Item | Value |
---|---|
geneid | 2395 |
ensemblid | ENSG00000165060.15 |
hgncid | 3951 |
symbol | FXN |
name | frataxin |
refseq_nuc | NM_000144.5 |
refseq_prot | NP_000135.2 |
ensembl_nuc | ENST00000484259.3 |
ensembl_prot | ENSP00000419243.2 |
mane_status | MANE Select |
chr | chr9 |
start | 69035752 |
end | 69079076 |
strand | + |
ver | v1.2 |
region | chr9:69035752-69079076 |
region5000 | chr9:69030752-69084076 |
regionname0 | FXN_chr9_69035752_69079076 |
regionname5000 | FXN_chr9_69030752_69084076 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 210 | 418 | 85 | 70 | 200 | 18 | 43 | 159 | FXN_chr9_69030752_69084076 | FXN | MWTLG others(205): Show |
chr9 | 69030752 | 69084076 |
a0002 | 0/0 | 210 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | MWTLG others(205): Show |
chr9 | 69030752 | 69084076 |
a0003 | 0/0 | 210 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | MWTLG others(205): Show |
chr9 | 69030752 | 69084076 |
a0004 | 0/0 | 210 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | MWTLG others(205): Show |
chr9 | 69030752 | 69084076 |
a0005 | 0/0 | 210 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | MWTLG others(205): Show |
chr9 | 69030752 | 69084076 |
a0006 | 0/0 | 210 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | MWTLG others(205): Show |
chr9 | 69030752 | 69084076 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 630 | 403 | 75 | 70 | 197 | 18 | 42 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0001c0002 | 1/0 | 630 | 11 | 10 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0001c0005 | 0/0 | 630 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0001c0008 | 0/0 | 630 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0002c0003 | 0/0 | 630 | 7 | 7 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0003c0004 | 0/0 | 630 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0004c0007 | 0/0 | 630 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0005c0009 | 0/0 | 630 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 | ||
a0006c0006 | 0/0 | 630 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | ATGTG others(625): Show |
chr9 | 69030752 | 69084076 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6983 | 70 | 2 | 18 | 47 | 0 | 3 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0002 | 0/0 | 6977 | 65 | 9 | 9 | 36 | 1 | 10 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0003 | 0/0 | 6982 | 53 | 2 | 7 | 37 | 3 | 4 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0004 | 0/0 | 6978 | 31 | 0 | 6 | 25 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0005 | 0/0 | 6982 | 28 | 14 | 1 | 5 | 5 | 3 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0006 | 0/0 | 6983 | 27 | 11 | 7 | 2 | 3 | 4 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0007 | 0/0 | 6986 | 14 | 3 | 0 | 9 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0008 | 0/0 | 6978 | 11 | 2 | 5 | 0 | 2 | 2 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0009 | 0/0 | 6975 | 10 | 9 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6970): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0010 | 0/0 | 6976 | 6 | 0 | 2 | 2 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6971): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0012 | 0/0 | 6983 | 5 | 1 | 0 | 0 | 2 | 2 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0013 | 0/0 | 6984 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6979): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0014 | 0/0 | 6991 | 4 | 3 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6986): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0015 | 0/0 | 6986 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0016 | 0/0 | 6986 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0017 | 0/0 | 6983 | 4 | 3 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0018 | 0/0 | 6977 | 3 | 0 | 1 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0019 | 0/0 | 6977 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0020 | 0/0 | 6977 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0022 | 0/0 | 6977 | 3 | 0 | 3 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0024 | 0/0 | 6985 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6980): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0025 | 0/0 | 6977 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0026 | 0/0 | 6976 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6971): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0027 | 0/0 | 6977 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0028 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0029 | 0/0 | 6986 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0030 | 0/0 | 6979 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6974): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0031 | 0/0 | 6982 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0035 | 0/0 | 6977 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0036 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0037 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0038 | 0/1 | 6977 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0039 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0040 | 0/0 | 6977 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0041 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0042 | 0/0 | 6977 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0043 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0044 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0045 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0046 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0047 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0049 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6970): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0050 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0052 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6970): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0053 | 0/0 | 6986 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0054 | 0/0 | 6986 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0055 | 0/0 | 6986 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0056 | 0/0 | 6990 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6985): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0057 | 0/0 | 6987 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6982): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0058 | 0/0 | 6983 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0059 | 0/0 | 6983 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0060 | 0/0 | 6979 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6974): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0061 | 0/0 | 6983 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0062 | 0/0 | 6983 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0063 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0064 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0065 | 0/0 | 6983 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0066 | 0/0 | 6984 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6979): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0067 | 0/0 | 6983 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6978): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0068 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6976): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0069 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6976): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0070 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6971): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0071 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0001t0072 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6976): Show |
chr9 | 69030752 | 69084076 |
a0001c0002t0005 | 0/0 | 6982 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0001c0002t0011 | 1/0 | 6978 | 5 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0002t0023 | 0/0 | 6999 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6994): Show |
chr9 | 69030752 | 69084076 |
a0001c0002t0034 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0002t0048 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0001c0005t0002 | 0/0 | 6977 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
a0001c0008t0074 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0002c0003t0008 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0002c0003t0015 | 0/0 | 6986 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6981): Show |
chr9 | 69030752 | 69084076 |
a0002c0003t0032 | 0/0 | 6984 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6979): Show |
chr9 | 69030752 | 69084076 |
a0002c0003t0051 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6973): Show |
chr9 | 69030752 | 69084076 |
a0002c0003t0073 | 0/0 | 6980 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6975): Show |
chr9 | 69030752 | 69084076 |
a0003c0004t0021 | 0/0 | 6973 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6968): Show |
chr9 | 69030752 | 69084076 |
a0003c0004t0033 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6968): Show |
chr9 | 69030752 | 69084076 |
a0004c0007t0005 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0005c0009t0028 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6977): Show |
chr9 | 69030752 | 69084076 |
a0006c0006t0002 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | AGGGC others(6972): Show |
chr9 | 69030752 | 69084076 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0021 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0001 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0010 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0006 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0015g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0017g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0017g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0017g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0018g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0018g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0019g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0020g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0020g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0022g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0022g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0022g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0024g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0025g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0026g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0026g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0027g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0028g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0029g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0029g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0030g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0031g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0031g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0035g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0036g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0037g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0038g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0039g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0040g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0041g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0042g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0043g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0044g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0045g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0046g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0047g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0049g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0050g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0052g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0053g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0054g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0055g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0056g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0057g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0058g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0059g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0060g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0061g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0062g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0063g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0064g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0065g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0066g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0067g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0068g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0069g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0070g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0071g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0072g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0011g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0011g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0023g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0023g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0034g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0048g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0005t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0005t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0005t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0008t0074g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0032g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0032g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0051g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0073g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0003c0004t0021g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0003c0004t0021g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0003c0004t0033g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0004c0007t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0005c0009t0028g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0006c0006t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0301 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0281 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0340 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0203 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0221 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0169 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00642 | hp1 | a0001 | c0001 | t0055 | g0046 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0343 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00673 | hp1 | a0001 | c0001 | t0019 | g0002 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00673 | hp2 | a0004 | c0007 | t0005 | g0284 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00738 | hp2 | a0001 | c0001 | t0045 | g0217 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0339 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0338 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0299 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0334 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0348 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0220 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01109 | hp2 | a0001 | c0001 | t0043 | g0110 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01167 | hp1 | a0001 | c0001 | t0010 | g0120 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01167 | hp2 | a0001 | c0001 | t0050 | g0346 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01168 | hp1 | a0001 | c0001 | t0059 | g0291 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0226 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0300 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01243 | hp2 | a0001 | c0001 | t0061 | g0283 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0219 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0238 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01346 | hp1 | a0001 | c0001 | t0046 | g0167 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01358 | hp1 | a0001 | c0001 | t0018 | g0022 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0006 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01496 | hp1 | a0001 | c0001 | t0014 | g0215 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01496 | hp2 | a0001 | c0001 | t0039 | g0124 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0208 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0206 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0207 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01516 | hp2 | a0001 | c0001 | t0018 | g0020 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01517 | hp1 | a0001 | c0001 | t0018 | g0020 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0209 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01884 | hp1 | a0001 | c0001 | t0068 | g0225 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01884 | hp2 | a0001 | c0002 | t0023 | g0055 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01891 | hp2 | a0002 | c0003 | t0015 | g0049 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01928 | hp2 | a0001 | c0001 | t0022 | g0111 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01943 | hp1 | a0001 | c0001 | t0062 | g0173 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01975 | hp2 | a0001 | c0001 | t0022 | g0168 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02040 | hp1 | a0001 | c0001 | t0069 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02040 | hp2 | a0001 | c0001 | t0024 | g0013 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0328 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0239 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0336 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02083 | hp1 | a0001 | c0001 | t0027 | g0028 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02145 | hp1 | a0001 | c0001 | t0040 | g0131 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0341 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0326 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0303 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02258 | hp1 | a0001 | c0001 | t0020 | g0036 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02280 | hp1 | a0001 | c0001 | t0020 | g0036 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0330 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02451 | hp1 | a0002 | c0003 | t0015 | g0053 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02572 | hp1 | a0001 | c0001 | t0014 | g0178 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0275 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02602 | hp2 | a0001 | c0001 | t0026 | g0022 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0182 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0329 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02622 | hp1 | a0001 | c0002 | t0048 | g0056 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02622 | hp2 | a0003 | c0004 | t0033 | g0014 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02630 | hp1 | a0001 | c0001 | t0052 | g0237 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02647 | hp2 | a0002 | c0003 | t0032 | g0050 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02683 | hp2 | a0001 | c0001 | t0042 | g0121 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02698 | hp2 | a0001 | c0008 | t0074 | g0232 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02717 | hp1 | a0001 | c0002 | t0023 | g0015 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0016 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02723 | hp1 | a0001 | c0002 | t0023 | g0015 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02723 | hp2 | a0002 | c0003 | t0051 | g0082 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0222 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02735 | hp2 | a0001 | c0001 | t0035 | g0141 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02738 | hp1 | a0001 | c0001 | t0072 | g0172 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0347 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0323 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0016 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0236 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02895 | hp1 | a0001 | c0001 | t0067 | g0064 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0322 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02896 | hp1 | a0001 | c0002 | t0034 | g0295 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02896 | hp2 | a0003 | c0004 | t0021 | g0014 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0345 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02897 | hp2 | a0003 | c0004 | t0021 | g0014 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0325 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02976 | hp1 | a0001 | c0002 | t0011 | g0008 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0202 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0342 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03041 | hp1 | a0002 | c0003 | t0008 | g0078 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03041 | hp2 | a0001 | c0001 | t0060 | g0161 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0080 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0333 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03195 | hp1 | a0002 | c0003 | t0032 | g0051 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03195 | hp2 | a0001 | c0002 | t0011 | g0008 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03209 | hp1 | a0001 | c0001 | t0053 | g0081 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0324 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0176 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03486 | hp1 | a0001 | c0001 | t0054 | g0059 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03486 | hp2 | a0003 | c0004 | t0021 | g0344 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03490 | hp1 | a0001 | c0001 | t0030 | g0033 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0337 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03491 | hp1 | a0001 | c0001 | t0058 | g0037 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03492 | hp1 | a0001 | c0001 | t0030 | g0033 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03516 | hp1 | a0002 | c0003 | t0073 | g0048 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0079 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0310 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0313 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03688 | hp1 | a0001 | c0001 | t0012 | g0320 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03704 | hp1 | a0001 | c0001 | t0071 | g0196 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03704 | hp2 | a0001 | c0001 | t0010 | g0089 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03710 | hp1 | a0005 | c0009 | t0028 | g0309 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0292 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03834 | hp2 | a0001 | c0001 | t0010 | g0090 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0223 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0335 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04184 | hp1 | a0001 | c0001 | t0028 | g0311 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0218 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0230 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04228 | hp2 | a0001 | c0001 | t0026 | g0128 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18747 | hp1 | a0001 | c0001 | t0027 | g0028 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18906 | hp2 | a0001 | c0002 | t0011 | g0008 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18939 | hp1 | a0001 | c0005 | t0002 | g0153 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18942 | hp1 | a0001 | c0001 | t0024 | g0013 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0245 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0242 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18949 | hp2 | a0001 | c0001 | t0036 | g0143 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18951 | hp1 | a0006 | c0006 | t0002 | g0180 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18953 | hp1 | a0001 | c0001 | t0070 | g0152 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18959 | hp2 | a0001 | c0001 | t0016 | g0302 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18963 | hp2 | a0001 | c0001 | t0056 | g0246 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18964 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18965 | hp1 | a0001 | c0001 | t0065 | g0276 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18967 | hp2 | a0001 | c0001 | t0066 | g0044 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18968 | hp2 | a0001 | c0001 | t0037 | g0019 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0243 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18971 | hp1 | a0001 | c0001 | t0024 | g0013 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18972 | hp1 | a0001 | c0001 | t0025 | g0025 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18978 | hp2 | a0001 | c0001 | t0029 | g0350 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18981 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18984 | hp1 | a0001 | c0001 | t0031 | g0197 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18987 | hp1 | a0001 | c0001 | t0013 | g0158 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18997 | hp1 | a0001 | c0001 | t0041 | g0157 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19002 | hp2 | a0001 | c0005 | t0002 | g0071 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19004 | hp1 | a0001 | c0001 | t0031 | g0165 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19009 | hp1 | a0001 | c0001 | t0013 | g0175 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19011 | hp1 | a0001 | c0001 | t0016 | g0307 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0148 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0280 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0314 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19043 | hp2 | a0001 | c0002 | t0005 | g0057 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0331 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19058 | hp2 | a0001 | c0001 | t0010 | g0070 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19070 | hp1 | a0001 | c0001 | t0025 | g0025 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19070 | hp2 | a0001 | c0001 | t0013 | g0042 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19075 | hp1 | a0001 | c0001 | t0019 | g0069 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19078 | hp1 | a0001 | c0001 | t0017 | g0279 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19078 | hp2 | a0001 | c0001 | t0019 | g0068 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19079 | hp1 | a0001 | c0001 | t0029 | g0351 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19080 | hp1 | a0001 | c0001 | t0007 | g0312 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19080 | hp2 | a0001 | c0001 | t0063 | g0060 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19081 | hp1 | a0001 | c0001 | t0016 | g0306 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19082 | hp2 | a0001 | c0001 | t0064 | g0187 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19083 | hp1 | a0001 | c0001 | t0016 | g0305 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19087 | hp1 | a0001 | c0001 | t0013 | g0261 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19090 | hp1 | a0001 | c0005 | t0002 | g0154 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19090 | hp2 | a0001 | c0001 | t0013 | g0042 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19240 | hp1 | a0001 | c0001 | t0044 | g0088 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20129 | hp1 | a0001 | c0002 | t0011 | g0008 | AFR | ASW | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | ASW | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0282 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20805 | hp1 | a0001 | c0001 | t0012 | g0316 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0298 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0317 | SAS | GIH | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | GIH | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02486 | hp2 | a0001 | c0001 | t0057 | g0063 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02559 | hp1 | a0001 | c0001 | t0017 | g0315 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02559 | hp2 | a0001 | c0001 | t0049 | g0011 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0321 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03471 | hp2 | a0001 | c0001 | t0047 | g0304 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0231 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
homoSapiens | chm13v2 | a0001 | c0001 | t0038 | g0108 | REF | REF | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
homoSapiens | grch38p0 | a0001 | c0002 | t0011 | g0296 | REF | REF | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035868 | G | A | 1 | a0006 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.86G>A | p.Arg29Gln | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/5 | 117/6978 | 86/633 | 29/210 | chr9 | 69035868 | |||
chr9:69046398 | G | A | 1 | a0004 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.179G>A | p.Arg60His | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/5 | 210/6978 | 179/633 | 60/210 | chr9 | 69046398 | |||
chr9:69046445 | A | G | 1 | a0002 | 7 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.226A>G | p.Met76Val | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/5 | 257/6978 | 226/633 | 76/210 | chr9 | 69046445 | |||
chr9:69053175 | A | C | 1 | a0005 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.299A>C | p.Glu100Ala | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/5 | 330/6978 | 299/633 | 100/210 | chr9 | 69053175 | |||
chr9:69072755 | A | G | 1 | a0003 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.626A>G | p.Asp209Gly | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 657/6978 | 626/633 | 209/210 | chr9 | 69072755 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035836 | A | G | 8 | a0001c0001 a0001c0005 a0001c0008 others(5): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
synonymous_variant | LOW | c.54A>G | p.Pro18Pro | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/5 | 85/6978 | 54/633 | 18/210 | chr9 | 69035836 | |||
chr9:69053233 | G | A | 1 | a0001c0005 | 3 | NA18939.hp1 NA19002.hp2 NA19090.hp1 |
synonymous_variant | LOW | c.357G>A | p.Thr119Thr | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/5 | 388/6978 | 357/633 | 119/210 | chr9 | 69053233 | |||
chr9:69065021 | A | G | 1 | a0001c0008 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.468A>G | p.Leu156Leu | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/5 | 499/6978 | 468/633 | 156/210 | chr9 | 69065021 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035776 | G | A | 1 | a0001c0001t0018 | 3 | HG01358.hp1 HG01516.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-7G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/5 | 7 | chr9 | 69035776 | ||||||
chr9:69072839 | TTTG | T | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*92_*94delGTT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 92 | INFO_REALIGN_3_PRIME | chr9 | 69072839 | |||||
chr9:69073008 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*246C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 246 | chr9 | 69073008 | ||||||
chr9:69073156 | G | A | 1 | a0003c0004t0033 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*394G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 394 | chr9 | 69073156 | ||||||
chr9:69073185 | A | G | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*423A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 423 | chr9 | 69073185 | ||||||
chr9:69073202 | A | G | 1 | a0001c0001t0057 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 440 | chr9 | 69073202 | ||||||
chr9:69073244 | T | C | 15 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0015 others(12): Show |
41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*482T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 482 | chr9 | 69073244 | ||||||
chr9:69073245 | G | A | 1 | a0001c0001t0053 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 483 | chr9 | 69073245 | ||||||
chr9:69073302 | T | C | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*540T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 540 | chr9 | 69073302 | ||||||
chr9:69073318 | C | T | 12 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 others(9): Show |
33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*556C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 556 | chr9 | 69073318 | ||||||
chr9:69073384 | A | G | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*622A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 622 | chr9 | 69073384 | ||||||
chr9:69073395 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*633C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 633 | chr9 | 69073395 | ||||||
chr9:69073402 | G | C | 1 | a0001c0002t0034 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*640G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 640 | chr9 | 69073402 | ||||||
chr9:69073557 | G | T | 2 | a0001c0001t0022 a0001c0001t0027 |
5 | HG00639.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*795G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 795 | chr9 | 69073557 | ||||||
chr9:69073560 | T | G | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(17): Show |
132 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*798T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 798 | chr9 | 69073560 | ||||||
chr9:69073679 | C | G | 1 | a0001c0001t0052 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 917 | chr9 | 69073679 | ||||||
chr9:69073760 | A | G | 1 | a0001c0001t0043 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 998 | chr9 | 69073760 | ||||||
chr9:69073830 | T | A | 2 | a0003c0004t0021 a0003c0004t0033 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1068T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1068 | chr9 | 69073830 | ||||||
chr9:69073834 | A | G | 2 | a0003c0004t0021 a0003c0004t0033 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1072A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1072 | chr9 | 69073834 | ||||||
chr9:69073861 | G | A | 15 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0015 others(12): Show |
41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1099G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1099 | chr9 | 69073861 | ||||||
chr9:69074037 | T | A | 1 | a0001c0001t0058 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1275 | chr9 | 69074037 | ||||||
chr9:69074042 | G | A | 12 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 others(9): Show |
33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1280G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1280 | chr9 | 69074042 | ||||||
chr9:69074077 | T | C | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1315T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1315 | chr9 | 69074077 | ||||||
chr9:69074088 | A | G | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1326 | chr9 | 69074088 | ||||||
chr9:69074129 | A | G | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1367A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1367 | chr9 | 69074129 | ||||||
chr9:69074129 | A | T | 1 | a0001c0008t0074 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1367 | chr9 | 69074129 | ||||||
chr9:69074200 | T | TAAA | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1439_*1440insAAA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1440 | INFO_REALIGN_3_PRIME | chr9 | 69074200 | |||||
chr9:69074261 | A | G | 1 | a0001c0001t0042 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1499 | chr9 | 69074261 | ||||||
chr9:69074287 | C | T | 1 | a0002c0003t0051 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1525C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1525 | chr9 | 69074287 | ||||||
chr9:69074295 | T | G | 1 | a0001c0001t0012 | 5 | HG00140.hp2 HG02145.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1533T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1533 | chr9 | 69074295 | ||||||
chr9:69074352 | A | T | 2 | a0002c0003t0032 a0002c0003t0073 |
3 | HG02647.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1590A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1590 | chr9 | 69074352 | ||||||
chr9:69074439 | C | T | 3 | a0001c0001t0016 a0001c0001t0027 a0001c0001t0031 |
8 | HG02083.hp1 NA18747.hp1 NA18959.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1677C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1677 | chr9 | 69074439 | ||||||
chr9:69074459 | A | G | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1697A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1697 | chr9 | 69074459 | ||||||
chr9:69074470 | G | T | 2 | a0001c0001t0071 a0001c0001t0072 |
2 | HG02738.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1708G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1708 | chr9 | 69074470 | ||||||
chr9:69074497 | G | A | 3 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0059 |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1735G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1735 | chr9 | 69074497 | ||||||
chr9:69074499 | G | A | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1737G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1737 | chr9 | 69074499 | ||||||
chr9:69074506 | C | T | 1 | a0001c0001t0041 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1744C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1744 | chr9 | 69074506 | ||||||
chr9:69074519 | CA | C | 3 | a0001c0001t0010 a0001c0001t0026 a0001c0001t0050 |
9 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1771delA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1771 | INFO_REALIGN_3_PRIME | chr9 | 69074519 | |||||
chr9:69074532 | AAG | A | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1771_*1772delAG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1771 | chr9 | 69074532 | ||||||
chr9:69074549 | G | A | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1787G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1787 | chr9 | 69074549 | ||||||
chr9:69074594 | A | G | 1 | a0001c0001t0059 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1832A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1832 | chr9 | 69074594 | ||||||
chr9:69074717 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1955C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1955 | chr9 | 69074717 | ||||||
chr9:69074743 | G | GA | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(24): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*1990dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1991 | INFO_REALIGN_3_PRIME | chr9 | 69074743 | |||||
chr9:69074789 | T | G | 1 | a0001c0001t0057 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2027T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2027 | chr9 | 69074789 | ||||||
chr9:69074840 | T | C | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*2078T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2078 | chr9 | 69074840 | ||||||
chr9:69074964 | G | A | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2202G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2202 | chr9 | 69074964 | ||||||
chr9:69075228 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2466C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2466 | chr9 | 69075228 | ||||||
chr9:69075229 | A | G | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2467A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2467 | chr9 | 69075229 | ||||||
chr9:69075234 | T | G | 79 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(76): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
3_prime_UTR_variant | MODIFIER | c.*2472T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2472 | chr9 | 69075234 | ||||||
chr9:69075241 | T | G | 1 | a0002c0003t0051 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2479T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2479 | chr9 | 69075241 | ||||||
chr9:69075266 | T | C | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2504T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2504 | chr9 | 69075266 | ||||||
chr9:69075287 | G | A | 1 | a0001c0001t0026 | 2 | HG02602.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2525G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2525 | chr9 | 69075287 | ||||||
chr9:69075320 | C | T | 1 | a0001c0001t0067 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2558C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2558 | chr9 | 69075320 | ||||||
