Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23408 |
| ensemblid | ENSG00000124523.17 |
| hgncid | 14933 |
| symbol | SIRT5 |
| name | sirtuin 5 |
| refseq_nuc | NM_012241.5 |
| refseq_prot | NP_036373.1 |
| ensembl_nuc | ENST00000606117.2 |
| ensembl_prot | ENSP00000476228.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 13574601 |
| end | 13615158 |
| strand | + |
| ver | v1.2 |
| region | chr6:13574601-13615158 |
| region5000 | chr6:13569601-13620158 |
| regionname0 | SIRT5_chr6_13574601_13615158 |
| regionname5000 | SIRT5_chr6_13569601_13620158 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 310 | 369 | 77 | 64 | 178 | 15 | 33 | 140 | SIRT5_chr6_13569601_13620158 | SIRT5 | MRPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| a0002 | 0/0 | 310 | 14 | 2 | 9 | 0 | 1 | 2 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | MRPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| a0003 | 0/0 | 310 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | MRPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| a0004 | 0/0 | 310 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | MRPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| a0005 | 0/0 | 310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | MQPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| a0006 | 0/0 | 310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | MRPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| a0007 | 0/0 | 310 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | MRPLQ others(305): Show |
chr6 | 13569601 | 13620158 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 930 | 299 | 74 | 47 | 140 | 12 | 25 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0001c0002 | 0/1 | 930 | 64 | 2 | 13 | 38 | 3 | 7 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0001c0005 | 0/0 | 930 | 6 | 1 | 4 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0002c0003 | 0/0 | 930 | 13 | 2 | 8 | 0 | 1 | 2 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0002c0009 | 0/0 | 930 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0003c0004 | 0/0 | 930 | 7 | 7 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0004c0007 | 0/0 | 930 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0005c0006 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCA others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0006c0010 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 | ||
| a0007c0008 | 0/0 | 930 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATGCG others(925): Show |
chr6 | 13569601 | 13620158 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4564 | 87 | 14 | 14 | 49 | 4 | 5 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0002 | 0/0 | 4564 | 13 | 9 | 1 | 2 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0003 | 0/0 | 4565 | 75 | 13 | 8 | 44 | 2 | 8 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0004 | 0/0 | 4564 | 32 | 9 | 10 | 7 | 3 | 3 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0005 | 0/0 | 4564 | 25 | 2 | 1 | 20 | 0 | 2 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0007 | 0/0 | 4564 | 5 | 0 | 0 | 5 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0008 | 0/0 | 4564 | 5 | 0 | 3 | 0 | 2 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0009 | 0/0 | 4564 | 3 | 1 | 1 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0010 | 0/0 | 4563 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4558): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0011 | 0/0 | 4565 | 3 | 0 | 0 | 3 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0012 | 0/0 | 4564 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0013 | 0/0 | 4564 | 3 | 0 | 3 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0014 | 0/0 | 4564 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0015 | 0/0 | 4565 | 3 | 0 | 1 | 0 | 0 | 2 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0016 | 0/0 | 4564 | 2 | 0 | 1 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0017 | 0/0 | 4564 | 2 | 1 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0018 | 0/0 | 4564 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0019 | 0/0 | 4565 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0020 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0021 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0022 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0023 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0024 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0025 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0026 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0027 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0028 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0029 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0031 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0032 | 0/0 | 4565 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0033 | 0/0 | 4565 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0034 | 0/0 | 4565 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0035 | 0/0 | 4565 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0036 | 0/0 | 4565 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0037 | 0/0 | 4565 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0038 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4558): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0041 | 0/0 | 4565 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0043 | 0/0 | 4565 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0044 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0045 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0046 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0047 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0048 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0049 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0050 | 0/0 | 4565 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0051 | 0/0 | 4565 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4560): Show |
chr6 | 13569601 | 13620158 |
| a0001c0001t0052 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0002t0002 | 0/1 | 4564 | 51 | 2 | 11 | 27 | 3 | 7 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0002t0004 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0002t0006 | 0/0 | 4564 | 11 | 0 | 0 | 11 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0002t0030 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0001c0005t0004 | 0/0 | 4564 | 6 | 1 | 4 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0002c0003t0002 | 0/0 | 4564 | 12 | 2 | 7 | 0 | 1 | 2 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0002c0003t0042 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0002c0009t0002 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0003c0004t0001 | 0/0 | 4564 | 7 | 7 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0004c0007t0039 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4558): Show |
chr6 | 13569601 | 13620158 |
| a0005c0006t0004 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0006c0010t0040 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| a0007c0008t0004 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | ATTCG others(4559): Show |
chr6 | 13569601 | 13620158 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 1 | 1 | 9 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0036 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0002 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0014 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0006 | 0/0 | 6 | 0 | 3 | 1 | 1 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0008g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0009g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0010g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0011g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0012g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0013g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0013g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0014g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0015g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0015g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0015g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0016g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0016g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0017g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0018g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0019g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0021g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0022g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0023g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0024g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0025g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0026g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0027g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0028g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0029g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0031g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0032g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0033g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0034g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0035g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0036g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0037g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0038g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0041g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0043g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0044g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0045g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0046g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0047g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0048g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0049g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0050g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0051g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0001t0052g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0020 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0002t0030g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0005t0004g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0005t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0005t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0001c0005t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0010 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0003t0042g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0002c0009t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0003c0004t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0003c0004t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0003c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0004c0007t0039g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0005c0006t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0006c0010t0040g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| a0007c0008t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0009 | g0159 | EUR | GBR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | GBR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0096 | EUR | FIN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0205 | EUR | FIN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00609 | hp2 | a0001 | c0001 | t0016 | g0141 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00735 | hp2 | a0004 | c0007 | t0039 | g0229 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0253 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0094 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01099 | hp1 | a0001 | c0001 | t0033 | g0014 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0255 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01109 | hp2 | a0001 | c0001 | t0016 | g0138 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01168 | hp1 | a0002 | c0003 | t0002 | g0252 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01175 | hp2 | a0002 | c0003 | t0002 | g0249 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01192 | hp1 | a0001 | c0001 | t0041 | g0087 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01192 | hp2 | a0001 | c0002 | t0030 | g0247 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01243 | hp1 | a0001 | c0001 | t0027 | g0109 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0093 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01261 | hp1 | a0001 | c0005 | t0004 | g0008 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0009 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0100 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0086 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01496 | hp1 | a0001 | c0001 | t0017 | g0107 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0079 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0023 | EUR | IBS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0046 | EUR | IBS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0225 | EUR | IBS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0167 | EUR | IBS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0023 | EUR | IBS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | IBS | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01891 | hp1 | a0001 | c0001 | t0014 | g0048 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0029 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01928 | hp2 | a0002 | c0003 | t0002 | g0010 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01934 | hp2 | a0002 | c0003 | t0002 | g0256 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01943 | hp1 | a0001 | c0001 | t0013 | g0025 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01952 | hp1 | a0002 | c0003 | t0042 | g0021 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01975 | hp2 | a0002 | c0003 | t0002 | g0010 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01978 | hp1 | a0001 | c0005 | t0004 | g0098 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0206 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02004 | hp2 | a0001 | c0005 | t0004 | g0097 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02027 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02055 | hp2 | a0001 | c0001 | t0038 | g0120 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02071 | hp1 | a0001 | c0001 | t0037 | g0002 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02074 | hp2 | a0001 | c0001 | t0043 | g0133 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | CDX | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | CDX | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02165 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | CDX | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02257 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02273 | hp2 | a0002 | c0009 | t0002 | g0021 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0011 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02280 | hp2 | a0003 | c0004 | t0001 | g0113 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02293 | hp1 | a0001 | c0001 | t0013 | g0025 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02293 | hp2 | a0001 | c0005 | t0004 | g0008 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02300 | hp1 | a0001 | c0001 | t0015 | g0069 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0181 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02602 | hp2 | a0001 | c0001 | t0015 | g0084 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02615 | hp2 | a0001 | c0001 | t0045 | g0053 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02622 | hp1 | a0001 | c0001 | t0050 | g0051 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02622 | hp2 | a0001 | c0001 | t0044 | g0050 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0131 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02738 | hp2 | a0002 | c0003 | t0002 | g0254 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0048 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02818 | hp2 | a0001 | c0001 | t0028 | g0101 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0269 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02896 | hp2 | a0001 | c0001 | t0029 | g0057 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03017 | hp1 | a0001 | c0001 | t0015 | g0070 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03098 | hp1 | a0001 | c0001 | t0048 | g0266 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03130 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03139 | hp1 | a0001 | c0001 | t0018 | g0011 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | ESN | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03239 | hp1 | a0001 | c0005 | t0004 | g0092 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03486 | hp2 | a0006 | c0010 | t0040 | g0028 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03579 | hp1 | a0001 | c0001 | t0049 | g0055 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03654 | hp1 | a0002 | c0003 | t0002 | g0021 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03669 | hp2 | a0001 | c0001 | t0024 | g0009 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03688 | hp1 | a0001 | c0001 | t0051 | g0006 | SAS | STU | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03688 | hp2 | a0001 | c0001 | t0036 | g0004 | SAS | STU | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03704 | hp1 | a0007 | c0008 | t0004 | g0080 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03831 | hp1 | a0001 | c0001 | t0047 | g0058 | SAS | BEB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0088 | SAS | BEB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0078 | SAS | BEB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0103 | SAS | STU | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0224 | SAS | STU | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0068 | SAS | STU | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | YRI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18906 | hp2 | a0001 | c0001 | t0052 | g0083 | AFR | YRI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18954 | hp2 | a0001 | c0001 | t0011 | g0016 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18971 | hp1 | a0001 | c0002 | t0006 | g0212 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18972 | hp2 | a0001 | c0002 | t0006 | g0220 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18975 | hp1 | a0001 | c0001 | t0021 | g0037 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18978 | hp1 | a0001 | c0001 | t0031 | g0171 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18986 | hp1 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18987 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18988 | hp2 | a0001 | c0002 | t0006 | g0127 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18999 | hp2 | a0001 | c0002 | t0006 | g0044 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19009 | hp1 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19011 | hp1 | a0001 | c0001 | t0023 | g0005 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19011 | hp2 | a0001 | c0002 | t0006 | g0264 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19043 | hp2 | a0001 | c0001 | t0025 | g0102 | AFR | LWK | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19056 | hp2 | a0001 | c0001 | t0011 | g0016 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19062 | hp2 | a0001 | c0001 | t0035 | g0032 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19067 | hp2 | a0001 | c0002 | t0006 | g0210 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19068 | hp1 | a0001 | c0001 | t0046 | g0062 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19070 | hp1 | a0001 | c0002 | t0006 | g0211 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19079 | hp2 | a0001 | c0002 | t0006 | g0214 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19083 | hp1 | a0001 | c0002 | t0006 | g0197 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19086 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19088 | hp2 | a0001 | c0001 | t0022 | g0037 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19089 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | YRI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0130 | AFR | ASW | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20129 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | ASW | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20752 | hp2 | a0002 | c0003 | t0002 | g0010 | EUR | TSI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20805 | hp1 | a0001 | c0001 | t0008 | g0026 | EUR | TSI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | GIH | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | GIH | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02109 | hp1 | a0001 | c0001 | t0034 | g0132 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02486 | hp1 | a0001 | c0001 | t0032 | g0017 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0029 | AFR | ACB | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG03471 | hp2 | a0005 | c0006 | t0004 | g0265 | AFR | MSL | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | USA | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0246 | AFR | USA | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0248 | AFR | USA | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0008 | AFR | USA | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0191 | REF | REF | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0036 | REF | REF | SIRT5_chr6_13569601_13620158 | SIRT5 | chr6 | 13569601 | 13620158 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13584115 | G | A | 1 | a0005 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.5G>A | p.Arg2Gln | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/10 | 343/4564 | 5/933 | 2/310 | chr6 | 13584115 | |||
| chr6:13595518 | G | A | 1 | a0004 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.517G>A | p.Ala173Thr | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/10 | 855/4564 | 517/933 | 173/310 | chr6 | 13595518 | |||
| chr6:13595552 | T | C | 1 | a0007 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.551T>C | p.Leu184Ser | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/10 | 889/4564 | 551/933 | 184/310 | chr6 | 13595552 | |||
| chr6:13600897 | G | A | 1 | a0006 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.805G>A | p.Val269Met | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/10 | 1143/4564 | 805/933 | 269/310 | chr6 | 13600897 | |||
| chr6:13600947 | C | A | 1 | a0003 | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.855C>A | p.Phe285Leu | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/10 | 1193/4564 | 855/933 | 285/310 | chr6 | 13600947 | |||
| chr6:13611846 | A | G | 1 | a0002 | 14 | HG01069.hp2 HG01099.hp2 HG01168.hp1 others(11): Show |
missense_variant | MODERATE | c.914A>G | p.Glu305Gly | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1252/4564 | 914/933 | 305/310 | chr6 | 13611846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13584138 | C | A | 1 | a0004c0007 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.28C>A | p.Arg10Arg | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/10 | 366/4564 | 28/933 | 10/310 | chr6 | 13584138 | |||
| chr6:13599053 | G | A | 1 | a0002c0009 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.639G>A | p.Gly213Gly | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/10 | 977/4564 | 639/933 | 213/310 | chr6 | 13599053 | |||
| chr6:13599071 | C | T | 1 | a0001c0002 | 63 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
synonymous_variant | LOW | c.657C>T | p.His219His | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/10 | 995/4564 | 657/933 | 219/310 | chr6 | 13599071 | |||
| chr6:13599074 | C | T | 2 | a0001c0005 a0007c0008 |
7 | HG01261.hp1 HG01978.hp1 HG02004.hp2 others(4): Show |
synonymous_variant | LOW | c.660C>T | p.Val220Val | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/10 | 998/4564 | 660/933 | 220/310 | chr6 | 13599074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13574636 | C | T | 1 | a0001c0001t0052 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-303C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/10 | 9475 | chr6 | 13574636 | ||||||
| chr6:13574703 | C | T | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0012 others(19): Show |
91 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-236C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/10 | 9408 | chr6 | 13574703 | ||||||
| chr6:13579524 | T | C | 1 | a0001c0001t0012 | 3 | HG02109.hp2 HG03041.hp1 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-121T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/10 | 4587 | chr6 | 13579524 | ||||||
| chr6:13579596 | A | C | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(19): Show |
95 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-49A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/10 | 4515 | chr6 | 13579596 | ||||||
| chr6:13584083 | C | T | 1 | a0001c0001t0011 | 3 | NA18954.hp2 NA19056.hp2 NA19086.hp2 |
5_prime_UTR_variant | MODIFIER | c.-28C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/10 | 28 | chr6 | 13584083 | ||||||
| chr6:13611883 | G | T | 2 | a0001c0001t0017 a0006c0010t0040 |
3 | HG01496.hp1 HG02055.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 18 | chr6 | 13611883 | ||||||
| chr6:13611984 | C | T | 1 | a0001c0002t0006 | 11 | NA18971.hp1 NA18972.hp2 NA18986.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*119C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 119 | chr6 | 13611984 | ||||||
| chr6:13612031 | CA | C | 3 | a0001c0001t0010 a0001c0001t0038 a0004c0007t0039 |
5 | HG00735.hp2 HG02055.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*169delA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 169 | INFO_REALIGN_3_PRIME | chr6 | 13612031 | |||||
| chr6:13612200 | T | C | 1 | a0001c0001t0019 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 335 | chr6 | 13612200 | ||||||
| chr6:13612258 | T | A | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 393 | chr6 | 13612258 | ||||||
| chr6:13612260 | T | C | 1 | a0001c0001t0009 | 3 | HG00099.hp1 HG01261.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 395 | chr6 | 13612260 | ||||||
| chr6:13612261 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 396 | chr6 | 13612261 | ||||||
| chr6:13612262 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 397 | chr6 | 13612262 | ||||||
| chr6:13612264 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 399 | chr6 | 13612264 | ||||||
| chr6:13612265 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 400 | chr6 | 13612265 | ||||||
| chr6:13612266 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 401 | chr6 | 13612266 | ||||||
| chr6:13612267 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 402 | chr6 | 13612267 | ||||||
| chr6:13612268 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*403A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 403 | chr6 | 13612268 | ||||||
| chr6:13612269 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 404 | chr6 | 13612269 | ||||||
| chr6:13612271 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 406 | chr6 | 13612271 | ||||||
| chr6:13612273 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*408A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 408 | chr6 | 13612273 | ||||||
| chr6:13612274 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 409 | chr6 | 13612274 | ||||||
| chr6:13612276 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 411 | chr6 | 13612276 | ||||||
| chr6:13612278 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 413 | chr6 | 13612278 | ||||||
| chr6:13612279 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 414 | chr6 | 13612279 | ||||||
| chr6:13612280 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 415 | chr6 | 13612280 | ||||||
| chr6:13612282 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*417C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 417 | chr6 | 13612282 | ||||||
| chr6:13612285 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 420 | chr6 | 13612285 | ||||||
| chr6:13612286 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*421A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 421 | chr6 | 13612286 | ||||||
| chr6:13612287 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 422 | chr6 | 13612287 | ||||||
| chr6:13612289 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*424A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 424 | chr6 | 13612289 | ||||||
