hp2 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18950 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18954 | hp1 | a0001 | c0002 | t0012 | g0357 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18954 | hp2 | a0001 | c0001 | t0017 | g0325 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18960 | hp1 | a0001 | c0002 | t0036 | g0270 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18963 | hp2 | a0001 | c0002 | t0011 | g0256 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18965 | hp1 | a0001 | c0002 | t0012 | g0213 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18965 | hp2 | a0001 | c0001 | t0056 | g0001 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0336 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18967 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0362 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18971 | hp1 | a0001 | c0003 | t0007 | g0063 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18975 | hp2 | a0001 | c0001 | t0017 | g0202 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18984 | hp1 | a0005 | c0009 | t0033 | g0364 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0041 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18992 | hp2 | a0001 | c0001 | t0025 | g0108 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18998 | hp1 | a0001 | c0002 | t0011 | g0201 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19000 | hp1 | a0001 | c0002 | t0011 | g0257 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0350 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0338 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19030 | hp2 | a0002 | c0005 | t0023 | g0179 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19043 | hp1 | a0001 | c0002 | t0012 | g0225 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0333 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19058 | hp2 | a0001 | c0001 | t0061 | g0274 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19066 | hp2 | a0001 | c0001 | t0014 | g0183 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0139 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19070 | hp1 | a0001 | c0001 | t0014 | g0184 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19078 | hp1 | a0001 | c0002 | t0035 | g0344 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0360 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19082 | hp2 | a0001 | c0002 | t0021 | g0262 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0319 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19084 | hp2 | a0001 | c0001 | t0024 | g0247 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19091 | hp2 | a0001 | c0001 | t0014 | g0186 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA19240 | hp2 | a0001 | c0002 | t0030 | g0169 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0351 | AFR | ASW | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0277 | AFR | ASW | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0137 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0175 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20905 | hp1 | a0001 | c0001 | t0054 | g0081 | SAS | GIH | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0302 | SAS | GIH | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02109 | hp2 | a0001 | c0002 | t0064 | g0148 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0289 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0243 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG02559 | hp2 | a0001 | c0001 | t0026 | g0234 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03471 | hp1 | a0001 | c0001 | t0013 | g0252 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG03471 | hp2 | a0001 | c0002 | t0041 | g0146 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG06807 | hp1 | a0001 | c0004 | t0006 | g0149 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0058 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA18955 | hp2 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA20300 | hp2 | a0001 | c0001 | t0019 | g0059 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0134 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0349 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0095 | REF | REF | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0051 | g0340 | REF | REF | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:175492168
|
T | C | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.65T>C | p.Ile22Thr | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 154/4066 | 65/969 | 22/322 | chr5 | 175492168 | ||
chr5:175492180
|
A | G | 1 | a0002 | 2 | HG02896.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.77A>G | p.Asn26Ser | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 166/4066 | 77/969 | 26/322 | chr5 | 175492180 | ||
chr5:175510161
|
G | A | 1 | a0003 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.388G>A | p.Val130Ile | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/11 | 477/4066 | 388/969 | 130/322 | chr5 | 175510161 | ||
chr5:175513470
|
A | C | 1 | a0005 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.604A>C | p.Lys202Gln | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/11 | 693/4066 | 604/969 | 202/322 | chr5 | 175513470 | ||
chr5:175521940
|
C | T | 1 | a0004 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.796C>T | p.Pro266Ser | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/11 | 885/4066 | 796/969 | 266/322 | chr5 | 175521940 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:175492215
|
C | T | 1 | a0001c0012 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.112C>T | p.Leu38Leu | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 201/4066 | 112/969 | 38/322 | chr5 | 175492215 | ||
chr5:175492244
|
G | A | 2 | a0001c0004a0001c0007 | 3 | HG02647.hp2 HG03579.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.141G>A | p.Ala47Ala | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 230/4066 | 141/969 | 47/322 | chr5 | 175492244 | ||
chr5:175509035
|
A | G | 2 | a0001c0003a0004c0011 | 13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
synonymous_variant | LOW | c.168A>G | p.Gln56Gln | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/11 | 257/4066 | 168/969 | 56/322 | chr5 | 175509035 | ||
chr5:175510160
|
C | T | 1 | a0001c0010 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.387C>T | p.Ala129Ala | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/11 | 476/4066 | 387/969 | 129/322 | chr5 | 175510160 | ||
chr5:175510190
|
C | T | 5 | a0001c0002a0001c0004a0002c0005others(2): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
synonymous_variant | LOW | c.417C>T | p.Asp139Asp | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/11 | 506/4066 | 417/969 | 139/322 | chr5 | 175510190 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:175526740
|
G | A | 28 | a0001c0001t0002a0001c0001t0020a0001c0002t0002others(25): Show | 113 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*6G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 6 | chr5 | 175526740 | |||||
chr5:175526774
|
A | C | 1 | a0001c0002t0064 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 40 | chr5 | 175526774 | |||||
chr5:175526788
|
A | G | 6 | a0001c0002t0015a0001c0002t0039a0001c0002t0041others(3): Show | 9 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*54A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 54 | chr5 | 175526788 | |||||
chr5:175526944
|
T | C | 1 | a0001c0004t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 210 | chr5 | 175526944 | |||||
chr5:175527060
|
T | C | 1 | a0001c0002t0027 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 326 | chr5 | 175527060 | |||||
chr5:175527180
|
C | A | 1 | a0001c0002t0011 | 5 | NA18945.hp2 NA18955.hp2 NA18963.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*446C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 446 | chr5 | 175527180 | |||||
chr5:175527210
|
AC | A | 32 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(29): Show | 136 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*479delC | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 479 | INFO_REALIGN_3_PRIME | chr5 | 175527210 | ||||
chr5:175527304
|
C | T | 1 | a0001c0001t0062 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 570 | chr5 | 175527304 | |||||
chr5:175527399
|
G | A | 1 | a0001c0002t0028 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 665 | chr5 | 175527399 | |||||
chr5:175527544
|
A | G | 1 | a0001c0001t0061 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*810A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 810 | chr5 | 175527544 | |||||
chr5:175527849
|
A | G | 1 | a0001c0002t0037 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1115A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1115 | chr5 | 175527849 | |||||
chr5:175527858
|
T | C | 40 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(37): Show | 152 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1124T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1124 | chr5 | 175527858 | |||||
chr5:175527915
|
A | AT | 30 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(27): Show | 137 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1203dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1204 | INFO_REALIGN_3_PRIME | chr5 | 175527915 | ||||
chr5:175527915
|
A | ATT | 8 | a0001c0001t0063a0001c0002t0006a0001c0002t0035others(5): Show | 14 | HG00621.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1202_*1203dupTT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1204 | INFO_REALIGN_3_PRIME | chr5 | 175527915 | ||||
chr5:175527915
|
AT | A | 5 | a0001c0001t0013a0001c0001t0019a0001c0001t0044others(2): Show | 18 | HG00423.hp2 HG01099.hp2 HG01192.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1203delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1203 | INFO_REALIGN_3_PRIME | chr5 | 175527915 | ||||
chr5:175527941
|
A | T | 1 | a0001c0002t0034 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1207A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1207 | chr5 | 175527941 | |||||
chr5:175528012
|
C | T | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1278C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1278 | chr5 | 175528012 | |||||
chr5:175528069
|
C | T | 3 | a0001c0002t0015a0001c0002t0039a0001c0002t0042 | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1335C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1335 | chr5 | 175528069 | |||||
chr5:175528152
|
G | A | 2 | a0001c0003t0007a0001c0003t0043 | 9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1418G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1418 | chr5 | 175528152 | |||||
chr5:175528171
|
G | A | 28 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(25): Show | 128 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1437G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1437 | chr5 | 175528171 | |||||
chr5:175528201
|
A | G | 1 | a0002c0005t0023 | 2 | HG02896.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1467A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1467 | chr5 | 175528201 | |||||
chr5:175528204
|
C | A | 1 | a0001c0003t0043 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1470 | chr5 | 175528204 | |||||
chr5:175528205
|
G | C | 28 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(25): Show | 128 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1471G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1471 | chr5 | 175528205 | |||||
chr5:175528205
|
G | T | 1 | a0001c0002t0021 | 2 | NA18949.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1471G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1471 | chr5 | 175528205 | |||||
chr5:175528442
|
G | A | 2 | a0001c0001t0014a0001c0002t0036 | 6 | HG02155.hp2 NA18939.hp2 NA18960.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1708G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1708 | chr5 | 175528442 | |||||
chr5:175528475
|
G | T | 1 | a0001c0002t0032 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1741 | chr5 | 175528475 | |||||
chr5:175528532
|
T | A | 1 | a0001c0002t0029 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1798T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1798 | chr5 | 175528532 | |||||
chr5:175528569
|
A | T | 31 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(28): Show | 131 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1835A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1835 | chr5 | 175528569 | |||||
chr5:175528581
|
C | T | 29 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(26): Show | 125 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1847C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1847 | chr5 | 175528581 | |||||
chr5:175528667
|
G | C | 2 | a0001c0001t0026a0001c0001t0059 | 3 | HG02559.hp2 HG02738.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1933G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1933 | chr5 | 175528667 | |||||
chr5:175528673
|
C | T | 2 | a0001c0001t0058a0001c0003t0060 | 2 | HG03688.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1939C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1939 | chr5 | 175528673 | |||||
chr5:175528743
|
G | A | 1 | a0001c0002t0030 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2009 | chr5 | 175528743 | |||||
chr5:175528743
|
G | C | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(21): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2009G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2009 | chr5 | 175528743 | |||||
chr5:175528791
|
G | A | 28 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(25): Show | 124 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2057G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2057 | chr5 | 175528791 | |||||
chr5:175528934
|
T | C | 1 | a0001c0001t0014 | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2200T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2200 | chr5 | 175528934 | |||||
chr5:175529036
|
G | T | 29 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(26): Show | 125 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2302G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2302 | chr5 | 175529036 | |||||
chr5:175529064
|
C | T | 1 | a0001c0004t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2330C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2330 | chr5 | 175529064 | |||||
chr5:175529077
|
C | T | 1 | a0001c0002t0064 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2343C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2343 | chr5 | 175529077 | |||||
chr5:175529108
|
G | A | 1 | a0001c0001t0052 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2374G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2374 | chr5 | 175529108 | |||||
chr5:175529120
|
T | G | 1 | a0001c0001t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2386T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2386 | chr5 | 175529120 | |||||
chr5:175529260
|
T | C | 29 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(26): Show | 125 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2526T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2526 | chr5 | 175529260 | |||||
chr5:175529326
|
G | A | 1 | a0001c0001t0056 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2592G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2592 | chr5 | 175529326 | |||||
chr5:175529338
|
C | CA | 5 | a0001c0001t0013a0001c0001t0019a0001c0001t0047others(2): Show | 18 | HG00423.hp2 HG01099.hp2 HG01993.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2618dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2619 | INFO_REALIGN_3_PRIME | chr5 | 175529338 | ||||
chr5:175529338
|
CA | C | 3 | a0001c0001t0018a0001c0001t0020a0001c0001t0057 | 7 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2618delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2618 | INFO_REALIGN_3_PRIME | chr5 | 175529338 | ||||
chr5:175529351
|
A | G | 1 | a0001c0001t0055 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2617A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2617 | chr5 | 175529351 | |||||
chr5:175529430
|
T | C | 2 | a0001c0001t0005a0001c0001t0063 | 14 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2696T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2696 | chr5 | 175529430 | |||||
chr5:175529464
|
A | G | 34 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(31): Show | 143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2730A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2730 | chr5 | 175529464 | |||||
chr5:175529484
|
T | TAAAC | 39 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(36): Show | 153 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2750_*2751insAAAC | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2751 | chr5 | 175529484 | |||||
chr5:175529531
|
GA | G | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0017others(8): Show | 83 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2806delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2806 | INFO_REALIGN_3_PRIME | chr5 | 175529531 | ||||
chr5:175529569
|
G | T | 1 | a0001c0001t0054 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2835 | chr5 | 175529569 | |||||
chr5:175529619
|
G | T | 2 | a0001c0001t0046a0001c0001t0053 | 2 | HG02965.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2885G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2885 | chr5 | 175529619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:175478673
|
TG | T | 192 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.-10+38delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175478673 | |||||
chr5:175478748
|
G | T | 1 | a0001c0002t0002g0365 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-10+109G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478748 | ||||||
chr5:175478758
|
C | T | 1 | a0001c0001t0014g0197 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-10+119C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478758 | ||||||
chr5:175478808
|
C | CG | 72 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(69): Show | 72 | HG00280.hp1 HG00544.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10+179dupG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175478808 | |||||
chr5:175478808
|
CG | C | 23 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0009g0177others(20): Show | 23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10+179delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175478808 | |||||
chr5:175478817
|
G | T | 19 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0014g0183others(16): Show | 19 | HG01884.hp1 HG02145.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+178G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478817 | ||||||
chr5:175478827
|
C | T | 1 | a0001c0001t0003g0175 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-10+188C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478827 | ||||||
chr5:175478862
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+223C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478862 | ||||||
chr5:175478865
|
C | T | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+226C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478865 | ||||||
chr5:175478892
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0045g0195 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-10+253C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478892 | ||||||
chr5:175478912
|
T | C | 18 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0014g0183others(15): Show | 18 | HG02145.hp2 HG02155.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-10+273T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478912 | ||||||
chr5:175479308
|
T | C | 12 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0014g0183others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+669T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479308 | ||||||
chr5:175479370
|
G | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-10+731G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479370 | ||||||
chr5:175479448
|
A | G | 12 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0014g0183others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+809A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479448 | ||||||
chr5:175479651
|
C | T | 1 | a0001c0002t0002g0363 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-10+1012C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479651 | ||||||
chr5:175479780
|
C | T | 1 | a0001c0002t0030g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-10+1141C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479780 | ||||||
chr5:175479861
|
T | G | 11 | a0001c0001t0020g0192a0001c0001t0020g0193a0001c0002t0002g0050others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+1222T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479861 | ||||||
chr5:175479862
|
T | C | 163 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-10+1223T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479862 | ||||||
chr5:175479901
|
C | G | 1 | a0001c0001t0003g0362 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-10+1262C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479901 | ||||||
chr5:175479903
|
G | A | 122 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-10+1264G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479903 | ||||||
chr5:175479923
|
G | A | 2 | a0001c0002t0002g0238a0001c0002t0002g0363 | 2 | HG01515.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-10+1284G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479923 | ||||||
chr5:175479997
|
A | G | 11 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0014g0183others(8): Show | 11 | HG02145.hp2 HG02155.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+1358A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479997 | ||||||
chr5:175480100
|
T | G | 11 | a0001c0001t0020g0192a0001c0001t0020g0193a0001c0002t0002g0050others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+1461T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480100 | ||||||
chr5:175480139
|
C | T | 1 | a0001c0002t0012g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10+1500C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480139 | ||||||
chr5:175480153
|
G | T | 1 | a0001c0001t0016g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10+1514G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480153 | ||||||
chr5:175480176
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0138a0001c0001t0001g0140others(1): Show | 4 | NA18747.hp1 NA18968.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+1537C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480176 | ||||||
chr5:175480227
|
C | T | 1 | a0001c0002t0002g0361 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-10+1588C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480227 | ||||||
chr5:175480245
|
C | CA | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1612dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175480245 | |||||
chr5:175480257
|