chr9:69075327 | G | A | 3 | a0001c0001t0015 a0001c0001t0054 a0002c0003t0015 |
5 | HG01891.hp2 HG02451.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2565G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2565 | chr9 | 69075327 | ||||||
chr9:69075330 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2568C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2568 | chr9 | 69075330 | ||||||
chr9:69075454 | C | T | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*2692C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2692 | chr9 | 69075454 | ||||||
chr9:69075459 | C | CAAAT | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(34): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2717_*2720dupTAAA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2721 | INFO_REALIGN_3_PRIME | chr9 | 69075459 | |||||
chr9:69075459 | C | CAAATAAA others(1): Show |
3 | a0001c0001t0014 a0001c0001t0056 a0002c0003t0032 |
7 | HG01496.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2713_*2720dupTAAA others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2721 | INFO_REALIGN_3_PRIME | chr9 | 69075459 | |||||
chr9:69075459 | C | CAAATAAA others(9): Show |
1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2705_*2720dupTAAA others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2721 | INFO_REALIGN_3_PRIME | chr9 | 69075459 | |||||
chr9:69075536 | T | A | 57 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(54): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*2774T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2774 | chr9 | 69075536 | ||||||
chr9:69075566 | T | G | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(55): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*2804T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2804 | chr9 | 69075566 | ||||||
chr9:69075585 | A | G | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*2823A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2823 | chr9 | 69075585 | ||||||
chr9:69075648 | T | A | 1 | a0001c0001t0057 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2886T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2886 | chr9 | 69075648 | ||||||
chr9:69075659 | G | T | 1 | a0001c0001t0025 | 2 | NA18972.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2897G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2897 | chr9 | 69075659 | ||||||
chr9:69075768 | G | T | 78 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(75): Show |
425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
3_prime_UTR_variant | MODIFIER | c.*3006G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3006 | chr9 | 69075768 | ||||||
chr9:69075797 | C | CAA | 3 | a0001c0001t0014 a0001c0001t0057 a0001c0002t0023 |
8 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3037_*3038dupAA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3039 | INFO_REALIGN_3_PRIME | chr9 | 69075797 | |||||
chr9:69075822 | C | T | 1 | a0001c0001t0054 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3060C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3060 | chr9 | 69075822 | ||||||
chr9:69075829 | T | G | 1 | a0001c0001t0058 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3067T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3067 | chr9 | 69075829 | ||||||
chr9:69076017 | CTAT | C | 3 | a0001c0001t0009 a0001c0001t0049 a0001c0001t0052 |
12 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3260_*3262delATT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3260 | INFO_REALIGN_3_PRIME | chr9 | 69076017 | |||||
chr9:69076047 | A | C | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3285A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3285 | chr9 | 69076047 | ||||||
chr9:69076058 | A | G | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3296A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3296 | chr9 | 69076058 | ||||||
chr9:69076114 | G | C | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3352G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3352 | chr9 | 69076114 | ||||||
chr9:69076145 | T | C | 3 | a0001c0001t0009 a0001c0001t0049 a0001c0001t0052 |
12 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3383T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3383 | chr9 | 69076145 | ||||||
chr9:69076217 | GT | G | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(18): Show |
133 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*3469delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3469 | INFO_REALIGN_3_PRIME | chr9 | 69076217 | |||||
chr9:69076220 | T | G | 1 | a0001c0001t0044 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3458T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3458 | chr9 | 69076220 | ||||||
chr9:69076231 | T | A | 1 | a0001c0001t0030 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3469T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3469 | chr9 | 69076231 | ||||||
chr9:69076231 | T | TTTA | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(22): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*3469_*3470insTTA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3470 | chr9 | 69076231 | ||||||
chr9:69076231 | T | TTTTA | 14 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 others(11): Show |
36 | HG00642.hp1 HG01891.hp2 HG02451.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3469_*3470insTTTA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3470 | chr9 | 69076231 | ||||||
chr9:69076323 | G | A | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3561G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3561 | chr9 | 69076323 | ||||||
chr9:69076704 | C | G | 1 | a0001c0001t0013 | 5 | NA18987.hp1 NA19009.hp1 NA19070.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3942C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3942 | chr9 | 69076704 | ||||||
chr9:69076704 | C | T | 4 | a0001c0001t0009 a0001c0001t0049 a0001c0001t0052 others(1): Show |
13 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3942C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3942 | chr9 | 69076704 | ||||||
chr9:69076752 | G | A | 1 | a0001c0001t0019 | 3 | HG00673.hp1 NA19075.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3990G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3990 | chr9 | 69076752 | ||||||
chr9:69076767 | C | A | 1 | a0001c0001t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4005C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4005 | chr9 | 69076767 | ||||||
chr9:69076886 | C | T | 2 | a0003c0004t0021 a0003c0004t0033 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4124C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4124 | chr9 | 69076886 | ||||||
chr9:69077000 | C | T | 1 | a0001c0001t0040 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4238C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4238 | chr9 | 69077000 | ||||||
chr9:69077001 | G | A | 4 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0029 others(1): Show |
10 | HG02040.hp2 NA18942.hp1 NA18949.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4239G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4239 | chr9 | 69077001 | ||||||
chr9:69077019 | A | G | 9 | a0001c0001t0003 a0001c0001t0030 a0001c0001t0031 others(6): Show |
63 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4257A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4257 | chr9 | 69077019 | ||||||
chr9:69077164 | C | G | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*4402C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4402 | chr9 | 69077164 | ||||||
chr9:69077192 | G | A | 1 | a0001c0001t0063 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4430G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4430 | chr9 | 69077192 | ||||||
chr9:69077221 | T | G | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(24): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*4459T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4459 | chr9 | 69077221 | ||||||
chr9:69077469 | A | G | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(43): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*4707A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4707 | chr9 | 69077469 | ||||||
chr9:69077491 | T | G | 1 | a0001c0001t0055 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4729T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4729 | chr9 | 69077491 | ||||||
chr9:69077564 | A | C | 5 | a0001c0001t0009 a0001c0001t0049 a0001c0001t0052 others(2): Show |
14 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4802A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4802 | chr9 | 69077564 | ||||||
chr9:69077658 | G | A | 2 | a0003c0004t0021 a0003c0004t0033 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4896G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4896 | chr9 | 69077658 | ||||||
chr9:69077765 | A | T | 2 | a0001c0001t0039 a0001c0001t0040 |
2 | HG01496.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5003A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5003 | chr9 | 69077765 | ||||||
chr9:69077786 | TGGCC | T | 2 | a0003c0004t0021 a0003c0004t0033 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5026_*5029delGCCG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5026 | INFO_REALIGN_3_PRIME | chr9 | 69077786 | |||||
chr9:69077789 | C | G | 76 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(73): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
3_prime_UTR_variant | MODIFIER | c.*5027C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5027 | chr9 | 69077789 | ||||||
chr9:69077895 | A | T | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5133A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5133 | chr9 | 69077895 | ||||||
chr9:69077896 | C | G | 5 | a0001c0001t0001 a0001c0001t0058 a0001c0001t0062 others(2): Show |
74 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*5134C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5134 | chr9 | 69077896 | ||||||
chr9:69077908 | T | C | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(40): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*5146T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5146 | chr9 | 69077908 | ||||||
chr9:69077930 | A | G | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5168A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5168 | chr9 | 69077930 | ||||||
chr9:69077946 | G | A | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5184G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5184 | chr9 | 69077946 | ||||||
chr9:69077981 | A | G | 1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5219A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5219 | chr9 | 69077981 | ||||||
chr9:69078028 | A | C | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5266A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5266 | chr9 | 69078028 | ||||||
chr9:69078163 | C | G | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5401C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5401 | chr9 | 69078163 | ||||||
chr9:69078212 | G | C | 79 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(76): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
3_prime_UTR_variant | MODIFIER | c.*5450G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5450 | chr9 | 69078212 | ||||||
chr9:69078227 | T | A | 13 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 others(10): Show |
34 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5465T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5465 | chr9 | 69078227 | ||||||
chr9:69078351 | C | T | 1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5589C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5589 | chr9 | 69078351 | ||||||
chr9:69078376 | G | A | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5614G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5614 | chr9 | 69078376 | ||||||
chr9:69078500 | AG | A | 16 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(13): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5740delG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5740 | INFO_REALIGN_3_PRIME | chr9 | 69078500 | |||||
chr9:69078504 | A | T | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(14): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5742A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5742 | chr9 | 69078504 | ||||||
chr9:69078505 | A | T | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(14): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5743A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5743 | chr9 | 69078505 | ||||||
chr9:69078506 | T | A | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(14): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5744T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5744 | chr9 | 69078506 | ||||||
chr9:69078508 | T | C | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(14): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5746T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5746 | chr9 | 69078508 | ||||||
chr9:69078531 | G | A | 1 | a0001c0001t0049 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5769G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5769 | chr9 | 69078531 | ||||||
chr9:69078565 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5803C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5803 | chr9 | 69078565 | ||||||
chr9:69078608 | A | G | 1 | a0001c0001t0020 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5846A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5846 | chr9 | 69078608 | ||||||
chr9:69078685 | AT | A | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*5927delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5927 | INFO_REALIGN_3_PRIME | chr9 | 69078685 | |||||
chr9:69078693 | G | A | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*5931G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5931 | chr9 | 69078693 | ||||||
chr9:69078746 | T | G | 1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5984T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5984 | chr9 | 69078746 | ||||||
chr9:69078808 | C | T | 2 | a0002c0003t0032 a0002c0003t0073 |
3 | HG02647.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6046C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6046 | chr9 | 69078808 | ||||||
chr9:69078861 | C | T | 45 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(42): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*6099C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6099 | chr9 | 69078861 | ||||||
chr9:69078958 | T | C | 2 | a0003c0004t0021 a0003c0004t0033 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6196T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6196 | chr9 | 69078958 | ||||||
chr9:69078977 | A | T | 1 | a0001c0001t0037 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6215A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6215 | chr9 | 69078977 | ||||||
chr9:69079050 | G | T | 1 | a0001c0001t0046 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6288G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6288 | chr9 | 69079050 |
view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035962 | C | T | 2 | a0001c0001t0029g0350 a0001c0001t0029g0351 |
2 | NA18978.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.165+15C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69035962 | |||||||
chr9:69035969 | AGCCGCGG others(7): Show |
A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0002t0005g0057 others(8): Show |
12 | HG01257.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+42_165+55delGG others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69035969 | ||||||
chr9:69036071 | C | G | 2 | a0001c0001t0003g0348 a0001c0001t0003g0349 |
2 | HG01106.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.165+124C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036071 | |||||||
chr9:69036130 | C | T | 1 | a0001c0001t0007g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+183C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036130 | |||||||
chr9:69036170 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+223G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036170 | |||||||
chr9:69036325 | G | A | 1 | a0001c0001t0054g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+378G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036325 | |||||||
chr9:69036453 | G | A | 3 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0063g0060 |
3 | HG02071.hp2 HG02132.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.165+506G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036453 | |||||||
chr9:69036689 | A | G | 59 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0002g0332 others(56): Show |
64 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.165+742A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036689 | |||||||
chr9:69036965 | T | C | 4 | a0001c0001t0006g0298 a0001c0001t0006g0299 a0001c0001t0006g0300 others(1): Show |
4 | HG00099.hp1 HG01081.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1018T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036965 | |||||||
chr9:69036995 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.165+1048C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036995 | |||||||
chr9:69037043 | G | A | 353 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(350): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.165+1096G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037043 | |||||||
chr9:69037045 | A | G | 1 | a0001c0001t0004g0294 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.165+1098A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037045 | |||||||
chr9:69037203 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.165+1256C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037203 | |||||||
chr9:69037284 | A | AAAAAAGA others(2): Show |
6 | a0001c0001t0007g0347 a0001c0001t0017g0016 a0001c0001t0029g0350 others(3): Show |
7 | HG02486.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(11): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAAGA others(5): Show |
11 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
11 | HG02074.hp2 HG03688.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAGAA others(1): Show |
27 | a0001c0001t0005g0314 a0001c0001t0007g0045 a0001c0001t0007g0046 others(24): Show |
31 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(10): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAGAA others(4): Show |
105 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(102): Show |
126 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(13): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAGAA others(13): Show |
1 | a0001c0001t0012g0316 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(22): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAGAA others(31): Show |
1 | a0001c0001t0006g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(40): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAGAA others(34): Show |
2 | a0001c0001t0002g0318 a0001c0001t0002g0319 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(43): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAAGAA others(37): Show |
1 | a0001c0001t0012g0320 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(46): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(3): Show |
5 | a0001c0001t0001g0166 a0001c0001t0002g0170 a0001c0001t0022g0168 others(2): Show |
5 | HG00639.hp2 HG01346.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(18): Show |
5 | a0001c0001t0006g0321 a0001c0001t0006g0322 a0001c0001t0006g0323 others(2): Show |
5 | HG02818.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(27): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(21): Show |
1 | a0001c0001t0006g0326 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(30): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(24): Show |
1 | a0001c0001t0006g0327 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(33): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(27): Show |
4 | a0001c0001t0006g0328 a0001c0001t0006g0329 a0001c0001t0006g0330 others(1): Show |
4 | HG02055.hp1 HG02300.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(36): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(30): Show |
2 | a0001c0001t0002g0332 a0001c0001t0006g0333 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(39): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(33): Show |
1 | a0001c0001t0006g0334 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.165+1339_165+1340i others(42): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(36): Show |
3 | a0001c0001t0006g0298 a0001c0001t0006g0336 a0001c0001t0012g0335 |
