Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 94081 |
| ensemblid | ENSG00000164466.13 |
| hgncid | 16085 |
| symbol | SFXN1 |
| name | sideroflexin 1 |
| refseq_nuc | NM_022754.7 |
| refseq_prot | NP_073591.2 |
| ensembl_nuc | ENST00000321442.10 |
| ensembl_prot | ENSP00000316905.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 175478560 |
| end | 175529742 |
| strand | + |
| ver | v1.2 |
| region | chr5:175478560-175529742 |
| region5000 | chr5:175473560-175534742 |
| regionname0 | SFXN1_chr5_175478560_175529742 |
| regionname5000 | SFXN1_chr5_175473560_175534742 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 322 | 366 | 89 | 69 | 146 | 14 | 46 | 110 | SFXN1_chr5_175473560_175534742 | SFXN1 | MSGEL others(317): Show |
chr5 | 175473560 | 175534742 |
| a0002 | 0/0 | 322 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | MSGEL others(317): Show |
chr5 | 175473560 | 175534742 |
| a0003 | 0/0 | 322 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | MSGEL others(317): Show |
chr5 | 175473560 | 175534742 |
| a0004 | 0/0 | 322 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | MSGEL others(317): Show |
chr5 | 175473560 | 175534742 |
| a0005 | 0/0 | 322 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | MSGEL others(317): Show |
chr5 | 175473560 | 175534742 |
| a0006 | 0/0 | 322 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | MSGEL others(317): Show |
chr5 | 175473560 | 175534742 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 966 | 244 | 47 | 52 | 109 | 11 | 23 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0001c0002 | 0/0 | 966 | 105 | 39 | 12 | 33 | 3 | 18 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0001c0003 | 0/0 | 966 | 12 | 0 | 5 | 3 | 0 | 4 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0001c0004 | 0/0 | 966 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0001c0007 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0001c0010 | 0/0 | 966 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0001c0012 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0002c0005 | 0/0 | 966 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0003c0011 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0004c0006 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0005c0008 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 | ||
| a0006c0009 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | ATGTC others(961): Show |
chr5 | 175473560 | 175534742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4066 | 68 | 7 | 20 | 27 | 8 | 5 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0002 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0003 | 0/0 | 4065 | 64 | 1 | 16 | 36 | 2 | 9 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0004 | 0/0 | 4066 | 28 | 0 | 4 | 23 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0005 | 0/0 | 4070 | 13 | 10 | 3 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0008 | 0/0 | 4067 | 6 | 0 | 1 | 4 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0009 | 0/0 | 4065 | 6 | 3 | 2 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0010 | 0/0 | 4067 | 6 | 0 | 2 | 3 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0013 | 0/0 | 4070 | 5 | 5 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0014 | 0/0 | 4070 | 5 | 0 | 0 | 5 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0016 | 0/0 | 4066 | 4 | 4 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0017 | 0/0 | 4066 | 4 | 1 | 0 | 3 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0018 | 0/0 | 4069 | 4 | 3 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4064): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0019 | 0/0 | 4070 | 3 | 3 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0020 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4064): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0024 | 0/0 | 4065 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0025 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0026 | 0/0 | 4066 | 2 | 1 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0044 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0045 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0046 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0047 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0048 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0049 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0050 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0051 | 1/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0052 | 0/0 | 4066 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0053 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0054 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0055 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0056 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0057 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4064): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0058 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0059 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0061 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0062 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0001t0063 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0002 | 0/0 | 4070 | 66 | 23 | 11 | 18 | 3 | 11 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0003 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0006 | 0/0 | 4071 | 7 | 3 | 0 | 1 | 0 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0011 | 0/0 | 4066 | 5 | 0 | 0 | 5 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0012 | 0/0 | 4069 | 5 | 1 | 0 | 3 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4064): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0015 | 0/0 | 4070 | 4 | 4 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0021 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0022 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0027 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0028 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0029 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0030 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0031 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0032 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0034 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0035 | 0/0 | 4072 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4067): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0036 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0037 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0039 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4064): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0041 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0042 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0002t0064 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0003t0004 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0003t0007 | 0/0 | 4070 | 8 | 0 | 2 | 3 | 0 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0003t0008 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0003t0043 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4064): Show |
chr5 | 175473560 | 175534742 |
| a0001c0003t0060 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4062): Show |
chr5 | 175473560 | 175534742 |
| a0001c0004t0006 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4066): Show |
chr5 | 175473560 | 175534742 |
| a0001c0004t0038 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0007t0040 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0001c0010t0001 | 0/0 | 4066 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0001c0012t0004 | 0/0 | 4066 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0002c0005t0023 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0003c0011t0004 | 0/0 | 4066 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4061): Show |
chr5 | 175473560 | 175534742 |
| a0004c0006t0003 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4060): Show |
chr5 | 175473560 | 175534742 |
| a0005c0008t0022 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| a0006c0009t0033 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | GGGAG others(4065): Show |
chr5 | 175473560 | 175534742 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0009g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0010g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0013g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0014g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0014g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0014g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0016g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0016g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0016g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0017g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0017g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0018g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0018g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0018g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0018g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0019g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0019g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0019g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0020g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0020g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0024g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0024g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0025g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0026g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0026g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0044g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0045g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0046g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0047g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0048g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0049g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0050g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0051g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0052g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0053g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0054g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0055g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0056g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0057g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0058g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0059g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0061g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0062g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0001t0063g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0001 | 0/0 | 7 | 1 | 0 | 2 | 1 | 3 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0011g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0011g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0012g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0012g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0012g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0012g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0021g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0021g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0022g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0027g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0028g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0029g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0030g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0031g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0032g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0034g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0035g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0036g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0037g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0039g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0041g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0042g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0002t0064g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0008g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0043g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0003t0060g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0004t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0004t0038g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0007t0040g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0010t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0001c0012t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0002c0005t0023g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0002c0005t0023g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0003c0011t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0004c0006t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0005c0008t0022g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| a0006c0009t0033g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0275 | EUR | GBR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0305 | EUR | FIN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00423 | hp1 | a0001 | c0002 | t0022 | g0012 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00423 | hp2 | a0001 | c0003 | t0007 | g0073 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00544 | hp2 | a0001 | c0001 | t0025 | g0133 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00621 | hp1 | a0001 | c0002 | t0006 | g0213 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | CHS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00738 | hp1 | a0001 | c0002 | t0029 | g0319 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG00741 | hp2 | a0001 | c0003 | t0008 | g0023 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0268 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0267 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01099 | hp2 | a0001 | c0003 | t0007 | g0231 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01109 | hp2 | a0001 | c0001 | t0063 | g0146 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0279 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0161 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01192 | hp2 | a0001 | c0001 | t0044 | g0019 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01256 | hp1 | a0001 | c0001 | t0049 | g0262 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0318 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01257 | hp1 | a0001 | c0003 | t0004 | g0072 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0224 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01261 | hp1 | a0001 | c0003 | t0043 | g0022 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01433 | hp2 | a0001 | c0001 | t0018 | g0238 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0345 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01884 | hp1 | a0001 | c0001 | t0050 | g0199 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0313 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01928 | hp2 | a0001 | c0001 | t0010 | g0286 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01943 | hp2 | a0003 | c0011 | t0004 | g0074 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01993 | hp2 | a0001 | c0003 | t0007 | g0078 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02055 | hp1 | a0001 | c0001 | t0057 | g0179 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02055 | hp2 | a0001 | c0002 | t0006 | g0315 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0156 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02071 | hp2 | a0001 | c0001 | t0024 | g0219 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02074 | hp2 | a0001 | c0001 | t0017 | g0296 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02080 | hp1 | a0001 | c0002 | t0037 | g0328 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02080 | hp2 | a0001 | c0001 | t0062 | g0049 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0347 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0322 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02155 | hp2 | a0001 | c0001 | t0014 | g0200 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02165 | hp1 | a0001 | c0003 | t0007 | g0140 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | CDX | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02257 | hp1 | a0001 | c0002 | t0015 | g0082 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0063 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02280 | hp1 | a0001 | c0002 | t0015 | g0085 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0269 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02300 | hp2 | a0001 | c0001 | t0010 | g0123 | AMR | PEL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02451 | hp1 | a0001 | c0001 | t0019 | g0064 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02451 | hp2 | a0001 | c0001 | t0052 | g0097 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02602 | hp1 | a0001 | c0002 | t0012 | g0230 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02615 | hp1 | a0001 | c0002 | t0039 | g0024 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02615 | hp2 | a0001 | c0002 | t0027 | g0059 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02622 | hp1 | a0001 | c0002 | t0042 | g0084 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02622 | hp2 | a0001 | c0002 | t0031 | g0256 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0079 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02647 | hp2 | a0001 | c0004 | t0038 | g0038 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0314 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02717 | hp2 | a0004 | c0006 | t0003 | g0086 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0281 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02738 | hp1 | a0001 | c0001 | t0059 | g0207 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02738 | hp2 | a0001 | c0010 | t0001 | g0027 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0241 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0240 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02886 | hp1 | a0001 | c0002 | t0015 | g0081 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02886 | hp2 | a0001 | c0002 | t0015 | g0096 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02896 | hp1 | a0002 | c0005 | t0023 | g0184 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0195 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02965 | hp2 | a0001 | c0001 | t0053 | g0090 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0248 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0311 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03041 | hp2 | a0001 | c0001 | t0055 | g0087 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0080 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0155 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03130 | hp1 | a0001 | c0002 | t0028 | g0190 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0092 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0191 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0229 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0127 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0193 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03225 | hp2 | a0001 | c0001 | t0045 | g0198 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0173 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0196 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03490 | hp1 | a0001 | c0001 | t0010 | g0061 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03516 | hp2 | a0001 | c0001 | t0047 | g0247 | AFR | ESN | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0312 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0334 | AFR | GWD | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0180 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03579 | hp2 | a0001 | c0007 | t0040 | g0181 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03654 | hp1 | a0001 | c0002 | t0034 | g0338 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0222 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03669 | hp2 | a0001 | c0003 | t0007 | g0077 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03688 | hp1 | a0001 | c0001 | t0058 | g0036 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0278 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0343 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03710 | hp1 | a0001 | c0001 | t0026 | g0069 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03710 | hp2 | a0001 | c0002 | t0006 | g0280 | SAS | PJL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03831 | hp1 | a0001 | c0002 | t0006 | g0008 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03927 | hp1 | a0001 | c0001 | t0046 | g0089 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0223 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03942 | hp1 | a0001 | c0003 | t0007 | g0021 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03942 | hp2 | a0001 | c0002 | t0006 | g0012 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04115 | hp1 | a0001 | c0002 | t0032 | g0172 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0167 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04184 | hp1 | a0001 | c0003 | t0060 | g0076 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04184 | hp2 | a0001 | c0001 | t0048 | g0018 | SAS | BEB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0212 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG04228 | hp2 | a0001 | c0003 | t0007 | g0075 | SAS | STU | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0194 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18939 | hp1 | a0001 | c0012 | t0004 | g0337 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18939 | hp2 | a0001 | c0001 | t0014 | g0188 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18945 | hp2 | a0001 | c0002 | t0011 | g0003 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18947 | hp2 | a0005 | c0008 | t0022 | g0208 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18948 | hp2 | a0001 | c0002 | t0012 | g0016 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18949 | hp1 | a0001 | c0002 | t0021 | g0257 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18949 | hp2 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0047 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18954 | hp1 | a0001 | c0002 | t0012 | g0339 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18954 | hp2 | a0001 | c0001 | t0017 | g0310 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18960 | hp1 | a0001 | c0002 | t0036 | g0266 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18963 | hp2 | a0001 | c0002 | t0011 | g0003 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18965 | hp1 | a0001 | c0002 | t0012 | g0214 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18965 | hp2 | a0001 | c0001 | t0056 | g0006 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18971 | hp1 | a0001 | c0003 | t0007 | g0070 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18975 | hp2 | a0001 | c0001 | t0017 | g0205 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18984 | hp1 | a0006 | c0009 | t0033 | g0346 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18988 | hp1 | a0001 | c0001 | t0008 | g0048 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18992 | hp2 | a0001 | c0001 | t0025 | g0114 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18998 | hp1 | a0001 | c0002 | t0011 | g0204 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19000 | hp1 | a0001 | c0002 | t0011 | g0253 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0321 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19030 | hp2 | a0002 | c0005 | t0023 | g0182 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19043 | hp1 | a0001 | c0002 | t0012 | g0226 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0317 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19058 | hp2 | a0001 | c0001 | t0061 | g0270 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19066 | hp2 | a0001 | c0001 | t0014 | g0186 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19068 | hp1 | a0001 | c0001 | t0010 | g0144 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19070 | hp1 | a0001 | c0001 | t0014 | g0187 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19078 | hp1 | a0001 | c0002 | t0035 | g0327 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19082 | hp2 | a0001 | c0002 | t0021 | g0258 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0304 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19084 | hp2 | a0001 | c0001 | t0024 | g0246 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19091 | hp2 | a0001 | c0001 | t0014 | g0189 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA19240 | hp2 | a0001 | c0002 | t0030 | g0174 | AFR | YRI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | ASW | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | ASW | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0142 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0178 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20905 | hp1 | a0001 | c0001 | t0054 | g0088 | SAS | GIH | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | GIH | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02109 | hp2 | a0001 | c0002 | t0064 | g0153 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG02559 | hp2 | a0001 | c0001 | t0026 | g0233 | AFR | ACB | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0249 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG03471 | hp2 | a0001 | c0002 | t0041 | g0151 | AFR | MSL | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG06807 | hp1 | a0001 | c0004 | t0006 | g0154 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0065 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA18955 | hp2 | a0001 | c0002 | t0011 | g0003 | EAS | JPT | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA20300 | hp2 | a0001 | c0001 | t0019 | g0066 | AFR | USA | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0139 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0331 | AFR | LWK | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0098 | REF | REF | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0051 | g0271 | REF | REF | SFXN1_chr5_175473560_175534742 | SFXN1 | chr5 | 175473560 | 175534742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175492168 | T | C | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.65T>C | p.Ile22Thr | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 154/4066 | 65/969 | 22/322 | chr5 | 175492168 | |||
| chr5:175492180 | A | G | 1 | a0002 | 2 | HG02896.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.77A>G | p.Asn26Ser | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 166/4066 | 77/969 | 26/322 | chr5 | 175492180 | |||
| chr5:175510161 | G | A | 1 | a0005 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.388G>A | p.Val130Ile | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/11 | 477/4066 | 388/969 | 130/322 | chr5 | 175510161 | |||
| chr5:175513470 | A | C | 1 | a0006 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.604A>C | p.Lys202Gln | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/11 | 693/4066 | 604/969 | 202/322 | chr5 | 175513470 | |||
| chr5:175521940 | C | T | 1 | a0003 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.796C>T | p.Pro266Ser | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/11 | 885/4066 | 796/969 | 266/322 | chr5 | 175521940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175492215 | C | T | 1 | a0001c0012 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.112C>T | p.Leu38Leu | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 201/4066 | 112/969 | 38/322 | chr5 | 175492215 | |||
| chr5:175492244 | G | A | 2 | a0001c0004 a0001c0007 |
3 | HG02647.hp2 HG03579.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.141G>A | p.Ala47Ala | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/11 | 230/4066 | 141/969 | 47/322 | chr5 | 175492244 | |||
| chr5:175509035 | A | G | 2 | a0001c0003 a0003c0011 |
13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
synonymous_variant | LOW | c.168A>G | p.Gln56Gln | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/11 | 257/4066 | 168/969 | 56/322 | chr5 | 175509035 | |||
| chr5:175510160 | C | T | 1 | a0001c0010 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.387C>T | p.Ala129Ala | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/11 | 476/4066 | 387/969 | 129/322 | chr5 | 175510160 | |||
| chr5:175510190 | C | T | 5 | a0001c0002 a0001c0004 a0002c0005 others(2): Show |
111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
synonymous_variant | LOW | c.417C>T | p.Asp139Asp | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/11 | 506/4066 | 417/969 | 139/322 | chr5 | 175510190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175526740 | G | A | 28 | a0001c0001t0002 a0001c0001t0020 a0001c0002t0002 others(25): Show |
113 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*6G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 6 | chr5 | 175526740 | ||||||