T | C | 1 | a0001c0001t0018g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10+1618T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480257 | ||||||
chr5:175480261
|
C | T | 1 | a0001c0001t0018g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10+1622C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480261 | ||||||
chr5:175480288
|
C | G | 1 | a0001c0001t0003g0360 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-10+1649C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480288 | ||||||
chr5:175480294
|
G | A | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10+1655G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480294 | ||||||
chr5:175480363
|
T | C | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+1724T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480363 | ||||||
chr5:175480396
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0010g0054others(2): Show | 5 | HG01192.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1757G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480396 | ||||||
chr5:175480400
|
T | TA | 20 | a0001c0001t0001g0011a0001c0001t0001g0194a0001c0001t0003g0182others(17): Show | 20 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10+1774dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175480400 | |||||
chr5:175480438
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1799A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480438 | ||||||
chr5:175480457
|
T | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-10+1818T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480457 | ||||||
chr5:175480581
|
C | T | 1 | a0001c0003t0007g0135 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-10+1942C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480581 | ||||||
chr5:175480745
|
ACC | A | 8 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0016g0134others(5): Show | 8 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+2108_-10+2109d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175480745 | |||||
chr5:175480780
|
C | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+2141C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480780 | ||||||
chr5:175480796
|
C | T | 2 | a0001c0001t0003g0358a0001c0001t0003g0359 | 2 | NA18999.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-10+2157C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480796 | ||||||
chr5:175480860
|
A | G | 1 | a0001c0001t0005g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+2221A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480860 | ||||||
chr5:175480904
|
C | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+2265C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480904 | ||||||
chr5:175480921
|
G | A | 10 | a0001c0001t0013g0056a0001c0001t0014g0183a0001c0001t0014g0184others(7): Show | 10 | HG01884.hp1 HG02155.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+2282G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480921 | ||||||
chr5:175480942
|
A | G | 105 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-10+2303A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480942 | ||||||
chr5:175480974
|
G | A | 10 | a0001c0001t0013g0056a0001c0001t0014g0183a0001c0001t0014g0184others(7): Show | 10 | HG01884.hp1 HG02155.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+2335G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480974 | ||||||
chr5:175481001
|
T | C | 1 | a0002c0005t0023g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10+2362T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481001 | ||||||
chr5:175481091
|
T | C | 1 | a0001c0001t0003g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-10+2452T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481091 | ||||||
chr5:175481196
|
T | C | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2557T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481196 | ||||||
chr5:175481304
|
G | C | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2665G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481304 | ||||||
chr5:175481334
|
G | T | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2695G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481334 | ||||||
chr5:175481356
|
C | G | 5 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2717C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481356 | ||||||
chr5:175481391
|
A | G | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2752A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481391 | ||||||
chr5:175481462
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2823C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481462 | ||||||
chr5:175481480
|
C | T | 95 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-10+2841C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481480 | ||||||
chr5:175481505
|
G | A | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+2866G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481505 | ||||||
chr5:175481606
|
G | A | 37 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(34): Show | 37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+2967G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481606 | ||||||
chr5:175481645
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3006G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481645 | ||||||
chr5:175481682
|
G | T | 4 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+3043G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481682 | ||||||
chr5:175481715
|
G | C | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10+3076G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481715 | ||||||
chr5:175481798
|
A | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-10+3159A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481798 | ||||||
chr5:175481842
|
T | C | 14 | a0001c0001t0013g0251a0001c0001t0013g0252a0001c0001t0020g0192others(11): Show | 14 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+3203T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481842 | ||||||
chr5:175481877
|
A | AG | 37 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(34): Show | 37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+3240dupG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175481877 | |||||
chr5:175481880
|
C | A | 37 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(34): Show | 37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+3241C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481880 | ||||||
chr5:175481881
|
C | T | 37 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(34): Show | 37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+3242C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481881 | ||||||
chr5:175482193
|
C | G | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+3554C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482193 | ||||||
chr5:175482221
|
T | C | 199 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-10+3582T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482221 | ||||||
chr5:175482229
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3590A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482229 | ||||||
chr5:175482249
|
C | T | 1 | a0001c0002t0030g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-10+3610C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482249 | ||||||
chr5:175482299
|
T | C | 168 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-10+3660T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482299 | ||||||
chr5:175482485
|
C | A | 78 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10+3846C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482485 | ||||||
chr5:175482640
|
A | C | 200 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-10+4001A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482640 | ||||||
chr5:175482663
|
C | G | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+4024C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482663 | ||||||
chr5:175482708
|
A | C | 32 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(29): Show | 32 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+4069A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482708 | ||||||
chr5:175482865
|
T | C | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+4226T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482865 | ||||||
chr5:175483024
|
G | A | 1 | a0001c0002t0028g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+4385G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483024 | ||||||
chr5:175483084
|
A | G | 1 | a0001c0001t0019g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-10+4445A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483084 | ||||||
chr5:175483174
|
A | G | 37 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(34): Show | 37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+4535A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483174 | ||||||
chr5:175483207
|
G | T | 32 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(29): Show | 32 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+4568G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483207 | ||||||
chr5:175483593
|
C | T | 4 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+4954C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483593 | ||||||
chr5:175483616
|
A | G | 35 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(32): Show | 35 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+4977A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483616 | ||||||
chr5:175483621
|
A | T | 166 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-10+4982A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483621 | ||||||
chr5:175483637
|
C | T | 1 | a0001c0002t0002g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+4998C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483637 | ||||||
chr5:175483697
|
C | A | 77 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-10+5058C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483697 | ||||||
chr5:175483698
|
TG | T | 5 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5060delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483698 | ||||||
chr5:175483710
|
G | A | 14 | a0001c0001t0003g0245a0001c0002t0002g0064a0001c0003t0004g0065others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+5071G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483710 | ||||||
chr5:175483937
|
A | T | 1 | a0001c0002t0012g0357 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-10+5298A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483937 | ||||||
chr5:175483966
|
G | A | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+5327G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483966 | ||||||
chr5:175484026
|
G | A | 32 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(29): Show | 32 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+5387G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484026 | ||||||
chr5:175484083
|
C | CACA | 32 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(29): Show | 32 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+5444_-10+5445i others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484083 | ||||||
chr5:175484092
|
A | C | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+5453A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484092 | ||||||
chr5:175484119
|
A | G | 1 | a0001c0003t0008g0014 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-10+5480A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484119 | ||||||
chr5:175484129
|
G | A | 1 | a0001c0003t0007g0063 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-10+5490G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484129 | ||||||
chr5:175484130
|
C | T | 7 | a0001c0001t0003g0017a0001c0001t0003g0084a0001c0001t0003g0086others(4): Show | 7 | HG02886.hp2 HG03130.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+5491C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484130 | ||||||
chr5:175484148
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+5509G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484148 | ||||||
chr5:175484230
|
C | T | 32 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(29): Show | 32 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+5591C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484230 | ||||||
chr5:175484420
|
C | G | 196 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-10+5781C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484420 | ||||||
chr5:175484437
|
A | T | 7 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+5798A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484437 | ||||||
chr5:175484463
|
G | A | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(31): Show | 34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+5824G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484463 | ||||||
chr5:175484496
|
C | T | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(31): Show | 34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+5857C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484496 | ||||||
chr5:175484500
|
G | A | 1 | a0001c0002t0002g0254 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-10+5861G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484500 | ||||||
chr5:175484516
|
A | G | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(31): Show | 34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+5877A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484516 | ||||||
chr5:175484542
|
C | T | 56 | a0001c0001t0001g0147a0001c0001t0001g0235a0001c0001t0001g0236others(53): Show | 56 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.-10+5903C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484542 | ||||||
chr5:175484545
|
G | A | 2 | a0001c0002t0002g0145a0001c0002t0041g0146 | 2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+5906G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484545 | ||||||
chr5:175484558
|
G | C | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10+5919G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484558 | ||||||
chr5:175484598
|
A | G | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-10+5959A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484598 | ||||||
chr5:175484661
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-10+6022G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484661 | ||||||
chr5:175484666
|
G | A | 2 | a0001c0001t0016g0072a0001c0001t0016g0073 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+6027G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484666 | ||||||
chr5:175484672
|
T | C | 198 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-10+6033T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484672 | ||||||
chr5:175484706
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+6067C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484706 | ||||||
chr5:175484709
|
C | T | 1 | a0001c0002t0034g0356 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10+6070C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484709 | ||||||
chr5:175484719
|
C | T | 35 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(32): Show | 35 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+6080C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484719 | ||||||
chr5:175484749
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10+6110C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484749 | ||||||
chr5:175484760
|
A | G | 1 | a0001c0001t0003g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+6121A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484760 | ||||||
chr5:175484847
|
C | T | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+6208C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484847 | ||||||
chr5:175484994
|
C | T | 1 | a0001c0012t0004g0355 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-10+6355C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484994 | ||||||
chr5:175484998
|
C | T | 1 | a0001c0001t0003g0354 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-10+6359C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484998 | ||||||
chr5:175484999
|
G | A | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(31): Show | 34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+6360G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484999 | ||||||
chr5:175485035
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0025g0128 | 2 | HG00544.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-10+6396C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485035 | ||||||
chr5:175485037
|
GTT | G | 6 | a0001c0001t0001g0255a0001c0001t0003g0258a0001c0002t0011g0002others(3): Show | 7 | NA18945.hp2 NA18955.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+6399_-10+6400d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485037 | ||||||
chr5:175485062
|
T | G | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+6423T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485062 | ||||||
chr5:175485199
|
T | C | 14 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+6560T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485199 | ||||||
chr5:175485336
|
T | C | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(31): Show | 34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+6697T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485336 | ||||||
chr5:175485394
|
T | A | 1 | a0001c0001t0003g0259 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-9-6701T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485394 | ||||||
chr5:175485570
|
A | G | 1 | a0001c0003t0007g0135 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9-6525A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485570 | ||||||
chr5:175485575
|
A | G | 1 | a0001c0001t0003g0353 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-9-6520A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485575 | ||||||
chr5:175485708
|
T | A | 1 | a0001c0004t0038g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9-6387T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485708 | ||||||
chr5:175485762
|
G | C | 162 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-9-6333G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485762 | ||||||
chr5:175485808
|
T | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-6287T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485808 | ||||||
chr5:175485869
|
C | T | 1 | a0001c0002t0002g0363 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-9-6226C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485869 | ||||||
chr5:175485886
|
C | T | 34 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(31): Show | 34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-9-6209C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485886 | ||||||
chr5:175485892
|
C | T | 2 | a0001c0001t0005g0351a0001c0002t0002g0352 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-9-6203C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485892 | ||||||
chr5:175485967
|
T | C | 162 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-9-6128T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485967 | ||||||
chr5:175486104
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5991A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486104 | ||||||
chr5:175486126
|
A | G | 1 | a0001c0001t0058g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9-5969A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486126 | ||||||
chr5:175486185
|
A | AG | 8 | a0001c0001t0003g0127a0001c0001t0005g0142a0001c0001t0005g0143others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-5909dupG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175486185 | |||||
chr5:175486186
|
GT | G | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5908delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486186 | ||||||
chr5:175486187
|
T | G | 190 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-9-5908T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486187 | ||||||
chr5:175486194
|
G | T | 15 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(12): Show | 15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-5901G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486194 | ||||||
chr5:175486355
|
C | G | 7 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-5740C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486355 | ||||||
chr5:175486395
|
A | G | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-5700A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486395 | ||||||
chr5:175486456
|
T | C | 1 | a0001c0002t0031g0260 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9-5639T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486456 | ||||||
chr5:175486910
|
C | T | 15 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(12): Show | 15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-5185C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486910 | ||||||
chr5:175486966
|
T | C | 2 | a0001c0002t0021g0261a0001c0002t0021g0262 | 2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-9-5129T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486966 | ||||||
chr5:175487005
|
G | A | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-5090G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487005 | ||||||
chr5:175487123
|
C | T | 1 | a0001c0002t0002g0350 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-9-4972C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487123 | ||||||
chr5:175487124
|
G | A | 1 | a0006c0006t0003g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9-4971G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487124 | ||||||
chr5:175487134
|
A | G | 10 | a0001c0001t0003g0175a0001c0001t0013g0056a0001c0001t0019g0057others(7): Show | 10 | HG02258.hp2 HG02451.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-4961A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487134 | ||||||
chr5:175487268
|
C | T | 1 | a0001c0002t0002g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9-4827C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487268 | ||||||
chr5:175487444
|
C | T | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-4651C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487444 | ||||||
chr5:175487523
|
C | T | 5 | a0001c0001t0003g0026a0001c0001t0003g0123a0001c0001t0003g0124others(2): Show | 5 | HG01192.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4572C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487523 | ||||||
chr5:175487634
|
G | A | 2 | a0001c0003t0004g0065a0001c0003t0008g0014 | 2 | HG00741.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-9-4461G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487634 | ||||||
chr5:175487662
|
A | G | 1 | a0006c0006t0003g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9-4433A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487662 | ||||||
chr5:175487681
|
A | G | 5 | a0001c0001t0005g0025a0001c0001t0005g0122a0001c0002t0002g0119others(2): Show | 5 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4414A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487681 | ||||||