| chr6:13612290 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 425 | chr6 | 13612290 | ||||||
| chr6:13612291 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 426 | chr6 | 13612291 | ||||||
| chr6:13612294 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*429A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 429 | chr6 | 13612294 | ||||||
| chr6:13612297 | T | A | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 432 | chr6 | 13612297 | ||||||
| chr6:13612301 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 436 | chr6 | 13612301 | ||||||
| chr6:13612303 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 438 | chr6 | 13612303 | ||||||
| chr6:13612314 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 449 | chr6 | 13612314 | ||||||
| chr6:13612315 | C | A | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 450 | chr6 | 13612315 | ||||||
| chr6:13612316 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 451 | chr6 | 13612316 | ||||||
| chr6:13612318 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*453C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 453 | chr6 | 13612318 | ||||||
| chr6:13612319 | A | G | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 454 | chr6 | 13612319 | ||||||
| chr6:13612324 | A | C | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 459 | chr6 | 13612324 | ||||||
| chr6:13612328 | C | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*463C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 463 | chr6 | 13612328 | ||||||
| chr6:13612329 | T | G | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*464T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 464 | chr6 | 13612329 | ||||||
| chr6:13612330 | T | G | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 465 | chr6 | 13612330 | ||||||
| chr6:13612332 | A | T | 1 | a0001c0001t0020 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*467A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 467 | chr6 | 13612332 | ||||||
| chr6:13612340 | C | CT | 14 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0015 others(11): Show |
92 | HG00544.hp2 HG00558.hp2 HG00741.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*492dupT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 493 | INFO_REALIGN_3_PRIME | chr6 | 13612340 | |||||
| chr6:13612489 | T | C | 2 | a0001c0001t0038 a0001c0001t0044 |
2 | HG02055.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*624T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 624 | chr6 | 13612489 | ||||||
| chr6:13612490 | A | G | 33 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(30): Show |
163 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*625A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 625 | chr6 | 13612490 | ||||||
| chr6:13612533 | T | C | 1 | a0001c0001t0032 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 668 | chr6 | 13612533 | ||||||
| chr6:13612571 | C | T | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(15): Show |
141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 706 | chr6 | 13612571 | ||||||
| chr6:13612629 | C | T | 1 | a0001c0001t0024 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 764 | chr6 | 13612629 | ||||||
| chr6:13612635 | C | T | 1 | a0001c0001t0035 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*770C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 770 | chr6 | 13612635 | ||||||
| chr6:13612721 | G | A | 1 | a0001c0001t0033 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 856 | chr6 | 13612721 | ||||||
| chr6:13612779 | T | C | 1 | a0004c0007t0039 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 914 | chr6 | 13612779 | ||||||
| chr6:13612898 | G | A | 1 | a0001c0002t0030 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1033G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1033 | chr6 | 13612898 | ||||||
| chr6:13612936 | G | C | 1 | a0001c0001t0045 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1071 | chr6 | 13612936 | ||||||
| chr6:13613064 | G | A | 3 | a0001c0001t0025 a0001c0001t0038 a0001c0001t0048 |
3 | HG02055.hp2 HG03098.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1199G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1199 | chr6 | 13613064 | ||||||
| chr6:13613079 | C | T | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(16): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1214C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1214 | chr6 | 13613079 | ||||||
| chr6:13613080 | C | T | 3 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0029 |
7 | HG01891.hp1 HG02647.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1215C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1215 | chr6 | 13613080 | ||||||
| chr6:13613124 | C | A | 1 | a0001c0001t0018 | 2 | HG02280.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1259C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1259 | chr6 | 13613124 | ||||||
| chr6:13613203 | C | T | 2 | a0001c0001t0028 a0001c0001t0044 |
2 | HG02622.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1338C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1338 | chr6 | 13613203 | ||||||
| chr6:13613347 | A | T | 1 | a0001c0001t0046 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1482A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1482 | chr6 | 13613347 | ||||||
| chr6:13613551 | A | G | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(20): Show |
150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1686A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1686 | chr6 | 13613551 | ||||||
| chr6:13613564 | A | G | 6 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(3): Show |
35 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1699A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 1699 | chr6 | 13613564 | ||||||
| chr6:13614283 | C | A | 1 | a0001c0001t0010 | 3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2418C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 2418 | chr6 | 13614283 | ||||||
| chr6:13614477 | T | G | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | NA18975.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2612T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 2612 | chr6 | 13614477 | ||||||
| chr6:13614545 | T | C | 1 | a0001c0001t0023 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2680T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 2680 | chr6 | 13614545 | ||||||
| chr6:13614684 | C | G | 1 | a0001c0001t0017 | 2 | HG01496.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2819C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 2819 | chr6 | 13614684 | ||||||
| chr6:13615126 | C | T | 4 | a0001c0001t0025 a0001c0001t0028 a0001c0001t0038 others(1): Show |
4 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3261C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 3261 | chr6 | 13615126 | ||||||
| chr6:13615141 | C | T | 1 | a0001c0001t0022 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3276C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 3276 | chr6 | 13615141 | ||||||
| chr6:13615154 | G | T | 1 | a0001c0001t0017 | 2 | HG01496.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3289G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 10/10 | 3289 | chr6 | 13615154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:13574784 | C | T | 2 | a0001c0001t0014g0048 a0001c0001t0014g0269 |
3 | HG01891.hp1 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-195+40C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13574784 | |||||||
| chr6:13574861 | A | T | 2 | a0001c0001t0014g0048 a0001c0001t0014g0269 |
3 | HG01891.hp1 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-195+117A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13574861 | |||||||
| chr6:13574908 | C | T | 2 | a0001c0002t0002g0267 a0001c0002t0002g0268 |
2 | HG02071.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.-195+164C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13574908 | |||||||
| chr6:13574910 | T | C | 8 | a0001c0001t0004g0049 a0001c0001t0005g0052 a0001c0001t0005g0054 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-195+166T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13574910 | |||||||
| chr6:13574995 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-195+251T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13574995 | |||||||
| chr6:13575118 | G | C | 1 | a0001c0001t0029g0057 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-195+374G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575118 | |||||||
| chr6:13575450 | G | A | 56 | a0001c0001t0003g0099 a0001c0001t0004g0006 a0001c0001t0004g0008 others(53): Show |
81 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.-195+706G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575450 | |||||||
| chr6:13575527 | T | G | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-195+783T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575527 | |||||||
| chr6:13575581 | G | A | 2 | a0001c0002t0002g0103 a0001c0002t0002g0104 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-195+837G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575581 | |||||||
| chr6:13575650 | C | T | 1 | a0001c0001t0008g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-195+906C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575650 | |||||||
| chr6:13575661 | C | T | 68 | a0001c0001t0003g0099 a0001c0001t0004g0006 a0001c0001t0004g0008 others(65): Show |
96 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-195+917C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575661 | |||||||
| chr6:13575742 | C | G | 1 | a0001c0001t0029g0057 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-195+998C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575742 | |||||||
| chr6:13575768 | C | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-195+1024C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575768 | |||||||
| chr6:13575857 | A | G | 1 | a0001c0001t0007g0263 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-195+1113A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575857 | |||||||
| chr6:13575901 | G | A | 77 | a0001c0001t0001g0105 a0001c0001t0002g0108 a0001c0001t0003g0099 others(74): Show |
105 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.-195+1157G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575901 | |||||||
| chr6:13575947 | T | C | 67 | a0001c0001t0003g0099 a0001c0001t0004g0006 a0001c0001t0004g0008 others(64): Show |
95 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.-195+1203T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13575947 | |||||||
| chr6:13576095 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-195+1351G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576095 | |||||||
| chr6:13576405 | A | G | 18 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0001t0002g0257 others(15): Show |
22 | HG01069.hp2 HG01099.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-195+1661A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576405 | |||||||
| chr6:13576476 | T | G | 59 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(56): Show |
85 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.-195+1732T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576476 | |||||||
| chr6:13576571 | A | G | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-195+1827A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576571 | |||||||
| chr6:13576671 | C | G | 7 | a0001c0001t0001g0105 a0001c0001t0002g0108 a0001c0001t0003g0106 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-195+1927C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576671 | |||||||
| chr6:13576955 | A | G | 1 | a0001c0001t0010g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-195+2211A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576955 | |||||||
| chr6:13576998 | C | G | 1 | a0001c0002t0030g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-195+2254C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13576998 | |||||||
| chr6:13577012 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0003g0111 |
2 | HG02015.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-195+2268G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577012 | |||||||
| chr6:13577014 | C | T | 6 | a0001c0001t0003g0014 a0001c0001t0003g0047 a0001c0001t0003g0244 others(3): Show |
9 | HG01099.hp1 HG01106.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-195+2270C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577014 | |||||||
| chr6:13577141 | T | G | 5 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-194-2310T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577141 | |||||||
| chr6:13577518 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-194-1933T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577518 | |||||||
| chr6:13577722 | T | G | 7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-194-1729T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577722 | |||||||
| chr6:13577849 | C | G | 1 | a0001c0001t0001g0243 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-194-1602C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577849 | |||||||
| chr6:13577928 | G | A | 1 | a0003c0004t0001g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-194-1523G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13577928 | |||||||
| chr6:13578402 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-194-1049C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578402 | |||||||
| chr6:13578477 | G | A | 2 | a0001c0001t0003g0118 a0001c0001t0003g0119 |
2 | NA18939.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-194-974G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578477 | |||||||
| chr6:13578480 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-194-971C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578480 | |||||||
| chr6:13578573 | C | T | 2 | a0001c0001t0004g0027 a0001c0005t0004g0098 |
3 | HG01069.hp1 HG01071.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-194-878C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578573 | |||||||
| chr6:13578574 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-194-877G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578574 | |||||||