| chr5:175526774 | A | C | 1 | a0001c0002t0064 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*40A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 40 | chr5 | 175526774 | ||||||
| chr5:175526788 | A | G | 6 | a0001c0002t0015 a0001c0002t0039 a0001c0002t0041 others(3): Show |
9 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*54A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 54 | chr5 | 175526788 | ||||||
| chr5:175526944 | T | C | 1 | a0001c0004t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 210 | chr5 | 175526944 | ||||||
| chr5:175527060 | T | C | 1 | a0001c0002t0027 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 326 | chr5 | 175527060 | ||||||
| chr5:175527180 | C | A | 1 | a0001c0002t0011 | 5 | NA18945.hp2 NA18955.hp2 NA18963.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*446C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 446 | chr5 | 175527180 | ||||||
| chr5:175527210 | AC | A | 32 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(29): Show |
136 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*479delC | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 479 | INFO_REALIGN_3_PRIME | chr5 | 175527210 | |||||
| chr5:175527304 | C | T | 1 | a0001c0001t0062 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 570 | chr5 | 175527304 | ||||||
| chr5:175527399 | G | A | 1 | a0001c0002t0028 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 665 | chr5 | 175527399 | ||||||
| chr5:175527544 | A | G | 1 | a0001c0001t0061 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*810A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 810 | chr5 | 175527544 | ||||||
| chr5:175527849 | A | G | 1 | a0001c0002t0037 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1115A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1115 | chr5 | 175527849 | ||||||
| chr5:175527858 | T | C | 40 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(37): Show |
152 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1124T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1124 | chr5 | 175527858 | ||||||
| chr5:175527915 | A | AT | 30 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(27): Show |
137 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1203dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1204 | INFO_REALIGN_3_PRIME | chr5 | 175527915 | |||||
| chr5:175527915 | A | ATT | 8 | a0001c0001t0063 a0001c0002t0006 a0001c0002t0035 others(5): Show |
14 | HG00621.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1202_*1203dupTT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1204 | INFO_REALIGN_3_PRIME | chr5 | 175527915 | |||||
| chr5:175527915 | AT | A | 5 | a0001c0001t0013 a0001c0001t0019 a0001c0001t0044 others(2): Show |
18 | HG00423.hp2 HG01099.hp2 HG01192.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1203delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1203 | INFO_REALIGN_3_PRIME | chr5 | 175527915 | |||||
| chr5:175527941 | A | T | 1 | a0001c0002t0034 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1207A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1207 | chr5 | 175527941 | ||||||
| chr5:175528012 | C | T | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(36): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1278C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1278 | chr5 | 175528012 | ||||||
| chr5:175528069 | C | T | 3 | a0001c0002t0015 a0001c0002t0039 a0001c0002t0042 |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1335C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1335 | chr5 | 175528069 | ||||||
| chr5:175528152 | G | A | 2 | a0001c0003t0007 a0001c0003t0043 |
9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1418G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1418 | chr5 | 175528152 | ||||||
| chr5:175528171 | G | A | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(25): Show |
128 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1437G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1437 | chr5 | 175528171 | ||||||
| chr5:175528201 | A | G | 1 | a0002c0005t0023 | 2 | HG02896.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1467A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1467 | chr5 | 175528201 | ||||||
| chr5:175528204 | C | A | 1 | a0001c0003t0043 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1470 | chr5 | 175528204 | ||||||
| chr5:175528205 | G | C | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(25): Show |
128 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1471G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1471 | chr5 | 175528205 | ||||||
| chr5:175528205 | G | T | 1 | a0001c0002t0021 | 2 | NA18949.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1471G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1471 | chr5 | 175528205 | ||||||
| chr5:175528442 | G | A | 2 | a0001c0001t0014 a0001c0002t0036 |
6 | HG02155.hp2 NA18939.hp2 NA18960.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1708G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1708 | chr5 | 175528442 | ||||||
| chr5:175528475 | G | T | 1 | a0001c0002t0032 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1741 | chr5 | 175528475 | ||||||
| chr5:175528532 | T | A | 1 | a0001c0002t0029 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1798T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1798 | chr5 | 175528532 | ||||||
| chr5:175528569 | A | T | 31 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(28): Show |
131 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1835A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1835 | chr5 | 175528569 | ||||||
| chr5:175528581 | C | T | 29 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(26): Show |
125 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1847C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1847 | chr5 | 175528581 | ||||||
| chr5:175528667 | G | C | 2 | a0001c0001t0026 a0001c0001t0059 |
3 | HG02559.hp2 HG02738.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1933G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1933 | chr5 | 175528667 | ||||||
| chr5:175528673 | C | T | 2 | a0001c0001t0058 a0001c0003t0060 |
2 | HG03688.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1939C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 1939 | chr5 | 175528673 | ||||||
| chr5:175528743 | G | A | 1 | a0001c0002t0030 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2009 | chr5 | 175528743 | ||||||
| chr5:175528743 | G | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(21): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2009G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2009 | chr5 | 175528743 | ||||||
| chr5:175528791 | G | A | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(25): Show |
124 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2057G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2057 | chr5 | 175528791 | ||||||
| chr5:175528934 | T | C | 1 | a0001c0001t0014 | 5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2200T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2200 | chr5 | 175528934 | ||||||
| chr5:175529036 | G | T | 29 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(26): Show |
125 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2302G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2302 | chr5 | 175529036 | ||||||
| chr5:175529064 | C | T | 1 | a0001c0004t0038 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2330C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2330 | chr5 | 175529064 | ||||||
| chr5:175529077 | C | T | 1 | a0001c0002t0064 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2343C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2343 | chr5 | 175529077 | ||||||
| chr5:175529108 | G | A | 1 | a0001c0001t0052 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2374G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2374 | chr5 | 175529108 | ||||||
| chr5:175529120 | T | G | 1 | a0001c0001t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2386T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2386 | chr5 | 175529120 | ||||||
| chr5:175529260 | T | C | 29 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(26): Show |
125 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2526T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2526 | chr5 | 175529260 | ||||||
| chr5:175529326 | G | A | 1 | a0001c0001t0056 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2592G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2592 | chr5 | 175529326 | ||||||
| chr5:175529338 | C | CA | 5 | a0001c0001t0013 a0001c0001t0019 a0001c0001t0047 others(2): Show |
18 | HG00423.hp2 HG01099.hp2 HG01993.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2618dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2619 | INFO_REALIGN_3_PRIME | chr5 | 175529338 | |||||
| chr5:175529338 | CA | C | 3 | a0001c0001t0018 a0001c0001t0020 a0001c0001t0057 |
7 | HG01433.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2618delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2618 | INFO_REALIGN_3_PRIME | chr5 | 175529338 | |||||
| chr5:175529351 | A | G | 1 | a0001c0001t0055 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2617A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2617 | chr5 | 175529351 | ||||||
| chr5:175529430 | T | C | 2 | a0001c0001t0005 a0001c0001t0063 |
14 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2696T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2696 | chr5 | 175529430 | ||||||
| chr5:175529464 | A | G | 34 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(31): Show |
143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2730A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2730 | chr5 | 175529464 | ||||||
| chr5:175529484 | T | TAAAC | 39 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(36): Show |
153 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2750_*2751insAAAC | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2751 | chr5 | 175529484 | ||||||
| chr5:175529531 | GA | G | 11 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0017 others(8): Show |
83 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2806delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2806 | INFO_REALIGN_3_PRIME | chr5 | 175529531 | |||||
| chr5:175529569 | G | T | 1 | a0001c0001t0054 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2835 | chr5 | 175529569 | ||||||
| chr5:175529619 | G | T | 2 | a0001c0001t0046 a0001c0001t0053 |
2 | HG02965.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2885G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 11/11 | 2885 | chr5 | 175529619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175478673 | TG | T | 188 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0020 others(185): Show |
191 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.-10+38delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175478673 | ||||||
| chr5:175478748 | G | T | 1 | a0001c0002t0002g0347 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-10+109G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478748 | |||||||
| chr5:175478758 | C | T | 1 | a0001c0001t0014g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-10+119C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478758 | |||||||
| chr5:175478808 | C | CG | 71 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0028 others(68): Show |
72 | HG00280.hp1 HG00544.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10+179dupG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175478808 | ||||||
| chr5:175478808 | CG | C | 23 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0009g0180 others(20): Show |
23 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10+179delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175478808 | ||||||
| chr5:175478817 | G | T | 19 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0014g0186 others(16): Show |
19 | HG01884.hp1 HG02145.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+178G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478817 | |||||||
| chr5:175478827 | C | T | 1 | a0001c0001t0003g0178 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-10+188C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478827 | |||||||
| chr5:175478862 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+223C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478862 | |||||||
| chr5:175478865 | C | T | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+226C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478865 | |||||||
| chr5:175478892 | C | G | 2 | a0001c0001t0001g0197 a0001c0001t0045g0198 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-10+253C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478892 | |||||||
| chr5:175478912 | T | C | 18 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0014g0186 others(15): Show |
18 | HG02145.hp2 HG02155.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-10+273T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175478912 | |||||||
| chr5:175479308 | T | C | 12 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0014g0186 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+669T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479308 | |||||||
| chr5:175479370 | G | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-10+731G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479370 | |||||||
| chr5:175479448 | A | G | 12 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0014g0186 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+809A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479448 | |||||||
| chr5:175479651 | C | T | 1 | a0001c0002t0002g0345 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-10+1012C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479651 | |||||||
| chr5:175479780 | C | T | 1 | a0001c0002t0030g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-10+1141C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479780 | |||||||
| chr5:175479861 | T | G | 11 | a0001c0001t0020g0195 a0001c0001t0020g0196 a0001c0002t0002g0057 others(8): Show |
11 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+1222T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479861 | |||||||
| chr5:175479862 | T | C | 159 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(156): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-10+1223T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479862 | |||||||
| chr5:175479901 | C | G | 1 | a0001c0001t0003g0344 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-10+1262C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479901 | |||||||