chr5:175487746
|
G | A | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-4349G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487746 | ||||||
chr5:175487777
|
G | C | 1 | a0001c0002t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9-4318G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487777 | ||||||
chr5:175487784
|
G | A | 33 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(30): Show | 33 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9-4311G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487784 | ||||||
chr5:175487832
|
C | G | 6 | a0001c0002t0002g0076a0001c0002t0015g0074a0001c0002t0015g0075others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-4263C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487832 | ||||||
chr5:175487833
|
C | T | 7 | a0001c0001t0001g0227a0001c0001t0001g0343a0001c0002t0002g0345others(4): Show | 7 | HG00597.hp1 HG00609.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-4262C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487833 | ||||||
chr5:175487834
|
A | T | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-4261A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487834 | ||||||
chr5:175487836
|
C | T | 1 | a0001c0001t0003g0342 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-9-4259C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487836 | ||||||
chr5:175487968
|
C | T | 1 | a0001c0002t0002g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9-4127C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487968 | ||||||
chr5:175487992
|
T | G | 9 | a0001c0001t0003g0003a0001c0001t0003g0166a0001c0001t0003g0203others(6): Show | 10 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-4103T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487992 | ||||||
chr5:175488213
|
C | T | 1 | a0001c0001t0004g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-9-3882C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488213 | ||||||
chr5:175488236
|
A | G | 2 | a0001c0001t0016g0072a0001c0001t0016g0073 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-3859A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488236 | ||||||
chr5:175488262
|
G | A | 6 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-3833G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488262 | ||||||
chr5:175488305
|
C | CTT | 7 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-3777_-9-3776dup others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175488305 | |||||
chr5:175488305
|
C | CTTT | 27 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(24): Show | 27 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9-3778_-9-3776dup others(3): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175488305 | |||||
chr5:175488332
|
C | T | 1 | a0001c0001t0003g0341 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-9-3763C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488332 | ||||||
chr5:175488349
|
C | G | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-3746C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488349 | ||||||
chr5:175488352
|
G | T | 1 | a0001c0001t0008g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-9-3743G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488352 | ||||||
chr5:175488366
|
G | A | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-3729G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488366 | ||||||
chr5:175488500
|
C | T | 35 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(32): Show | 35 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9-3595C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488500 | ||||||
chr5:175488510
|
G | A | 1 | a0001c0003t0007g0066 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9-3585G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488510 | ||||||
chr5:175488519
|
G | C | 13 | a0001c0003t0004g0065a0001c0003t0007g0012a0001c0003t0007g0063others(10): Show | 13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-3576G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488519 | ||||||
chr5:175488591
|
G | A | 22 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(19): Show | 22 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9-3504G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488591 | ||||||
chr5:175488695
|
C | CT | 15 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(12): Show | 15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-3397dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175488695 | |||||
chr5:175488761
|
T | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-3334T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488761 | ||||||
chr5:175488948
|
G | T | 1 | a0001c0001t0009g0168 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-9-3147G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488948 | ||||||
chr5:175488968
|
G | C | 1 | a0001c0002t0002g0061 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-9-3127G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488968 | ||||||
chr5:175489037
|
C | T | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-3058C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489037 | ||||||
chr5:175489119
|
C | T | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-2976C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489119 | ||||||
chr5:175489120
|
T | TA | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-2975_-9-2974ins others(1): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489120 | ||||||
chr5:175489281
|
G | A | 6 | a0001c0001t0003g0175a0001c0001t0014g0183a0001c0001t0014g0184others(3): Show | 6 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-2814G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489281 | ||||||
chr5:175489401
|
T | C | 163 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-9-2694T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489401 | ||||||
chr5:175489405
|
C | T | 3 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0118 | 3 | HG00735.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-9-2690C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489405 | ||||||
chr5:175489442
|
A | G | 87 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-9-2653A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489442 | ||||||
chr5:175489455
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-2640G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489455 | ||||||
chr5:175489456
|
A | G | 4 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-2639A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489456 | ||||||
chr5:175489537
|
A | G | 1 | a0001c0002t0002g0226 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-9-2558A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489537 | ||||||
chr5:175489599
|
G | A | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-2496G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489599 | ||||||
chr5:175489621
|
A | G | 1 | a0001c0001t0004g0045 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-9-2474A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489621 | ||||||
chr5:175489652
|
T | C | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-2443T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489652 | ||||||
chr5:175489749
|
A | G | 1 | a0001c0002t0034g0356 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-9-2346A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489749 | ||||||
chr5:175489907
|
C | T | 16 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(13): Show | 16 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-2188C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489907 | ||||||
chr5:175489943
|
T | G | 1 | a0001c0001t0003g0268 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-9-2152T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489943 | ||||||
chr5:175490130
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-9-1965T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490130 | ||||||
chr5:175490164
|
C | T | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9-1931C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490164 | ||||||
chr5:175490187
|
T | C | 1 | a0001c0001t0005g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9-1908T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490187 | ||||||
chr5:175490207
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-9-1888C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490207 | ||||||
chr5:175490421
|
T | C | 198 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9-1674T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490421 | ||||||
chr5:175490557
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1538A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490557 | ||||||
chr5:175490603
|
T | G | 191 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-9-1492T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490603 | ||||||
chr5:175490859
|
A | AT | 16 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(13): Show | 16 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-1236_-9-1235ins others(1): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490859 | ||||||
chr5:175490859
|
A | T | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1236A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490859 | ||||||
chr5:175490861
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1234A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490861 | ||||||
chr5:175490901
|
A | T | 1 | a0001c0002t0002g0350 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-9-1194A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490901 | ||||||
chr5:175490991
|
T | A | 15 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0084others(12): Show | 15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-1104T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490991 | ||||||
chr5:175491007
|
C | T | 178 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-9-1088C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491007 | ||||||
chr5:175491035
|
C | T | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-1060C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491035 | ||||||
chr5:175491256
|
T | A | 198 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-9-839T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491256 | ||||||
chr5:175491313
|
G | A | 146 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9-782G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491313 | ||||||
chr5:175491359
|
C | T | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-736C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491359 | ||||||
chr5:175491389
|
G | A | 162 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-9-706G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491389 | ||||||
chr5:175491408
|
G | A | 1 | a0001c0001t0003g0269 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-9-687G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491408 | ||||||
chr5:175491445
|
G | A | 1 | a0001c0002t0015g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9-650G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491445 | ||||||
chr5:175491477
|
C | CT | 14 | a0001c0001t0002g0164a0001c0001t0003g0258a0001c0001t0013g0251others(11): Show | 14 | HG02074.hp1 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-604dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175491477 | |||||
chr5:175491477
|
CT | C | 17 | a0001c0001t0003g0360a0001c0002t0036g0270a0001c0003t0004g0065others(14): Show | 17 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-604delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175491477 | |||||
chr5:175491488
|
T | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-607T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491488 | ||||||
chr5:175491540
|
T | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-555T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491540 | ||||||
chr5:175491629
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0010g0117 | 2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-9-466C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491629 | ||||||
chr5:175491687
|
G | A | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-408G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491687 | ||||||
chr5:175491720
|
C | T | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-375C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491720 | ||||||
chr5:175491777
|
G | A | 162 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-9-318G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491777 | ||||||
chr5:175491798
|
G | A | 365 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(362): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-9-297G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491798 | ||||||
chr5:175492053
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-42A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175492053 | ||||||
chr5:175492387
|
C | T | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+120C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492387 | ||||||
chr5:175492388
|
CA | C | 184 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.164+134delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175492388 | |||||
chr5:175492388
|
CAA | C | 14 | a0001c0001t0001g0115a0001c0001t0014g0186a0001c0003t0004g0065others(11): Show | 14 | HG00423.hp2 HG00558.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.164+133_164+134del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175492388 | |||||
chr5:175492427
|
T | C | 2 | a0001c0001t0003g0175a0001c0001t0054g0081 | 2 | NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.164+160T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492427 | ||||||
chr5:175492447
|
C | A | 79 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.164+180C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492447 | ||||||
chr5:175492456
|
G | C | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+189G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492456 | ||||||
chr5:175492641
|
G | A | 2 | a0001c0001t0004g0031a0001c0001t0004g0032 | 2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.164+374G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492641 | ||||||
chr5:175492741
|
C | T | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+474C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492741 | ||||||
chr5:175492792
|
G | A | 1 | a0001c0004t0006g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164+525G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492792 | ||||||
chr5:175492859
|
A | G | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.164+592A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492859 | ||||||
chr5:175492946
|
A | T | 1 | a0001c0002t0002g0244 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.164+679A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492946 | ||||||
chr5:175493012
|
G | A | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+745G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493012 | ||||||
chr5:175493035
|
C | T | 3 | a0001c0002t0002g0338a0001c0002t0006g0339a0001c0002t0031g0260 | 3 | HG02145.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.164+768C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493035 | ||||||
chr5:175493122
|
G | A | 6 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(3): Show | 6 | HG02258.hp2 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+855G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493122 | ||||||
chr5:175493126
|
G | A | 1 | a0001c0003t0008g0014 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.164+859G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493126 | ||||||
chr5:175493184
|
C | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.164+917C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493184 | ||||||
chr5:175493190
|
C | T | 310 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(307): Show | 314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.164+923C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493190 | ||||||
chr5:175493248
|
A | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+981A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493248 | ||||||
chr5:175493269
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.164+1002A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493269 | ||||||
chr5:175493344
|
G | A | 1 | a0001c0001t0004g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.164+1077G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493344 | ||||||
chr5:175493517
|
A | C | 3 | a0001c0002t0002g0294a0001c0002t0002g0295a0001c0002t0012g0213 | 3 | NA18957.hp1 NA18965.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.164+1250A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493517 | ||||||
chr5:175493596
|
C | T | 7 | a0001c0002t0002g0076a0001c0002t0002g0180a0001c0002t0015g0074others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+1329C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493596 | ||||||
chr5:175493635
|
A | G | 1 | a0001c0001t0003g0337 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.164+1368A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493635 | ||||||
chr5:175493745
|
G | A | 12 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0091others(9): Show | 12 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+1478G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493745 | ||||||
chr5:175493818
|
A | G | 1 | a0001c0002t0041g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164+1551A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493818 | ||||||
chr5:175493821
|
C | G | 2 | a0001c0001t0001g0129a0001c0001t0025g0128 | 2 | HG00544.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.164+1554C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493821 | ||||||
chr5:175493830
|
TA | T | 15 | a0001c0001t0001g0147a0001c0001t0005g0023a0001c0001t0005g0024others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.164+1566delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175493830 | |||||
chr5:175493965
|
G | A | 1 | a0001c0004t0006g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164+1698G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493965 | ||||||
chr5:175494167
|
C | T | 181 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0255others(178): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.164+1900C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494167 | ||||||
chr5:175494184
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.164+1917A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494184 | ||||||
chr5:175494226
|
T | A | 1 | a0001c0001t0005g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.164+1959T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494226 | ||||||
chr5:175494428
|
A | G | 123 | a0001c0001t0003g0279a0001c0001t0009g0177a0001c0001t0013g0056others(120): Show | 127 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.164+2161A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494428 | ||||||
chr5:175494440
|
G | T | 1 | a0001c0012t0004g0355 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.164+2173G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494440 | ||||||
chr5:175494470
|
G | A | 4 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0035others(1): Show | 4 | HG00544.hp1 HG02155.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2203G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494470 | ||||||
chr5:175494515
|
A | G | 4 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0035others(1): Show | 4 | HG00544.hp1 HG02155.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2248A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494515 | ||||||
chr5:175494576
|
C | T | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+2309C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494576 | ||||||
chr5:175494580
|
T | C | 2 | a0001c0001t0004g0153a0001c0001t0004g0154 | 2 | NA18990.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.164+2313T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494580 | ||||||
chr5:175494612
|
C | T | 86 | a0001c0001t0013g0241a0001c0001t0013g0242a0001c0001t0018g0239others(83): Show | 90 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.164+2345C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494612 | ||||||
chr5:175494619
|
G | A | 6 | a0001c0002t0002g0007a0001c0002t0002g0345a0001c0002t0002g0347others(3): Show | 7 | HG00597.hp1 HG02080.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+2352G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494619 | ||||||
chr5:175494727
|
G | A | 4 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2460G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494727 | ||||||
chr5:175494739
|
C | T | 1 | a0001c0002t0012g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164+2472C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494739 | ||||||
chr5:175494748
|
A | G | 121 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(118): Show | 125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+2481A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494748 | ||||||
chr5:175494751
|
T | TA | 7 | a0001c0001t0008g0151a0001c0001t0014g0183a0001c0001t0014g0184others(4): Show | 7 | HG01109.hp2 HG02056.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+2498dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175494751 | |||||
chr5:175494793
|
A | G | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+2526A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494793 | ||||||
chr5:175494866
|
G | A | 22 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(19): Show | 22 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.164+2599G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494866 | ||||||
chr5:175494876
|
A | G | 1 | a0001c0001t0005g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.164+2609A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494876 | ||||||
chr5:175495046
|
G | A | 119 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(116): Show | 123 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.164+2779G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495046 | ||||||
chr5:175495094
|
T | C | 4 | a0001c0001t0018g0239a0001c0001t0018g0326a0001c0001t0018g0327others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2827T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495094 | ||||||
chr5:175495174
|
A | G | 15 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.164+2907A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495174 | ||||||
chr5:175495207
|
G | C | 1 | a0001c0001t0003g0341 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.164+2940G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495207 | ||||||
chr5:175495247
|
G | C | 2 | a0001c0001t0009g0177a0001c0002t0064g0148 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.164+2980G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495247 | ||||||