| chr6:13578580 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-194-871G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578580 | |||||||
| chr6:13578616 | C | CA | 14 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0124 others(11): Show |
16 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-194-814dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 13578616 | ||||||
| chr6:13578616 | CA | C | 29 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0117 others(26): Show |
29 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-194-814delA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 13578616 | ||||||
| chr6:13578638 | G | C | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-194-813G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578638 | |||||||
| chr6:13578641 | A | G | 67 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(64): Show |
95 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.-194-810A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578641 | |||||||
| chr6:13578658 | CTGCTTTA others(6): Show |
C | 67 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(64): Show |
95 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.-194-790_-194-778d others(15): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 13578658 | ||||||
| chr6:13578805 | C | T | 1 | a0001c0001t0003g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-194-646C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578805 | |||||||
| chr6:13578852 | G | T | 77 | a0001c0001t0001g0112 a0001c0001t0001g0208 a0001c0001t0001g0221 others(74): Show |
94 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-194-599G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578852 | |||||||
| chr6:13578863 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(3): Show |
6 | HG01496.hp1 HG02055.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-194-588G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578863 | |||||||
| chr6:13578872 | C | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-194-579C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578872 | |||||||
| chr6:13578887 | T | C | 1 | a0001c0001t0005g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-194-564T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578887 | |||||||
| chr6:13578906 | G | A | 67 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(64): Show |
95 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.-194-545G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13578906 | |||||||
| chr6:13579430 | T | G | 1 | a0001c0001t0011g0002 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-194-21T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 1/9 | chr6 | 13579430 | |||||||
| chr6:13579676 | T | G | 157 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0129 others(154): Show |
202 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-36+67T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13579676 | |||||||
| chr6:13579713 | T | C | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-36+104T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13579713 | |||||||
| chr6:13579805 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-36+196G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13579805 | |||||||
| chr6:13579982 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-36+373C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13579982 | |||||||
| chr6:13580233 | A | G | 2 | a0001c0001t0014g0048 a0001c0001t0014g0269 |
3 | HG01891.hp1 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-36+624A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580233 | |||||||
| chr6:13580296 | C | A | 3 | a0003c0004t0001g0012 a0003c0004t0001g0029 a0003c0004t0001g0113 |
7 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+687C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580296 | |||||||
| chr6:13580353 | G | C | 157 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0129 others(154): Show |
202 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-36+744G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580353 | |||||||
| chr6:13580554 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0010g0130 a0001c0001t0010g0131 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+945T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580554 | |||||||
| chr6:13580609 | C | T | 1 | a0001c0001t0049g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-36+1000C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580609 | |||||||
| chr6:13580653 | C | T | 67 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(64): Show |
95 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.-36+1044C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580653 | |||||||
| chr6:13580693 | A | T | 1 | a0001c0001t0048g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-36+1084A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580693 | |||||||
| chr6:13580898 | T | C | 1 | a0001c0002t0002g0192 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-36+1289T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580898 | |||||||
| chr6:13580944 | T | C | 221 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0110 others(218): Show |
288 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.-36+1335T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580944 | |||||||
| chr6:13580981 | G | A | 1 | a0001c0001t0007g0263 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-36+1372G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13580981 | |||||||
| chr6:13581043 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+1434C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581043 | |||||||
| chr6:13581128 | A | G | 1 | a0001c0001t0002g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36+1519A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581128 | |||||||
| chr6:13581134 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG00673.hp2 HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-36+1525A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581134 | |||||||
| chr6:13581455 | G | A | 11 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(8): Show |
21 | HG00597.hp1 NA18941.hp1 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.-36+1846G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581455 | |||||||
| chr6:13581612 | T | C | 59 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(56): Show |
85 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.-36+2003T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581612 | |||||||
| chr6:13581647 | A | G | 1 | a0001c0001t0005g0094 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-36+2038A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581647 | |||||||
| chr6:13581674 | G | C | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-36+2065G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581674 | |||||||
| chr6:13581720 | C | A | 7 | a0001c0001t0001g0105 a0001c0001t0002g0108 a0001c0001t0003g0106 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36+2111C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13581720 | |||||||
| chr6:13582031 | C | T | 1 | a0001c0001t0049g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-35-2045C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582031 | |||||||
| chr6:13582160 | A | G | 1 | a0001c0001t0005g0067 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-35-1916A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582160 | |||||||
| chr6:13582208 | T | C | 1 | a0001c0001t0009g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-35-1868T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582208 | |||||||
| chr6:13582237 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0003g0111 |
2 | HG02015.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-35-1839A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582237 | |||||||
| chr6:13582392 | T | C | 1 | a0001c0001t0044g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-35-1684T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582392 | |||||||
| chr6:13582611 | C | CA | 34 | a0001c0001t0001g0160 a0001c0001t0002g0193 a0001c0001t0002g0250 others(31): Show |
40 | HG00733.hp1 HG01069.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.-35-1445dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13582611 | ||||||
| chr6:13582611 | C | CAA | 55 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0011 others(52): Show |
80 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-35-1446_-35-1445d others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13582611 | ||||||
| chr6:13582734 | T | C | 7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
11 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35-1342T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582734 | |||||||
| chr6:13582795 | A | C | 1 | a0001c0001t0003g0244 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-35-1281A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582795 | |||||||
| chr6:13582817 | C | T | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-1259C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13582817 | |||||||
| chr6:13583062 | C | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0225 |
3 | HG01175.hp1 HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-35-1014C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583062 | |||||||
| chr6:13583267 | C | CT | 63 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0024 others(60): Show |
88 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.-35-807dupT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13583267 | ||||||
| chr6:13583267 | C | CTT | 3 | a0001c0001t0004g0011 a0001c0001t0004g0091 a0001c0001t0018g0011 |
5 | HG01884.hp2 HG02280.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-808_-35-807dup others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13583267 | ||||||
| chr6:13583269 | TC | T | 5 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-806delC | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583269 | |||||||
| chr6:13583270 | C | T | 155 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0208 others(152): Show |
200 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.-35-806C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583270 | |||||||
| chr6:13583289 | C | CT | 17 | a0001c0001t0001g0129 a0001c0001t0001g0156 a0001c0001t0001g0184 others(14): Show |
17 | HG01884.hp1 HG02145.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.-35-765dupT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13583289 | ||||||
| chr6:13583289 | CT | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0135 a0001c0001t0001g0161 others(14): Show |
17 | HG01256.hp1 HG01943.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-35-765delT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13583289 | ||||||
| chr6:13583364 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0003g0137 others(2): Show |
5 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-712G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583364 | |||||||
| chr6:13583390 | G | A | 1 | a0005c0006t0004g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35-686G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583390 | |||||||
| chr6:13583598 | A | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-35-478A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583598 | |||||||
| chr6:13583743 | C | G | 69 | a0001c0001t0002g0108 a0001c0001t0004g0006 a0001c0001t0004g0008 others(66): Show |
97 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-35-333C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583743 | |||||||
| chr6:13583765 | G | A | 2 | a0001c0002t0002g0040 a0001c0002t0002g0195 |
3 | HG03017.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-35-311G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583765 | |||||||
| chr6:13583839 | G | GGCACCTC others(1): Show |
8 | a0001c0001t0004g0049 a0001c0001t0005g0052 a0001c0001t0005g0054 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35-228_-35-221dup others(8): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr6 | 13583839 | ||||||
| chr6:13583962 | A | C | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-114A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583962 | |||||||
| chr6:13583969 | T | C | 76 | a0001c0001t0001g0105 a0001c0001t0002g0108 a0001c0001t0003g0106 others(73): Show |
104 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.-35-107T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583969 | |||||||
| chr6:13583975 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-101G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13583975 | |||||||
| chr6:13584009 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-35-67A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13584009 | |||||||
| chr6:13584041 | T | C | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-35-35T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 2/9 | chr6 | 13584041 | |||||||
| chr6:13584351 | A | G | 157 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0129 others(154): Show |
202 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.115+126A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13584351 | |||||||
| chr6:13584358 | C | CT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0155 a0001c0001t0001g0183 others(2): Show |
7 | NA18942.hp2 NA18945.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+144dupT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 13584358 | ||||||
| chr6:13584374 | C | T | 1 | a0001c0001t0005g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.115+149C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13584374 | |||||||
| chr6:13584643 | C | T | 1 | a0001c0001t0004g0089 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.115+418C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13584643 | |||||||
| chr6:13584770 | CAT | C | 79 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0208 others(76): Show |
96 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.115+546_115+547del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13584770 | |||||||
| chr6:13584895 | C | T | 1 | a0001c0002t0002g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.115+670C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13584895 | |||||||