| chr5:175479903 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-10+1264G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479903 | |||||||
| chr5:175479923 | G | A | 2 | a0001c0002t0002g0237 a0001c0002t0002g0345 |
2 | HG01515.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-10+1284G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479923 | |||||||
| chr5:175479997 | A | G | 11 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0014g0186 others(8): Show |
11 | HG02145.hp2 HG02155.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+1358A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175479997 | |||||||
| chr5:175480100 | T | G | 11 | a0001c0001t0020g0195 a0001c0001t0020g0196 a0001c0002t0002g0057 others(8): Show |
11 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+1461T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480100 | |||||||
| chr5:175480139 | C | T | 1 | a0001c0002t0012g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10+1500C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480139 | |||||||
| chr5:175480153 | G | T | 1 | a0001c0001t0016g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10+1514G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480153 | |||||||
| chr5:175480176 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0143 a0001c0001t0001g0145 others(1): Show |
4 | NA18747.hp1 NA18968.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+1537C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480176 | |||||||
| chr5:175480227 | C | T | 1 | a0001c0002t0002g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-10+1588C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480227 | |||||||
| chr5:175480245 | C | CA | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1612dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175480245 | ||||||
| chr5:175480257 | T | C | 1 | a0001c0001t0018g0238 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10+1618T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480257 | |||||||
| chr5:175480261 | C | T | 1 | a0001c0001t0018g0238 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10+1622C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480261 | |||||||
| chr5:175480288 | C | G | 1 | a0001c0001t0003g0342 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-10+1649C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480288 | |||||||
| chr5:175480294 | G | A | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10+1655G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480294 | |||||||
| chr5:175480363 | T | C | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+1724T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480363 | |||||||
| chr5:175480396 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0010g0061 others(2): Show |
5 | HG01192.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1757G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480396 | |||||||
| chr5:175480400 | T | TA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0197 a0001c0001t0003g0185 others(17): Show |
20 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10+1774dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175480400 | ||||||
| chr5:175480438 | A | G | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1799A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480438 | |||||||
| chr5:175480457 | T | C | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-10+1818T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480457 | |||||||
| chr5:175480581 | C | T | 1 | a0001c0003t0007g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-10+1942C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480581 | |||||||
| chr5:175480745 | ACC | A | 8 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0016g0139 others(5): Show |
8 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+2108_-10+2109d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175480745 | ||||||
| chr5:175480780 | C | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+2141C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480780 | |||||||
| chr5:175480796 | C | T | 2 | a0001c0001t0003g0340 a0001c0001t0003g0341 |
2 | NA18999.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-10+2157C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480796 | |||||||
| chr5:175480860 | A | G | 1 | a0001c0001t0005g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10+2221A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480860 | |||||||
| chr5:175480904 | C | A | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+2265C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480904 | |||||||
| chr5:175480921 | G | A | 10 | a0001c0001t0013g0063 a0001c0001t0014g0186 a0001c0001t0014g0187 others(7): Show |
10 | HG01884.hp1 HG02155.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+2282G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480921 | |||||||
| chr5:175480942 | A | G | 101 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(98): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.-10+2303A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480942 | |||||||
| chr5:175480974 | G | A | 10 | a0001c0001t0013g0063 a0001c0001t0014g0186 a0001c0001t0014g0187 others(7): Show |
10 | HG01884.hp1 HG02155.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+2335G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175480974 | |||||||
| chr5:175481001 | T | C | 1 | a0002c0005t0023g0182 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10+2362T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481001 | |||||||
| chr5:175481091 | T | C | 1 | a0001c0001t0003g0171 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-10+2452T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481091 | |||||||
| chr5:175481196 | T | C | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2557T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481196 | |||||||
| chr5:175481304 | G | C | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2665G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481304 | |||||||
| chr5:175481334 | G | T | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2695G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481334 | |||||||
| chr5:175481356 | C | G | 5 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2717C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481356 | |||||||
| chr5:175481391 | A | G | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+2752A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481391 | |||||||
| chr5:175481462 | C | T | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2823C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481462 | |||||||
| chr5:175481480 | C | T | 91 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(88): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-10+2841C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481480 | |||||||
| chr5:175481505 | G | A | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+2866G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481505 | |||||||
| chr5:175481606 | G | A | 37 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(34): Show |
37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+2967G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481606 | |||||||
| chr5:175481645 | G | A | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3006G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481645 | |||||||
| chr5:175481682 | G | T | 4 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+3043G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481682 | |||||||
| chr5:175481715 | G | C | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10+3076G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481715 | |||||||
| chr5:175481798 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-10+3159A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481798 | |||||||
| chr5:175481842 | T | C | 14 | a0001c0001t0013g0248 a0001c0001t0013g0249 a0001c0001t0020g0195 others(11): Show |
14 | HG01884.hp2 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+3203T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481842 | |||||||
| chr5:175481877 | A | AG | 37 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(34): Show |
37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+3240dupG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175481877 | ||||||
| chr5:175481880 | C | A | 37 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(34): Show |
37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+3241C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481880 | |||||||
| chr5:175481881 | C | T | 37 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(34): Show |
37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+3242C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175481881 | |||||||
| chr5:175482193 | C | G | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+3554C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482193 | |||||||
| chr5:175482221 | T | C | 194 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(191): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-10+3582T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482221 | |||||||
| chr5:175482229 | A | G | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+3590A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482229 | |||||||
| chr5:175482249 | C | T | 1 | a0001c0002t0030g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-10+3610C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482249 | |||||||
| chr5:175482299 | T | C | 163 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(160): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-10+3660T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482299 | |||||||
| chr5:175482485 | C | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(71): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-10+3846C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482485 | |||||||
| chr5:175482640 | A | C | 195 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(192): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-10+4001A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482640 | |||||||
| chr5:175482663 | C | G | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+4024C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482663 | |||||||
| chr5:175482708 | A | C | 32 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(29): Show |
32 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+4069A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482708 | |||||||
| chr5:175482865 | T | C | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+4226T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175482865 | |||||||
| chr5:175483024 | G | A | 1 | a0001c0002t0028g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+4385G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483024 | |||||||
| chr5:175483084 | A | G | 1 | a0001c0001t0019g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-10+4445A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483084 | |||||||
| chr5:175483174 | A | G | 37 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(34): Show |
37 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10+4535A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483174 | |||||||
| chr5:175483207 | G | T | 32 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(29): Show |
32 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+4568G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483207 | |||||||
| chr5:175483593 | C | T | 4 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+4954C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483593 | |||||||
| chr5:175483616 | A | G | 34 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(31): Show |
35 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+4977A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483616 | |||||||
| chr5:175483621 | A | T | 161 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-10+4982A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483621 | |||||||
| chr5:175483637 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+4998C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483637 | |||||||
| chr5:175483697 | C | A | 73 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(70): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.-10+5058C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483697 | |||||||
| chr5:175483698 | TG | T | 5 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+5060delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483698 | |||||||
| chr5:175483710 | G | A | 14 | a0001c0001t0003g0244 a0001c0002t0002g0071 a0001c0003t0004g0072 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+5071G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483710 | |||||||
| chr5:175483937 | A | T | 1 | a0001c0002t0012g0339 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-10+5298A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483937 | |||||||
| chr5:175483966 | G | A | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+5327G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175483966 | |||||||
| chr5:175484026 | G | A | 32 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(29): Show |
32 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+5387G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484026 | |||||||
| chr5:175484083 | C | CACA | 32 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(29): Show |
32 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+5444_-10+5445i others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484083 | |||||||
| chr5:175484092 | A | C | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+5453A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484092 | |||||||
| chr5:175484119 | A | G | 1 | a0001c0003t0008g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-10+5480A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484119 | |||||||
| chr5:175484129 | G | A | 1 | a0001c0003t0007g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-10+5490G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484129 | |||||||
| chr5:175484130 | C | T | 7 | a0001c0001t0003g0026 a0001c0001t0003g0091 a0001c0001t0003g0093 others(4): Show |
7 | HG02886.hp2 HG03130.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+5491C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484130 | |||||||
| chr5:175484148 | G | A | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+5509G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484148 | |||||||