3 | HG02056.hp2 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(45): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(39): Show |
3 | a0001c0001t0006g0299 a0001c0001t0006g0300 a0001c0001t0006g0337 |
3 | HG01081.hp2 HG01192.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(48): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(42): Show |
3 | a0001c0001t0006g0301 a0001c0001t0006g0338 a0001c0001t0006g0339 |
3 | HG00099.hp1 HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(51): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(45): Show |
2 | a0001c0001t0012g0340 a0001c0001t0012g0341 |
2 | HG00140.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(54): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(48): Show |
1 | a0001c0001t0006g0342 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.165+1339_165+1340i others(57): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAAGAAG others(69): Show |
1 | a0001c0001t0006g0343 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.165+1339_165+1340i others(78): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAGAAG | 70 | a0001c0001t0002g0184 a0001c0001t0003g0001 a0001c0001t0003g0004 others(67): Show |
93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.165+1352_165+1357d others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAGAAGA others(2): Show |
65 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(62): Show |
82 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+1349_165+1357d others(11): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAGAAGA others(5): Show |
1 | a0001c0001t0009g0280 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+1346_165+1357d others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAGAAGA others(17): Show |
1 | a0001c0001t0006g0345 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.165+1357_165+1358i others(26): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAAGAAGA others(38): Show |
1 | a0001c0001t0050g0346 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.165+1357_165+1358i others(47): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAGAAG | 6 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0285 others(3): Show |
6 | HG00140.hp1 HG00673.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1338_165+1339i others(7): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037284 | A | AAGAAGAA others(4): Show |
6 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0289 others(3): Show |
6 | HG01168.hp1 HG02132.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1338_165+1339i others(13): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | ||||||
chr9:69037286 | AG | A | 3 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0002c0003t0008g0078 |
3 | HG02280.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.165+1340delG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037286 | |||||||
chr9:69037287 | G | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1340G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037287 | |||||||
chr9:69037289 | A | G | 1 | a0001c0001t0006g0343 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.165+1342A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037289 | |||||||
chr9:69037334 | C | T | 1 | a0002c0003t0051g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+1387C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037334 | |||||||
chr9:69037369 | G | C | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1422G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037369 | |||||||
chr9:69037468 | AAATAAT | A | 34 | a0001c0001t0002g0184 a0001c0001t0003g0001 a0001c0001t0003g0004 others(31): Show |
51 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.165+1530_165+1535d others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037468 | ||||||
chr9:69037477 | T | TA | 5 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0003c0004t0021g0014 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1532dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037477 | ||||||
chr9:69037517 | C | T | 74 | a0001c0001t0002g0184 a0001c0001t0003g0001 a0001c0001t0003g0004 others(71): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.165+1570C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037517 | |||||||
chr9:69037572 | GCAGACAT others(5): Show |
G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1626_165+1637d others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037572 | |||||||
chr9:69037605 | C | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1658C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037605 | |||||||
chr9:69037614 | C | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1667C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037614 | |||||||
chr9:69037619 | A | C | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1672A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037619 | |||||||
chr9:69037620 | T | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1673T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037620 | |||||||
chr9:69037632 | C | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1685C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037632 | |||||||
chr9:69037634 | C | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1687C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037634 | |||||||
chr9:69037642 | G | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1695G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037642 | |||||||
chr9:69037646 | A | C | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1699A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037646 | |||||||
chr9:69037652 | T | G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1705T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037652 | |||||||
chr9:69037653 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1706G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037653 | |||||||
chr9:69037654 | G | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1707G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037654 | |||||||
chr9:69037656 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1709T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037656 | |||||||
chr9:69037659 | T | G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1712T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037659 | |||||||
chr9:69037660 | C | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1713C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037660 | |||||||
chr9:69037672 | G | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1725G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037672 | |||||||
chr9:69037673 | T | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1726T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037673 | |||||||
chr9:69037677 | G | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1730G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037677 | |||||||
chr9:69037682 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1735G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037682 | |||||||
chr9:69037695 | A | G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1748A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037695 | |||||||
chr9:69037700 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1753T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037700 | |||||||
chr9:69037702 | C | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1755C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037702 | |||||||
chr9:69037711 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1764T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037711 | |||||||
chr9:69037729 | G | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1782G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037729 | |||||||
chr9:69037733 | C | G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1786C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037733 | |||||||
chr9:69037734 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1787T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037734 | |||||||
chr9:69037735 | C | G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1788C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037735 | |||||||
chr9:69037741 | C | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1794C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037741 | |||||||
chr9:69037742 | A | G | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1795A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037742 | |||||||
chr9:69037746 | C | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1799C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037746 | |||||||
chr9:69037748 | C | A | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1801C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037748 | |||||||
chr9:69038062 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.165+2115G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038062 | |||||||
chr9:69038125 | G | T | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.165+2178G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038125 | |||||||
chr9:69038228 | G | A | 4 | a0001c0001t0004g0083 a0001c0001t0004g0084 a0001c0001t0004g0085 others(1): Show |
4 | NA18950.hp1 NA18973.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2281G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038228 | |||||||
chr9:69038281 | T | A | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.165+2334T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038281 | |||||||
chr9:69038667 | A | C | 163 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0065 others(160): Show |
190 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.165+2720A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038667 | |||||||
chr9:69038813 | A | G | 1 | a0001c0001t0005g0286 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.165+2866A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038813 | |||||||
chr9:69038836 | C | A | 1 | a0001c0001t0004g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.165+2889C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038836 | |||||||
chr9:69038999 | T | A | 1 | a0001c0001t0016g0302 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.165+3052T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038999 | |||||||
chr9:69039039 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(142): Show |
184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.165+3092G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039039 | |||||||
chr9:69039128 | C | A | 158 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0065 others(155): Show |
184 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.165+3181C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039128 | |||||||
chr9:69039231 | G | A | 1 | a0001c0001t0014g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165+3284G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039231 | |||||||
chr9:69039401 | A | G | 1 | a0001c0001t0054g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+3454A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039401 | |||||||
chr9:69039519 | AC | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0065 others(124): Show |
149 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.165+3574delC | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69039519 | ||||||
chr9:69039595 | T | A | 2 | a0001c0001t0010g0089 a0001c0001t0010g0090 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.165+3648T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039595 | |||||||
chr9:69039721 | G | A | 1 | a0001c0001t0015g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.165+3774G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039721 | |||||||
chr9:69039723 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(143): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.165+3776A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039723 | |||||||
chr9:69039745 | A | G | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.165+3798A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039745 | |||||||
chr9:69039765 | T | C | 127 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0065 others(124): Show |
149 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.165+3818T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039765 | |||||||
chr9:69040008 | T | C | 1 | a0001c0002t0023g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165+4061T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040008 | |||||||
chr9:69040050 | C | A | 1 | a0002c0003t0015g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.165+4103C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040050 | |||||||
chr9:69040057 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.165+4110C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040057 | |||||||
chr9:69040194 | A | G | 1 | a0001c0001t0006g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.165+4247A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040194 | |||||||
chr9:69040565 | C | T | 2 | a0001c0001t0003g0233 a0001c0008t0074g0232 |
2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.165+4618C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040565 | |||||||
chr9:69040602 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(143): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.165+4655A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040602 | |||||||
chr9:69040668 | A | G | 5 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0003c0004t0021g0014 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+4721A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040668 | |||||||
chr9:69040672 | A | G | 22 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0006g0298 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+4725A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040672 | |||||||
chr9:69040678 | AT | A | 5 | a0001c0001t0001g0037 a0001c0001t0002g0256 a0001c0001t0013g0042 others(2): Show |
6 | HG03654.hp1 NA18987.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4732delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040678 | |||||||
chr9:69040679 | T | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(71): Show |
81 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.165+4732T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040679 | |||||||
chr9:69040683 | T | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0234 a0001c0001t0009g0011 others(9): Show |
13 | HG01255.hp2 HG02015.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+4736T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040683 | |||||||
chr9:69040750 | C | T | 1 | a0001c0001t0027g0028 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.165+4803C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040750 | |||||||
chr9:69040968 | C | G | 5 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0003c0004t0021g0014 others(2): Show |
6 | HG02280.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+5021C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040968 | |||||||
chr9:69041238 | A | G | 1 | a0001c0001t0020g0036 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.166-5147A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041238 | |||||||
chr9:69041309 | T | A | 1 | a0001c0001t0001g0240 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.166-5076T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041309 | |||||||
chr9:69041411 | A | C | 1 | a0001c0001t0004g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.166-4974A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041411 | |||||||
chr9:69041416 | C | G | 1 | a0001c0001t0031g0165 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.166-4969C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041416 | |||||||
chr9:69041672 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-4713G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041672 | |||||||
chr9:69041822 | G | T | 3 | a0001c0001t0004g0027 a0001c0001t0004g0162 a0001c0001t0004g0163 |
4 | HG01981.hp1 HG01993.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-4563G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041822 | |||||||
chr9:69041899 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(3): Show |
8 | HG00544.hp2 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4486G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041899 | |||||||
chr9:69041945 | A | G | 2 | a0001c0001t0001g0277 a0001c0001t0065g0276 |
2 | NA18965.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.166-4440A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041945 | |||||||
chr9:69041971 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.166-4414G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041971 | |||||||
chr9:69042205 | T | A | 153 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(150): Show |
179 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.166-4180T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042205 | |||||||
chr9:69042206 | C | T | 153 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(150): Show |
179 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.166-4179C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042206 | |||||||
chr9:69042239 | G | GA | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.166-4131dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69042239 | ||||||
chr9:69042264 | C | T | 2 | a0001c0001t0004g0155 a0001c0001t0025g0025 |
3 | NA18944.hp2 NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.166-4121C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042264 | |||||||
chr9:69042302 | C | G | 1 | a0001c0001t0054g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-4083C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042302 | |||||||
chr9:69042481 | G | A | 155 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(152): Show |
180 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.166-3904G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042481 | |||||||
chr9:69042568 | A | G | 3 | a0001c0005t0002g0071 a0001c0005t0002g0153 a0001c0005t0002g0154 |
3 | NA18939.hp1 NA19002.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.166-3817A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042568 | |||||||
chr9:69042637 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.166-3748G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042637 | |||||||
chr9:69042641 | C | T | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-3744C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042641 | |||||||
chr9:69042691 | A | AAC | 31 | a0001c0001t0002g0164 a0001c0001t0007g0045 a0001c0001t0007g0046 others(28): Show |
36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.166-3680_166-3679d others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69042691 | ||||||
chr9:69042854 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.166-3531T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042854 | |||||||
chr9:69043095 | G | A | 1 | a0001c0001t0003g0097 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.166-3290G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043095 | |||||||
chr9:69043222 | T | A | 1 | a0001c0001t0003g0183 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.166-3163T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043222 | |||||||
chr9:69043231 | G | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-3154G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043231 | |||||||
chr9:69043279 | C | G | 39 | a0001c0001t0002g0184 a0001c0001t0003g0001 a0001c0001t0003g0004 others(36): Show |
59 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.166-3106C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043279 | |||||||
chr9:69043520 | G | A | 32 | a0001c0001t0002g0332 a0001c0001t0006g0298 a0001c0001t0006g0299 others(29): Show |
32 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.166-2865G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043520 | |||||||
chr9:69043565 | C | T | 1 | a0001c0001t0070g0152 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.166-2820C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043565 | |||||||
chr9:69043591 | T | C | 6 | a0001c0001t0014g0182 a0002c0003t0015g0049 a0002c0003t0015g0053 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-2794T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043591 | |||||||
chr9:69043646 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.166-2739C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043646 | |||||||