chr5:175495278
|
G | T | 1 | a0001c0002t0041g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164+3011G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495278 | ||||||
chr5:175495369
|
A | G | 286 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.164+3102A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495369 | ||||||
chr5:175495383
|
T | C | 85 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.164+3116T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495383 | ||||||
chr5:175495447
|
G | T | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3180G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495447 | ||||||
chr5:175495492
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+3225G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495492 | ||||||
chr5:175495518
|
C | T | 98 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(95): Show | 102 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.164+3251C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495518 | ||||||
chr5:175495675
|
C | G | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3408C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495675 | ||||||
chr5:175495687
|
C | T | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164+3420C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495687 | ||||||
chr5:175495694
|
A | G | 1 | a0001c0001t0003g0220 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.164+3427A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495694 | ||||||
chr5:175495728
|
C | CA | 107 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.164+3473dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495728 | |||||
chr5:175495728
|
CA | C | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3473delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495728 | |||||
chr5:175495767
|
C | T | 96 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(93): Show | 100 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.164+3500C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495767 | ||||||
chr5:175495796
|
C | A | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3529C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495796 | ||||||
chr5:175495891
|
G | A | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3624G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495891 | ||||||
chr5:175495903
|
C | CT | 8 | a0001c0001t0001g0049a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 8 | HG00597.hp2 HG02300.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+3650dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495903 | |||||
chr5:175495903
|
CTT | C | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3649_164+3650d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495903 | |||||
chr5:175495977
|
A | G | 197 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(194): Show | 201 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.164+3710A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495977 | ||||||
chr5:175495986
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.164+3719C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495986 | ||||||
chr5:175496041
|
C | T | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3774C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496041 | ||||||
chr5:175496109
|
A | G | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3842A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496109 | ||||||
chr5:175496138
|
T | G | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164+3871T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496138 | ||||||
chr5:175496247
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.164+3980C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496247 | ||||||
chr5:175496251
|
C | T | 2 | a0001c0001t0009g0177a0001c0002t0064g0148 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.164+3984C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496251 | ||||||
chr5:175496278
|
G | A | 1 | a0001c0002t0021g0261 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.164+4011G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496278 | ||||||
chr5:175496299
|
G | A | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164+4032G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496299 | ||||||
chr5:175496358
|
G | A | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+4091G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496358 | ||||||
chr5:175496376
|
A | G | 17 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(14): Show | 17 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.164+4109A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496376 | ||||||
chr5:175496384
|
T | C | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+4117T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496384 | ||||||
chr5:175496401
|
A | G | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+4134A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496401 | ||||||
chr5:175496702
|
C | G | 2 | a0001c0001t0009g0177a0001c0002t0064g0148 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.164+4435C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496702 | ||||||
chr5:175496756
|
GAATCCCT others(909): Show |
G | 1 | a0001c0001t0016g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164+4496_164+5411d others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175496756 | |||||
chr5:175496898
|
C | CT | 126 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0300others(123): Show | 130 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.164+4642dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175496898 | |||||
chr5:175496950
|
G | A | 2 | a0001c0004t0038g0029a0001c0007t0040g0178 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164+4683G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496950 | ||||||
chr5:175496967
|
T | C | 286 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.164+4700T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496967 | ||||||
chr5:175497035
|
A | G | 121 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(118): Show | 125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+4768A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497035 | ||||||
chr5:175497043
|
T | C | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+4776T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497043 | ||||||
chr5:175497364
|
T | G | 1 | a0001c0001t0003g0302 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.164+5097T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497364 | ||||||
chr5:175497644
|
C | T | 121 | a0001c0001t0001g0132a0001c0001t0009g0177a0001c0001t0013g0056others(118): Show | 125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+5377C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497644 | ||||||
chr5:175497657
|
A | G | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164+5390A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497657 | ||||||
chr5:175497717
|
T | G | 1 | a0001c0002t0002g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.164+5450T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497717 | ||||||
chr5:175497764
|
G | A | 198 | a0001c0001t0001g0132a0001c0001t0002g0164a0001c0001t0004g0001others(195): Show | 202 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.164+5497G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497764 | ||||||
chr5:175497788
|
G | A | 7 | a0001c0001t0013g0056a0001c0001t0013g0251a0001c0001t0013g0252others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+5521G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497788 | ||||||
chr5:175497873
|
T | A | 2 | a0001c0002t0006g0339a0001c0002t0031g0260 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.164+5606T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497873 | ||||||
chr5:175497936
|
G | GA | 22 | a0001c0001t0001g0214a0001c0001t0001g0227a0001c0001t0001g0235others(19): Show | 22 | HG00597.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.164+5688dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175497936 | |||||
chr5:175497936
|
GA | G | 105 | a0001c0001t0001g0132a0001c0001t0001g0194a0001c0001t0003g0323others(102): Show | 109 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.164+5688delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175497936 | |||||
chr5:175497967
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164+5700G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497967 | ||||||
chr5:175497988
|
T | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+5721T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497988 | ||||||
chr5:175498059
|
A | AAAAT | 121 | a0001c0001t0001g0132a0001c0001t0009g0177a0001c0001t0013g0056others(118): Show | 125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+5795_164+5796i others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175498059 | |||||
chr5:175498084
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0010g0054 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.164+5817G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498084 | ||||||
chr5:175498086
|
AATTAATG others(21): Show |
A | 2 | a0001c0001t0016g0072a0001c0001t0016g0073 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.164+5838_164+5865d others(30): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175498086 | |||||
chr5:175498102
|
A | G | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+5835A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498102 | ||||||
chr5:175498163
|
A | C | 3 | a0001c0002t0002g0199a0001c0002t0002g0243a0001c0002t0002g0244 | 3 | HG01167.hp2 HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.164+5896A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498163 | ||||||
chr5:175498172
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+5905G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498172 | ||||||
chr5:175498282
|
A | G | 1 | a0001c0002t0015g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.164+6015A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498282 | ||||||
chr5:175498313
|
T | C | 1 | a0001c0003t0007g0063 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.164+6046T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498313 | ||||||
chr5:175498346
|
A | AC | 14 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.164+6080dupC | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175498346 | |||||
chr5:175498420
|
C | T | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+6153C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498420 | ||||||
chr5:175498493
|
A | G | 16 | a0001c0001t0001g0132a0001c0001t0009g0177a0001c0002t0064g0148others(13): Show | 16 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.164+6226A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498493 | ||||||
chr5:175498650
|
A | G | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.164+6383A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498650 | ||||||
chr5:175498713
|
G | A | 119 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(116): Show | 123 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.164+6446G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498713 | ||||||
chr5:175498715
|
A | G | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+6448A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498715 | ||||||
chr5:175498824
|
A | G | 120 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(117): Show | 124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+6557A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498824 | ||||||
chr5:175498838
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.164+6571G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498838 | ||||||
chr5:175499002
|
C | T | 25 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(22): Show | 25 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.164+6735C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499002 | ||||||
chr5:175499134
|
T | A | 14 | a0001c0002t0064g0148a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.164+6867T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499134 | ||||||
chr5:175499138
|
C | T | 23 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(20): Show | 23 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.164+6871C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499138 | ||||||
chr5:175499234
|
A | G | 23 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(20): Show | 23 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.164+6967A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499234 | ||||||
chr5:175499248
|
C | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+6981C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499248 | ||||||
chr5:175499257
|
GA | G | 114 | a0001c0001t0005g0144a0001c0001t0013g0056a0001c0001t0013g0241others(111): Show | 118 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.164+7002delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175499257 | |||||
chr5:175499270
|
G | A | 19 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(16): Show | 19 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.164+7003G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499270 | ||||||
chr5:175499273
|
A | G | 40 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(37): Show | 40 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.164+7006A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499273 | ||||||
chr5:175499312
|
G | A | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164+7045G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499312 | ||||||
chr5:175499378
|
A | T | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.164+7111A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499378 | ||||||
chr5:175499451
|
G | C | 1 | a0001c0001t0003g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164+7184G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499451 | ||||||
chr5:175499660
|
C | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0038 | 2 | NA18982.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.164+7393C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499660 | ||||||
chr5:175499680
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.164+7413T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499680 | ||||||
chr5:175499835
|
G | A | 2 | a0001c0001t0013g0241a0001c0001t0013g0242 | 2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.164+7568G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499835 | ||||||
chr5:175499879
|
T | C | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+7612T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499879 | ||||||
chr5:175500294
|
T | A | 5 | a0001c0002t0011g0002a0001c0002t0011g0201a0001c0002t0011g0256others(2): Show | 6 | NA18945.hp2 NA18955.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+8027T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175500294 | ||||||
chr5:175500403
|
A | AAC | 70 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.164+8186_164+8187d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
A | AACAC | 18 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0111others(15): Show | 18 | HG00597.hp2 HG01192.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.164+8184_164+8187d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
A | AACACAC | 7 | a0001c0001t0001g0022a0001c0001t0003g0047a0001c0001t0003g0175others(4): Show | 7 | HG00741.hp1 HG01981.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+8182_164+8187d others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
A | AACACACA others(3): Show |
1 | a0001c0001t0009g0277 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164+8178_164+8187d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AAC | A | 40 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0235others(37): Show | 40 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.164+8186_164+8187d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACAC | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0170a0001c0001t0001g0171others(16): Show | 19 | HG00423.hp2 HG00741.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.164+8184_164+8187d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACAC | A | 12 | a0001c0001t0001g0194a0001c0001t0001g0231a0001c0001t0001g0232others(9): Show | 12 | HG01243.hp1 HG02109.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.164+8182_164+8187d others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(1): Show |
A | 12 | a0001c0001t0004g0039a0001c0001t0005g0024a0001c0001t0005g0351others(9): Show | 12 | HG01169.hp2 HG02155.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+8180_164+8187d others(10): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(3): Show |
A | 21 | a0001c0001t0005g0023a0001c0001t0005g0025a0001c0001t0005g0091others(18): Show | 21 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.164+8178_164+8187d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(5): Show |
A | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.164+8176_164+8187d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(7): Show |
A | 8 | a0001c0001t0020g0192a0001c0001t0020g0193a0001c0002t0002g0053others(5): Show | 8 | HG00621.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+8174_164+8187d others(16): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(9): Show |
A | 8 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0060others(5): Show | 8 | HG00673.hp1 HG01884.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+8172_164+8187d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(11): Show |
A | 77 | a0001c0001t0018g0239a0001c0001t0018g0326a0001c0001t0018g0327others(74): Show | 81 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.164+8170_164+8187d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(13): Show |
A | 1 | a0001c0002t0032g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164+8168_164+8187d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500403
|
AACACACA others(15): Show |
A | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+8166_164+8187d others(24): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | |||||
chr5:175500789
|
G | A | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165-8243G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175500789 | ||||||
chr5:175501063
|
A | AT | 37 | a0001c0001t0001g0094a0001c0001t0001g0140a0001c0001t0001g0200others(34): Show | 37 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.165-7946dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501063
|
A | ATT | 8 | a0001c0001t0020g0192a0001c0001t0020g0193a0001c0001t0063g0141others(5): Show | 8 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-7947_165-7946d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501063
|
A | ATTT | 18 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(15): Show | 18 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.165-7948_165-7946d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501063
|
A | ATTTT | 7 | a0001c0001t0005g0093a0001c0001t0005g0118a0001c0001t0009g0177others(4): Show | 7 | HG00735.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-7949_165-7946d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501063
|
AT | A | 12 | a0001c0001t0001g0095a0001c0002t0002g0224a0001c0002t0002g0289others(9): Show | 12 | HG00621.hp1 HG01258.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.165-7946delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501063
|
ATT | A | 84 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(81): Show | 88 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.165-7947_165-7946d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501063
|
ATTT | A | 22 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(19): Show | 22 | HG00741.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.165-7948_165-7946d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | |||||
chr5:175501129
|
C | T | 92 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(89): Show | 96 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.165-7903C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501129 | ||||||
chr5:175501192
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | NA18747.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.165-7840C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501192 | ||||||
chr5:175501194
|
G | A | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7838G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501194 | ||||||
chr5:175501195
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.165-7837A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501195 | ||||||
chr5:175501225
|
C | A | 1 | a0004c0011t0004g0067 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.165-7807C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501225 | ||||||
chr5:175501244
|
A | AT | 4 | a0001c0001t0018g0239a0001c0001t0018g0326a0001c0001t0018g0327others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-7783dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501244 | |||||
chr5:175501261
|
G | A | 4 | a0001c0002t0002g0331a0001c0002t0002g0336a0001c0002t0012g0332others(1): Show | 4 | NA18948.hp2 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-7771G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501261 | ||||||
chr5:175501306
|
T | G | 4 | a0001c0002t0002g0206a0001c0002t0002g0207a0001c0002t0002g0208others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-7726T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501306 | ||||||
chr5:175501320
|
G | A | 1 | a0001c0001t0010g0299 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.165-7712G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501320 | ||||||
chr5:175501360
|
G | A | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.165-7672G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501360 | ||||||
chr5:175501615
|
A | G | 13 | a0001c0003t0004g0065a0001c0003t0007g0012a0001c0003t0007g0063others(10): Show | 13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-7417A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501615 | ||||||
chr5:175501796
|
C | T | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165-7236C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501796 | ||||||
chr5:175501803
|
T | G | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7229T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501803 | ||||||
chr5:175501925
|
A | T | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7107A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501925 | ||||||
chr5:175501996
|
C | G | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7036C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501996 | ||||||
chr5:175502153
|
G | A | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-6879G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502153 | ||||||
chr5:175502223
|
G | T | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-6809G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502223 | ||||||