| chr5:175484230 | C | T | 32 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(29): Show |
32 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+5591C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484230 | |||||||
| chr5:175484420 | C | G | 191 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(188): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-10+5781C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484420 | |||||||
| chr5:175484437 | A | T | 7 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+5798A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484437 | |||||||
| chr5:175484463 | G | A | 34 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(31): Show |
34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+5824G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484463 | |||||||
| chr5:175484496 | C | T | 34 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(31): Show |
34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+5857C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484496 | |||||||
| chr5:175484500 | G | A | 1 | a0001c0002t0002g0251 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-10+5861G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484500 | |||||||
| chr5:175484516 | A | G | 34 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(31): Show |
34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+5877A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484516 | |||||||
| chr5:175484542 | C | T | 55 | a0001c0001t0001g0152 a0001c0001t0001g0234 a0001c0001t0001g0235 others(52): Show |
56 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.-10+5903C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484542 | |||||||
| chr5:175484545 | G | A | 2 | a0001c0002t0002g0150 a0001c0002t0041g0151 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+5906G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484545 | |||||||
| chr5:175484558 | G | C | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10+5919G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484558 | |||||||
| chr5:175484598 | A | G | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-10+5959A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484598 | |||||||
| chr5:175484661 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-10+6022G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484661 | |||||||
| chr5:175484666 | G | A | 2 | a0001c0001t0016g0079 a0001c0001t0016g0080 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+6027G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484666 | |||||||
| chr5:175484672 | T | C | 193 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(190): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-10+6033T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484672 | |||||||
| chr5:175484706 | C | T | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+6067C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484706 | |||||||
| chr5:175484709 | C | T | 1 | a0001c0002t0034g0338 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10+6070C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484709 | |||||||
| chr5:175484719 | C | T | 34 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(31): Show |
35 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+6080C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484719 | |||||||
| chr5:175484749 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10+6110C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484749 | |||||||
| chr5:175484760 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+6121A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484760 | |||||||
| chr5:175484847 | C | T | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+6208C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484847 | |||||||
| chr5:175484994 | C | T | 1 | a0001c0012t0004g0337 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-10+6355C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484994 | |||||||
| chr5:175484998 | C | T | 1 | a0001c0001t0003g0336 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-10+6359C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484998 | |||||||
| chr5:175484999 | G | A | 34 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(31): Show |
34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+6360G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175484999 | |||||||
| chr5:175485035 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0025g0133 |
2 | HG00544.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-10+6396C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485035 | |||||||
| chr5:175485037 | GTT | G | 5 | a0001c0001t0001g0252 a0001c0001t0003g0254 a0001c0002t0011g0003 others(2): Show |
7 | NA18945.hp2 NA18955.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+6399_-10+6400d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485037 | |||||||
| chr5:175485062 | T | G | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+6423T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485062 | |||||||
| chr5:175485199 | T | C | 14 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+6560T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485199 | |||||||
| chr5:175485336 | T | C | 34 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(31): Show |
34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10+6697T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485336 | |||||||
| chr5:175485394 | T | A | 1 | a0001c0001t0003g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-9-6701T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485394 | |||||||
| chr5:175485570 | A | G | 1 | a0001c0003t0007g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9-6525A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485570 | |||||||
| chr5:175485575 | A | G | 1 | a0001c0001t0003g0335 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-9-6520A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485575 | |||||||
| chr5:175485708 | T | A | 1 | a0001c0004t0038g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9-6387T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485708 | |||||||
| chr5:175485762 | G | C | 157 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-9-6333G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485762 | |||||||
| chr5:175485808 | T | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-6287T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485808 | |||||||
| chr5:175485869 | C | T | 1 | a0001c0002t0002g0345 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-9-6226C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485869 | |||||||
| chr5:175485886 | C | T | 34 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(31): Show |
34 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.-9-6209C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485886 | |||||||
| chr5:175485892 | C | T | 2 | a0001c0001t0005g0333 a0001c0002t0002g0334 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-9-6203C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485892 | |||||||
| chr5:175485967 | T | C | 157 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-9-6128T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175485967 | |||||||
| chr5:175486104 | A | G | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5991A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486104 | |||||||
| chr5:175486126 | A | G | 1 | a0001c0001t0058g0036 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9-5969A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486126 | |||||||
| chr5:175486185 | A | AG | 8 | a0001c0001t0003g0099 a0001c0001t0005g0147 a0001c0001t0005g0148 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-5909dupG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175486185 | ||||||
| chr5:175486186 | GT | G | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5908delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486186 | |||||||
| chr5:175486187 | T | G | 185 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(182): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-9-5908T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486187 | |||||||
| chr5:175486194 | G | T | 15 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(12): Show |
15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-5901G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486194 | |||||||
| chr5:175486355 | C | G | 7 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-5740C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486355 | |||||||
| chr5:175486395 | A | G | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-5700A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486395 | |||||||
| chr5:175486456 | T | C | 1 | a0001c0002t0031g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9-5639T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486456 | |||||||
| chr5:175486910 | C | T | 15 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(12): Show |
15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-5185C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486910 | |||||||
| chr5:175486966 | T | C | 2 | a0001c0002t0021g0257 a0001c0002t0021g0258 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-9-5129T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175486966 | |||||||
| chr5:175487005 | G | A | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-5090G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487005 | |||||||
| chr5:175487123 | C | T | 1 | a0001c0002t0002g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-9-4972C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487123 | |||||||
| chr5:175487124 | G | A | 1 | a0004c0006t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9-4971G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487124 | |||||||
| chr5:175487134 | A | G | 10 | a0001c0001t0003g0178 a0001c0001t0013g0063 a0001c0001t0019g0064 others(7): Show |
10 | HG02258.hp2 HG02451.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-4961A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487134 | |||||||
| chr5:175487268 | C | T | 1 | a0001c0002t0002g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9-4827C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487268 | |||||||
| chr5:175487444 | C | T | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-4651C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487444 | |||||||
| chr5:175487523 | C | T | 5 | a0001c0001t0003g0035 a0001c0001t0003g0129 a0001c0001t0003g0130 others(2): Show |
5 | HG01192.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4572C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487523 | |||||||
| chr5:175487634 | G | A | 2 | a0001c0003t0004g0072 a0001c0003t0008g0023 |
2 | HG00741.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-9-4461G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487634 | |||||||
| chr5:175487662 | A | G | 1 | a0004c0006t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9-4433A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487662 | |||||||
| chr5:175487681 | A | G | 5 | a0001c0001t0005g0034 a0001c0001t0005g0128 a0001c0002t0002g0125 others(2): Show |
5 | HG02723.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-4414A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487681 | |||||||
| chr5:175487746 | G | A | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-4349G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487746 | |||||||
| chr5:175487777 | G | C | 1 | a0001c0002t0002g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-9-4318G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487777 | |||||||
| chr5:175487784 | G | A | 33 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(30): Show |
33 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9-4311G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487784 | |||||||
| chr5:175487832 | C | G | 6 | a0001c0002t0002g0083 a0001c0002t0015g0081 a0001c0002t0015g0082 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-4263C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487832 | |||||||
| chr5:175487833 | C | T | 7 | a0001c0001t0001g0228 a0001c0001t0001g0325 a0001c0002t0002g0326 others(4): Show |
7 | HG00597.hp1 HG00609.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-4262C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487833 | |||||||
| chr5:175487834 | A | T | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-9-4261A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487834 | |||||||
| chr5:175487836 | C | T | 1 | a0001c0001t0003g0324 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-9-4259C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487836 | |||||||
| chr5:175487968 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-9-4127C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487968 | |||||||
| chr5:175487992 | T | G | 9 | a0001c0001t0003g0011 a0001c0001t0003g0171 a0001c0001t0003g0206 others(6): Show |
10 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-4103T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175487992 | |||||||
| chr5:175488213 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-9-3882C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488213 | |||||||
| chr5:175488236 | A | G | 2 | a0001c0001t0016g0079 a0001c0001t0016g0080 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-3859A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488236 | |||||||
| chr5:175488262 | G | A | 6 | a0001c0001t0005g0147 a0001c0001t0005g0148 a0001c0001t0005g0149 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-3833G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488262 | |||||||
| chr5:175488305 | C | CTT | 7 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-3777_-9-3776dup others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175488305 | ||||||
| chr5:175488305 | C | CTTT | 27 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(24): Show |
27 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9-3778_-9-3776dup others(3): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175488305 | ||||||
| chr5:175488332 | C | T | 1 | a0001c0001t0003g0323 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-9-3763C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488332 | |||||||
| chr5:175488349 | C | G | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-3746C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488349 | |||||||
| chr5:175488352 | G | T | 1 | a0001c0001t0008g0053 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-9-3743G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488352 | |||||||
