Item | Value |
---|---|
geneid | 23409 |
ensemblid | ENSG00000089163.4 |
hgncid | 14932 |
symbol | SIRT4 |
name | sirtuin 4 |
refseq_nuc | NM_012240.3 |
refseq_prot | NP_036372.1 |
ensembl_nuc | ENST00000202967.4 |
ensembl_prot | ENSP00000202967.4 |
mane_status | MANE Select |
chr | chr12 |
start | 120302321 |
end | 120313249 |
strand | + |
ver | v1.2 |
region | chr12:120302321-120313249 |
region5000 | chr12:120297321-120318249 |
regionname0 | SIRT4_chr12_120302321_120313249 |
regionname5000 | SIRT4_chr12_120297321_120318249 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 314 | 373 | 89 | 68 | 154 | 16 | 44 | 115 | SIRT4_chr12_120297321_120318249 | SIRT4 | MKMSF others(309): Show |
chr12 | 120297321 | 120318249 |
a0002 | 0/0 | 314 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | MKMSF others(309): Show |
chr12 | 120297321 | 120318249 |
a0003 | 0/0 | 314 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | MKMSF others(309): Show |
chr12 | 120297321 | 120318249 |
a0004 | 0/0 | 314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | MKMSF others(309): Show |
chr12 | 120297321 | 120318249 |
a0005 | 0/0 | 165 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | MKMSF others(160): Show |
chr12 | 120297321 | 120318249 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 942 | 341 | 88 | 59 | 137 | 16 | 39 | SIRT4_chr12_120297321_120318249 | SIRT4 | ATGAA others(937): Show |
chr12 | 120297321 | 120318249 | ||
a0001c0002 | 0/0 | 942 | 32 | 1 | 9 | 17 | 0 | 5 | SIRT4_chr12_120297321_120318249 | SIRT4 | ATGAA others(937): Show |
chr12 | 120297321 | 120318249 | ||
a0002c0003 | 0/0 | 942 | 4 | 4 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | ATGAA others(937): Show |
chr12 | 120297321 | 120318249 | ||
a0003c0006 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | ATGAA others(937): Show |
chr12 | 120297321 | 120318249 | ||
a0004c0005 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | ATGAA others(937): Show |
chr12 | 120297321 | 120318249 | ||
a0005c0004 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | ATGAA others(492): Show |
chr12 | 120297321 | 120318249 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1216 | 341 | 88 | 59 | 137 | 16 | 39 | SIRT4_chr12_120297321_120318249 | SIRT4 | GCAAA others(1211): Show |
chr12 | 120297321 | 120318249 |
a0001c0002t0001 | 0/0 | 1216 | 32 | 1 | 9 | 17 | 0 | 5 | SIRT4_chr12_120297321_120318249 | SIRT4 | GCAAA others(1211): Show |
chr12 | 120297321 | 120318249 |
a0002c0003t0001 | 0/0 | 1216 | 4 | 4 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | GCAAA others(1211): Show |
chr12 | 120297321 | 120318249 |
a0003c0006t0001 | 0/0 | 1216 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | GCAAA others(1211): Show |
chr12 | 120297321 | 120318249 |
a0004c0005t0001 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | GCAAA others(1211): Show |
chr12 | 120297321 | 120318249 |
a0005c0004t0002 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | GCAAA others(550): Show |
chr12 | 120297321 | 120318249 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 69 | 0 | 20 | 37 | 3 | 9 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0002 | 0/0 | 58 | 10 | 3 | 38 | 3 | 4 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0003 | 0/0 | 19 | 17 | 2 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0005 | 0/0 | 17 | 4 | 7 | 0 | 4 | 2 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0006 | 0/0 | 16 | 1 | 3 | 7 | 0 | 5 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0007 | 0/0 | 11 | 1 | 2 | 7 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0008 | 0/0 | 10 | 0 | 0 | 7 | 0 | 3 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0009 | 0/0 | 7 | 2 | 0 | 3 | 0 | 2 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0011 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0024 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0004 | 0/0 | 18 | 1 | 6 | 7 | 0 | 4 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0023 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0002c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0002c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0003c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0004c0005t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
a0005c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02074 | hp1 | a0003 | c0006 | t0001 | g0041 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02145 | hp2 | a0002 | c0003 | t0001 | g0083 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02809 | hp1 | a0004 | c0005 | t0001 | g0002 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02970 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18906 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | YRI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18974 | hp2 | a0005 | c0004 | t0002 | g0045 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | USA | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0058 | REF | REF | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0024 | REF | REF | SIRT4_chr12_120297321_120318249 | SIRT4 | chr12 | 120297321 | 120318249 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120303641 | C | T | 1 | a0003 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.80C>T | p.Ala27Val | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/4 | 139/1217 | 80/945 | 27/314 | chr12 | 120303641 | |||
chr12:120303733 | C | T | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.172C>T | p.Leu58Phe | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/4 | 231/1217 | 172/945 | 58/314 | chr12 | 120303733 | |||
chr12:120303865 | C | T | 1 | a0002 | 4 | HG02145.hp2 HG02970.hp2 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.304C>T | p.Arg102Cys | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/4 | 363/1217 | 304/945 | 102/314 | chr12 | 120303865 | |||
chr12:120312031 | CCAGCACT others(1243): Show |
C | 1 | a0005 | 1 | NA18974.hp2 | exon_loss_variant | HIGH | c.498-424_*245del | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 3/4 | chr12 | 120312031 | |||||||
chr12:120312661 | G | A | 1 | a0001 | 3 | NA18948.hp2 NA18982.hp1 NA19005.hp1 |
missense_variant | MODERATE | c.703G>A | p.Gly235Arg | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 3/4 | 762/1217 | 703/945 | 235/314 | chr12 | 120312661 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120303579 | G | A | 1 | a0001c0002 | 32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
synonymous_variant | LOW | c.18G>A | p.Ala6Ala | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/4 | 77/1217 | 18/945 | 6/314 | chr12 | 120303579 | |||
chr12:120312570 | C | T | 1 | a0001c0001 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.612C>T | p.Asp204Asp | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 3/4 | 671/1217 | 612/945 | 204/314 | chr12 | 120312570 | |||
chr12:120312618 | C | T | 1 | a0001c0001 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.660C>T | p.Cys220Cys | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 3/4 | 719/1217 | 660/945 | 220/314 | chr12 | 120312618 | |||
chr12:120312714 | A | G | 1 | a0001c0002 | 32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
synonymous_variant | LOW | c.756A>G | p.Glu252Glu | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 3/4 | 815/1217 | 756/945 | 252/314 | chr12 | 120312714 | |||
chr12:120312943 | A | T | 2 | a0001c0001 a0002c0003 |
9 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
synonymous_variant | LOW | c.852A>T | p.Ile284Ile | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 4/4 | 911/1217 | 852/945 | 284/314 | chr12 | 120312943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120313186 | G | A | 1 | a0001c0001t0001 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 4/4 | 150 | chr12 | 120313186 | ||||||