| chr6:13584910 | G | A | 71 | a0001c0001t0002g0108 a0001c0001t0004g0006 a0001c0001t0004g0008 others(68): Show |
99 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.115+685G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13584910 | |||||||
| chr6:13585033 | G | A | 1 | a0001c0002t0002g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.115+808G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585033 | |||||||
| chr6:13585050 | T | C | 76 | a0001c0001t0001g0105 a0001c0001t0002g0108 a0001c0001t0003g0106 others(73): Show |
104 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.115+825T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585050 | |||||||
| chr6:13585404 | C | A | 7 | a0001c0001t0004g0049 a0001c0001t0005g0052 a0001c0001t0005g0054 others(4): Show |
9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+1179C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585404 | |||||||
| chr6:13585406 | C | T | 1 | a0001c0001t0004g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.115+1181C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585406 | |||||||
| chr6:13585570 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.115+1345A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585570 | |||||||
| chr6:13585642 | C | T | 221 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0110 others(218): Show |
288 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.115+1417C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585642 | |||||||
| chr6:13585758 | G | A | 1 | a0001c0001t0005g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.115+1533G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585758 | |||||||
| chr6:13585960 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115+1735C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585960 | |||||||
| chr6:13585961 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115+1736T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585961 | |||||||
| chr6:13585977 | A | G | 1 | a0001c0001t0049g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.115+1752A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585977 | |||||||
| chr6:13585998 | G | T | 68 | a0001c0001t0002g0108 a0001c0001t0004g0006 a0001c0001t0004g0008 others(65): Show |
96 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.115+1773G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13585998 | |||||||
| chr6:13586262 | T | C | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 |
3 | HG00423.hp1 HG02155.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.115+2037T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13586262 | |||||||
| chr6:13586751 | C | G | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.116-1580C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13586751 | |||||||
| chr6:13586760 | G | T | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.116-1571G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13586760 | |||||||
| chr6:13586813 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.116-1518G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13586813 | |||||||
| chr6:13586933 | A | G | 1 | a0001c0001t0026g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.116-1398A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13586933 | |||||||
| chr6:13587001 | C | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.116-1330C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587001 | |||||||
| chr6:13587083 | A | T | 7 | a0001c0001t0004g0049 a0001c0001t0005g0052 a0001c0001t0005g0054 others(4): Show |
9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-1248A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587083 | |||||||
| chr6:13587088 | GCTCCACA others(74): Show |
G | 7 | a0001c0001t0004g0049 a0001c0001t0005g0052 a0001c0001t0005g0054 others(4): Show |
9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-1241_116-1161d others(83): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 13587088 | ||||||
| chr6:13587123 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.116-1208C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587123 | |||||||
| chr6:13587502 | G | GA | 75 | a0001c0001t0001g0112 a0001c0001t0001g0208 a0001c0001t0001g0221 others(72): Show |
92 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.116-823dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 13587502 | ||||||
| chr6:13587526 | C | G | 1 | a0001c0001t0005g0094 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.116-805C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587526 | |||||||
| chr6:13587526 | C | T | 1 | a0001c0001t0005g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.116-805C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587526 | |||||||
| chr6:13587539 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.116-792G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587539 | |||||||
| chr6:13587603 | A | C | 1 | a0001c0001t0001g0180 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.116-728A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587603 | |||||||
| chr6:13587748 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
363 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(360): Show |
intron_variant | MODIFIER | c.116-583C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587748 | |||||||
| chr6:13587774 | T | C | 5 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-557T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587774 | |||||||
| chr6:13587812 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.116-519G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13587812 | |||||||
| chr6:13588063 | C | T | 3 | a0001c0001t0001g0179 a0001c0002t0002g0103 a0001c0002t0002g0104 |
3 | HG02056.hp2 HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.116-268C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 3/9 | chr6 | 13588063 | |||||||
| chr6:13588487 | TA | T | 4 | a0001c0001t0008g0026 a0001c0001t0008g0086 a0001c0001t0008g0100 others(1): Show |
5 | HG01192.hp1 HG01361.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+27delA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 13588487 | ||||||
| chr6:13588761 | C | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0198 a0001c0002t0002g0223 |
4 | NA18942.hp1 NA18949.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+297C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13588761 | |||||||
| chr6:13588880 | C | A | 1 | a0001c0001t0003g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+416C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13588880 | |||||||
| chr6:13588909 | C | T | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 |
3 | HG00423.hp1 HG02155.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.249+445C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13588909 | |||||||
| chr6:13588966 | A | G | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.249+502A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13588966 | |||||||
| chr6:13588984 | T | G | 1 | a0001c0001t0015g0070 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.249+520T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13588984 | |||||||
| chr6:13589336 | G | T | 1 | a0001c0001t0004g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.249+872G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589336 | |||||||
| chr6:13589420 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0003g0106 a0001c0001t0017g0028 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+956G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589420 | |||||||
| chr6:13589445 | C | T | 8 | a0001c0001t0001g0116 a0001c0001t0001g0129 a0001c0001t0002g0108 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+981C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589445 | |||||||
| chr6:13589503 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.249+1039C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589503 | |||||||
| chr6:13589621 | C | T | 1 | a0001c0001t0003g0134 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.249+1157C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589621 | |||||||
| chr6:13589641 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(79): Show |
115 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.249+1177G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589641 | |||||||
| chr6:13589663 | G | A | 2 | a0001c0001t0017g0028 a0006c0010t0040g0028 |
2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.249+1199G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589663 | |||||||
| chr6:13589685 | G | A | 1 | a0001c0001t0004g0071 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.249+1221G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589685 | |||||||
| chr6:13589781 | C | T | 4 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1317C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589781 | |||||||
| chr6:13589827 | G | A | 1 | a0001c0001t0004g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.249+1363G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589827 | |||||||
| chr6:13589830 | C | T | 1 | a0001c0001t0007g0039 | 2 | NA18983.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.249+1366C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589830 | |||||||
| chr6:13589953 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0038 others(162): Show |
216 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.249+1489A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13589953 | |||||||
| chr6:13590000 | A | G | 3 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 |
3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.249+1536A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13590000 | |||||||
| chr6:13590051 | G | A | 2 | a0001c0001t0004g0088 a0001c0001t0005g0094 |
2 | HG01071.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.249+1587G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13590051 | |||||||
| chr6:13590265 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.250-1404C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13590265 | |||||||
| chr6:13590269 | A | C | 1 | a0001c0002t0002g0206 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.250-1400A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13590269 | |||||||
| chr6:13590559 | G | GTA | 117 | a0001c0001t0001g0155 a0001c0001t0001g0175 a0001c0001t0001g0208 others(114): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.250-1108_250-1107d others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 13590559 | ||||||
| chr6:13590799 | TTG | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0225 |
3 | HG01175.hp1 HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.250-858_250-857del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 13590799 | ||||||
| chr6:13590892 | CAT | C | 52 | a0001c0001t0001g0208 a0001c0001t0002g0193 a0001c0001t0002g0204 others(49): Show |
65 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.250-774_250-773del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 13590892 | ||||||
| chr6:13590948 | GTGT | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0135 others(45): Show |
68 | HG00544.hp2 HG00558.hp2 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.250-719_250-717del others(3): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 13590948 | ||||||
| chr6:13590959 | G | T | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.250-710G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13590959 | |||||||
| chr6:13591009 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.250-660G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591009 | |||||||
| chr6:13591013 | G | A | 1 | a0001c0001t0028g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.250-656G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591013 | |||||||
| chr6:13591022 | T | C | 3 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 |
3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.250-647T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591022 | |||||||
| chr6:13591148 | G | A | 1 | a0001c0001t0005g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250-521G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591148 | |||||||
| chr6:13591323 | A | G | 1 | a0002c0003t0002g0256 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.250-346A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591323 | |||||||
| chr6:13591454 | C | G | 1 | a0001c0001t0049g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250-215C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591454 | |||||||
| chr6:13591568 | C | G | 1 | a0001c0001t0002g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250-101C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591568 | |||||||
| chr6:13591646 | C | G | 1 | a0001c0001t0052g0083 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.250-23C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 4/9 | chr6 | 13591646 | |||||||
| chr6:13591903 | C | T | 67 | a0001c0001t0002g0193 a0001c0001t0002g0204 a0001c0001t0002g0218 others(64): Show |
85 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.475+9C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13591903 | |||||||
| chr6:13592429 | G | A | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475+535G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13592429 | |||||||
| chr6:13592663 | G | A | 18 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(15): Show |
29 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.475+769G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13592663 | |||||||
| chr6:13592875 | A | AT | 107 | a0001c0001t0001g0155 a0001c0001t0001g0208 a0001c0001t0002g0146 others(104): Show |
134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.475+987dupT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 13592875 | ||||||
| chr6:13592915 | A | AT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0112 others(97): Show |
140 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.475+1037dupT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 13592915 | ||||||
| chr6:13592915 | A | ATT | 10 | a0001c0001t0002g0193 a0001c0001t0003g0099 a0001c0001t0003g0154 others(7): Show |
10 | HG00733.hp1 HG01516.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+1036_475+1037d others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 13592915 | ||||||