| chr5:175488366 | G | A | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-3729G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488366 | |||||||
| chr5:175488500 | C | T | 34 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(31): Show |
35 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9-3595C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488500 | |||||||
| chr5:175488510 | G | A | 1 | a0001c0003t0007g0073 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9-3585G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488510 | |||||||
| chr5:175488519 | G | C | 13 | a0001c0003t0004g0072 a0001c0003t0007g0021 a0001c0003t0007g0070 others(10): Show |
13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-3576G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488519 | |||||||
| chr5:175488591 | G | A | 22 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(19): Show |
22 | HG01109.hp2 HG01952.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-9-3504G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488591 | |||||||
| chr5:175488695 | C | CT | 15 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(12): Show |
15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-3397dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175488695 | ||||||
| chr5:175488761 | T | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-3334T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488761 | |||||||
| chr5:175488948 | G | T | 1 | a0001c0001t0009g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-9-3147G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488948 | |||||||
| chr5:175488968 | G | C | 1 | a0001c0002t0002g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-9-3127G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175488968 | |||||||
| chr5:175489037 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-3058C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489037 | |||||||
| chr5:175489119 | C | T | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-9-2976C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489119 | |||||||
| chr5:175489120 | T | TA | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-9-2975_-9-2974ins others(1): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489120 | |||||||
| chr5:175489281 | G | A | 6 | a0001c0001t0003g0178 a0001c0001t0014g0186 a0001c0001t0014g0187 others(3): Show |
6 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-2814G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489281 | |||||||
| chr5:175489401 | T | C | 158 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(155): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-9-2694T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489401 | |||||||
| chr5:175489405 | C | T | 3 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0124 |
3 | HG00735.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-9-2690C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489405 | |||||||
| chr5:175489442 | A | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(80): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-9-2653A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489442 | |||||||
| chr5:175489455 | G | A | 6 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-2640G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489455 | |||||||
| chr5:175489456 | A | G | 4 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-2639A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489456 | |||||||
| chr5:175489537 | A | G | 1 | a0001c0002t0002g0227 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-9-2558A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489537 | |||||||
| chr5:175489599 | G | A | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-9-2496G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489599 | |||||||
| chr5:175489621 | A | G | 1 | a0001c0001t0004g0052 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-9-2474A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489621 | |||||||
| chr5:175489652 | T | C | 192 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-9-2443T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489652 | |||||||
| chr5:175489749 | A | G | 1 | a0001c0002t0034g0338 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-9-2346A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489749 | |||||||
| chr5:175489907 | C | T | 16 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(13): Show |
16 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-2188C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489907 | |||||||
| chr5:175489943 | T | G | 1 | a0001c0001t0003g0264 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-9-2152T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175489943 | |||||||
| chr5:175490130 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-9-1965T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490130 | |||||||
| chr5:175490164 | C | T | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9-1931C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490164 | |||||||
| chr5:175490187 | T | C | 1 | a0001c0001t0005g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9-1908T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490187 | |||||||
| chr5:175490207 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-9-1888C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490207 | |||||||
| chr5:175490421 | T | C | 193 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(190): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-1674T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490421 | |||||||
| chr5:175490557 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1538A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490557 | |||||||
| chr5:175490603 | T | G | 186 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(183): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-9-1492T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490603 | |||||||
| chr5:175490859 | A | AT | 16 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(13): Show |
16 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-1236_-9-1235ins others(1): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490859 | |||||||
| chr5:175490859 | A | T | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1236A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490859 | |||||||
| chr5:175490861 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1234A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490861 | |||||||
| chr5:175490901 | A | T | 1 | a0001c0002t0002g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-9-1194A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490901 | |||||||
| chr5:175490991 | T | A | 15 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0091 others(12): Show |
15 | HG01952.hp2 HG02258.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-1104T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175490991 | |||||||
| chr5:175491007 | C | T | 173 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(170): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-9-1088C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491007 | |||||||
| chr5:175491035 | C | T | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-1060C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491035 | |||||||
| chr5:175491256 | T | A | 193 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(190): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-9-839T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491256 | |||||||
| chr5:175491313 | G | A | 141 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(138): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-9-782G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491313 | |||||||
| chr5:175491359 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-736C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491359 | |||||||
| chr5:175491389 | G | A | 157 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-9-706G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491389 | |||||||
| chr5:175491408 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-9-687G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491408 | |||||||
| chr5:175491445 | G | A | 1 | a0001c0002t0015g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9-650G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491445 | |||||||
| chr5:175491477 | C | CT | 14 | a0001c0001t0002g0169 a0001c0001t0003g0254 a0001c0001t0013g0248 others(11): Show |
14 | HG02074.hp1 HG02572.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-604dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175491477 | ||||||
| chr5:175491477 | CT | C | 17 | a0001c0001t0003g0342 a0001c0002t0036g0266 a0001c0003t0004g0072 others(14): Show |
17 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-604delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 175491477 | ||||||
| chr5:175491488 | T | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-607T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491488 | |||||||
| chr5:175491540 | T | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-555T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491540 | |||||||
| chr5:175491629 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0010g0123 |
2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-9-466C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491629 | |||||||
| chr5:175491687 | G | A | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-408G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491687 | |||||||
| chr5:175491720 | C | T | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-375C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491720 | |||||||
| chr5:175491777 | G | A | 157 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-9-318G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175491777 | |||||||
| chr5:175492053 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-42A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 1/10 | chr5 | 175492053 | |||||||
| chr5:175492387 | C | T | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+120C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492387 | |||||||
| chr5:175492388 | CA | C | 179 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(176): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.164+134delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175492388 | ||||||
| chr5:175492388 | CAA | C | 14 | a0001c0001t0001g0121 a0001c0001t0014g0189 a0001c0003t0004g0072 others(11): Show |
14 | HG00423.hp2 HG00558.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.164+133_164+134del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175492388 | ||||||
| chr5:175492427 | T | C | 2 | a0001c0001t0003g0178 a0001c0001t0054g0088 |
2 | NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.164+160T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492427 | |||||||
| chr5:175492447 | C | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.164+180C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492447 | |||||||
| chr5:175492456 | G | C | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+189G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492456 | |||||||
| chr5:175492641 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0041 |
2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.164+374G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492641 | |||||||
| chr5:175492741 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+474C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492741 | |||||||
| chr5:175492792 | G | A | 1 | a0001c0004t0006g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164+525G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492792 | |||||||
| chr5:175492859 | A | G | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.164+592A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492859 | |||||||
| chr5:175492946 | A | T | 1 | a0001c0002t0002g0243 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.164+679A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175492946 | |||||||
| chr5:175493012 | G | A | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+745G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493012 | |||||||
| chr5:175493035 | C | T | 3 | a0001c0002t0002g0321 a0001c0002t0006g0322 a0001c0002t0031g0256 |
3 | HG02145.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.164+768C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493035 | |||||||
| chr5:175493122 | G | A | 6 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(3): Show |
6 | HG02258.hp2 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+855G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493122 | |||||||
| chr5:175493126 | G | A | 1 | a0001c0003t0008g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.164+859G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493126 | |||||||
| chr5:175493184 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.164+917C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493184 | |||||||
| chr5:175493190 | C | T | 300 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(297): Show |
313 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.164+923C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493190 | |||||||
| chr5:175493248 | A | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+981A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493248 | |||||||
| chr5:175493269 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.164+1002A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493269 | |||||||
| chr5:175493344 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.164+1077G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493344 | |||||||
| chr5:175493517 | A | C | 3 | a0001c0002t0002g0284 a0001c0002t0002g0285 a0001c0002t0012g0214 |
3 | NA18957.hp1 NA18965.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.164+1250A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493517 | |||||||
| chr5:175493596 | C | T | 7 | a0001c0002t0002g0083 a0001c0002t0002g0183 a0001c0002t0015g0081 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+1329C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493596 | |||||||
| chr5:175493635 | A | G | 1 | a0001c0001t0003g0320 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.164+1368A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493635 | |||||||
| chr5:175493745 | G | A | 11 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(8): Show |