chr12:120313219 | T | A | 1 | a0001c0001t0001 | 5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 4/4 | 183 | chr12 | 120313219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:120302559 | C | G | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(8): Show |
32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-2+181C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302559 | |||||||
chr12:120302566 | T | G | 1 | a0001c0001t0001g0013 | 4 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+188T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302566 | |||||||
chr12:120302576 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2+198C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302576 | |||||||
chr12:120302720 | C | CT | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(8): Show |
12 | HG00438.hp2 HG01070.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+359dupT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 120302720 | ||||||
chr12:120302720 | CT | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0005c0004t0002g0045 |
9 | HG00558.hp1 HG02027.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+359delT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 120302720 | ||||||
chr12:120302726 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0009 |
24 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2+348T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302726 | |||||||
chr12:120302845 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-2+467T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302845 | |||||||
chr12:120302874 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.-2+496A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302874 | |||||||
chr12:120302942 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-2+564C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120302942 | |||||||
chr12:120303053 | G | T | 1 | a0001c0001t0001g0040 | 2 | HG00639.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-1-508G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120303053 | |||||||
chr12:120303444 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-1-117T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | chr12 | 120303444 | |||||||
chr12:120303510 | G | GA | 3 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0057 |
6 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-39dupA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 120303510 | ||||||
chr12:120303510 | G | GAA | 10 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(7): Show |
31 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1-40_-1-39dupAA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 120303510 | ||||||
chr12:120304324 | C | T | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(8): Show |
32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.497+266C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304324 | |||||||
chr12:120304341 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(21): Show |
87 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.497+283A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304341 | |||||||
chr12:120304381 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG00609.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.497+323G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304381 | |||||||
chr12:120304387 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.497+329C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304387 | |||||||
chr12:120304432 | A | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0096 others(11): Show |
38 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.497+374A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304432 | |||||||
chr12:120304456 | C | G | 1 | a0001c0001t0001g0042 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.497+398C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304456 | |||||||
chr12:120304506 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497+448C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304506 | |||||||
chr12:120304507 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.497+449A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304507 | |||||||
chr12:120304531 | TC | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0002c0003t0001g0016 others(1): Show |
7 | HG02145.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+476delC | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304531 | ||||||
chr12:120304752 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0082 |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+694C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304752 | |||||||
chr12:120304803 | T | TTA | 1 | a0001c0001t0001g0017 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.497+777_497+778dup others(2): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304803 | ||||||
chr12:120304803 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497+769_497+778dup others(10): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304803 | ||||||
chr12:120304803 | T | TTATATAT others(5): Show |
1 | a0001c0002t0001g0100 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.497+767_497+778dup others(12): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304803 | ||||||
chr12:120304803 | T | TTATATAT others(7): Show |
2 | a0001c0002t0001g0098 a0001c0002t0001g0099 |
2 | NA18965.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.497+765_497+778dup others(14): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304803 | ||||||
chr12:120304803 | T | TTATATAT others(9): Show |
1 | a0001c0002t0001g0044 | 2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.497+763_497+778dup others(16): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304803 | ||||||
chr12:120304803 | T | TTATATAT others(11): Show |
1 | a0001c0002t0001g0043 | 2 | HG03710.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.497+761_497+778dup others(18): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304803 | ||||||
chr12:120304819 | ATATATAT others(19): Show |
A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01069.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.497+763_497+788del others(26): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304819 | ||||||
chr12:120304822 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
27 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.497+764T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304822 | |||||||
chr12:120304823 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.497+767_497+783del others(17): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304823 | ||||||
chr12:120304824 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(28): Show |
142 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.497+766T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304824 | |||||||
chr12:120304825 | ATATATAT others(6): Show |
A | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.497+769_497+781del others(13): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304825 | ||||||
chr12:120304825 | ATATATAT others(8): Show |
A | 3 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0104 |
6 | HG00741.hp2 HG01070.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+769_497+783del others(15): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304825 | ||||||
chr12:120304825 | ATATATAT others(9): Show |
A | 1 | a0001c0002t0001g0004 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.497+769_497+784del others(16): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304825 | ||||||
chr12:120304825 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.497+769_497+785del others(17): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304825 | ||||||
chr12:120304825 | ATATATAT others(12): Show |