chr9:69043647 | G | A | 1 | a0001c0001t0017g0279 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.166-2738G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043647 | |||||||
chr9:69043679 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.166-2706A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043679 | |||||||
chr9:69043772 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.166-2613C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043772 | |||||||
chr9:69043773 | G | A | 1 | a0001c0001t0005g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.166-2612G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043773 | |||||||
chr9:69043877 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.166-2508C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043877 | |||||||
chr9:69044030 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0004g0098 |
3 | HG02071.hp1 HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.166-2355G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044030 | |||||||
chr9:69044172 | T | A | 2 | a0001c0001t0005g0281 a0001c0001t0005g0282 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.166-2213T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044172 | |||||||
chr9:69044176 | G | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(172): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.166-2209G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044176 | |||||||
chr9:69044364 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(55): Show |
73 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.166-2021C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044364 | |||||||
chr9:69044655 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.166-1730C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044655 | |||||||
chr9:69044691 | C | G | 1 | a0001c0001t0002g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.166-1694C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044691 | |||||||
chr9:69044694 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0043 others(20): Show |
31 | HG00438.hp2 HG01099.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.166-1691C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044694 | |||||||
chr9:69044704 | C | T | 10 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0145 others(7): Show |
12 | HG02083.hp2 NA18939.hp1 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1681C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044704 | |||||||
chr9:69045193 | G | A | 146 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(143): Show |
169 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.166-1192G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045193 | |||||||
chr9:69045249 | A | AC | 358 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(355): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.166-1136_166-1135i others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045249 | |||||||
chr9:69045274 | TA | T | 21 | a0001c0001t0001g0166 a0001c0001t0001g0240 a0001c0001t0009g0011 others(18): Show |
24 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-1098delA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69045274 | ||||||
chr9:69045317 | T | C | 333 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(330): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.166-1068T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045317 | |||||||
chr9:69045464 | G | T | 7 | a0002c0003t0008g0078 a0002c0003t0015g0049 a0002c0003t0015g0053 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-921G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045464 | |||||||
chr9:69045474 | T | A | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.166-911T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045474 | |||||||
chr9:69045475 | C | T | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.166-910C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045475 | |||||||
chr9:69045517 | C | T | 2 | a0001c0001t0005g0230 a0001c0001t0017g0279 |
2 | HG04199.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.166-868C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045517 | |||||||
chr9:69045547 | C | T | 2 | a0001c0001t0005g0038 a0001c0001t0061g0283 |
3 | HG01243.hp2 HG02056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-838C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045547 | |||||||
chr9:69045548 | G | A | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.166-837G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045548 | |||||||
chr9:69045549 | T | C | 358 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(355): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.166-836T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045549 | |||||||
chr9:69045611 | C | T | 5 | a0001c0001t0006g0298 a0001c0001t0006g0299 a0001c0001t0006g0300 others(2): Show |
5 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-774C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045611 | |||||||
chr9:69045612 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.166-773C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045612 | |||||||
chr9:69045612 | C | CA | 8 | a0001c0001t0004g0083 a0002c0003t0008g0078 a0002c0003t0015g0049 others(5): Show |
8 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-762dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69045612 | ||||||
chr9:69045622 | A | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(173): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.166-763A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045622 | |||||||
chr9:69045650 | G | A | 1 | a0001c0001t0020g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-735G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045650 | |||||||
chr9:69045869 | G | A | 1 | a0001c0001t0003g0348 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.166-516G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045869 | |||||||
chr9:69046200 | G | A | 85 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0010 others(82): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.166-185G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69046200 | |||||||
chr9:69046540 | C | G | 2 | a0001c0001t0005g0228 a0001c0001t0005g0229 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.263+58C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046540 | |||||||
chr9:69046625 | G | C | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+143G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046625 | |||||||
chr9:69046626 | A | C | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+144A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046626 | |||||||
chr9:69046627 | A | C | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+145A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046627 | |||||||
chr9:69046628 | A | C | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+146A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046628 | |||||||
chr9:69046629 | T | G | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+147T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046629 | |||||||
chr9:69046667 | C | T | 1 | a0001c0001t0057g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.263+185C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046667 | |||||||
chr9:69046743 | G | A | 4 | a0001c0001t0006g0330 a0001c0001t0006g0337 a0001c0001t0006g0338 others(1): Show |
4 | HG01070.hp2 HG02300.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+261G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046743 | |||||||
chr9:69046753 | C | T | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+271C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046753 | |||||||
chr9:69046880 | A | T | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+398A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046880 | |||||||
chr9:69046973 | G | A | 2 | a0001c0001t0005g0285 a0004c0007t0005g0284 |
2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.263+491G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046973 | |||||||
chr9:69047106 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.263+624G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047106 | |||||||
chr9:69047116 | A | T | 2 | a0001c0001t0004g0155 a0001c0001t0025g0025 |
3 | NA18944.hp2 NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.263+634A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047116 | |||||||
chr9:69047117 | T | G | 2 | a0001c0001t0004g0155 a0001c0001t0025g0025 |
3 | NA18944.hp2 NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.263+635T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047117 | |||||||
chr9:69047139 | A | G | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+657A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047139 | |||||||
chr9:69047224 | C | T | 155 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(152): Show |
179 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.263+742C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047224 | |||||||
chr9:69047262 | A | C | 28 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(25): Show |
32 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.263+780A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047262 | |||||||
chr9:69047301 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.263+819T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047301 | |||||||
chr9:69047330 | G | GACACAGA others(7): Show |
1 | a0001c0001t0002g0144 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.263+868_263+881dup others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047330 | ||||||
chr9:69047344 | C | T | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+862C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047344 | |||||||
chr9:69047350 | G | C | 1 | a0001c0001t0007g0045 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.263+868G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047350 | |||||||
chr9:69047350 | G | GAC | 33 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0102 others(30): Show |
38 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.263+897_263+898dup others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047350 | ||||||
chr9:69047350 | G | GACAC | 6 | a0001c0001t0002g0099 a0001c0001t0014g0176 a0001c0001t0014g0178 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+895_263+898dup others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047350 | ||||||
chr9:69047350 | GAC | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0043 others(28): Show |
40 | HG00438.hp2 HG01099.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.263+897_263+898del others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047350 | ||||||
chr9:69047433 | C | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | NA18947.hp2 NA18994.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.263+951C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047433 | |||||||
chr9:69047712 | C | T | 1 | a0001c0001t0007g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.263+1230C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047712 | |||||||
chr9:69047781 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0043g0110 |
2 | HG00323.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.263+1299G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047781 | |||||||
chr9:69047863 | G | A | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+1381G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047863 | |||||||
chr9:69047933 | G | A | 1 | a0001c0001t0005g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.263+1451G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047933 | |||||||
chr9:69047960 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.263+1478C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047960 | |||||||
chr9:69047961 | G | A | 1 | a0001c0001t0022g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.263+1479G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047961 | |||||||
chr9:69047983 | G | C | 1 | a0002c0003t0051g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+1501G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047983 | |||||||
chr9:69048288 | G | A | 1 | a0001c0001t0012g0320 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.263+1806G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048288 | |||||||
chr9:69048343 | G | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+1861G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048343 | |||||||
chr9:69048465 | C | T | 1 | a0002c0003t0051g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+1983C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048465 | |||||||
chr9:69048590 | C | T | 3 | a0001c0001t0005g0224 a0001c0001t0005g0226 a0001c0001t0068g0225 |
3 | HG01175.hp1 HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.263+2108C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048590 | |||||||
chr9:69048773 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0159 a0001c0001t0001g0174 |
3 | NA18950.hp2 NA19065.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.263+2291C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048773 | |||||||
chr9:69048973 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.263+2491T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048973 | |||||||
chr9:69049146 | C | T | 1 | a0001c0001t0006g0331 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.263+2664C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049146 | |||||||
chr9:69049245 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.263+2763G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049245 | |||||||
chr9:69049290 | T | C | 2 | a0001c0001t0005g0210 a0001c0001t0005g0211 |
2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.263+2808T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049290 | |||||||
chr9:69049812 | C | G | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-3328C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049812 | |||||||
chr9:69049838 | C | T | 6 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0221 others(3): Show |
6 | HG00323.hp1 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-3302C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049838 | |||||||
chr9:69049844 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.264-3296G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049844 | |||||||
chr9:69049864 | A | T | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.264-3276A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049864 | |||||||
chr9:69050181 | A | T | 86 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0010 others(83): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2959A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050181 | |||||||
chr9:69050220 | A | G | 33 | a0001c0001t0002g0332 a0001c0001t0006g0203 a0001c0001t0006g0298 others(30): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.264-2920A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050220 | |||||||
chr9:69050259 | G | C | 29 | a0001c0001t0001g0249 a0001c0001t0007g0045 a0001c0001t0007g0046 others(26): Show |
33 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(30): Show |
intron_variant | MODIFIER | c.264-2881G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050259 | |||||||
chr9:69050407 | TAAGAGTG others(227): Show |
T | 353 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(350): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.264-2716_264-2483d others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69050407 | ||||||
chr9:69050783 | T | C | 2 | a0001c0001t0005g0212 a0001c0001t0005g0213 |
2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.264-2357T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050783 | |||||||
chr9:69050784 | C | CT | 200 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(197): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.264-2343dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69050784 | ||||||
chr9:69050834 | G | A | 1 | a0001c0001t0004g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.264-2306G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050834 | |||||||
chr9:69050844 | G | A | 2 | a0001c0001t0003g0349 a0001c0002t0034g0295 |
2 | HG02896.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.264-2296G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050844 | |||||||
chr9:69050905 | C | T | 1 | a0001c0001t0024g0013 | 3 | HG02040.hp2 NA18942.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.264-2235C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050905 | |||||||
chr9:69051000 | G | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-2140G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051000 | |||||||
chr9:69051023 | G | A | 1 | a0002c0003t0051g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.264-2117G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051023 | |||||||
chr9:69051026 | C | T | 28 | a0001c0001t0001g0249 a0001c0001t0007g0045 a0001c0001t0007g0046 others(25): Show |
32 | HG00642.hp1 HG02040.hp2 HG02809.hp1 others(29): Show |
intron_variant | MODIFIER | c.264-2114C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051026 | |||||||
chr9:69051040 | G | A | 77 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0010 others(74): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.264-2100G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051040 | |||||||
chr9:69051081 | G | A | 16 | a0001c0001t0004g0005 a0001c0001t0004g0018 a0001c0001t0004g0027 others(13): Show |
21 | HG00438.hp1 HG01943.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.264-2059G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051081 | |||||||
chr9:69051161 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.264-1979G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051161 | |||||||
chr9:69051419 | CT | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0073 others(6): Show |
9 | HG00639.hp2 HG01515.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1708delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69051419 | ||||||
chr9:69051420 | T | C | 1 | a0001c0001t0003g0262 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.264-1720T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051420 | |||||||
chr9:69051638 | C | T | 1 | a0001c0001t0008g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.264-1502C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051638 | |||||||
chr9:69051772 | G | A | 1 | a0001c0001t0007g0347 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.264-1368G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051772 | |||||||
chr9:69051869 | C | T | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.264-1271C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051869 | |||||||
chr9:69051935 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.264-1205C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051935 | |||||||
chr9:69052007 | C | T | 1 | a0001c0001t0008g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.264-1133C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052007 | |||||||
chr9:69052036 | C | T | 1 | a0001c0002t0034g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.264-1104C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052036 | |||||||
chr9:69052149 | A | AT | 10 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(7): Show |
11 | HG01109.hp1 HG01255.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-977dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052149 | ||||||
chr9:69052149 | A | T | 1 | a0001c0001t0057g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.264-991A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052149 | |||||||
chr9:69052149 | AT | A | 21 | a0001c0001t0002g0142 a0001c0001t0008g0177 a0001c0001t0008g0303 others(18): Show |
23 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.264-977delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052149 | ||||||
chr9:69052149 | ATT | A | 115 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(112): Show |
134 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.264-978_264-977del others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052149 | ||||||
chr9:69052537 | AT | A | 287 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(284): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.264-580delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052537 | ||||||
chr9:69052537 | ATT | A | 49 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0072 others(46): Show |