12 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+1478G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493745 | |||||||
| chr5:175493818 | A | G | 1 | a0001c0002t0041g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164+1551A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493818 | |||||||
| chr5:175493821 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0025g0133 |
2 | HG00544.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.164+1554C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493821 | |||||||
| chr5:175493830 | TA | T | 14 | a0001c0001t0001g0152 a0001c0001t0005g0005 a0001c0001t0005g0032 others(11): Show |
15 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.164+1566delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175493830 | ||||||
| chr5:175493965 | G | A | 1 | a0001c0004t0006g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164+1698G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175493965 | |||||||
| chr5:175494167 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0252 others(168): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.164+1900C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494167 | |||||||
| chr5:175494184 | A | G | 1 | a0001c0001t0003g0025 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.164+1917A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494184 | |||||||
| chr5:175494226 | T | A | 1 | a0001c0001t0005g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.164+1959T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494226 | |||||||
| chr5:175494428 | A | G | 117 | a0001c0001t0003g0276 a0001c0001t0009g0180 a0001c0001t0013g0063 others(114): Show |
127 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.164+2161A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494428 | |||||||
| chr5:175494440 | G | T | 1 | a0001c0012t0004g0337 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.164+2173G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494440 | |||||||
| chr5:175494470 | G | A | 3 | a0001c0001t0004g0004 a0001c0001t0004g0042 a0001c0001t0004g0157 |
4 | HG00544.hp1 HG02155.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2203G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494470 | |||||||
| chr5:175494515 | A | G | 3 | a0001c0001t0004g0004 a0001c0001t0004g0042 a0001c0001t0004g0157 |
4 | HG00544.hp1 HG02155.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2248A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494515 | |||||||
| chr5:175494576 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+2309C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494576 | |||||||
| chr5:175494580 | T | C | 2 | a0001c0001t0004g0158 a0001c0001t0004g0159 |
2 | NA18990.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.164+2313T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494580 | |||||||
| chr5:175494612 | C | T | 80 | a0001c0001t0013g0240 a0001c0001t0013g0241 a0001c0001t0018g0238 others(77): Show |
90 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.164+2345C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494612 | |||||||
| chr5:175494619 | G | A | 6 | a0001c0002t0002g0015 a0001c0002t0002g0326 a0001c0002t0002g0329 others(3): Show |
7 | HG00597.hp1 HG02080.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+2352G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494619 | |||||||
| chr5:175494727 | G | A | 4 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2460G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494727 | |||||||
| chr5:175494739 | C | T | 1 | a0001c0002t0012g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164+2472C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494739 | |||||||
| chr5:175494748 | A | G | 115 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(112): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+2481A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494748 | |||||||
| chr5:175494751 | T | TA | 7 | a0001c0001t0008g0156 a0001c0001t0014g0186 a0001c0001t0014g0187 others(4): Show |
7 | HG01109.hp2 HG02056.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+2498dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175494751 | ||||||
| chr5:175494793 | A | G | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+2526A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494793 | |||||||
| chr5:175494866 | G | A | 22 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(19): Show |
22 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.164+2599G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494866 | |||||||
| chr5:175494876 | A | G | 1 | a0001c0001t0005g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.164+2609A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175494876 | |||||||
| chr5:175495046 | G | A | 113 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(110): Show |
123 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.164+2779G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495046 | |||||||
| chr5:175495094 | T | C | 4 | a0001c0001t0018g0238 a0001c0001t0018g0311 a0001c0001t0018g0312 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2827T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495094 | |||||||
| chr5:175495174 | A | G | 14 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(11): Show |
15 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.164+2907A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495174 | |||||||
| chr5:175495207 | G | C | 1 | a0001c0001t0003g0323 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.164+2940G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495207 | |||||||
| chr5:175495247 | G | C | 2 | a0001c0001t0009g0180 a0001c0002t0064g0153 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.164+2980G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495247 | |||||||
| chr5:175495278 | G | T | 1 | a0001c0002t0041g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164+3011G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495278 | |||||||
| chr5:175495369 | A | G | 275 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(272): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.164+3102A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495369 | |||||||
| chr5:175495383 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(79): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.164+3116T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495383 | |||||||
| chr5:175495447 | G | T | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3180G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495447 | |||||||
| chr5:175495492 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+3225G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495492 | |||||||
| chr5:175495518 | C | T | 92 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(89): Show |
102 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.164+3251C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495518 | |||||||
| chr5:175495675 | C | G | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3408C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495675 | |||||||
| chr5:175495687 | C | T | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164+3420C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495687 | |||||||
| chr5:175495694 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.164+3427A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495694 | |||||||
| chr5:175495728 | C | CA | 104 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(101): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.164+3473dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495728 | ||||||
| chr5:175495728 | CA | C | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3473delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495728 | ||||||
| chr5:175495767 | C | T | 90 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(87): Show |
100 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.164+3500C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495767 | |||||||
| chr5:175495796 | C | A | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3529C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495796 | |||||||
| chr5:175495891 | G | A | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3624G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495891 | |||||||
| chr5:175495903 | C | CT | 8 | a0001c0001t0001g0056 a0001c0001t0001g0215 a0001c0001t0001g0216 others(5): Show |
8 | HG00597.hp2 HG02300.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+3650dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495903 | ||||||
| chr5:175495903 | CTT | C | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3649_164+3650d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175495903 | ||||||
| chr5:175495977 | A | G | 189 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(186): Show |
201 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.164+3710A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495977 | |||||||
| chr5:175495986 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.164+3719C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175495986 | |||||||
| chr5:175496041 | C | T | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3774C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496041 | |||||||
| chr5:175496109 | A | G | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+3842A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496109 | |||||||
| chr5:175496138 | T | G | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164+3871T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496138 | |||||||
| chr5:175496247 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.164+3980C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496247 | |||||||
| chr5:175496251 | C | T | 2 | a0001c0001t0009g0180 a0001c0002t0064g0153 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.164+3984C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496251 | |||||||
| chr5:175496278 | G | A | 1 | a0001c0002t0021g0257 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.164+4011G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496278 | |||||||
| chr5:175496299 | G | A | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164+4032G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496299 | |||||||
| chr5:175496358 | G | A | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+4091G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496358 | |||||||
| chr5:175496376 | A | G | 16 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(13): Show |
17 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.164+4109A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496376 | |||||||
| chr5:175496384 | T | C | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+4117T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496384 | |||||||
| chr5:175496401 | A | G | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+4134A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496401 | |||||||
| chr5:175496702 | C | G | 2 | a0001c0001t0009g0180 a0001c0002t0064g0153 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.164+4435C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496702 | |||||||
| chr5:175496756 | GAATCCCT others(909): Show |
G | 1 | a0001c0001t0016g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164+4496_164+5411d others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175496756 | ||||||
| chr5:175496898 | C | CT | 120 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0287 others(117): Show |
130 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.164+4642dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175496898 | ||||||
| chr5:175496950 | G | A | 2 | a0001c0004t0038g0038 a0001c0007t0040g0181 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164+4683G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496950 | |||||||
| chr5:175496967 | T | C | 275 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(272): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.164+4700T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175496967 | |||||||
| chr5:175497035 | A | G | 115 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(112): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+4768A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497035 | |||||||
| chr5:175497043 | T | C | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+4776T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497043 | |||||||
| chr5:175497364 | T | G | 1 | a0001c0001t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.164+5097T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497364 | |||||||
| chr5:175497644 | C | T | 115 | a0001c0001t0001g0137 a0001c0001t0009g0180 a0001c0001t0013g0063 others(112): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+5377C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497644 | |||||||
| chr5:175497657 | A | G | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164+5390A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497657 | |||||||
| chr5:175497717 | T | G | 1 | a0001c0002t0002g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.164+5450T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497717 | |||||||
| chr5:175497764 | G | A | 190 | a0001c0001t0001g0137 a0001c0001t0002g0169 a0001c0001t0004g0004 others(187): Show |
202 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.164+5497G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497764 | |||||||
| chr5:175497788 | G | A | 7 | a0001c0001t0013g0063 a0001c0001t0013g0248 a0001c0001t0013g0249 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+5521G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497788 | |||||||
| chr5:175497873 | T | A | 2 | a0001c0002t0006g0322 a0001c0002t0031g0256 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.164+5606T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497873 | |||||||
| chr5:175497936 | G | GA | 22 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0234 others(19): Show |
22 | HG00597.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.164+5688dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175497936 | ||||||
| chr5:175497936 | GA | G | 99 | a0001c0001t0001g0137 a0001c0001t0001g0197 a0001c0001t0003g0308 others(96): Show |
109 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.164+5688delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175497936 | ||||||
| chr5:175497967 | G | A | 1 | a0001c0001t0005g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.164+5700G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497967 | |||||||