A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0002c0003t0001g0016 others(1): Show |
7 | HG02145.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+769_497+787del others(19): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304825 | ||||||
chr12:120304826 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(15): Show |
50 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.497+768T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304826 | |||||||
chr12:120304827 | ATATATAT others(7): Show |
A | 1 | a0001c0002t0001g0004 | 2 | HG01496.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.497+771_497+784del others(14): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304827 | ||||||
chr12:120304827 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0013 a0001c0002t0001g0004 |
3 | HG01109.hp2 HG01981.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.497+771_497+785del others(15): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304827 | ||||||
chr12:120304827 | ATATATAT others(10): Show |
A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(11): Show |
54 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.497+771_497+787del others(17): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304827 | ||||||
chr12:120304827 | ATATATAT others(11): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(15): Show |
87 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.497+771_497+788del others(18): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304827 | ||||||
chr12:120304827 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+771_497+789del others(19): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304827 | ||||||
chr12:120304828 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.497+770T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304828 | |||||||
chr12:120304829 | ATATATAT others(8): Show |
A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0022 others(5): Show |
23 | HG01169.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.497+773_497+787del others(15): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304829 | ||||||
chr12:120304829 | ATATATAT others(9): Show |
A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0027 others(7): Show |
27 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.497+773_497+788del others(16): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304829 | ||||||
chr12:120304830 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0080 |
4 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+772T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304830 | |||||||
chr12:120304831 | ATATATTT others(7): Show |
A | 1 | a0001c0001t0001g0026 | 2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.497+775_497+788del others(14): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304831 | ||||||
chr12:120304833 | ATATTTTT others(3): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0007 |
2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497+777_497+786del others(10): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304833 | ||||||
chr12:120304833 | ATATTTTT others(4): Show |
A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0080 |
4 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+777_497+787del others(11): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304833 | ||||||
chr12:120304833 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.497+777_497+788del others(12): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304833 | ||||||
chr12:120304835 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0004 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.497+778_497+779ins others(11): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304835 | A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0023 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.497+778_497+779ins others(13): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304835 | A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.497+778_497+779ins others(15): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304835 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0004 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.497+778_497+779ins others(17): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304835 | A | ATATATAT others(9): Show |
1 | a0001c0002t0001g0103 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.497+778_497+779ins others(16): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304835 | ATTTT | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(7): Show |
18 | HG00597.hp1 HG01099.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.497+798_497+801del others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304835 | ATTTTTT | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(10): Show |
59 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.497+796_497+801del others(6): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120304835 | ||||||
chr12:120304836 | T | TA | 3 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0051 |
8 | HG03225.hp1 HG03516.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.497+778_497+779ins others(1): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304836 | |||||||
chr12:120304836 | T | TATA | 2 | a0001c0001t0001g0010 a0001c0001t0001g0020 |
3 | HG01516.hp2 HG01517.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.497+778_497+779ins others(3): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304836 | |||||||
chr12:120304836 | T | TATATATA others(4): Show |
1 | a0001c0002t0001g0004 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.497+778_497+779ins others(11): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304836 | |||||||
chr12:120304836 | T | TATATATA others(6): Show |
2 | a0001c0002t0001g0004 a0001c0002t0001g0101 |
2 | HG00621.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.497+778_497+779ins others(13): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304836 | |||||||
chr12:120304836 | T | TATATATA others(8): Show |
2 | a0001c0002t0001g0004 a0001c0002t0001g0102 |
2 | NA18948.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.497+778_497+779ins others(15): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304836 | |||||||
chr12:120304836 | T | TATATATA others(10): Show |
1 | a0001c0002t0001g0004 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.497+778_497+779ins others(17): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304836 | |||||||
chr12:120304837 | T | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0020 others(14): Show |
21 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.497+779T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304837 | |||||||
chr12:120304838 | T | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(8): Show |
21 | HG00621.hp2 HG01243.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+780T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304838 | |||||||
chr12:120304839 | T | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(16): Show |
22 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.497+781T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304839 | |||||||
chr12:120304840 | T | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(9): Show |
23 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.497+782T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304840 | |||||||
chr12:120304841 | T | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(20): Show |
32 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.497+783T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304841 | |||||||
chr12:120304842 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(5): Show |
19 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.497+784T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304842 | |||||||