chr5:175502286
|
A | T | 1 | a0001c0002t0002g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165-6746A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502286 | ||||||
chr5:175502373
|
A | G | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-6659A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502373 | ||||||
chr5:175502553
|
G | A | 1 | a0001c0002t0002g0350 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.165-6479G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502553 | ||||||
chr5:175502597
|
G | A | 1 | a0001c0002t0015g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.165-6435G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502597 | ||||||
chr5:175502656
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-6376A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502656 | ||||||
chr5:175502698
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.165-6334G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502698 | ||||||
chr5:175502829
|
A | G | 53 | a0001c0001t0001g0132a0001c0001t0009g0177a0001c0001t0013g0056others(50): Show | 53 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.165-6203A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502829 | ||||||
chr5:175502861
|
T | TAATA | 28 | a0001c0001t0001g0132a0001c0001t0013g0056a0001c0001t0013g0241others(25): Show | 28 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.165-6157_165-6154d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175502861 | |||||
chr5:175502988
|
G | A | 2 | a0001c0001t0020g0192a0001c0001t0020g0193 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.165-6044G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502988 | ||||||
chr5:175503237
|
A | G | 14 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-5795A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503237 | ||||||
chr5:175503316
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.165-5716C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503316 | ||||||
chr5:175503396
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.165-5636C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503396 | ||||||
chr5:175503449
|
G | A | 176 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(173): Show | 180 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.165-5583G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503449 | ||||||
chr5:175503453
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0003g0182a0001c0001t0045g0195 | 3 | HG02486.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.165-5579A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503453 | ||||||
chr5:175503661
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.165-5371C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503661 | ||||||
chr5:175503744
|
C | T | 113 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(110): Show | 113 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.165-5288C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503744 | ||||||
chr5:175503745
|
A | G | 199 | a0001c0001t0001g0132a0001c0001t0002g0164a0001c0001t0004g0001others(196): Show | 203 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.165-5287A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503745 | ||||||
chr5:175503831
|
C | T | 21 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(18): Show | 21 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.165-5201C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503831 | ||||||
chr5:175503870
|
G | A | 1 | a0001c0001t0003g0313 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.165-5162G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503870 | ||||||
chr5:175503875
|
G | A | 1 | a0001c0001t0017g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165-5157G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503875 | ||||||
chr5:175503904
|
T | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-5128T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503904 | ||||||
chr5:175503912
|
G | A | 1 | a0001c0002t0002g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.165-5120G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503912 | ||||||
chr5:175503927
|
CT | C | 62 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5104delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503927 | ||||||
chr5:175503928
|
T | C | 23 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(20): Show | 23 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.165-5104T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503928 | ||||||
chr5:175503929
|
G | C | 62 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5103G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503929 | ||||||
chr5:175503931
|
G | C | 62 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5101G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503931 | ||||||
chr5:175503932
|
A | T | 62 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5100A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503932 | ||||||
chr5:175503959
|
C | T | 84 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(81): Show | 88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165-5073C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503959 | ||||||
chr5:175503972
|
T | C | 20 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-5060T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503972 | ||||||
chr5:175503993
|
C | T | 84 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(81): Show | 88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165-5039C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503993 | ||||||
chr5:175504003
|
C | CAA | 23 | a0001c0001t0005g0024a0001c0001t0013g0056a0001c0001t0013g0241others(20): Show | 23 | HG01169.hp2 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.165-5013_165-5012d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | |||||
chr5:175504003
|
C | CAAA | 28 | a0001c0001t0005g0023a0001c0001t0005g0025a0001c0001t0005g0091others(25): Show | 28 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.165-5014_165-5012d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | |||||
chr5:175504003
|
C | CAAAAA | 39 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(36): Show | 39 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.165-5016_165-5012d others(7): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | |||||
chr5:175504003
|
CA | C | 6 | a0001c0001t0001g0131a0001c0001t0003g0342a0001c0001t0003g0353others(3): Show | 6 | HG01257.hp2 HG01515.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-5012delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | |||||
chr5:175504023
|
G | A | 101 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(98): Show | 101 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.165-5009G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504023 | ||||||
chr5:175504054
|
G | A | 1 | a0001c0003t0008g0014 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.165-4978G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504054 | ||||||
chr5:175504416
|
AAC | A | 23 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(20): Show | 23 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.165-4612_165-4611d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504416 | |||||
chr5:175504429
|
A | G | 36 | a0001c0001t0009g0177a0001c0002t0002g0050a0001c0002t0002g0052others(33): Show | 36 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.165-4603A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504429 | ||||||
chr5:175504431
|
C | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-4601C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504431 | ||||||
chr5:175504443
|
C | T | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-4589C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504443 | ||||||
chr5:175504504
|
G | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-4528G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504504 | ||||||
chr5:175504573
|
C | CA | 9 | a0001c0001t0003g0219a0001c0001t0014g0183a0001c0001t0014g0184others(6): Show | 10 | HG02109.hp2 HG02155.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.165-4445dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504573 | |||||
chr5:175504573
|
CA | C | 12 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(9): Show | 12 | HG01256.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.165-4445delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504573 | |||||
chr5:175504577
|
A | C | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-4455A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504577 | ||||||
chr5:175504768
|
G | T | 1 | a0001c0001t0013g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165-4264G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504768 | ||||||
chr5:175504821
|
C | T | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0014g0183others(2): Show | 5 | NA18747.hp2 NA18939.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-4211C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504821 | ||||||
chr5:175504829
|
C | T | 5 | a0001c0001t0003g0026a0001c0001t0003g0123a0001c0001t0003g0124others(2): Show | 5 | HG01192.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-4203C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504829 | ||||||
chr5:175504874
|
G | A | 12 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(9): Show | 12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-4158G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504874 | ||||||
chr5:175504936
|
G | T | 60 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.165-4096G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504936 | ||||||
chr5:175505008
|
A | G | 119 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(116): Show | 123 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.165-4024A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505008 | ||||||
chr5:175505020
|
A | G | 137 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(134): Show | 141 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.165-4012A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505020 | ||||||
chr5:175505026
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.165-4006C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505026 | ||||||
chr5:175505067
|
C | T | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165-3965C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505067 | ||||||
chr5:175505083
|
C | T | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-3949C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505083 | ||||||
chr5:175505125
|
A | T | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165-3907A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505125 | ||||||
chr5:175505206
|
A | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0094others(3): Show | 6 | HG01106.hp2 HG01433.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-3826A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505206 | ||||||
chr5:175505218
|
A | G | 1 | a0001c0002t0002g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.165-3814A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505218 | ||||||
chr5:175505312
|
A | C | 1 | a0001c0002t0002g0282 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.165-3720A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505312 | ||||||
chr5:175505390
|
A | G | 6 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-3642A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505390 | ||||||
chr5:175505536
|
A | T | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-3496A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505536 | ||||||
chr5:175505537
|
C | CAAT | 13 | a0001c0001t0001g0147a0001c0001t0003g0016a0001c0001t0003g0136others(10): Show | 13 | HG01952.hp2 HG02165.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-3461_165-3459d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
C | CAATAAT | 9 | a0001c0001t0001g0255a0001c0001t0003g0026a0001c0001t0003g0123others(6): Show | 9 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-3464_165-3459d others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
C | CAATAATA others(2): Show |
21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(18): Show | 21 | HG00558.hp2 HG00609.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.165-3467_165-3459d others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
C | CAATAATA others(5): Show |
52 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.165-3470_165-3459d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
C | CAATAATA others(8): Show |
19 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0048others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.165-3473_165-3459d others(17): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
C | CAATAATA others(11): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0095others(3): Show | 6 | HG00558.hp1 HG00642.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-3476_165-3459d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
C | CAATAATA others(17): Show |
1 | a0001c0001t0014g0186 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.165-3482_165-3459d others(26): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
CAAT | C | 57 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(54): Show | 57 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.165-3461_165-3459d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
CAATAATA others(2): Show |
C | 2 | a0001c0002t0002g0007a0001c0002t0064g0148 | 3 | HG02109.hp2 NA18969.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.165-3467_165-3459d others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505537
|
CAATAATA others(5): Show |
C | 114 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(111): Show | 117 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.165-3470_165-3459d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | |||||
chr5:175505582
|
T | G | 108 | a0001c0001t0009g0177a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 112 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.165-3450T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505582 | ||||||
chr5:175505663
|
G | C | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-3369G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505663 | ||||||
chr5:175505671
|
T | C | 1 | a0001c0001t0003g0313 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.165-3361T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505671 | ||||||
chr5:175505711
|
A | G | 136 | a0001c0001t0001g0132a0001c0001t0009g0177a0001c0001t0013g0056others(133): Show | 140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.165-3321A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505711 | ||||||
chr5:175505809
|
T | C | 131 | a0001c0001t0001g0132a0001c0001t0009g0177a0001c0001t0013g0056others(128): Show | 135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.165-3223T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505809 | ||||||
chr5:175505875
|
A | G | 4 | a0001c0001t0003g0219a0001c0001t0003g0245a0001c0001t0003g0323others(1): Show | 4 | HG02083.hp1 NA18981.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-3157A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505875 | ||||||
chr5:175505937
|
T | C | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-3095T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505937 | ||||||
chr5:175505961
|
C | T | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-3071C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505961 | ||||||
chr5:175506060
|
T | C | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2972T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506060 | ||||||
chr5:175506088
|
G | C | 118 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(115): Show | 122 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.165-2944G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506088 | ||||||
chr5:175506339
|
G | A | 2 | a0001c0001t0024g0217a0001c0002t0064g0148 | 2 | HG02071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.165-2693G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506339 | ||||||
chr5:175506362
|
A | T | 8 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-2670A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506362 | ||||||
chr5:175506410
|
G | A | 1 | a0001c0001t0055g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165-2622G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506410 | ||||||
chr5:175506459
|
T | C | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-2573T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506459 | ||||||
chr5:175506479
|
C | A | 2 | a0001c0002t0006g0339a0001c0002t0031g0260 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.165-2553C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506479 | ||||||
chr5:175506576
|
T | C | 1 | a0001c0001t0016g0072 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165-2456T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506576 | ||||||
chr5:175506653
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.165-2379A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506653 | ||||||
chr5:175506659
|
T | A | 197 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(194): Show | 201 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.165-2373T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506659 | ||||||
chr5:175506728
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2304A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506728 | ||||||
chr5:175506754
|
C | T | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2278C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506754 | ||||||
chr5:175506817
|
A | C | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2215A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506817 | ||||||
chr5:175506924
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2108A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506924 | ||||||
chr5:175506953
|
C | T | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-2079C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506953 | ||||||
chr5:175506961
|
G | A | 1 | a0006c0006t0003g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165-2071G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506961 | ||||||
chr5:175507043
|
A | G | 1 | a0001c0001t0013g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165-1989A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507043 | ||||||
chr5:175507059
|
A | G | 97 | a0001c0001t0009g0177a0001c0002t0002g0004a0001c0002t0002g0005others(94): Show | 101 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.165-1973A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507059 | ||||||
chr5:175507122
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1910A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507122 | ||||||
chr5:175507128
|
C | T | 2 | a0001c0002t0002g0211a0001c0002t0002g0281 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.165-1904C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507128 | ||||||
chr5:175507168
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.165-1864A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507168 | ||||||
chr5:175507198
|
A | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0173others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-1834A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507198 | ||||||
chr5:175507211
|
A | G | 7 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-1821A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507211 | ||||||
chr5:175507333
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1699A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507333 | ||||||
chr5:175507434
|
A | G | 14 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1598A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507434 | ||||||
chr5:175507435
|
A | T | 14 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1597A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507435 | ||||||
chr5:175507473
|
A | C | 14 | a0001c0001t0001g0132a0001c0003t0004g0065a0001c0003t0007g0012others(11): Show | 14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1559A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507473 | ||||||
chr5:175507479
|
A | G | 60 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.165-1553A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507479 | ||||||
chr5:175507553
|
T | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1479T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507553 | ||||||
chr5:175507554
|
A | G | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165-1478A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507554 | ||||||
chr5:175507586
|
A | T | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1446A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507586 | ||||||
chr5:175507594
|
T | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1438T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507594 | ||||||
chr5:175507620
|
C | T | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1412C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507620 | ||||||
chr5:175507627
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165-1405C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507627 | ||||||
chr5:175507652
|
A | G | 40 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(37): Show | 40 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.165-1380A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507652 | ||||||
chr5:175507658
|
C | T | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1374C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507658 | ||||||
chr5:175507663
|
A | G | 1 | a0006c0006t0003g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165-1369A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507663 | ||||||
chr5:175507682
|
G | A | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-1350G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507682 | ||||||
chr5:175507804
|
C | T | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-1228C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507804 | ||||||
chr5:175507850
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-1182A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507850 | ||||||
chr5:175507970
|
C | CT | 39 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(36): Show | 39 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.165-1059dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507970 | |||||
chr5:175507973
|
T | TAAAAAAA | 10 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(7): Show | 10 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.165-1046_165-1040d others(9): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | |||||
chr5:175507973
|
T | TAAAATAA others(2): Show |
16 | a0001c0002t0002g0050a0001c0002t0002g0076a0001c0002t0002g0145others(13): Show | 16 | HG01884.hp2 HG02080.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.165-1055_165-1054i others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | |||||