56 | HG00642.hp1 HG01070.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.264-581_264-580del others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052537 | ||||||
chr9:69052582 | G | T | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-558G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052582 | |||||||
chr9:69052605 | C | T | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-535C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052605 | |||||||
chr9:69052612 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.264-528G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052612 | |||||||
chr9:69052734 | G | T | 2 | a0002c0003t0015g0053 a0002c0003t0073g0048 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264-406G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052734 | |||||||
chr9:69052755 | G | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.264-385G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052755 | |||||||
chr9:69052807 | G | A | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.264-333G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052807 | |||||||
chr9:69052873 | C | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-267C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052873 | |||||||
chr9:69053070 | G | A | 126 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(123): Show |
146 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.264-70G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69053070 | |||||||
chr9:69053281 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(175): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.384+21T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053281 | |||||||
chr9:69053368 | GT | G | 5 | a0001c0001t0004g0113 a0001c0001t0004g0115 a0001c0001t0004g0116 others(2): Show |
5 | NA18612.hp2 NA18994.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+109delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053368 | |||||||
chr9:69053371 | G | A | 1 | a0001c0001t0057g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.384+111G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053371 | |||||||
chr9:69053419 | C | A | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+159C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053419 | |||||||
chr9:69053458 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(53): Show |
71 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.384+198G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053458 | |||||||
chr9:69053471 | A | AGATG | 153 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(150): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.384+247_384+250dup others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | ||||||
chr9:69053471 | A | AGATGGAT others(1): Show |
80 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(77): Show |
89 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.384+243_384+250dup others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | ||||||
chr9:69053471 | A | AGATGGAT others(5): Show |
12 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0258 others(9): Show |
12 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.384+239_384+250dup others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | ||||||
chr9:69053471 | A | AGATGGAT others(9): Show |
2 | a0001c0001t0005g0281 a0001c0001t0005g0282 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.384+235_384+250dup others(16): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | ||||||
chr9:69053471 | A | G | 16 | a0001c0001t0003g0233 a0001c0001t0009g0011 a0001c0001t0009g0202 others(13): Show |
18 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.384+211A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053471 | |||||||
chr9:69053499 | GGATGGAT others(9): Show |
G | 1 | a0001c0001t0002g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.384+243_384+258del others(16): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053499 | ||||||
chr9:69053507 | GGATA | G | 7 | a0001c0001t0006g0330 a0001c0001t0047g0304 a0002c0003t0015g0049 others(4): Show |
7 | HG01891.hp2 HG02300.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+273_384+276del others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053507 | ||||||
chr9:69053511 | A | G | 345 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(342): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.384+251A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053511 | |||||||
chr9:69053515 | A | G | 130 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(127): Show |
150 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.384+255A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053515 | |||||||
chr9:69053519 | A | G | 8 | a0001c0001t0001g0094 a0001c0001t0001g0270 a0001c0001t0014g0176 others(5): Show |
8 | HG00735.hp1 HG02080.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+259A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053519 | |||||||
chr9:69053523 | A | G | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+263A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053523 | |||||||
chr9:69053529 | A | G | 4 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+269A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053529 | |||||||
chr9:69053559 | TAAGAC | T | 3 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0290 |
3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.384+305_384+309del others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053559 | ||||||
chr9:69053856 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.384+596C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053856 | |||||||
chr9:69053926 | C | T | 1 | a0001c0001t0006g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.384+666C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053926 | |||||||
chr9:69054159 | C | T | 5 | a0001c0001t0006g0298 a0001c0001t0006g0299 a0001c0001t0006g0300 others(2): Show |
5 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+899C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054159 | |||||||
chr9:69054173 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.384+913G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054173 | |||||||
chr9:69054200 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+940A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054200 | |||||||
chr9:69054219 | C | T | 1 | a0001c0001t0044g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.384+959C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054219 | |||||||
chr9:69054242 | C | G | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+982C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054242 | |||||||
chr9:69054441 | T | TAAAGTAG others(344): Show |
1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+1197_384+1198i others(353): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69054441 | ||||||
chr9:69054581 | A | G | 1 | a0001c0001t0031g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.384+1321A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054581 | |||||||
chr9:69054797 | G | A | 1 | a0002c0003t0051g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.384+1537G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054797 | |||||||
chr9:69054839 | G | A | 5 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+1579G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054839 | |||||||
chr9:69054866 | G | A | 1 | a0001c0001t0005g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384+1606G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054866 | |||||||
chr9:69054881 | A | T | 1 | a0001c0001t0004g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.384+1621A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054881 | |||||||
chr9:69055096 | A | C | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+1836A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055096 | |||||||
chr9:69055272 | C | A | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.384+2012C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055272 | |||||||
chr9:69055370 | G | C | 1 | a0001c0001t0047g0304 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.384+2110G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055370 | |||||||
chr9:69055491 | T | A | 5 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+2231T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055491 | |||||||
chr9:69055496 | C | CT | 24 | a0001c0001t0002g0140 a0001c0001t0002g0170 a0001c0001t0006g0323 others(21): Show |
26 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.384+2251dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69055496 | ||||||
chr9:69055571 | G | A | 2 | a0001c0001t0005g0281 a0001c0001t0005g0282 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.384+2311G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055571 | |||||||
chr9:69055590 | T | G | 1 | a0001c0001t0002g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.384+2330T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055590 | |||||||
chr9:69055594 | A | C | 1 | a0001c0001t0003g0034 | 2 | HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.384+2334A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055594 | |||||||
chr9:69055646 | ACAATACA others(494): Show |
A | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.384+2387_384+2887d others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055646 | |||||||
chr9:69055649 | A | G | 116 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(113): Show |
135 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.384+2389A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055649 | |||||||
chr9:69055862 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.384+2602T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055862 | |||||||
chr9:69056117 | G | A | 1 | a0001c0001t0008g0177 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.384+2857G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056117 | |||||||
chr9:69056147 | G | A | 357 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(354): Show |
425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.384+2887G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056147 | |||||||
chr9:69056174 | C | T | 27 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(24): Show |
31 | HG00642.hp1 HG02040.hp2 HG02809.hp1 others(28): Show |
intron_variant | MODIFIER | c.384+2914C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056174 | |||||||
chr9:69056196 | G | A | 1 | a0001c0001t0005g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.384+2936G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056196 | |||||||
chr9:69056200 | G | A | 156 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(153): Show |
181 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.384+2940G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056200 | |||||||
chr9:69056330 | C | T | 31 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(28): Show |
36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.384+3070C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056330 | |||||||
chr9:69056404 | G | A | 2 | a0001c0001t0007g0242 a0001c0001t0007g0243 |
2 | NA18946.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.384+3144G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056404 | |||||||
chr9:69056617 | A | G | 1 | a0001c0001t0016g0302 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.384+3357A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056617 | |||||||
chr9:69056713 | T | G | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+3453T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056713 | |||||||
chr9:69056740 | CT | C | 5 | a0001c0001t0003g0262 a0001c0001t0010g0070 a0003c0004t0021g0014 others(2): Show |
6 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+3494delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69056740 | ||||||
chr9:69056773 | TGCTCTGT others(202): Show |
T | 1 | a0001c0001t0002g0123 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.384+3514_384+3722d others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056773 | |||||||
chr9:69056795 | T | C | 33 | a0001c0001t0001g0249 a0001c0001t0005g0210 a0001c0001t0007g0045 others(30): Show |
38 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(35): Show |
intron_variant | MODIFIER | c.384+3535T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056795 | |||||||
chr9:69056820 | G | A | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+3560G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056820 | |||||||
chr9:69056823 | A | T | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+3563A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056823 | |||||||
chr9:69056830 | C | T | 1 | a0001c0001t0003g0001 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.384+3570C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056830 | |||||||
chr9:69056916 | T | A | 1 | a0003c0004t0033g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.384+3656T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056916 | |||||||
chr9:69057109 | C | G | 1 | a0001c0001t0013g0175 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.384+3849C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057109 | |||||||
chr9:69057153 | G | A | 1 | a0001c0001t0006g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.384+3893G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057153 | |||||||
chr9:69057309 | C | T | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+4049C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057309 | |||||||
chr9:69057515 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.384+4255A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057515 | |||||||
chr9:69057535 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.384+4275G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057535 | |||||||
chr9:69057579 | A | G | 87 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0010 others(84): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.384+4319A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057579 | |||||||
chr9:69057837 | G | C | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.384+4577G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057837 | |||||||
chr9:69057942 | C | T | 31 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(28): Show |
36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.384+4682C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057942 | |||||||
chr9:69058031 | T | C | 1 | a0001c0001t0006g0336 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.384+4771T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058031 | |||||||
chr9:69058077 | C | T | 2 | a0001c0001t0047g0304 a0002c0003t0051g0082 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.384+4817C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058077 | |||||||
chr9:69058114 | C | T | 31 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(28): Show |
36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.384+4854C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058114 | |||||||
chr9:69058117 | G | A | 122 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(119): Show |
141 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.384+4857G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058117 | |||||||
chr9:69058369 | C | A | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+5109C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058369 | |||||||
chr9:69058397 | C | CT | 31 | a0001c0001t0006g0298 a0001c0001t0006g0299 a0001c0001t0006g0300 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+5145dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69058397 | ||||||
chr9:69058407 | C | A | 1 | a0001c0002t0048g0056 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.384+5147C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058407 | |||||||
chr9:69058490 | T | A | 2 | a0001c0001t0017g0016 a0001c0001t0067g0064 |
3 | HG02717.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.384+5230T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058490 | |||||||
chr9:69058600 | T | TA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(90): Show |
108 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.384+5354dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69058600 | ||||||
chr9:69058704 | G | A | 17 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(14): Show |
19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+5444G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058704 | |||||||
chr9:69058796 | C | T | 7 | a0001c0001t0002g0122 a0001c0001t0002g0138 a0001c0001t0002g0139 others(4): Show |
8 | HG00639.hp2 HG01928.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.384+5536C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058796 | |||||||
chr9:69058801 | C | G | 1 | a0001c0001t0005g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.384+5541C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058801 | |||||||
chr9:69058806 | C | T | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.384+5546C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058806 | |||||||
chr9:69058840 | G | A | 28 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(25): Show |
32 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.384+5580G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058840 | |||||||
chr9:69058871 | A | G | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+5611A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058871 | |||||||
chr9:69058929 | G | A | 28 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(25): Show |
32 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.384+5669G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058929 | |||||||
chr9:69058954 | G | A | 16 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(13): Show |
18 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.384+5694G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058954 | |||||||
chr9:69059000 | G | A | 31 | a0001c0001t0006g0298 a0001c0001t0006g0299 a0001c0001t0006g0300 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+5740G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059000 | |||||||
chr9:69059055 | G | C | 4 | a0001c0001t0005g0314 a0001c0001t0017g0016 a0001c0001t0017g0315 others(1): Show |
5 | HG02559.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+5795G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059055 | |||||||
chr9:69059063 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.384+5803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059063 | |||||||
chr9:69059152 | G | A | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-5786G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059152 | |||||||
chr9:69059209 | G | A | 120 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(117): Show |
139 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.385-5729G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059209 | |||||||
chr9:69059218 | T | A | 1 | a0001c0001t0008g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.385-5720T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059218 | |||||||
chr9:69059224 | T | C | 16 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(13): Show |
18 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-5714T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059224 | |||||||
chr9:69059391 | C | CT | 45 | a0001c0001t0005g0204 a0001c0001t0006g0298 a0001c0001t0006g0299 others(42): Show |
48 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.385-5520dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | C | CTT | 55 | a0001c0001t0001g0234 a0001c0001t0001g0252 a0001c0001t0001g0253 others(52): Show |
61 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.385-5521_385-5520d others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | C | CTTT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0037 others(79): Show |
107 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.385-5522_385-5520d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | C | CTTTT | 34 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0058 others(31): Show |
46 | HG00099.hp2 HG00280.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.385-5523_385-5520d others(6): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | C | CTTTTT | 67 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0091 others(64): Show |
80 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.385-5524_385-5520d others(7): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | C | CTTTTTT | 32 | a0001c0001t0001g0093 a0001c0001t0002g0024 a0001c0001t0002g0029 others(29): Show |