chr12:120304843 | T | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(18): Show |
46 | HG00544.hp2 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.497+785T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304843 | |||||||
chr12:120304844 | T | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0074 |
9 | HG01168.hp1 HG03017.hp2 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+786T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304844 | |||||||
chr12:120304845 | T | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02559.hp2 HG03540.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+787T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304845 | |||||||
chr12:120304847 | T | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02559.hp2 HG03540.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.497+789T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304847 | |||||||
chr12:120304932 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497+874T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304932 | |||||||
chr12:120304997 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.497+939T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120304997 | |||||||
chr12:120305110 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.497+1052T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305110 | |||||||
chr12:120305172 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.497+1114G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305172 | |||||||
chr12:120305242 | C | CGT | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0096 |
3 | HG00438.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.497+1209_497+1210d others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120305242 | ||||||
chr12:120305242 | CGT | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.497+1209_497+1210d others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120305242 | ||||||
chr12:120305242 | CGTGTGT | C | 12 | a0001c0001t0001g0085 a0001c0002t0001g0004 a0001c0002t0001g0023 others(9): Show |
33 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.497+1205_497+1210d others(8): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120305242 | ||||||
chr12:120305249 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.497+1191G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305249 | |||||||
chr12:120305414 | C | A | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(8): Show |
32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.497+1356C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305414 | |||||||
chr12:120305670 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0025 others(19): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.497+1612G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305670 | |||||||
chr12:120305725 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.497+1667T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305725 | |||||||
chr12:120305751 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.497+1693G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305751 | |||||||
chr12:120305839 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+1781C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305839 | |||||||
chr12:120305883 | A | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0035 others(16): Show |
46 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.497+1825A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120305883 | |||||||
chr12:120306007 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+1949G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306007 | |||||||
chr12:120306011 | CA | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
7 | HG01169.hp1 HG01192.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.497+1969delA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120306011 | ||||||
chr12:120306028 | G | A | 12 | a0001c0001t0001g0064 a0001c0002t0001g0004 a0001c0002t0001g0023 others(9): Show |
33 | HG00621.hp2 HG00639.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.497+1970G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306028 | |||||||
chr12:120306029 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.497+1971A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306029 | |||||||
chr12:120306263 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.497+2205G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306263 | |||||||
chr12:120306288 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497+2230C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306288 | |||||||
chr12:120306301 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497+2243C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306301 | |||||||
chr12:120306318 | A | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0080 |
4 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+2260A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306318 | |||||||
chr12:120306349 | C | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0093 |
2 | HG01255.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.497+2291C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306349 | |||||||
chr12:120306367 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0039 others(1): Show |
16 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.497+2309C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306367 | |||||||
chr12:120306416 | G | A | 1 | a0002c0003t0001g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.497+2358G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306416 | |||||||
chr12:120306459 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0082 |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+2401G>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306459 | |||||||
chr12:120306477 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.497+2419C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306477 | |||||||
chr12:120306478 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.497+2420G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306478 | |||||||
chr12:120306480 | C | CA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0016 others(12): Show |
41 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.497+2433dupA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120306480 | ||||||
chr12:120306488 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.497+2430A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306488 | |||||||
chr12:120306592 | A | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0082 |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+2534A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306592 | |||||||
chr12:120306675 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497+2617C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306675 | |||||||
chr12:120306888 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.497+2830G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120306888 | |||||||
chr12:120307090 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.497+3032A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307090 | |||||||
chr12:120307282 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.497+3224G>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307282 | |||||||
chr12:120307341 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(13): Show |
75 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.497+3283T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307341 | |||||||
chr12:120307362 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+3304G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307362 | |||||||
chr12:120307522 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0082 |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+3464C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307522 | |||||||