chr5:175507973
|
T | TAAAATAA others(3): Show |
3 | a0001c0002t0002g0052a0001c0002t0015g0075a0001c0002t0041g0146 | 3 | HG02257.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.165-1055_165-1054i others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | |||||
chr5:175507973
|
TA | T | 103 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(100): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.165-1040delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | |||||
chr5:175507974
|
A | AAAATAAA others(3): Show |
6 | a0001c0002t0015g0074a0001c0002t0015g0078a0001c0002t0015g0089others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-1055_165-1054i others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507974 | |||||
chr5:175507975
|
A | AAATAAAA others(2): Show |
77 | a0001c0001t0009g0177a0001c0002t0002g0004a0001c0002t0002g0005others(74): Show | 81 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.165-1055_165-1054i others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507975 | |||||
chr5:175507992
|
A | G | 3 | a0001c0002t0002g0224a0001c0002t0002g0335a0001c0002t0029g0334 | 3 | HG00738.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.165-1040A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507992 | ||||||
chr5:175507994
|
T | C | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-1038T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507994 | ||||||
chr5:175508080
|
A | G | 3 | a0001c0003t0004g0065a0001c0003t0008g0014a0004c0011t0004g0067 | 3 | HG00741.hp2 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.165-952A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508080 | ||||||
chr5:175508110
|
A | G | 13 | a0001c0003t0004g0065a0001c0003t0007g0012a0001c0003t0007g0063others(10): Show | 13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-922A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508110 | ||||||
chr5:175508156
|
A | G | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-876A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508156 | ||||||
chr5:175508217
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-815A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508217 | ||||||
chr5:175508222
|
A | AT | 54 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.165-784dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | |||||
chr5:175508222
|
A | ATT | 12 | a0001c0001t0002g0164a0001c0001t0004g0156a0001c0001t0004g0157others(9): Show | 12 | HG00621.hp2 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-785_165-784dup others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | |||||
chr5:175508222
|
AT | A | 221 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(218): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.165-784delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | |||||
chr5:175508222
|
ATT | A | 16 | a0001c0001t0003g0084a0001c0001t0014g0183a0001c0001t0014g0184others(13): Show | 16 | HG02155.hp2 HG02717.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-785_165-784del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | |||||
chr5:175508222
|
ATTTT | A | 11 | a0001c0003t0007g0063a0001c0003t0007g0066a0001c0003t0007g0068others(8): Show | 11 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.165-787_165-784del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | |||||
chr5:175508222
|
ATTTTT | A | 10 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(7): Show | 10 | HG01257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.165-788_165-784del others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | |||||
chr5:175508281
|
A | G | 2 | a0001c0002t0002g0347a0001c0002t0002g0348 | 2 | HG00597.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.165-751A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508281 | ||||||
chr5:175508291
|
T | C | 1 | a0001c0002t0002g0191 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165-741T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508291 | ||||||
chr5:175508319
|
G | A | 2 | a0001c0002t0002g0206a0001c0002t0064g0148 | 2 | HG01993.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.165-713G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508319 | ||||||
chr5:175508325
|
A | C | 2 | a0001c0001t0001g0276a0001c0001t0061g0274 | 2 | NA18946.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.165-707A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508325 | ||||||
chr5:175508416
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-616A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508416 | ||||||
chr5:175508443
|
A | C | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-589A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508443 | ||||||
chr5:175508457
|
A | G | 13 | a0001c0003t0004g0065a0001c0003t0007g0012a0001c0003t0007g0063others(10): Show | 13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-575A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508457 | ||||||
chr5:175508474
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-558A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508474 | ||||||
chr5:175508526
|
C | T | 4 | a0001c0001t0016g0072a0001c0001t0016g0073a0001c0001t0016g0150others(1): Show | 4 | HG01884.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-506C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508526 | ||||||
chr5:175508568
|
A | G | 117 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-464A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508568 | ||||||
chr5:175508610
|
C | G | 1 | a0001c0004t0038g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165-422C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508610 | ||||||
chr5:175508645
|
A | AT | 117 | a0001c0001t0005g0142a0001c0001t0009g0177a0001c0001t0013g0056others(114): Show | 121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-376dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508645 | |||||
chr5:175508793
|
G | A | 108 | a0001c0001t0009g0177a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 112 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.165-239G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508793 | ||||||
chr5:175508826
|
C | T | 27 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(24): Show | 27 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.165-206C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508826 | ||||||
chr5:175508857
|
T | G | 108 | a0001c0001t0009g0177a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 112 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.165-175T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508857 | ||||||
chr5:175508913
|
A | G | 135 | a0001c0001t0009g0177a0001c0001t0013g0056a0001c0001t0013g0241others(132): Show | 139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.165-119A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508913 | ||||||
chr5:175508973
|
T | A | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-59T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508973 | ||||||
chr5:175509230
|
T | C | 23 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(20): Show | 23 | HG00621.hp2 HG00673.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.335+28T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509230 | ||||||
chr5:175509309
|
T | G | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.335+107T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509309 | ||||||
chr5:175509315
|
GACAA | G | 3 | a0001c0002t0064g0148a0002c0005t0023g0179a0002c0005t0023g0181 | 3 | HG02109.hp2 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.335+118_335+121del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 175509315 | |||||
chr5:175509364
|
A | G | 13 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(10): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.335+162A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509364 | ||||||
chr5:175509455
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.335+253A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509455 | ||||||
chr5:175509517
|
C | CT | 8 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 8 | HG01981.hp1 HG01981.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+326dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 175509517 | |||||
chr5:175509559
|
T | C | 12 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(9): Show | 12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.335+357T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509559 | ||||||
chr5:175509699
|
A | G | 92 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(89): Show | 96 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.336-410A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509699 | ||||||
chr5:175509699
|
A | T | 12 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(9): Show | 12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.336-410A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509699 | ||||||
chr5:175510061
|
C | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.336-48C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175510061 | ||||||
chr5:175510417
|
T | C | 1 | a0001c0001t0046g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434+210T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510417 | ||||||
chr5:175510480
|
T | G | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.434+273T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510480 | ||||||
chr5:175510500
|
A | G | 1 | a0001c0002t0041g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.434+293A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510500 | ||||||
chr5:175510520
|
G | A | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.434+313G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510520 | ||||||
chr5:175510732
|
TA | T | 8 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.434+535delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 175510732 | |||||
chr5:175510772
|
G | A | 104 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(101): Show | 108 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.434+565G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510772 | ||||||
chr5:175510795
|
A | T | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.434+588A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510795 | ||||||
chr5:175510972
|
T | C | 135 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(132): Show | 139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.435-479T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510972 | ||||||
chr5:175510980
|
CTT | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0115a0001c0001t0001g0129others(4): Show | 7 | HG00558.hp1 NA18747.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-470_435-469del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510980 | ||||||
chr5:175511009
|
T | G | 104 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(101): Show | 108 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.435-442T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175511009 | ||||||
chr5:175511141
|
G | T | 1 | a0001c0001t0005g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.435-310G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175511141 | ||||||
chr5:175511439
|
T | C | 1 | a0001c0001t0004g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.435-12T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175511439 | ||||||
chr5:175511691
|
A | T | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+165A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511691 | ||||||
chr5:175511740
|
CTG | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.510+218_510+219del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511740 | |||||
chr5:175511763
|
C | G | 1 | a0001c0002t0012g0213 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510+237C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511763 | ||||||
chr5:175511817
|
A | T | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.510+291A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511817 | ||||||
chr5:175511821
|
C | G | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-290C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511821 | ||||||
chr5:175511822
|
T | C | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-289T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511822 | ||||||
chr5:175511823
|
C | A | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-288C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511823 | ||||||
chr5:175511824
|
T | G | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-287T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511824 | ||||||
chr5:175511838
|
A | C | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-273A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511838 | ||||||
chr5:175511839
|
G | A | 1 | a0001c0001t0024g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-272G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511839 | ||||||
chr5:175511841
|
A | ATC | 3 | a0001c0002t0064g0148a0002c0005t0023g0179a0002c0005t0023g0181 | 3 | HG02109.hp2 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-249_511-248dup others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | |||||
chr5:175511841
|
A | ATCTCTC | 90 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(87): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.511-253_511-248dup others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | |||||
chr5:175511841
|
A | ATCTCTCT others(1): Show |
9 | a0001c0002t0002g0293a0001c0002t0002g0294a0001c0002t0002g0295others(6): Show | 9 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-255_511-248dup others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | |||||
chr5:175511841
|
A | ATCTCTCT others(3): Show |
1 | a0001c0002t0006g0339 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.511-257_511-248dup others(10): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | |||||
chr5:175511841
|
A | ATCTCTCT others(5): Show |
2 | a0001c0002t0031g0260a0001c0004t0038g0029 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.511-259_511-248dup others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | |||||
chr5:175511860
|
TCTCC | T | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.511-249_511-246del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511860 | |||||
chr5:175511862
|
TCC | T | 19 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(16): Show | 19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.511-246_511-245del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511862 | |||||
chr5:175511864
|
C | T | 101 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(98): Show | 105 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.511-247C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511864 | ||||||
chr5:175512013
|
A | T | 2 | a0001c0001t0003g0305a0001c0001t0003g0318 | 2 | NA18984.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.511-98A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175512013 | ||||||
chr5:175512075
|
A | G | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-36A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175512075 | ||||||
chr5:175512211
|
C | T | 107 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(104): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.596+15C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512211 | ||||||
chr5:175512223
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+27G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512223 | ||||||
chr5:175512334
|
A | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.596+138A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512334 | ||||||
chr5:175512387
|
G | A | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+191G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512387 | ||||||
chr5:175512424
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(104): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.596+228G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512424 | ||||||
chr5:175512461
|
C | T | 352 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(349): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.596+265C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512461 | ||||||
chr5:175512631
|
G | T | 27 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(24): Show | 27 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.596+435G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512631 | ||||||
chr5:175512636
|
A | G | 4 | a0001c0001t0018g0239a0001c0001t0018g0326a0001c0001t0018g0327others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+440A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512636 | ||||||
chr5:175512692
|
G | A | 12 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0076others(9): Show | 12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.596+496G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512692 | ||||||
chr5:175512703
|
G | T | 5 | a0001c0001t0013g0241a0001c0001t0013g0242a0001c0001t0013g0251others(2): Show | 5 | HG02809.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+507G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512703 | ||||||
chr5:175512780
|
T | C | 1 | a0001c0007t0040g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.596+584T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512780 | ||||||
chr5:175512855
|
A | C | 4 | a0001c0002t0002g0076a0001c0002t0002g0145a0001c0002t0002g0188others(1): Show | 4 | HG02572.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-608A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512855 | ||||||
chr5:175513000
|
A | T | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.597-463A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513000 | ||||||
chr5:175513027
|
G | A | 1 | a0001c0003t0007g0230 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.597-436G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513027 | ||||||
chr5:175513138
|
T | TAAAAATA others(337): Show |
1 | a0001c0001t0004g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.597-308_597-307ins others(344): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513138 | |||||
chr5:175513175
|
C | T | 19 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(16): Show | 19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.597-288C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513175 | ||||||
chr5:175513177
|
G | A | 19 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(16): Show | 19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.597-286G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513177 | ||||||
chr5:175513191
|
T | C | 2 | a0001c0002t0006g0339a0001c0002t0031g0260 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.597-272T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513191 | ||||||
chr5:175513193
|
G | T | 1 | a0001c0004t0038g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.597-270G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513193 | ||||||
chr5:175513233
|
A | G | 135 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(132): Show | 139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.597-230A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513233 | ||||||
chr5:175513294
|
TGTAAAAA others(8): Show |
T | 1 | a0001c0003t0004g0065 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.597-168_597-154del others(15): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513294 | ||||||
chr5:175513296
|
TA | T | 73 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0055others(70): Show | 75 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.597-139delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513296
|
TAA | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.597-140_597-139del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513296
|
TAAA | T | 54 | a0001c0001t0002g0164a0001c0001t0004g0032a0001c0001t0004g0036others(51): Show | 57 | HG00099.hp1 HG00597.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-141_597-139del others(3): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513296
|
TAAAA | T | 83 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(80): Show | 84 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.597-142_597-139del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513296
|
TAAAAA | T | 15 | a0001c0001t0004g0035a0001c0001t0004g0278a0001c0001t0026g0234others(12): Show | 15 | HG00140.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-143_597-139del others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513296
|
TAAAAAA | T | 8 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(5): Show | 8 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-144_597-139del others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513296
|
TAAAAAAA others(6): Show |
T | 18 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(15): Show | 18 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.597-151_597-139del others(13): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | |||||
chr5:175513310
|
A | C | 1 | a0001c0001t0003g0362 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.597-153A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513310 | ||||||
chr5:175513313
|
A | C | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.597-150A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513313 | ||||||
chr5:175513366
|
G | C | 3 | a0001c0002t0002g0294a0001c0002t0002g0295a0001c0002t0012g0213 | 3 | NA18957.hp1 NA18965.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.597-97G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513366 | ||||||
chr5:175513394
|
A | G | 1 | a0001c0001t0009g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.597-69A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513394 | ||||||
chr5:175513678
|
C | T | 5 | a0001c0001t0013g0241a0001c0001t0013g0242a0001c0001t0013g0251others(2): Show | 5 | HG02809.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+88C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513678 | ||||||
chr5:175513691
|
A | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+101A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513691 | ||||||
chr5:175513787
|
G | A | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.724+197G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513787 | ||||||
chr5:175513789
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+199G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513789 | ||||||
chr5:175513795
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | NA18948.hp1 NA18969.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.724+205G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513795 | ||||||
chr5:175513849
|
T | A | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.724+259T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513849 | ||||||
chr5:175513996
|
C | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0115a0001c0001t0001g0129others(4): Show | 7 | HG00558.hp1 NA18747.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+406C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513996 | ||||||
chr5:175514036
|
C | T | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.724+446C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514036 | ||||||
chr5:175514136
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.724+546G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514136 | ||||||
chr5:175514222
|
G | A | 21 | a0001c0001t0003g0086a0001c0001t0014g0183a0001c0001t0014g0184others(18): Show | 21 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.724+632G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514222 | ||||||
chr5:175514347
|
C | G | 96 | a0001c0001t0002g0164a0001c0002t0002g0004a0001c0002t0002g0005others(93): Show | 100 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.724+757C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514347 | ||||||
chr5:175514421
|
C | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+831C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514421 | ||||||
chr5:175514435
|
G | A | 1 | a0006c0006t0003g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.724+845G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514435 | ||||||
chr5:175514633
|
G | A | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.724+1043G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514633 | ||||||
chr5:175514687
|
AG | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+1099delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 175514687 | |||||
chr5:175514715
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+1125G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514715 | ||||||
chr5:175514807
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.724+1217C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514807 | ||||||
chr5:175514862
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0104 | 2 | HG00099.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.724+1272G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514862 | ||||||
chr5:175514882
|
A | G | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.724+1292A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514882 | ||||||
chr5:175514929
|
A | G | 19 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(16): Show | 19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.724+1339A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514929 | ||||||
chr5:175514936
|
T | A | 2 | a0001c0002t0002g0329a0001c0002t0002g0333 | 2 | HG02683.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.724+1346T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514936 | ||||||
chr5:175514974
|
C | T | 5 | a0001c0002t0002g0060a0001c0002t0002g0223a0001c0002t0002g0228others(2): Show | 5 | HG02723.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+1384C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514974 | ||||||
chr5:175515026
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.724+1436T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515026 | ||||||
chr5:175515069
|
C | T | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.724+1479C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515069 | ||||||
chr5:175515176
|
C | G | 107 | a0001c0001t0002g0164a0001c0001t0057g0176a0001c0002t0002g0004others(104): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.725-1438C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515176 | ||||||
chr5:175515205
|
CAG | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.725-1408_725-1407d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515205 | ||||||
chr5:175515302
|
C | T | 1 | a0001c0001t0003g0337 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.725-1312C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515302 | ||||||
chr5:175515303
|
G | A | 1 | a0001c0001t0062g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.725-1311G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515303 | ||||||
chr5:175515323
|
T | C | 1 | a0001c0001t0003g0304 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.725-1291T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515323 | ||||||
chr5:175515365
|
T | A | 39 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(36): Show | 39 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1249T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515365 | ||||||
chr5:175515381
|
G | C | 6 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.725-1233G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515381 | ||||||
chr5:175515470
|
T | C | 12 | a0001c0003t0004g0065a0001c0003t0007g0012a0001c0003t0007g0063others(9): Show | 12 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.725-1144T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515470 | ||||||
chr5:175515496
|
T | C | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.725-1118T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515496 | ||||||
chr5:175515515
|
T | C | 4 | a0001c0001t0013g0056a0001c0001t0019g0057a0001c0001t0019g0058others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.725-1099T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515515 | ||||||
chr5:175515516
|
G | A | 1 | a0001c0001t0003g0302 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.725-1098G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515516 | ||||||
chr5:175515554
|
G | A | 1 | a0001c0002t0002g0284 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.725-1060G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515554 | ||||||
chr5:175515858
|
C | T | 59 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(56): Show | 59 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.725-756C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515858 | ||||||
chr5:175515915
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG02647.hp1 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.725-699G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515915 | ||||||
chr5:175516033
|
TAATGCGG others(42): Show |
T | 8 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-576_725-528del others(49): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 175516033 | |||||
chr5:175516035
|
A | G | 60 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.725-579A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516035 | ||||||
chr5:175516150
|
A | G | 16 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(13): Show | 16 | HG02155.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.725-464A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516150 | ||||||
chr5:175516218
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.725-396C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516218 | ||||||
chr5:175516261
|
T | C | 84 | a0001c0001t0002g0164a0001c0002t0002g0004a0001c0002t0002g0005others(81): Show | 88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.725-353T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516261 | ||||||
chr5:175516548
|
GA | G | 71 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(68): Show | 71 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.725-57delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 175516548 | |||||
chr5:175516738
|
G | C | 1 | a0001c0001t0005g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.774+75G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175516738 | ||||||
chr5:175516858
|
A | G | 1 | a0001c0001t0001g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.774+195A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175516858 | ||||||
chr5:175517088
|
A | T | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.774+425A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517088 | ||||||
chr5:175517237
|
G | A | 1 | a0001c0001t0053g0083 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.774+574G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517237 | ||||||
chr5:175517324
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.774+661C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517324 | ||||||
chr5:175517393
|
G | A | 1 | a0001c0003t0004g0065 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.774+730G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517393 | ||||||
chr5:175517528
|
C | G | 1 | a0001c0001t0004g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.774+865C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517528 | ||||||
chr5:175517611
|
A | G | 123 | a0001c0001t0002g0164a0001c0001t0013g0056a0001c0001t0013g0241others(120): Show | 127 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.774+948A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517611 | ||||||
chr5:175517836
|
C | T | 9 | a0001c0003t0007g0012a0001c0003t0007g0063a0001c0003t0007g0066others(6): Show | 9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+1173C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517836 | ||||||
chr5:175517905
|
G | A | 107 | a0001c0001t0002g0164a0001c0001t0057g0176a0001c0002t0002g0004others(104): Show | 111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.774+1242G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517905 | ||||||
chr5:175518033
|
C | A | 1 | a0001c0001t0003g0314 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.774+1370C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518033 | ||||||
chr5:175518050
|
C | T | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1387C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518050 | ||||||
chr5:175518300
|
A | G | 66 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.774+1637A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518300 | ||||||
chr5:175518383
|
GTT | G | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+1726_774+1727d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175518383 | |||||
chr5:175518462
|
C | T | 194 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(191): Show | 198 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.774+1799C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518462 | ||||||
chr5:175518490
|
A | G | 6 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1827A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518490 | ||||||
chr5:175518496
|
T | G | 2 | a0001c0001t0013g0251a0001c0001t0047g0250 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.774+1833T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518496 | ||||||
chr5:175518530
|
G | A | 1 | a0001c0001t0013g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.774+1867G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518530 | ||||||
chr5:175518558
|
G | T | 1 | a0001c0001t0016g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.774+1895G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518558 | ||||||
chr5:175518678
|
G | A | 2 | a0001c0002t0041g0146a0001c0007t0040g0178 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.774+2015G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518678 | ||||||
chr5:175518813
|
A | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+2150A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518813 | ||||||
chr5:175518827
|
C | T | 3 | a0001c0001t0009g0271a0001c0001t0009g0272a0001c0001t0010g0139 | 3 | HG01069.hp1 HG01070.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.774+2164C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518827 | ||||||
chr5:175518833
|
A | G | 8 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+2170A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518833 | ||||||
chr5:175518836
|
C | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+2173C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518836 | ||||||
chr5:175518899
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.774+2236T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518899 | ||||||
chr5:175519038
|
T | A | 1 | a0001c0001t0055g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.774+2375T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519038 | ||||||
chr5:175519082
|
C | G | 1 | a0001c0001t0001g0022 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.774+2419C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519082 | ||||||
chr5:175519180
|
A | G | 1 | a0001c0004t0038g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.774+2517A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519180 | ||||||
chr5:175519191
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+2528G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519191 | ||||||
chr5:175519388
|
A | T | 1 | a0001c0001t0003g0316 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.775-2531A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519388 | ||||||
chr5:175519468
|
C | T | 62 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.775-2451C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519468 | ||||||
chr5:175519480
|
A | G | 1 | a0001c0002t0031g0260 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.775-2439A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519480 | ||||||
chr5:175519538
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.775-2381G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519538 | ||||||
chr5:175519688
|
CAAG | C | 6 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-2228_775-2226d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519688 | |||||
chr5:175519858
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0045g0195 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.775-2061T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519858 | ||||||
chr5:175519864
|
C | CT | 51 | a0001c0001t0001g0055a0001c0001t0001g0101a0001c0001t0001g0104others(48): Show | 51 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.775-2031dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519864 | |||||
chr5:175519864
|
C | CTT | 6 | a0001c0001t0001g0343a0001c0001t0025g0108a0001c0002t0002g0189others(3): Show | 6 | HG00609.hp2 HG02109.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-2032_775-2031d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519864 | |||||
chr5:175519864
|
CT | C | 20 | a0001c0001t0001g0170a0001c0001t0003g0124a0001c0001t0003g0353others(17): Show | 20 | HG01167.hp1 HG01168.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-2031delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519864 | |||||
chr5:175519932
|
T | C | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1987T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519932 | ||||||
chr5:175520058
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.775-1861C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520058 | ||||||
chr5:175520220
|
T | C | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1699T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520220 | ||||||
chr5:175520260
|
A | C | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.775-1659A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520260 | ||||||
chr5:175520426
|
G | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0098a0001c0001t0001g0131others(1): Show | 4 | HG01081.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1493G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520426 | ||||||
chr5:175520428
|
G | A | 4 | a0001c0002t0002g0076a0001c0002t0002g0145a0001c0002t0002g0188others(1): Show | 4 | HG02572.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1491G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520428 | ||||||
chr5:175520538
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.775-1381C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520538 | ||||||
chr5:175520573
|
G | C | 1 | a0001c0001t0003g0084 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.775-1346G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520573 | ||||||
chr5:175520712
|
C | T | 1 | a0001c0004t0006g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.775-1207C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520712 | ||||||
chr5:175520745
|
A | G | 6 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(3): Show | 6 | HG02055.hp1 HG02155.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-1174A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520745 | ||||||
chr5:175520870
|
A | G | 9 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1049A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520870 | ||||||
chr5:175520925
|
G | A | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.775-994G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520925 | ||||||
chr5:175520945
|
C | T | 105 | a0001c0001t0002g0164a0001c0002t0002g0004a0001c0002t0002g0005others(102): Show | 109 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.775-974C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520945 | ||||||
chr5:175521003
|
T | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.775-916T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521003 | ||||||
chr5:175521026
|
C | T | 1 | a0001c0002t0002g0361 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.775-893C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521026 | ||||||
chr5:175521253
|
T | TA | 360 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(357): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.775-653dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175521253 | |||||
chr5:175521554
|
A | G | 152 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(149): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.775-365A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521554 | ||||||
chr5:175521709
|
T | C | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-210T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521709 | ||||||
chr5:175521813
|
A | C | 19 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(16): Show | 19 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-106A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521813 | ||||||
chr5:175521832
|
G | A | 16 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(13): Show | 16 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.775-87G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521832 | ||||||
chr5:175522093
|
G | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0010g0299 | 3 | HG01928.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.824+125G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522093 | ||||||
chr5:175522115
|
A | G | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.824+147A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522115 | ||||||
chr5:175522138
|
A | G | 9 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(6): Show | 9 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.824+170A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522138 | ||||||
chr5:175522203
|
T | C | 123 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(120): Show | 127 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.825-172T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522203 | ||||||
chr5:175522275
|
G | T | 1 | a0001c0001t0009g0168 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.825-100G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522275 | ||||||
chr5:175522287
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.825-88G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522287 | ||||||
chr5:175522290
|
G | A | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.825-85G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522290 | ||||||
chr5:175522472
|
C | A | 18 | a0001c0001t0013g0056a0001c0001t0013g0241a0001c0001t0013g0242others(15): Show | 18 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.872+50C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522472 | ||||||
chr5:175522476
|
T | C | 1 | a0001c0002t0030g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.872+54T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522476 | ||||||
chr5:175522482
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.872+60G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522482 | ||||||
chr5:175522649
|
C | CT | 123 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(120): Show | 127 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.872+230dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175522649 | |||||
chr5:175522736
|
C | G | 1 | a0001c0001t0003g0359 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.872+314C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522736 | ||||||
chr5:175522809
|
G | C | 1 | a0001c0001t0005g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.872+387G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522809 | ||||||
chr5:175522870
|
A | G | 143 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(140): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.872+448A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522870 | ||||||
chr5:175522882
|
G | A | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+460G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522882 | ||||||
chr5:175522885
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.872+463A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522885 | ||||||
chr5:175523117
|
G | A | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.872+695G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523117 | ||||||
chr5:175523173
|
A | G | 1 | a0001c0001t0018g0328 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.872+751A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523173 | ||||||
chr5:175523220
|
G | A | 2 | a0001c0001t0026g0234a0001c0001t0059g0204 | 2 | HG02559.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.872+798G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523220 | ||||||
chr5:175523236
|
A | G | 2 | a0002c0005t0023g0179a0002c0005t0023g0181 | 2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.872+814A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523236 | ||||||
chr5:175523671
|
C | T | 132 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(129): Show | 136 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+1249C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523671 | ||||||
chr5:175523767
|
G | A | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.872+1345G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523767 | ||||||
chr5:175523795
|
C | A | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.872+1373C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523795 | ||||||
chr5:175523875
|
C | G | 6 | a0001c0002t0015g0074a0001c0002t0015g0075a0001c0002t0015g0078others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+1453C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523875 | ||||||
chr5:175524003
|
A | G | 1 | a0001c0002t0012g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.872+1581A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524003 | ||||||
chr5:175524019
|
G | A | 1 | a0001c0001t0016g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.872+1597G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524019 | ||||||
chr5:175524111
|
AAAAAAAA others(27): Show |