| chr6:13592915 | A | ATTT | 94 | a0001c0001t0001g0155 a0001c0001t0001g0208 a0001c0001t0002g0146 others(91): Show |
121 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.475+1035_475+1037d others(5): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 13592915 | ||||||
| chr6:13592915 | A | ATTTT | 8 | a0001c0001t0002g0258 a0001c0001t0002g0262 a0001c0002t0002g0044 others(5): Show |
8 | HG02004.hp2 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.475+1034_475+1037d others(6): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 13592915 | ||||||
| chr6:13592915 | A | T | 1 | a0001c0001t0013g0079 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.475+1021A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13592915 | |||||||
| chr6:13593008 | G | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0195 |
3 | HG03017.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.475+1114G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593008 | |||||||
| chr6:13593213 | A | G | 3 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 |
3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.475+1319A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593213 | |||||||
| chr6:13593219 | A | C | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475+1325A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593219 | |||||||
| chr6:13593308 | G | C | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.475+1414G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593308 | |||||||
| chr6:13593556 | A | G | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475+1662A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593556 | |||||||
| chr6:13593588 | A | G | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.475+1694A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593588 | |||||||
| chr6:13593614 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.475+1720G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593614 | |||||||
| chr6:13593641 | G | A | 1 | a0001c0001t0005g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.475+1747G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13593641 | |||||||
| chr6:13594017 | C | T | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.476-1460C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594017 | |||||||
| chr6:13594021 | C | T | 1 | a0001c0002t0004g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.476-1456C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594021 | |||||||
| chr6:13594095 | C | T | 1 | a0001c0002t0002g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.476-1382C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594095 | |||||||
| chr6:13594122 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.476-1355G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594122 | |||||||
| chr6:13594434 | G | T | 34 | a0001c0001t0002g0146 a0001c0001t0004g0006 a0001c0001t0004g0008 others(31): Show |
48 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.476-1043G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594434 | |||||||
| chr6:13594598 | G | A | 5 | a0001c0002t0006g0127 a0001c0002t0006g0210 a0001c0002t0006g0211 others(2): Show |
5 | NA18971.hp1 NA18972.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-879G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594598 | |||||||
| chr6:13594630 | G | A | 14 | a0001c0001t0002g0108 a0001c0001t0002g0193 a0001c0001t0002g0250 others(11): Show |
18 | HG00733.hp1 HG01069.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.476-847G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594630 | |||||||
| chr6:13594897 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.476-580G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13594897 | |||||||
| chr6:13595240 | G | A | 26 | a0001c0001t0002g0146 a0001c0001t0004g0006 a0001c0001t0004g0008 others(23): Show |
37 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.476-237G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13595240 | |||||||
| chr6:13595334 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.476-143G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13595334 | |||||||
| chr6:13595373 | T | C | 1 | a0001c0001t0049g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.476-104T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 5/9 | chr6 | 13595373 | |||||||
| chr6:13595692 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0177 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.563+128G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13595692 | |||||||
| chr6:13595743 | TG | T | 8 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(5): Show |
8 | HG00735.hp2 HG01496.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.563+183delG | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 13595743 | ||||||
| chr6:13595816 | A | G | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.563+252A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13595816 | |||||||
| chr6:13595846 | G | A | 18 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(15): Show |
29 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.563+282G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13595846 | |||||||
| chr6:13596127 | T | C | 1 | a0001c0001t0008g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.563+563T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13596127 | |||||||
| chr6:13596452 | C | G | 1 | a0001c0001t0002g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.564-511C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13596452 | |||||||
| chr6:13596650 | C | A | 1 | a0001c0001t0003g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.564-313C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13596650 | |||||||
| chr6:13596749 | A | G | 54 | a0001c0001t0001g0208 a0001c0001t0002g0193 a0001c0001t0002g0204 others(51): Show |
67 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.564-214A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13596749 | |||||||
| chr6:13596953 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.564-10T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 6/9 | chr6 | 13596953 | |||||||
| chr6:13597063 | C | CA | 9 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(6): Show |
9 | HG00735.hp2 HG01496.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+58dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13597063 | ||||||
| chr6:13597270 | C | T | 1 | a0001c0001t0004g0077 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.617+254C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597270 | |||||||
| chr6:13597433 | T | TA | 18 | a0001c0001t0001g0169 a0001c0001t0003g0142 a0001c0001t0003g0147 others(15): Show |
19 | HG01243.hp1 HG01891.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.617+437dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13597433 | ||||||
| chr6:13597433 | TA | T | 20 | a0001c0001t0001g0162 a0001c0001t0001g0177 a0001c0001t0001g0178 others(17): Show |
21 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.617+437delA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13597433 | ||||||
| chr6:13597443 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.617+427A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597443 | |||||||
| chr6:13597489 | T | A | 2 | a0001c0001t0021g0037 a0001c0001t0022g0037 |
2 | NA18975.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.617+473T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597489 | |||||||
| chr6:13597540 | GTTTAT | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0166 others(3): Show |
8 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+538_617+542del others(5): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13597540 | ||||||
| chr6:13597572 | A | C | 1 | a0001c0002t0002g0219 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.617+556A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597572 | |||||||
| chr6:13597581 | TGTCACCC others(8): Show |
T | 1 | a0001c0001t0002g0218 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.617+568_617+582del others(15): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13597581 | ||||||
| chr6:13597598 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0135 others(58): Show |
83 | HG00544.hp2 HG00558.hp2 HG00741.hp2 others(80): Show |
intron_variant | MODIFIER | c.617+582T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597598 | |||||||
| chr6:13597608 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.617+592C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597608 | |||||||
| chr6:13597677 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.617+661C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597677 | |||||||
| chr6:13597677 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.617+661C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597677 | |||||||
| chr6:13597691 | G | A | 2 | a0001c0002t0002g0200 a0001c0002t0002g0201 |
2 | HG00423.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.617+675G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597691 | |||||||
| chr6:13597702 | C | T | 3 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 |
3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.617+686C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597702 | |||||||
| chr6:13597841 | C | T | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.617+825C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597841 | |||||||
| chr6:13597890 | G | A | 51 | a0001c0001t0002g0193 a0001c0002t0002g0007 a0001c0002t0002g0020 others(48): Show |
64 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.617+874G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597890 | |||||||
| chr6:13597920 | G | A | 1 | a0001c0002t0002g0223 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.617+904G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13597920 | |||||||
| chr6:13598068 | C | T | 3 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 |
3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.618-964C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598068 | |||||||
| chr6:13598079 | G | A | 1 | a0001c0001t0003g0157 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.618-953G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598079 | |||||||
| chr6:13598272 | A | T | 1 | a0001c0001t0003g0153 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.618-760A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598272 | |||||||
| chr6:13598317 | T | C | 6 | a0001c0001t0005g0052 a0001c0001t0005g0054 a0001c0001t0012g0015 others(3): Show |
8 | HG01109.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.618-715T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598317 | |||||||
| chr6:13598324 | A | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(42): Show |
68 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.618-708A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598324 | |||||||
| chr6:13598595 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0129 a0001c0001t0001g0162 others(1): Show |
5 | HG01884.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-437C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598595 | |||||||
| chr6:13598632 | C | T | 1 | a0001c0002t0004g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.618-400C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598632 | |||||||
| chr6:13598671 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0188 |
2 | HG00673.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.618-361A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598671 | |||||||
| chr6:13598779 | C | A | 1 | a0001c0001t0046g0062 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.618-253C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598779 | |||||||
| chr6:13598825 | C | CA | 28 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0003g0128 others(25): Show |
39 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.618-186dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13598825 | ||||||
| chr6:13598825 | CA | C | 11 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0237 others(8): Show |
11 | HG00323.hp1 HG00558.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.618-186delA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 13598825 | ||||||
| chr6:13598929 | G | A | 1 | a0001c0001t0004g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618-103G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 7/9 | chr6 | 13598929 | |||||||
| chr6:13599167 | C | T | 1 | a0001c0001t0005g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.741+12C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599167 | |||||||
| chr6:13599204 | T | G | 8 | a0001c0002t0002g0041 a0001c0002t0002g0042 a0001c0002t0002g0045 others(5): Show |
11 | HG00597.hp2 HG01258.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.741+49T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599204 | |||||||
| chr6:13599285 | C | T | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.741+130C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599285 | |||||||
| chr6:13599328 | T | C | 2 | a0001c0001t0021g0037 a0001c0001t0022g0037 |
2 | NA18975.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.741+173T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599328 | |||||||
| chr6:13599353 | A | C | 3 | a0001c0001t0017g0028 a0001c0001t0017g0107 a0006c0010t0040g0028 |
3 | HG01496.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.741+198A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599353 | |||||||
| chr6:13599565 | G | A | 1 | a0001c0001t0003g0150 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.741+410G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599565 | |||||||
| chr6:13599683 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.741+528C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599683 | |||||||
| chr6:13599924 | C | T | 3 | a0001c0001t0003g0034 a0001c0001t0003g0134 a0001c0001t0003g0153 |
4 | NA18955.hp1 NA18999.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+769C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13599924 | |||||||
| chr6:13600078 | C | T | 7 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(4): Show |