chr12:120307562 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0042 |
9 | HG02615.hp1 HG02723.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+3504C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307562 | |||||||
chr12:120307585 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.497+3527C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307585 | |||||||
chr12:120307588 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.497+3530G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307588 | |||||||
chr12:120307780 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.497+3722C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307780 | |||||||
chr12:120307806 | T | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0096 others(11): Show |
38 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.497+3748T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307806 | |||||||
chr12:120307815 | ACCATTGC others(3490): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497+3786_498-1116d others(2): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120307815 | ||||||
chr12:120307867 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0082 |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+3809A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120307867 | |||||||
chr12:120308024 | A | AT | 3 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0095 |
6 | HG01243.hp1 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.497+3977dupT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120308024 | ||||||
chr12:120308024 | A | T | 1 | a0001c0001t0001g0002 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.497+3966A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308024 | |||||||
chr12:120308024 | AT | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0002t0001g0004 others(9): Show |
36 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.497+3977delT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120308024 | ||||||
chr12:120308033 | T | C | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(8): Show |
32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.497+3975T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308033 | |||||||
chr12:120308056 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.497+3998T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308056 | |||||||
chr12:120308108 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0035 others(17): Show |
47 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.497+4050T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308108 | |||||||
chr12:120308117 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.497+4059A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308117 | |||||||
chr12:120308142 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.497+4084C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308142 | |||||||
chr12:120308165 | C | CT | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0034 others(11): Show |
34 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.497+4128dupT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120308165 | ||||||
chr12:120308165 | CT | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(44): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.497+4128delT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120308165 | ||||||
chr12:120308165 | CTT | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(6): Show |
12 | HG01168.hp2 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.497+4127_497+4128d others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120308165 | ||||||
chr12:120308193 | C | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0002t0001g0004 others(10): Show |
37 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.497+4135C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308193 | |||||||
chr12:120308256 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.497+4198G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308256 | |||||||
chr12:120308437 | C | T | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(8): Show |
32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.498-4019C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308437 | |||||||
chr12:120308464 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0040 |
4 | HG00639.hp2 HG02698.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-3992C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308464 | |||||||
chr12:120308522 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18968.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.498-3934C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308522 | |||||||
chr12:120308574 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(10): Show |
50 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.498-3882C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308574 | |||||||
chr12:120308888 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.498-3568C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308888 | |||||||
chr12:120308958 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-3498T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120308958 | |||||||
chr12:120309032 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3424A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309032 | |||||||
chr12:120309034 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3422C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309034 | |||||||
chr12:120309035 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3421C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309035 | |||||||
chr12:120309038 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3418G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309038 | |||||||
chr12:120309039 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3417C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309039 | |||||||
chr12:120309040 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3416A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309040 | |||||||
chr12:120309041 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3415T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309041 | |||||||
chr12:120309046 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3410G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309046 | |||||||
chr12:120309049 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3407C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309049 | |||||||
chr12:120309053 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3403C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309053 | |||||||
chr12:120309054 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3402C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309054 | |||||||
chr12:120309057 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3399T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309057 | |||||||
chr12:120309058 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3398A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309058 | |||||||
chr12:120309059 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3397A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309059 | |||||||
chr12:120309060 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3396T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309060 | |||||||
chr12:120309061 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3395C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309061 | |||||||
chr12:120309062 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3394C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309062 | |||||||
chr12:120309063 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3393C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309063 | |||||||