37 | HG00438.hp1 HG00544.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.385-5525_385-5520d others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | C | CTTTTTTT | 8 | a0001c0001t0002g0107 a0001c0001t0002g0137 a0001c0001t0002g0170 others(5): Show |
8 | HG03710.hp2 HG04184.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-5526_385-5520d others(9): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | CT | C | 7 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(4): Show |
8 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-5520delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059391 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0005g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.385-5529_385-5520d others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | ||||||
chr9:69059462 | C | T | 1 | a0001c0001t0063g0060 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.385-5476C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059462 | |||||||
chr9:69059547 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.385-5391G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059547 | |||||||
chr9:69059566 | AT | A | 349 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(346): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.385-5361delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059566 | ||||||
chr9:69059669 | G | A | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-5269G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059669 | |||||||
chr9:69059714 | C | T | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-5224C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059714 | |||||||
chr9:69059722 | C | T | 1 | a0001c0001t0039g0124 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.385-5216C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059722 | |||||||
chr9:69059785 | C | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-5153C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059785 | |||||||
chr9:69059873 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.385-5065G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059873 | |||||||
chr9:69060045 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.385-4893G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060045 | |||||||
chr9:69060046 | G | T | 1 | a0001c0001t0053g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385-4892G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060046 | |||||||
chr9:69060096 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG00735.hp1 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4842T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060096 | |||||||
chr9:69060106 | C | T | 2 | a0001c0002t0023g0015 a0001c0002t0023g0055 |
3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.385-4832C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060106 | |||||||
chr9:69060107 | G | A | 1 | a0001c0001t0044g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385-4831G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060107 | |||||||
chr9:69060135 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | NA18612.hp1 NA18942.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-4803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060135 | |||||||
chr9:69060154 | G | A | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4784G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060154 | |||||||
chr9:69060164 | C | G | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4774C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060164 | |||||||
chr9:69060173 | T | C | 45 | a0001c0001t0001g0252 a0001c0001t0003g0227 a0001c0001t0005g0206 others(42): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.385-4765T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060173 | |||||||
chr9:69060196 | G | A | 105 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0023 others(102): Show |
122 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.385-4742G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060196 | |||||||
chr9:69060231 | C | T | 1 | a0001c0001t0035g0141 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.385-4707C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060231 | |||||||
chr9:69060238 | G | T | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.385-4700G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060238 | |||||||
chr9:69060244 | G | A | 2 | a0001c0001t0002g0318 a0001c0001t0002g0319 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.385-4694G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060244 | |||||||
chr9:69060263 | C | T | 2 | a0001c0001t0002g0318 a0001c0001t0002g0319 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.385-4675C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060263 | |||||||
chr9:69060295 | C | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(172): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.385-4643C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060295 | |||||||
chr9:69060303 | A | G | 20 | a0001c0001t0007g0046 a0001c0001t0007g0047 a0001c0001t0007g0242 others(17): Show |
23 | HG00642.hp1 HG02040.hp2 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-4635A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060303 | |||||||
chr9:69060304 | G | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(177): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.385-4634G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060304 | |||||||
chr9:69060373 | A | G | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-4565A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060373 | |||||||
chr9:69060548 | T | G | 113 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(110): Show |
130 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.385-4390T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060548 | |||||||
chr9:69060644 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.385-4294T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060644 | |||||||
chr9:69060659 | TG | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0041 others(2): Show |
10 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.385-4274delG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69060659 | ||||||
chr9:69060674 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.385-4264A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060674 | |||||||
chr9:69060827 | T | C | 1 | a0001c0001t0053g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385-4111T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060827 | |||||||
chr9:69060892 | G | A | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-4046G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060892 | |||||||
chr9:69061022 | A | G | 1 | a0001c0001t0035g0141 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.385-3916A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061022 | |||||||
chr9:69061135 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(179): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.385-3803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061135 | |||||||
chr9:69061172 | C | T | 113 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(110): Show |
130 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.385-3766C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061172 | |||||||
chr9:69061178 | C | T | 1 | a0001c0002t0005g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-3760C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061178 | |||||||
chr9:69061270 | G | A | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.385-3668G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061270 | |||||||
chr9:69061276 | C | G | 1 | a0001c0001t0003g0185 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.385-3662C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061276 | |||||||
chr9:69061317 | G | A | 4 | a0001c0001t0016g0302 a0001c0001t0016g0305 a0001c0001t0016g0306 others(1): Show |
4 | NA18959.hp2 NA19011.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-3621G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061317 | |||||||
chr9:69061365 | A | C | 1 | a0001c0001t0003g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.385-3573A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061365 | |||||||
chr9:69061428 | C | A | 4 | a0001c0001t0008g0177 a0001c0001t0008g0303 a0001c0001t0044g0088 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-3510C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061428 | |||||||
chr9:69061440 | G | A | 113 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(110): Show |
130 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.385-3498G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061440 | |||||||
chr9:69061448 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0066g0044 |
2 | NA18967.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.385-3490C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061448 | |||||||
chr9:69061517 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.385-3421C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061517 | |||||||
chr9:69061529 | A | T | 2 | a0001c0001t0047g0304 a0002c0003t0051g0082 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-3409A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061529 | |||||||
chr9:69061555 | C | G | 14 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(11): Show |
15 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.385-3383C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061555 | |||||||
chr9:69061646 | G | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(240): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.385-3292G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061646 | |||||||
chr9:69061668 | C | T | 1 | a0001c0001t0024g0013 | 3 | HG02040.hp2 NA18942.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.385-3270C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061668 | |||||||
chr9:69061721 | C | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | NA18947.hp2 NA18994.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.385-3217C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061721 | |||||||
chr9:69062008 | C | T | 2 | a0001c0002t0023g0015 a0001c0002t0023g0055 |
3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.385-2930C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062008 | |||||||
chr9:69062149 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.385-2789T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062149 | |||||||
chr9:69062182 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0037g0019 |
2 | NA18968.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.385-2756G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062182 | |||||||
chr9:69062502 | T | C | 1 | a0001c0001t0040g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.385-2436T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062502 | |||||||
chr9:69062594 | GAAGTAGT others(3): Show |
G | 1 | a0001c0001t0060g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.385-2331_385-2322d others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69062594 | ||||||
chr9:69062720 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.385-2218A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062720 | |||||||
chr9:69062727 | A | G | 1 | a0001c0001t0030g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385-2211A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062727 | |||||||
chr9:69062745 | T | C | 1 | a0001c0001t0015g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-2193T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062745 | |||||||
chr9:69062791 | G | C | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2147G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062791 | |||||||
chr9:69062811 | G | A | 2 | a0001c0001t0047g0304 a0002c0003t0051g0082 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-2127G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062811 | |||||||
chr9:69062893 | TA | T | 46 | a0001c0001t0002g0077 a0001c0001t0002g0170 a0001c0001t0002g0319 others(43): Show |
52 | HG00642.hp1 HG01168.hp2 HG01255.hp2 others(49): Show |
intron_variant | MODIFIER | c.385-2031delA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69062893 | ||||||
chr9:69062960 | G | A | 1 | a0001c0001t0015g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-1978G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062960 | |||||||
chr9:69063023 | C | A | 1 | a0001c0001t0001g0269 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.385-1915C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063023 | |||||||
chr9:69063077 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.385-1861C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063077 | |||||||
chr9:69063412 | C | T | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-1526C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063412 | |||||||
chr9:69063529 | C | T | 37 | a0001c0001t0005g0212 a0001c0001t0005g0213 a0001c0001t0005g0214 others(34): Show |
42 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(39): Show |
intron_variant | MODIFIER | c.385-1409C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063529 | |||||||
chr9:69063550 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.385-1388T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063550 | |||||||
chr9:69063720 | G | GT | 89 | a0001c0001t0001g0255 a0001c0001t0003g0001 a0001c0001t0003g0004 others(86): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.385-1217dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69063720 | ||||||
chr9:69063723 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0142 |
2 | NA18956.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.385-1215G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063723 | |||||||
chr9:69063733 | G | T | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-1205G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063733 | |||||||
chr9:69063743 | G | A | 27 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(24): Show |
31 | HG00642.hp1 HG02040.hp2 HG02809.hp1 others(28): Show |
intron_variant | MODIFIER | c.385-1195G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063743 | |||||||
chr9:69063828 | C | T | 2 | a0001c0001t0005g0281 a0001c0001t0005g0282 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.385-1110C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063828 | |||||||
chr9:69063875 | G | A | 1 | a0001c0001t0004g0118 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.385-1063G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063875 | |||||||
chr9:69063890 | C | T | 1 | a0002c0003t0008g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-1048C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063890 | |||||||
chr9:69064046 | A | G | 3 | a0001c0001t0008g0177 a0001c0001t0008g0303 a0002c0003t0008g0078 |
3 | HG02257.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.385-892A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064046 | |||||||
chr9:69064079 | G | A | 2 | a0001c0001t0019g0068 a0001c0001t0019g0069 |
2 | NA19075.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.385-859G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064079 | |||||||
chr9:69064100 | A | G | 1 | a0001c0001t0008g0177 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-838A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064100 | |||||||
chr9:69064157 | C | A | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-781C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064157 | |||||||
chr9:69064249 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0266 |
2 | NA18964.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.385-689T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064249 | |||||||
chr9:69064341 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.385-597C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064341 | |||||||
chr9:69064432 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.385-506C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064432 | |||||||
chr9:69064522 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(241): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.385-416A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064522 | |||||||
chr9:69064529 | G | A | 1 | a0001c0001t0054g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.385-409G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064529 | |||||||
chr9:69064550 | A | C | 4 | a0001c0001t0003g0032 a0001c0001t0003g0034 a0001c0001t0003g0191 others(1): Show |
6 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-388A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064550 | |||||||
chr9:69064710 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385-228G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064710 | |||||||
chr9:69064725 | A | T | 5 | a0002c0003t0015g0049 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-213A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064725 | |||||||
chr9:69064858 | A | G | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-80A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064858 | |||||||
chr9:69065077 | A | G | 5 | a0001c0001t0047g0304 a0002c0003t0051g0082 a0003c0004t0021g0014 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+42A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065077 | |||||||
chr9:69065223 | A | G | 2 | a0001c0001t0006g0323 a0001c0001t0006g0324 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.482+188A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065223 | |||||||
chr9:69065476 | G | C | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+441G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065476 | |||||||
chr9:69065498 | G | A | 1 | a0001c0001t0006g0325 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.482+463G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065498 | |||||||
chr9:69065540 | C | CAA | 116 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0023 others(113): Show |
136 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.482+519_482+520dup others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69065540 | ||||||
chr9:69065540 | C | CAAAA | 21 | a0001c0001t0001g0052 a0001c0001t0001g0240 a0001c0001t0001g0258 others(18): Show |
21 | HG00323.hp1 HG00438.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.482+517_482+520dup others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69065540 | ||||||
chr9:69065561 | C | T | 1 | a0001c0002t0034g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.482+526C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065561 | |||||||
chr9:69065642 | A | G | 14 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(11): Show |
15 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.482+607A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065642 | |||||||
chr9:69066167 | C | T | 1 | a0001c0001t0004g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.482+1132C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066167 | |||||||
chr9:69066253 | G | A | 1 | a0001c0001t0015g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.482+1218G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066253 | |||||||
chr9:69066324 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(240): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.482+1289T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066324 | |||||||
chr9:69066337 | C | A | 224 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(221): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.482+1302C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066337 | |||||||
chr9:69066425 | G | C | 1 | a0001c0001t0004g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.482+1390G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066425 | |||||||
chr9:69066858 | C | CA | 7 | a0001c0001t0008g0177 a0001c0001t0008g0303 a0001c0001t0009g0236 others(4): Show |
7 | HG01255.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.482+1835dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69066858 | ||||||
chr9:69066867 | A | AT | 31 | a0001c0001t0003g0227 a0001c0001t0005g0035 a0001c0001t0005g0038 others(28): Show |
34 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.482+1832_482+1833i others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066867 | |||||||
chr9:69066867 | A | ATAT | 4 | a0001c0001t0002g0126 a0001c0001t0002g0135 a0001c0001t0002g0250 others(1): Show |