7 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-756C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600078 | |||||||
| chr6:13600227 | T | C | 55 | a0001c0001t0002g0108 a0001c0001t0002g0146 a0001c0001t0002g0218 others(52): Show |
73 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.742-607T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600227 | |||||||
| chr6:13600280 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.742-554G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600280 | |||||||
| chr6:13600284 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.742-550C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600284 | |||||||
| chr6:13600622 | A | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0173 |
2 | NA18979.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.742-212A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600622 | |||||||
| chr6:13600764 | G | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0155 a0001c0001t0001g0183 others(2): Show |
7 | NA18942.hp2 NA18945.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-70G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600764 | |||||||
| chr6:13600777 | A | G | 1 | a0002c0003t0002g0255 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.742-57A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 8/9 | chr6 | 13600777 | |||||||
| chr6:13601049 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.857+100A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13601049 | |||||||
| chr6:13601296 | T | C | 125 | a0001c0001t0001g0208 a0001c0001t0002g0108 a0001c0001t0002g0146 others(122): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.857+347T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13601296 | |||||||
| chr6:13601314 | T | C | 2 | a0001c0001t0004g0072 a0001c0001t0004g0077 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.857+365T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13601314 | |||||||
| chr6:13601322 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.857+373C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13601322 | |||||||
| chr6:13601755 | A | C | 1 | a0001c0001t0050g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.857+806A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13601755 | |||||||
| chr6:13601975 | T | C | 1 | a0001c0001t0003g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.857+1026T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13601975 | |||||||
| chr6:13602040 | A | G | 18 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(15): Show |
29 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.857+1091A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13602040 | |||||||
| chr6:13602075 | A | T | 1 | a0001c0002t0002g0194 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.857+1126A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13602075 | |||||||
| chr6:13602179 | T | A | 4 | a0001c0001t0014g0048 a0001c0001t0014g0269 a0001c0001t0029g0057 others(1): Show |
5 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.857+1230T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13602179 | |||||||
| chr6:13602500 | C | CA | 5 | a0001c0001t0003g0123 a0001c0001t0004g0023 a0001c0001t0047g0058 others(2): Show |
6 | HG01515.hp1 HG01517.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.857+1566dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13602500 | ||||||
| chr6:13602717 | C | G | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | NA18963.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.857+1768C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13602717 | |||||||
| chr6:13602789 | A | G | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.857+1840A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13602789 | |||||||
| chr6:13602947 | C | T | 1 | a0001c0001t0004g0089 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.857+1998C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13602947 | |||||||
| chr6:13603000 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.857+2051G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603000 | |||||||
| chr6:13603043 | C | T | 1 | a0005c0006t0004g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.857+2094C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603043 | |||||||
| chr6:13603086 | G | C | 1 | a0007c0008t0004g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.857+2137G>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603086 | |||||||
| chr6:13603104 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+2155C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603104 | |||||||
| chr6:13603105 | G | A | 2 | a0001c0001t0025g0102 a0001c0001t0028g0101 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.857+2156G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603105 | |||||||
| chr6:13603121 | C | G | 1 | a0001c0001t0002g0251 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.857+2172C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603121 | |||||||
| chr6:13603133 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.857+2184C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603133 | |||||||
| chr6:13603256 | G | A | 1 | a0001c0001t0048g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.857+2307G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603256 | |||||||
| chr6:13603271 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.857+2322C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603271 | |||||||
| chr6:13603276 | C | CA | 5 | a0001c0001t0003g0144 a0001c0001t0003g0151 a0001c0001t0004g0024 others(2): Show |
6 | HG03225.hp2 HG03831.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+2347dupA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13603276 | ||||||
| chr6:13603276 | CA | C | 10 | a0001c0001t0001g0164 a0001c0001t0002g0218 a0001c0001t0025g0102 others(7): Show |
10 | HG00323.hp2 HG01169.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.857+2347delA | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13603276 | ||||||
| chr6:13603410 | A | T | 1 | a0001c0001t0004g0074 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.857+2461A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603410 | |||||||
| chr6:13603629 | G | A | 3 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 |
3 | HG02647.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.857+2680G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603629 | |||||||
| chr6:13603676 | A | G | 1 | a0001c0001t0004g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.857+2727A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603676 | |||||||
| chr6:13603883 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.857+2934A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603883 | |||||||
| chr6:13603955 | T | C | 1 | a0001c0001t0003g0099 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.857+3006T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603955 | |||||||
| chr6:13603957 | T | C | 3 | a0001c0001t0017g0028 a0001c0001t0017g0107 a0006c0010t0040g0028 |
3 | HG01496.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857+3008T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603957 | |||||||
| chr6:13603970 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.857+3021T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13603970 | |||||||
| chr6:13604144 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.857+3195A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13604144 | |||||||
| chr6:13604426 | G | A | 1 | a0001c0001t0031g0171 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.857+3477G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13604426 | |||||||
| chr6:13604478 | A | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0225 |
3 | HG01175.hp1 HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.857+3529A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13604478 | |||||||
| chr6:13604627 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.857+3678G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13604627 | |||||||
| chr6:13604686 | T | C | 2 | a0001c0002t0002g0046 a0001c0002t0002g0225 |
3 | HG01175.hp1 HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.857+3737T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13604686 | |||||||
| chr6:13605387 | C | A | 2 | a0001c0001t0001g0208 a0001c0001t0002g0204 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.857+4438C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13605387 | |||||||
| chr6:13605426 | T | C | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.857+4477T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13605426 | |||||||
| chr6:13605478 | G | A | 6 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(3): Show |
6 | HG01496.hp1 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.857+4529G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13605478 | |||||||
| chr6:13605641 | T | A | 7 | a0001c0001t0014g0048 a0001c0001t0014g0269 a0001c0001t0027g0109 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.857+4692T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13605641 | |||||||
| chr6:13605673 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.857+4724C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13605673 | |||||||
| chr6:13606188 | G | A | 1 | a0001c0001t0045g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.857+5239G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13606188 | |||||||
| chr6:13606743 | G | A | 16 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(13): Show |
26 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858-5047G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13606743 | |||||||
| chr6:13606774 | C | T | 6 | a0001c0001t0014g0048 a0001c0001t0014g0269 a0001c0001t0025g0102 others(3): Show |
7 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.858-5016C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13606774 | |||||||
| chr6:13607082 | C | T | 1 | a0001c0002t0002g0201 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.858-4708C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607082 | |||||||
| chr6:13607158 | A | G | 1 | a0001c0002t0006g0043 | 2 | NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.858-4632A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607158 | |||||||
| chr6:13607758 | A | G | 114 | a0001c0001t0001g0155 a0001c0001t0001g0208 a0001c0001t0002g0108 others(111): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.858-4032A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607758 | |||||||
| chr6:13607822 | C | T | 2 | a0003c0004t0001g0012 a0003c0004t0001g0113 |
5 | HG02280.hp2 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-3968C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607822 | |||||||
| chr6:13607840 | G | A | 1 | a0001c0001t0005g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.858-3950G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607840 | |||||||
| chr6:13607906 | A | T | 1 | a0001c0001t0015g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.858-3884A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607906 | |||||||
| chr6:13607948 | C | T | 7 | a0001c0001t0014g0048 a0001c0001t0014g0269 a0001c0001t0025g0102 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.858-3842C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13607948 | |||||||
| chr6:13608018 | C | T | 1 | a0001c0002t0006g0220 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.858-3772C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608018 | |||||||
| chr6:13608019 | T | A | 1 | a0001c0002t0006g0220 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.858-3771T>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608019 | |||||||
| chr6:13608040 | T | C | 14 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(11): Show |
15 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.858-3750T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608040 | |||||||
| chr6:13608060 | T | C | 221 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0038 others(218): Show |
291 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.858-3730T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608060 | |||||||
| chr6:13608072 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.858-3718A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608072 | |||||||
| chr6:13608107 | A | T | 1 | a0001c0002t0006g0220 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.858-3683A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608107 | |||||||
| chr6:13608204 | T | C | 3 | a0001c0001t0027g0109 a0001c0001t0048g0266 a0001c0001t0052g0083 |
3 | HG01243.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.858-3586T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608204 | |||||||
| chr6:13608471 | G | A | 6 | a0001c0001t0014g0048 a0001c0001t0014g0269 a0001c0001t0025g0102 others(3): Show |
7 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.858-3319G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13608471 | |||||||
| chr6:13608821 | AT | A | 120 | a0001c0001t0001g0208 a0001c0001t0002g0108 a0001c0001t0002g0146 others(117): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.858-2955delT | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13608821 | ||||||
| chr6:13608821 | ATT | A | 8 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(5): Show |
8 | HG00735.hp2 HG01496.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.858-2956_858-2955d others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13608821 | ||||||
| chr6:13609487 | GGCCAGGG others(36): Show |
G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2302_858-2260d others(45): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609487 | |||||||
| chr6:13609507 | A | C | 1 | a0001c0001t0014g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.858-2283A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609507 | |||||||
| chr6:13609514 | A | G | 8 | a0001c0001t0010g0130 a0001c0001t0010g0131 a0001c0001t0010g0248 others(5): Show |
8 | HG00735.hp2 HG01496.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.858-2276A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609514 | |||||||
| chr6:13609538 | G | A | 2 | a0001c0001t0003g0226 a0001c0001t0003g0227 |