chr12:120309064 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3392A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309064 | |||||||
chr12:120309066 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3390C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309066 | |||||||
chr12:120309067 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3389T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309067 | |||||||
chr12:120309068 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3388A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309068 | |||||||
chr12:120309069 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3387C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309069 | |||||||
chr12:120309070 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3386T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309070 | |||||||
chr12:120309071 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3385C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309071 | |||||||
chr12:120309075 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3381A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309075 | |||||||
chr12:120309078 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3378C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309078 | |||||||
chr12:120309079 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3377T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309079 | |||||||
chr12:120309081 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3375A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309081 | |||||||
chr12:120309084 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3372C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309084 | |||||||
chr12:120309085 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3371A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309085 | |||||||
chr12:120309088 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3368A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309088 | |||||||
chr12:120309090 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3366A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309090 | |||||||
chr12:120309094 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-3362G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309094 | |||||||
chr12:120309100 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3356A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309100 | |||||||
chr12:120309107 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3349A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309107 | |||||||
chr12:120309110 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3346C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309110 | |||||||
chr12:120309113 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3343A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309113 | |||||||
chr12:120309116 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3340T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309116 | |||||||
chr12:120309117 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3339T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309117 | |||||||
chr12:120309121 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.498-3335G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309121 | |||||||
chr12:120309400 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.498-3056C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309400 | |||||||
chr12:120309413 | C | CT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(5): Show |
9 | HG00621.hp1 HG01192.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-3027dupT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120309413 | ||||||
chr12:120309505 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-2951G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309505 | |||||||
chr12:120309648 | G | A | 1 | a0001c0001t0001g0006 | 3 | HG00673.hp1 NA19010.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.498-2808G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309648 | |||||||
chr12:120309714 | C | CT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
13 | HG01346.hp2 HG02015.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-2723dupT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120309714 | ||||||
chr12:120309714 | C | CTT | 4 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0002c0003t0001g0016 others(1): Show |
6 | HG02145.hp2 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-2724_498-2723d others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120309714 | ||||||
chr12:120309714 | CT | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(12): Show |
38 | HG00621.hp2 HG00741.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.498-2723delT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120309714 | ||||||
chr12:120309877 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.498-2579G>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309877 | |||||||
chr12:120309978 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.498-2478A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120309978 | |||||||
chr12:120310007 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.498-2449G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310007 | |||||||
chr12:120310110 | G | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(14): Show |
77 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.498-2346G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310110 | |||||||
chr12:120310173 | T | C | 1 | a0001c0001t0001g0008 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.498-2283T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310173 | |||||||
chr12:120310184 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0082 |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-2272C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310184 | |||||||
chr12:120310198 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0065 |
5 | HG01070.hp1 HG01071.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-2258G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310198 | |||||||
chr12:120310259 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.498-2197G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310259 | |||||||
chr12:120310337 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.498-2119G>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310337 | |||||||
chr12:120310378 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0084 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.498-2078C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310378 | |||||||
chr12:120310390 | A | T | 1 | a0001c0001t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.498-2066A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310390 | |||||||
chr12:120310474 | C | T | 1 | a0001c0001t0001g0006 | 2 | NA18972.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.498-1982C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310474 | |||||||
chr12:120310521 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0087 |
3 | HG02976.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.498-1935G>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310521 | |||||||
chr12:120310554 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1902C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310554 | |||||||
chr12:120310557 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1899A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310557 | |||||||
chr12:120310560 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1896G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310560 | |||||||
chr12:120310561 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1895C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310561 | |||||||