4 | HG01109.hp2 HG02602.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1832_482+1833i others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066867 | |||||||
chr9:69066867 | A | T | 4 | a0001c0001t0007g0313 a0003c0004t0021g0014 a0003c0004t0021g0344 others(1): Show |
5 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.482+1832A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066867 | |||||||
chr9:69066869 | A | AAAT | 12 | a0001c0001t0002g0024 a0001c0001t0002g0095 a0001c0001t0002g0127 others(9): Show |
13 | HG00741.hp2 HG01175.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+1835_482+1836i others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69066869 | ||||||
chr9:69066869 | A | AT | 10 | a0001c0001t0005g0286 a0001c0001t0009g0011 a0001c0001t0009g0202 others(7): Show |
11 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+1834_482+1835i others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | |||||||
chr9:69066869 | A | ATAT | 86 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0023 others(83): Show |
101 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.482+1834_482+1835i others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | |||||||
chr9:69066869 | A | ATATAT | 2 | a0001c0001t0004g0027 a0001c0001t0004g0162 |
3 | HG01981.hp1 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.482+1834_482+1835i others(7): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | |||||||
chr9:69066869 | A | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(190): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+1834A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | |||||||
chr9:69066870 | AT | A | 3 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 |
3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.482+1836delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066870 | |||||||
chr9:69066871 | T | A | 1 | a0001c0001t0008g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482+1836T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066871 | |||||||
chr9:69066959 | A | G | 6 | a0001c0001t0005g0035 a0001c0001t0005g0204 a0001c0001t0005g0205 others(3): Show |
7 | HG01175.hp1 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1924A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066959 | |||||||
chr9:69066966 | C | T | 2 | a0001c0001t0002g0134 a0001c0001t0002g0332 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.482+1931C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066966 | |||||||
chr9:69066970 | G | A | 4 | a0001c0001t0008g0177 a0001c0001t0008g0303 a0001c0001t0044g0088 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1935G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066970 | |||||||
chr9:69066989 | C | T | 1 | a0001c0001t0006g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.482+1954C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066989 | |||||||
chr9:69067008 | G | A | 2 | a0001c0001t0005g0230 a0001c0001t0017g0279 |
2 | HG04199.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.482+1973G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067008 | |||||||
chr9:69067070 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(192): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+2035C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067070 | |||||||
chr9:69067199 | C | T | 8 | a0001c0001t0005g0038 a0001c0001t0005g0248 a0001c0001t0005g0281 others(5): Show |
9 | HG00140.hp1 HG00423.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+2164C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067199 | |||||||
chr9:69067249 | C | G | 1 | a0001c0001t0002g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482+2214C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067249 | |||||||
chr9:69067298 | C | A | 1 | a0001c0001t0054g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482+2263C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067298 | |||||||
chr9:69067366 | G | A | 113 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(110): Show |
130 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.482+2331G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067366 | |||||||
chr9:69067479 | G | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+2444G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067479 | |||||||
chr9:69067606 | C | A | 1 | a0001c0001t0003g0233 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.482+2571C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067606 | |||||||
chr9:69067611 | A | AAAC | 6 | a0001c0001t0044g0088 a0002c0003t0015g0049 a0002c0003t0015g0053 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+2594_482+2596d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69067611 | ||||||
chr9:69067629 | C | A | 1 | a0001c0001t0004g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.482+2594C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067629 | |||||||
chr9:69067815 | T | C | 1 | a0001c0001t0052g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482+2780T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067815 | |||||||
chr9:69067895 | G | A | 2 | a0001c0001t0005g0212 a0001c0001t0005g0213 |
2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.482+2860G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067895 | |||||||
chr9:69067951 | A | C | 1 | a0001c0001t0005g0286 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.482+2916A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067951 | |||||||
chr9:69068053 | GAGAC | G | 113 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(110): Show |
130 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.482+3023_482+3026d others(6): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69068053 | ||||||
chr9:69068199 | C | T | 1 | a0001c0001t0022g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.482+3164C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068199 | |||||||
chr9:69068258 | G | A | 2 | a0001c0001t0047g0304 a0002c0003t0051g0082 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.482+3223G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068258 | |||||||
chr9:69068371 | C | T | 4 | a0001c0001t0015g0079 a0001c0001t0015g0080 a0001c0001t0054g0059 others(1): Show |
4 | HG01891.hp2 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3336C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068371 | |||||||
chr9:69068373 | C | G | 2 | a0001c0001t0002g0129 a0001c0001t0002g0137 |
2 | HG04184.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.482+3338C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068373 | |||||||
chr9:69068396 | T | C | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+3361T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068396 | |||||||
chr9:69068490 | G | C | 1 | a0003c0004t0021g0344 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482+3455G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068490 | |||||||
chr9:69068505 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.482+3470C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068505 | |||||||
chr9:69068574 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.482+3539G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068574 | |||||||
chr9:69068773 | T | TA | 4 | a0001c0001t0006g0321 a0001c0001t0006g0326 a0001c0001t0006g0327 others(1): Show |
4 | HG02257.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3739dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69068773 | ||||||
chr9:69068776 | G | A | 5 | a0001c0001t0015g0079 a0001c0001t0015g0080 a0001c0001t0018g0020 others(2): Show |
6 | HG01516.hp2 HG01517.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+3741G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068776 | |||||||
chr9:69068824 | G | A | 3 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0042g0121 |
3 | HG01168.hp2 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.483-3788G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068824 | |||||||
chr9:69068913 | C | T | 1 | a0001c0001t0004g0086 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.483-3699C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068913 | |||||||
chr9:69069020 | C | T | 1 | a0001c0001t0003g0292 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.483-3592C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069020 | |||||||
chr9:69069046 | C | T | 1 | a0001c0001t0015g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.483-3566C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069046 | |||||||
chr9:69069222 | A | G | 29 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(26): Show |
33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.483-3390A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069222 | |||||||
chr9:69069254 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(211): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.483-3358G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069254 | |||||||
chr9:69069304 | G | A | 3 | a0003c0004t0021g0014 a0003c0004t0021g0344 a0003c0004t0033g0014 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-3308G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069304 | |||||||
chr9:69069320 | G | A | 2 | a0001c0002t0023g0015 a0001c0002t0023g0055 |
3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.483-3292G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069320 | |||||||
chr9:69069343 | C | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.483-3269C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069343 | |||||||
chr9:69069367 | AAAG | A | 5 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(2): Show |
6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.483-3244_483-3242d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069367 | |||||||
chr9:69069453 | G | A | 9 | a0001c0001t0008g0006 a0001c0001t0008g0208 a0001c0001t0008g0209 others(6): Show |
12 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.483-3159G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069453 | |||||||
chr9:69069471 | C | G | 1 | a0001c0008t0074g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.483-3141C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069471 | |||||||
chr9:69069511 | ACACT | A | 10 | a0001c0001t0008g0006 a0001c0001t0008g0208 a0001c0001t0008g0209 others(7): Show |
13 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.483-3097_483-3094d others(6): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69069511 | ||||||
chr9:69069675 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(211): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.483-2937T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069675 | |||||||
chr9:69069783 | G | A | 3 | a0001c0001t0003g0171 a0001c0001t0003g0190 a0001c0001t0003g0193 |
3 | NA18940.hp1 NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.483-2829G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069783 | |||||||
chr9:69069786 | G | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(187): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.483-2826G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069786 | |||||||
chr9:69069879 | A | G | 1 | a0001c0002t0034g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.483-2733A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069879 | |||||||
chr9:69069985 | T | G | 2 | a0001c0001t0047g0304 a0002c0003t0051g0082 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.483-2627T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069985 | |||||||
chr9:69069989 | G | A | 3 | a0001c0001t0005g0206 a0001c0001t0005g0207 a0001c0001t0005g0222 |
3 | HG01515.hp2 HG01516.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.483-2623G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069989 | |||||||
chr9:69070045 | A | G | 13 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(10): Show |
14 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.483-2567A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070045 | |||||||
chr9:69070096 | A | G | 19 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(16): Show |
21 | HG01255.hp2 HG01496.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.483-2516A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070096 | |||||||
chr9:69070118 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.483-2494A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070118 | |||||||
chr9:69070208 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.483-2404G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070208 | |||||||
chr9:69070236 | A | G | 1 | a0001c0002t0034g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.483-2376A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070236 | |||||||
chr9:69070242 | A | G | 1 | a0001c0001t0060g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.483-2370A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070242 | |||||||
chr9:69070275 | G | A | 5 | a0001c0001t0004g0098 a0002c0003t0015g0053 a0002c0003t0032g0050 others(2): Show |
5 | HG02071.hp1 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.483-2337G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070275 | |||||||
chr9:69070399 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.483-2213G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070399 | |||||||
chr9:69070400 | C | G | 1 | a0001c0001t0002g0142 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.483-2212C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070400 | |||||||
chr9:69070516 | T | G | 2 | a0001c0002t0023g0015 a0001c0002t0023g0055 |
3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.483-2096T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070516 | |||||||
chr9:69070598 | C | T | 35 | a0001c0001t0008g0006 a0001c0001t0008g0177 a0001c0001t0008g0208 others(32): Show |
40 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.483-2014C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070598 | |||||||
chr9:69070728 | T | A | 2 | a0001c0001t0006g0322 a0001c0001t0006g0345 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.483-1884T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070728 | |||||||
chr9:69070729 | G | GT | 17 | a0001c0001t0001g0271 a0001c0001t0003g0186 a0001c0001t0009g0011 others(14): Show |
18 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.483-1874dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070729 | ||||||
chr9:69070802 | GT | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-1800delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070802 | ||||||
chr9:69070883 | TTGGTCTG others(7): Show |
T | 35 | a0001c0001t0008g0006 a0001c0001t0008g0177 a0001c0001t0008g0208 others(32): Show |
40 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.483-1725_483-1712d others(16): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070883 | ||||||
chr9:69070946 | T | TG | 4 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(1): Show |
4 | HG01496.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-1663dupG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070946 | ||||||
chr9:69070980 | G | T | 1 | a0001c0001t0004g0113 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.483-1632G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070980 | |||||||
chr9:69070992 | T | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(236): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.483-1620T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070992 | |||||||
chr9:69071088 | GGGA | G | 2 | a0001c0001t0020g0036 a0001c0001t0020g0231 |
3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483-1523_483-1521d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071088 | |||||||
chr9:69071265 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(228): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.483-1347T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071265 | |||||||
chr9:69071499 | T | C | 1 | a0001c0001t0044g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-1113T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071499 | |||||||
chr9:69071560 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(171): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.483-1052G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071560 | |||||||
chr9:69071585 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483-1027G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071585 | |||||||
chr9:69071597 | C | T | 1 | a0001c0001t0007g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.483-1015C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071597 | |||||||
chr9:69071604 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(223): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.483-1008A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071604 | |||||||
chr9:69071641 | T | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(174): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.483-971T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071641 | |||||||
chr9:69071649 | C | A | 29 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(26): Show |
33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.483-963C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071649 | |||||||
chr9:69071716 | A | G | 1 | a0001c0001t0005g0216 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.483-896A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071716 | |||||||
chr9:69071786 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-826A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071786 | |||||||
chr9:69071803 | T | C | 36 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(33): Show |
41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.483-809T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071803 | |||||||
chr9:69071809 | A | G | 36 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(33): Show |
41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.483-803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071809 | |||||||
chr9:69071950 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-662G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071950 | |||||||
chr9:69072002 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-610G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072002 | |||||||
chr9:69072136 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-476G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072136 | |||||||
chr9:69072254 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.483-358G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072254 | |||||||
chr9:69072274 | A | G | 2 | a0001c0002t0023g0015 a0001c0002t0023g0055 |
3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.483-338A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072274 | |||||||
chr9:69072275 | C | T | 12 | a0001c0001t0009g0011 a0001c0001t0009g0202 a0001c0001t0009g0235 others(9): Show |
13 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-337C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072275 | |||||||
chr9:69072285 | C | A | 1 | a0001c0001t0009g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.483-327C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072285 | |||||||
chr9:69072307 | C | A | 4 | a0001c0001t0014g0176 a0001c0001t0014g0178 a0001c0001t0014g0182 others(1): Show |
4 | HG01496.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-305C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072307 | |||||||
chr9:69072381 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483-231G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072381 | |||||||
chr9:69072413 | T | C | 5 | a0001c0001t0005g0038 a0001c0001t0005g0248 a0001c0001t0005g0285 others(2): Show |
6 | HG00423.hp1 HG00673.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-199T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072413 | |||||||
chr9:69072437 | T | G | 30 | a0001c0001t0007g0045 a0001c0001t0007g0046 a0001c0001t0007g0047 others(27): Show |
34 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.483-175T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072437 | |||||||
chr9:69072443 | A | G | 1 | a0001c0001t0054g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.483-169A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072443 | |||||||
chr9:69072484 | C | CTG | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-127_483-126ins others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69072484 | ||||||
chr9:69072524 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(174): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.483-88C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072524 |