A | 1 | a0001c0002t0041g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872+1691_872+1724d others(36): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524111 | |||||
chr5:175524114
|
AAAAAAAA others(24): Show |
A | 1 | a0001c0002t0012g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.872+1694_872+1724d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524114 | |||||
chr5:175524115
|
AAAAAAAA others(25): Show |
A | 1 | a0001c0002t0002g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.872+1695_872+1726d others(34): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524115 | |||||
chr5:175524116
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0002t0034g0356 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.872+1696_872+1724d others(31): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524116 | |||||
chr5:175524116
|
AAAAAAAA others(24): Show |
A | 33 | a0001c0001t0002g0164a0001c0002t0002g0004a0001c0002t0002g0053others(30): Show | 34 | HG00099.hp1 HG01167.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.872+1696_872+1726d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524116 | |||||
chr5:175524116
|
AAAAAAAA others(28): Show |
A | 2 | a0001c0002t0002g0076a0001c0002t0002g0188 | 2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.872+1696_872+1730d others(37): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524116 | |||||
chr5:175524117
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0055g0080 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.872+1697_872+1712d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524117 | |||||
chr5:175524117
|
AAAAAAAA others(23): Show |
A | 2 | a0001c0002t0002g0285a0001c0002t0002g0291 | 2 | HG00673.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.872+1697_872+1726d others(32): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524117 | |||||
chr5:175524117
|
AAAAAAAA others(27): Show |
A | 1 | a0001c0002t0030g0169 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.872+1697_872+1730d others(36): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524117 | |||||
chr5:175524118
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0003g0341 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.872+1698_872+1718d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | |||||
chr5:175524118
|
AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0003g0136a0001c0001t0003g0216 | 2 | NA18985.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.872+1698_872+1722d others(27): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | |||||
chr5:175524118
|
AAAAAAAA others(24): Show |
A | 45 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(42): Show | 48 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.872+1698_872+1728d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | |||||
chr5:175524118
|
AAAAAAAA others(28): Show |
A | 9 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0145others(6): Show | 9 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.872+1698_872+1732d others(37): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | |||||
chr5:175524118
|
AAAAAAAA others(30): Show |
A | 1 | a0001c0002t0002g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.872+1698_872+1734d others(39): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | |||||
chr5:175524119
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0003g0269 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.872+1699_872+1708d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | |||||
chr5:175524119
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0003g0302a0001c0001t0003g0311 | 2 | HG01255.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.872+1699_872+1710d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | |||||
chr5:175524119
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0005g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.872+1699_872+1724d others(28): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | |||||
chr5:175524119
|
AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0005g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.872+1699_872+1726d others(30): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | |||||
chr5:175524119
|
AAAAAAAA others(23): Show |
A | 2 | a0001c0002t0002g0345a0001c0007t0040g0178 | 2 | HG03579.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.872+1699_872+1728d others(32): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | |||||
chr5:175524120
|
AAAAAAAT | A | 6 | a0001c0001t0003g0003a0001c0001t0003g0259a0001c0001t0003g0267others(3): Show | 7 | HG00735.hp2 HG01099.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+1700_872+1706d others(9): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(4): Show |
A | 5 | a0001c0001t0003g0218a0001c0001t0003g0310a0001c0001t0003g0320others(2): Show | 5 | HG00280.hp2 HG01109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1700_872+1710d others(13): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0004g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.872+1700_872+1712d others(15): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(10): Show |
A | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.872+1700_872+1716d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(12): Show |
A | 2 | a0001c0001t0001g0022a0001c0001t0001g0028 | 2 | NA18968.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.872+1700_872+1718d others(21): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0016g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.872+1700_872+1720d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(18): Show |
A | 1 | a0001c0001t0005g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.872+1700_872+1724d others(27): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(20): Show |
A | 4 | a0001c0001t0005g0143a0001c0001t0020g0192a0001c0001t0020g0193others(1): Show | 4 | HG01109.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1700_872+1726d others(29): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524120
|
AAAAAAAT others(24): Show |
A | 1 | a0001c0002t0002g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.872+1700_872+1730d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | |||||
chr5:175524121
|
A | T | 6 | a0001c0001t0003g0362a0001c0002t0015g0075a0001c0002t0015g0078others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+1699A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524121 | ||||||
chr5:175524121
|
AAAAAATA others(5): Show |
A | 9 | a0001c0001t0003g0006a0001c0001t0003g0016a0001c0001t0003g0047others(6): Show | 10 | HG01952.hp2 NA18945.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+1701_872+1712d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | |||||
chr5:175524121
|
AAAAAATA others(9): Show |
A | 1 | a0001c0001t0004g0159 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.872+1701_872+1716d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | |||||
chr5:175524121
|
AAAAAATA others(11): Show |
A | 8 | a0001c0001t0001g0110a0001c0001t0004g0278a0001c0001t0026g0062others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+1701_872+1718d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | |||||
chr5:175524121
|
AAAAAATA others(13): Show |
A | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.872+1701_872+1720d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | |||||
chr5:175524122
|
AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0103 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.872+1702_872+1716d others(17): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | |||||
chr5:175524122
|
AAAAATAT others(10): Show |
A | 3 | a0001c0001t0001g0111a0001c0001t0001g0255a0001c0001t0003g0084 | 3 | HG02004.hp2 HG03492.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.872+1702_872+1718d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | |||||
chr5:175524122
|
AAAAATAT others(12): Show |
A | 10 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0112others(7): Show | 10 | HG01243.hp1 HG01978.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.872+1702_872+1720d others(21): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | |||||
chr5:175524122
|
AAAAATAT others(14): Show |
A | 12 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0147others(9): Show | 12 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.872+1702_872+1722d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | |||||
chr5:175524122
|
AAAAATAT others(16): Show |
A | 1 | a0001c0001t0052g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.872+1702_872+1724d others(25): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | |||||
chr5:175524122
|
AAAAATAT others(20): Show |
A | 9 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0091others(6): Show | 9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.872+1702_872+1728d others(29): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | |||||
chr5:175524123
|
A | T | 9 | a0001c0001t0003g0087a0001c0001t0003g0258a0001c0001t0003g0362others(6): Show | 9 | HG02074.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+1701A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524123 | ||||||
chr5:175524123
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0003g0322 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.872+1703_872+1712d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524123
|
AAAATATA others(5): Show |
A | 1 | a0001c0001t0003g0315 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.872+1703_872+1714d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524123
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0008g0151 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.872+1703_872+1718d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524123
|
AAAATATA others(11): Show |
A | 22 | a0001c0001t0004g0001a0001c0001t0004g0030a0001c0001t0004g0031others(19): Show | 22 | HG00673.hp2 HG01175.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.872+1703_872+1720d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524123
|
AAAATATA others(13): Show |
A | 6 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0003g0026others(3): Show | 6 | HG00280.hp1 HG01192.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.872+1703_872+1722d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524123
|
AAAATATA others(15): Show |
A | 3 | a0001c0001t0001g0249a0001c0001t0010g0139a0001c0001t0016g0134 | 3 | HG01069.hp2 NA19068.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.872+1703_872+1724d others(24): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524123
|
AAAATATA others(21): Show |
A | 2 | a0001c0001t0018g0239a0001c0001t0018g0327 | 2 | HG01433.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.872+1703_872+1730d others(30): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | |||||
chr5:175524124
|
A | T | 1 | a0001c0001t0001g0343 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.872+1702A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524124 | ||||||
chr5:175524124
|
AAATATAT others(4): Show |
A | 2 | a0001c0001t0003g0309a0001c0001t0003g0314 | 2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.872+1704_872+1714d others(13): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | |||||
chr5:175524124
|
AAATATAT others(6): Show |
A | 1 | a0001c0001t0001g0275 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.872+1704_872+1716d others(15): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | |||||
chr5:175524124
|
AAATATAT others(10): Show |
A | 5 | a0001c0001t0004g0035a0001c0001t0008g0046a0001c0001t0009g0177others(2): Show | 5 | HG03579.hp1 NA18967.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1704_872+1720d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | |||||
chr5:175524124
|
AAATATAT others(12): Show |
A | 7 | a0001c0001t0001g0105a0001c0001t0001g0227a0001c0001t0001g0296others(4): Show | 7 | HG00544.hp1 HG00558.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+1704_872+1722d others(21): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | |||||
chr5:175524124
|
AAATATAT others(14): Show |
A | 46 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(43): Show | 46 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.872+1704_872+1724d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | |||||
chr5:175524124
|
AAATATAT others(20): Show |
A | 2 | a0001c0001t0005g0093a0001c0001t0018g0326 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.872+1704_872+1730d others(29): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | |||||
chr5:175524125
|
A | T | 19 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0166others(16): Show | 19 | HG02074.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+1703A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524125 | ||||||
chr5:175524125
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AATATATA others(3): Show |
A | 3 | a0001c0001t0003g0324a0001c0001t0013g0241a0001c0001t0013g0242 | 3 | HG00597.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.872+1740_872+1749d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | |||||
chr5:175524125
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AATATATA others(5): Show |
A | 9 | a0001c0003t0007g0012a0001c0003t0007g0063a0001c0003t0007g0066others(6): Show | 9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+1738_872+1749d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | |||||
chr5:175524125
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AATATATA others(11): Show |
A | 5 | a0001c0001t0001g0343a0001c0001t0004g0036a0001c0001t0004g0045others(2): Show | 5 | HG00609.hp2 HG00621.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+1732_872+1749d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | |||||
chr5:175524125
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AATATATA others(13): Show |
A | 4 | a0001c0001t0001g0094a0001c0001t0025g0108a0001c0001t0025g0128others(1): Show | 4 | HG00544.hp2 HG01433.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1730_872+1749d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | |||||
chr5:175524125
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AATATATA others(17): Show |
A | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+1726_872+1749d others(26): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | |||||
chr5:175524126
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ATATATAT others(10): Show |
A | 1 | a0002c0005t0023g0181 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.872+1705_872+1721d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524126 | ||||||
chr5:175524126
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ATATATAT others(14): Show |
A | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0116others(3): Show | 6 | HG00140.hp1 HG01106.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.872+1705_872+1725d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524126 | ||||||
chr5:175524127
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T | A | 2 | a0001c0001t0009g0273a0001c0002t0003g0221 | 2 | HG02280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.872+1705T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524127 | ||||||
chr5:175524129
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T | A | 1 | a0001c0001t0009g0273 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.872+1707T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524129 | ||||||
chr5:175524131
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T | A | 2 | a0001c0001t0047g0250a0001c0001t0057g0176 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.872+1709T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524131 | ||||||
chr5:175524133
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T | A | 4 | a0001c0001t0013g0251a0001c0001t0013g0252a0001c0001t0047g0250others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1711T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524133 | ||||||
chr5:175524135
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T | A | 4 | a0001c0001t0003g0305a0001c0001t0003g0318a0001c0001t0013g0251others(1): Show | 4 | HG02055.hp1 HG02976.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1713T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524135 | ||||||
chr5:175524137
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T | A | 4 | a0001c0001t0003g0324a0001c0001t0013g0241a0001c0001t0013g0242others(1): Show | 4 | HG00597.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1715T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524137 | ||||||
chr5:175524139
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T | A | 9 | a0001c0003t0007g0012a0001c0003t0007g0063a0001c0003t0007g0066others(6): Show | 9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+1717T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524139 | ||||||
chr5:175524141
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T | A | 4 | a0001c0003t0007g0066a0001c0003t0007g0071a0001c0003t0007g0230others(1): Show | 4 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1719T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524141 | ||||||
chr5:175524147
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T | A | 1 | a0001c0001t0050g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.872+1725T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524147 | ||||||
chr5:175524149
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T | A | 2 | a0001c0001t0001g0116a0001c0001t0010g0117 | 2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.872+1727T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524149 | ||||||
chr5:175524151
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T | A | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+1729T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524151 | ||||||
chr5:175524153
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T | A | 1 | a0001c0002t0064g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+1731T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524153 | ||||||
chr5:175524168
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A | C | 18 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0094others(15): Show | 18 | HG00140.hp1 HG00544.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.872+1746A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524168 | ||||||
chr5:175524170
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A | C | 19 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0094others(16): Show | 19 | HG00140.hp1 HG00544.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+1748A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524170 | ||||||
chr5:175524177
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A | G | 1 | a0001c0004t0006g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.872+1755A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524177 | ||||||
chr5:175524428
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T | C | 132 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(129): Show | 136 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+2006T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524428 | ||||||
chr5:175524446
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T | C | 1 | a0001c0001t0057g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.872+2024T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524446 | ||||||
chr5:175524673
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G | T | 152 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(149): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.873-1965G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524673 | ||||||
chr5:175524945
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A | T | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-1693A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524945 | ||||||
chr5:175525431
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A | G | 42 | a0001c0001t0002g0164a0001c0002t0002g0004a0001c0002t0002g0005others(39): Show | 44 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.873-1207A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175525431 | ||||||
chr5:175525881
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C | T | 194 | a0001c0001t0002g0164a0001c0001t0004g0001a0001c0001t0004g0030others(191): Show | 198 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.873-757C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175525881 | ||||||
chr5:175526114
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A | G | 1 | a0001c0002t0006g0286 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.873-524A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526114 | ||||||
chr5:175526124
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G | GT | 28 | a0001c0001t0001g0048a0001c0001t0001g0194a0001c0001t0003g0026others(25): Show | 28 | HG00741.hp1 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.873-498dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175526124 | |||||
chr5:175526124
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GT | G | 124 | a0001c0001t0002g0164a0001c0001t0005g0023a0001c0001t0005g0024others(121): Show | 128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.873-498delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175526124 | |||||
chr5:175526184
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TAC | T | 5 | a0001c0001t0014g0183a0001c0001t0014g0184a0001c0001t0014g0185others(2): Show | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-452_873-451del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175526184 | |||||
chr5:175526295
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G | A | 1 | a0001c0001t0003g0302 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.873-343G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526295 | ||||||
chr5:175526379
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G | A | 2 | a0001c0001t0003g0315a0001c0001t0003g0322 | 2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.873-259G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526379 | ||||||
chr5:175526502
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G | A | 7 | a0001c0001t0003g0016a0001c0002t0015g0074a0001c0002t0015g0075others(4): Show | 7 | HG01952.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-136G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526502 | ||||||
chr5:175526527
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C | T | 1 | a0001c0002t0006g0121 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.873-111C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526527 | ||||||
chr5:175526570
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T | C | 20 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(17): Show | 20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.873-68T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526570 | ||||||
chr5:175526626
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C | T | 1 | a0001c0002t0006g0286 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.873-12C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526626 |