chr12:120310563 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1893G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310563 | |||||||
chr12:120310564 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1892A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310564 | |||||||
chr12:120310567 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1889A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310567 | |||||||
chr12:120310583 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1873A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310583 | |||||||
chr12:120310584 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1872A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310584 | |||||||
chr12:120310584 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.498-1872A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310584 | |||||||
chr12:120310585 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1871A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310585 | |||||||
chr12:120310588 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1868A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310588 | |||||||
chr12:120310592 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1864T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310592 | |||||||
chr12:120310594 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1862G>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310594 | |||||||
chr12:120310631 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1825A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310631 | |||||||
chr12:120310634 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1822A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310634 | |||||||
chr12:120310635 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1821C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310635 | |||||||
chr12:120310636 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1820T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310636 | |||||||
chr12:120310642 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-1814A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310642 | |||||||
chr12:120310650 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1806T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310650 | |||||||
chr12:120310659 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1797C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310659 | |||||||
chr12:120310660 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1796T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310660 | |||||||
chr12:120310668 | C | A | 1 | a0001c0001t0001g0013 | 4 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-1788C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310668 | |||||||
chr12:120310669 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.498-1787G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310669 | |||||||
chr12:120310686 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1770T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310686 | |||||||
chr12:120310694 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1762C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310694 | |||||||
chr12:120310696 | ACTGCACT others(4): Show |
A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1759_498-1749d others(13): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310696 | |||||||
chr12:120310709 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1747T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310709 | |||||||
chr12:120310715 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1741C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310715 | |||||||
chr12:120310717 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1739A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310717 | |||||||
chr12:120310720 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1736A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310720 | |||||||
chr12:120310723 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1733C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310723 | |||||||
chr12:120310727 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1729G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310727 | |||||||
chr12:120310729 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1727C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310729 | |||||||
chr12:120310735 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1721C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310735 | |||||||
chr12:120310736 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1720C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310736 | |||||||
chr12:120310738 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1718G>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310738 | |||||||
chr12:120310742 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1714C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310742 | |||||||
chr12:120310744 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.498-1712T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310744 | |||||||
chr12:120310782 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(27): Show |
113 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.498-1674C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310782 | |||||||
chr12:120310829 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.498-1627G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310829 | |||||||
chr12:120310874 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.498-1582T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310874 | |||||||
chr12:120310875 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.498-1581A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310875 | |||||||
chr12:120310880 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-1576C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310880 | |||||||
chr12:120310884 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.498-1572C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310884 | |||||||
chr12:120310901 | A | T | 1 | a0001c0002t0001g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.498-1555A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310901 | |||||||
chr12:120310937 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(60): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.498-1519G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310937 | |||||||
chr12:120310948 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(60): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.498-1508G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310948 | |||||||
chr12:120310992 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.498-1464C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120310992 | |||||||
chr12:120311017 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.498-1439G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311017 | |||||||
chr12:120311041 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0028 |
6 | HG02004.hp2 HG02148.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-1415T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311041 | |||||||
chr12:120311048 | T | TA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(23): Show |
35 | HG00597.hp1 HG00735.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.498-1382dupA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311048 | ||||||
chr12:120311048 | T | TAA | 14 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(11): Show |
31 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.498-1383_498-1382d others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311048 | ||||||