2 | NA19000.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.858-2252G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609538 | |||||||
| chr6:13609574 | T | C | 1 | a0001c0002t0006g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.858-2216T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609574 | |||||||
| chr6:13609593 | C | G | 1 | a0001c0001t0004g0089 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.858-2197C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609593 | |||||||
| chr6:13609603 | C | A | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2187C>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609603 | |||||||
| chr6:13609631 | A | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2159A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609631 | |||||||
| chr6:13609640 | G | A | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2150G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609640 | |||||||
| chr6:13609642 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2148A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609642 | |||||||
| chr6:13609643 | T | C | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2147T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609643 | |||||||
| chr6:13609652 | C | CAGTTACT others(22): Show |
1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2138_858-2137i others(31): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609652 | |||||||
| chr6:13609725 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2065A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609725 | |||||||
| chr6:13609742 | A | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2048A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609742 | |||||||
| chr6:13609768 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2022A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609768 | |||||||
| chr6:13609773 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2017A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609773 | |||||||
| chr6:13609774 | A | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2016A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609774 | |||||||
| chr6:13609775 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2015A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609775 | |||||||
| chr6:13609776 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2014A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609776 | |||||||
| chr6:13609778 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2012A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609778 | |||||||
| chr6:13609780 | A | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2010A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609780 | |||||||
| chr6:13609783 | G | T | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2007G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609783 | |||||||
| chr6:13609784 | T | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2006T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609784 | |||||||
| chr6:13609788 | C | G | 1 | a0001c0002t0006g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.858-2002C>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609788 | |||||||
| chr6:13609956 | A | G | 127 | a0001c0001t0001g0208 a0001c0001t0002g0108 a0001c0001t0002g0146 others(124): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.858-1834A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13609956 | |||||||
| chr6:13610113 | C | T | 2 | a0001c0001t0038g0120 a0004c0007t0039g0229 |
2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.858-1677C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610113 | |||||||
| chr6:13610123 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0031g0171 |
2 | HG00609.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.858-1667C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610123 | |||||||
| chr6:13610153 | T | G | 1 | a0001c0001t0048g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.858-1637T>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610153 | |||||||
| chr6:13610518 | A | G | 1 | a0001c0001t0014g0269 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.858-1272A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610518 | |||||||
| chr6:13610528 | C | T | 1 | a0001c0001t0009g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.858-1262C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610528 | |||||||
| chr6:13610675 | A | C | 109 | a0001c0001t0002g0108 a0001c0001t0002g0146 a0001c0001t0002g0193 others(106): Show |
141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.858-1115A>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610675 | |||||||
| chr6:13610955 | T | C | 1 | a0001c0001t0049g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.858-835T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13610955 | |||||||
| chr6:13611052 | C | T | 1 | a0001c0001t0004g0081 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.858-738C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611052 | |||||||
| chr6:13611195 | A | ATG | 8 | a0001c0001t0003g0032 a0001c0001t0003g0119 a0001c0001t0003g0244 others(5): Show |
9 | HG02027.hp2 HG02080.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.858-583_858-582dup others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611195 | ||||||
| chr6:13611195 | ATG | A | 34 | a0001c0001t0002g0262 a0001c0001t0004g0011 a0001c0001t0004g0024 others(31): Show |
40 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.858-583_858-582del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611195 | ||||||
| chr6:13611203 | GTGTGTAT others(7): Show |
G | 4 | a0001c0001t0027g0109 a0001c0001t0038g0120 a0001c0001t0048g0266 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-585_858-572del others(14): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611203 | ||||||
| chr6:13611205 | G | A | 4 | a0001c0001t0004g0049 a0001c0001t0010g0130 a0001c0001t0010g0131 others(1): Show |
4 | HG02145.hp1 HG02647.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-585G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611205 | |||||||
| chr6:13611205 | G | GTA | 17 | a0001c0001t0002g0251 a0001c0001t0004g0008 a0001c0001t0004g0023 others(14): Show |
20 | HG00735.hp1 HG01168.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.858-584_858-583ins others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611205 | ||||||
| chr6:13611205 | G | GTATA | 20 | a0001c0001t0002g0146 a0001c0001t0002g0193 a0001c0001t0002g0257 others(17): Show |
20 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.858-584_858-583ins others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611205 | ||||||
| chr6:13611205 | G | GTATATA | 3 | a0001c0001t0002g0261 a0001c0001t0004g0090 a0002c0003t0002g0010 |
3 | HG01975.hp2 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-584_858-583ins others(6): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611205 | ||||||
| chr6:13611205 | GTGTATAT others(5): Show |
G | 16 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(13): Show |
26 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858-583_858-572del others(12): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611205 | ||||||
| chr6:13611207 | G | A | 73 | a0001c0001t0002g0108 a0001c0001t0002g0146 a0001c0001t0002g0193 others(70): Show |
98 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.858-583G>A | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611207 | |||||||
| chr6:13611207 | G | GTA | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(49): Show |
76 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.858-554_858-553dup others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611207 | ||||||
| chr6:13611207 | G | GTATA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00639.hp1 HG00738.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.858-556_858-553dup others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611207 | ||||||
| chr6:13611207 | G | GTATATA | 4 | a0001c0001t0001g0038 a0001c0001t0001g0160 a0001c0001t0003g0002 others(1): Show |
6 | HG01346.hp1 HG01358.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.858-558_858-553dup others(6): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611207 | ||||||
| chr6:13611207 | GTA | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0166 others(4): Show |
7 | HG00140.hp1 HG02004.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.858-554_858-553del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611207 | ||||||
| chr6:13611207 | GTATA | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
7 | HG01169.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.858-556_858-553del others(4): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611207 | ||||||
| chr6:13611209 | A | G | 8 | a0001c0001t0001g0241 a0001c0001t0003g0002 a0001c0001t0003g0004 others(5): Show |
8 | HG02135.hp2 HG02622.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.858-581A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611209 | |||||||
| chr6:13611211 | A | G | 1 | a0001c0001t0025g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.858-579A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611211 | |||||||
| chr6:13611212 | TATATATA others(23): Show |
T | 1 | a0001c0001t0002g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.858-576_858-547del others(30): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611212 | ||||||
| chr6:13611213 | A | G | 1 | a0001c0001t0025g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.858-577A>G | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611213 | |||||||
| chr6:13611220 | TATATATA others(15): Show |
T | 4 | a0001c0001t0014g0048 a0001c0001t0014g0269 a0001c0001t0029g0057 others(1): Show |
5 | HG01891.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-568_858-547del others(22): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611220 | ||||||
| chr6:13611224 | TATATATA others(15): Show |
T | 1 | a0004c0007t0039g0229 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.858-562_858-541del others(22): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611224 | ||||||
| chr6:13611230 | TATATATA others(5): Show |
T | 1 | a0007c0008t0004g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.858-558_858-547del others(12): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611230 | ||||||
| chr6:13611234 | T | C | 16 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(13): Show |
26 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858-556T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611234 | |||||||
| chr6:13611236 | T | C | 16 | a0001c0001t0005g0003 a0001c0001t0005g0022 a0001c0001t0005g0059 others(13): Show |
26 | HG00597.hp1 HG00609.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858-554T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611236 | |||||||
| chr6:13611236 | TAC | T | 13 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0142 others(10): Show |
13 | HG00544.hp2 HG02074.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.858-544_858-543del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611236 | ||||||
| chr6:13611236 | TACACAC | T | 6 | a0001c0001t0010g0131 a0001c0001t0027g0109 a0001c0001t0028g0101 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.858-548_858-543del others(6): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611236 | ||||||
| chr6:13611236 | TACACACA others(3): Show |
T | 1 | a0001c0001t0038g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.858-552_858-543del others(10): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611236 | ||||||
| chr6:13611238 | C | T | 164 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0112 others(161): Show |
214 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.858-552C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611238 | |||||||
| chr6:13611240 | C | T | 111 | a0001c0001t0002g0146 a0001c0001t0002g0193 a0001c0001t0002g0204 others(108): Show |
142 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.858-550C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611240 | |||||||
| chr6:13611242 | C | T | 111 | a0001c0001t0002g0146 a0001c0001t0002g0193 a0001c0001t0002g0204 others(108): Show |
141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.858-548C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611242 | |||||||
| chr6:13611244 | C | T | 2 | a0001c0001t0010g0131 a0001c0001t0010g0248 |
2 | HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.858-546C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611244 | |||||||
| chr6:13611248 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.858-542T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611248 | |||||||
| chr6:13611252 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0183 |
2 | NA18945.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.858-538C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611252 | |||||||
| chr6:13611260 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0183 |
2 | NA18945.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.858-530T>C | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611260 | |||||||
| chr6:13611360 | G | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG00673.hp2 HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.858-430G>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611360 | |||||||
| chr6:13611389 | C | T | 2 | a0001c0001t0005g0078 a0001c0001t0047g0058 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.858-401C>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611389 | |||||||
| chr6:13611401 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.858-389A>T | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611401 | |||||||
| chr6:13611574 | TC | T | 4 | a0001c0001t0004g0075 a0001c0001t0007g0174 a0001c0002t0002g0198 others(1): Show |
4 | NA18961.hp1 NA18963.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-211delC | SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 13611574 | ||||||
| chr6:13611578 | CCA | C | 27 | a0001c0001t0002g0146 a0001c0001t0002g0218 a0001c0001t0004g0006 others(24): Show |
38 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.858-211_858-210del others(2): Show |
SIRT5 | ENSG00000124523.17 | transcript | ENST00000606117.2 | protein_coding | 9/9 | chr6 | 13611578 |