chr12:120311048 | T | TAAA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0002t0001g0004 others(3): Show |
10 | HG00621.hp2 HG01109.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-1384_498-1382d others(5): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311048 | ||||||
chr12:120311048 | TA | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(31): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.498-1382delA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311048 | ||||||
chr12:120311048 | TAA | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(1): Show |
10 | HG00544.hp1 HG01074.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-1383_498-1382d others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311048 | ||||||
chr12:120311048 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-1391_498-1382d others(12): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311048 | ||||||
chr12:120311067 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1389A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311067 | |||||||
chr12:120311069 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1387A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311069 | |||||||
chr12:120311071 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1385A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311071 | |||||||
chr12:120311072 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1384A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311072 | |||||||
chr12:120311073 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1383A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311073 | |||||||
chr12:120311074 | A | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0081 |
2 | HG01358.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.498-1382A>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311074 | |||||||
chr12:120311075 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1381T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311075 | |||||||
chr12:120311087 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1369A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311087 | |||||||
chr12:120311096 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1360T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311096 | |||||||
chr12:120311125 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1331A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311125 | |||||||
chr12:120311150 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1306A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311150 | |||||||
chr12:120311181 | C | A | 1 | a0001c0001t0001g0002 | 3 | HG02486.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.498-1275C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311181 | |||||||
chr12:120311182 | C | A | 1 | a0001c0002t0001g0004 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.498-1274C>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311182 | |||||||
chr12:120311185 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-1271G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311185 | |||||||
chr12:120311223 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1233T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311223 | |||||||
chr12:120311225 | C | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1231C>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311225 | |||||||
chr12:120311226 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1230A>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311226 | |||||||
chr12:120311227 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1229T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311227 | |||||||
chr12:120311235 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1221A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311235 | |||||||
chr12:120311247 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.498-1209C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311247 | |||||||
chr12:120311269 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1187T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311269 | |||||||
chr12:120311272 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.498-1184T>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311272 | |||||||
chr12:120311454 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0035 others(17): Show |
47 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.498-1002A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311454 | |||||||
chr12:120311650 | G | A | 1 | a0001c0001t0001g0013 | 4 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-806G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311650 | |||||||
chr12:120311735 | CA | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0034 others(9): Show |
25 | HG00642.hp2 HG01106.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.498-692delA | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311735 | ||||||
chr12:120311735 | CAA | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(22): Show |
99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.498-693_498-692del others(2): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311735 | ||||||
chr12:120311735 | CAAA | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(14): Show |
37 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.498-694_498-692del others(3): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311735 | ||||||
chr12:120311735 | CAAAA | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
116 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.498-695_498-692del others(4): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311735 | ||||||
chr12:120311735 | CAAAAA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0022 others(12): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.498-696_498-692del others(5): Show |
SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120311735 | ||||||
chr12:120311780 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.498-676C>T | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311780 | |||||||
chr12:120311983 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG02523.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.498-473A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120311983 | |||||||
chr12:120312040 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.498-416T>C | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120312040 | |||||||
chr12:120312061 | T | A | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0043 others(8): Show |
32 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.498-395T>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120312061 | |||||||
chr12:120312147 | A | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0096 others(11): Show |
38 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.498-309A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120312147 | |||||||
chr12:120312249 | C | CT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0090 others(3): Show |
9 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-206dupT | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 120312249 | ||||||
chr12:120312307 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.498-149A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120312307 | |||||||
chr12:120312436 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(61): Show |
243 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.498-20A>G | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 2/3 | chr12 | 120312436 | |||||||
chr12:120312769 | G | A | 1 | a0001c0001t0001g0006 | 4 | HG00673.hp1 NA18939.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+19G>A | SIRT4 | ENSG00000089163.4 | transcript | ENST00000202967.4 | protein_coding | 3/3 | chr12 | 120312769 |