| chr5:175497988 | T | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+5721T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175497988 | |||||||
| chr5:175498059 | A | AAAAT | 115 | a0001c0001t0001g0137 a0001c0001t0009g0180 a0001c0001t0013g0063 others(112): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.164+5795_164+5796i others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175498059 | ||||||
| chr5:175498084 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0010g0061 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.164+5817G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498084 | |||||||
| chr5:175498086 | AATTAATG others(21): Show |
A | 2 | a0001c0001t0016g0079 a0001c0001t0016g0080 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.164+5838_164+5865d others(30): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175498086 | ||||||
| chr5:175498102 | A | G | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+5835A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498102 | |||||||
| chr5:175498163 | A | C | 3 | a0001c0002t0002g0202 a0001c0002t0002g0242 a0001c0002t0002g0243 |
3 | HG01167.hp2 HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.164+5896A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498163 | |||||||
| chr5:175498172 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+5905G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498172 | |||||||
| chr5:175498282 | A | G | 1 | a0001c0002t0015g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.164+6015A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498282 | |||||||
| chr5:175498313 | T | C | 1 | a0001c0003t0007g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.164+6046T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498313 | |||||||
| chr5:175498346 | A | AC | 14 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.164+6080dupC | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175498346 | ||||||
| chr5:175498420 | C | T | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.164+6153C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498420 | |||||||
| chr5:175498493 | A | G | 16 | a0001c0001t0001g0137 a0001c0001t0009g0180 a0001c0002t0064g0153 others(13): Show |
16 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.164+6226A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498493 | |||||||
| chr5:175498650 | A | G | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.164+6383A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498650 | |||||||
| chr5:175498713 | G | A | 113 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(110): Show |
123 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.164+6446G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498713 | |||||||
| chr5:175498715 | A | G | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+6448A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498715 | |||||||
| chr5:175498824 | A | G | 114 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(111): Show |
124 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.164+6557A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498824 | |||||||
| chr5:175498838 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.164+6571G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175498838 | |||||||
| chr5:175499002 | C | T | 25 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(22): Show |
25 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.164+6735C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499002 | |||||||
| chr5:175499134 | T | A | 14 | a0001c0002t0064g0153 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.164+6867T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499134 | |||||||
| chr5:175499138 | C | T | 23 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(20): Show |
23 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.164+6871C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499138 | |||||||
| chr5:175499234 | A | G | 23 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(20): Show |
23 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.164+6967A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499234 | |||||||
| chr5:175499248 | C | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+6981C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499248 | |||||||
| chr5:175499257 | GA | G | 108 | a0001c0001t0005g0149 a0001c0001t0013g0063 a0001c0001t0013g0240 others(105): Show |
118 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.164+7002delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175499257 | ||||||
| chr5:175499270 | G | A | 19 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(16): Show |
19 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.164+7003G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499270 | |||||||
| chr5:175499273 | A | G | 39 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(36): Show |
40 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.164+7006A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499273 | |||||||
| chr5:175499312 | G | A | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.164+7045G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499312 | |||||||
| chr5:175499378 | A | T | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.164+7111A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499378 | |||||||
| chr5:175499451 | G | C | 1 | a0001c0001t0003g0276 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164+7184G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499451 | |||||||
| chr5:175499660 | C | A | 2 | a0001c0001t0004g0039 a0001c0001t0004g0045 |
2 | NA18982.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.164+7393C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499660 | |||||||
| chr5:175499680 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.164+7413T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499680 | |||||||
| chr5:175499835 | G | A | 2 | a0001c0001t0013g0240 a0001c0001t0013g0241 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.164+7568G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499835 | |||||||
| chr5:175499879 | T | C | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+7612T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175499879 | |||||||
| chr5:175500294 | T | A | 4 | a0001c0002t0011g0003 a0001c0002t0011g0204 a0001c0002t0011g0253 others(1): Show |
6 | NA18945.hp2 NA18955.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.164+8027T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175500294 | |||||||
| chr5:175500403 | A | AAC | 68 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0029 others(65): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.164+8186_164+8187d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | A | AACAC | 18 | a0001c0001t0001g0037 a0001c0001t0001g0116 a0001c0001t0001g0117 others(15): Show |
18 | HG00597.hp2 HG01192.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.164+8184_164+8187d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | A | AACACAC | 7 | a0001c0001t0001g0031 a0001c0001t0003g0054 a0001c0001t0003g0178 others(4): Show |
7 | HG00741.hp1 HG01981.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+8182_164+8187d others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | A | AACACACA others(3): Show |
1 | a0001c0001t0009g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164+8178_164+8187d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AAC | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0137 a0001c0001t0001g0152 others(36): Show |
40 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.164+8186_164+8187d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACAC | A | 19 | a0001c0001t0001g0017 a0001c0001t0001g0175 a0001c0001t0001g0176 others(16): Show |
19 | HG00423.hp2 HG00741.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.164+8184_164+8187d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACAC | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0197 a0001c0001t0003g0221 others(8): Show |
12 | HG01243.hp1 HG02109.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.164+8182_164+8187d others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(1): Show |
A | 12 | a0001c0001t0004g0046 a0001c0001t0005g0033 a0001c0001t0005g0333 others(9): Show |
12 | HG01169.hp2 HG02155.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.164+8180_164+8187d others(10): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(3): Show |
A | 20 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0034 others(17): Show |
21 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.164+8178_164+8187d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(5): Show |
A | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.164+8176_164+8187d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(7): Show |
A | 8 | a0001c0001t0020g0195 a0001c0001t0020g0196 a0001c0002t0002g0060 others(5): Show |
8 | HG00621.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+8174_164+8187d others(16): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(9): Show |
A | 7 | a0001c0002t0002g0013 a0001c0002t0002g0057 a0001c0002t0002g0058 others(4): Show |
8 | HG00673.hp1 HG01884.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+8172_164+8187d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(11): Show |
A | 72 | a0001c0001t0018g0238 a0001c0001t0018g0311 a0001c0001t0018g0312 others(69): Show |
81 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.164+8170_164+8187d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(13): Show |
A | 1 | a0001c0002t0032g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164+8168_164+8187d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500403 | AACACACA others(15): Show |
A | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+8166_164+8187d others(24): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175500403 | ||||||
| chr5:175500789 | G | A | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165-8243G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175500789 | |||||||
| chr5:175501063 | A | AT | 37 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0145 others(34): Show |
37 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.165-7946dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501063 | A | ATT | 8 | a0001c0001t0020g0195 a0001c0001t0020g0196 a0001c0001t0063g0146 others(5): Show |
8 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-7947_165-7946d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501063 | A | ATTT | 18 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(15): Show |
18 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.165-7948_165-7946d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501063 | A | ATTTT | 7 | a0001c0001t0005g0005 a0001c0001t0005g0124 a0001c0001t0009g0180 others(4): Show |
7 | HG00735.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-7949_165-7946d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501063 | AT | A | 11 | a0001c0002t0002g0001 a0001c0002t0002g0224 a0001c0002t0002g0283 others(8): Show |
11 | HG00621.hp1 HG01258.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.165-7946delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501063 | ATT | A | 80 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(77): Show |
88 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.165-7947_165-7946d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501063 | ATTT | A | 22 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(19): Show |
22 | HG00741.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.165-7948_165-7946d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501063 | ||||||
| chr5:175501129 | C | T | 86 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(83): Show |
96 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.165-7903C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501129 | |||||||
| chr5:175501192 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18747.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.165-7840C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501192 | |||||||
| chr5:175501194 | G | A | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7838G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501194 | |||||||
| chr5:175501195 | A | G | 1 | a0001c0002t0002g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.165-7837A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501195 | |||||||
| chr5:175501225 | C | A | 1 | a0003c0011t0004g0074 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.165-7807C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501225 | |||||||
| chr5:175501244 | A | AT | 4 | a0001c0001t0018g0238 a0001c0001t0018g0311 a0001c0001t0018g0312 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-7783dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175501244 | ||||||
| chr5:175501261 | G | A | 4 | a0001c0002t0002g0016 a0001c0002t0002g0316 a0001c0002t0012g0016 others(1): Show |
4 | NA18948.hp2 NA18966.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-7771G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501261 | |||||||
| chr5:175501306 | T | G | 4 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-7726T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501306 | |||||||
| chr5:175501320 | G | A | 1 | a0001c0001t0010g0286 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.165-7712G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501320 | |||||||
| chr5:175501360 | G | A | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.165-7672G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501360 | |||||||
| chr5:175501615 | A | G | 13 | a0001c0003t0004g0072 a0001c0003t0007g0021 a0001c0003t0007g0070 others(10): Show |
13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-7417A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501615 | |||||||
| chr5:175501796 | C | T | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165-7236C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501796 | |||||||
| chr5:175501803 | T | G | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7229T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501803 | |||||||
| chr5:175501925 | A | T | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7107A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501925 | |||||||
| chr5:175501996 | C | G | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-7036C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175501996 | |||||||
| chr5:175502153 | G | A | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-6879G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502153 | |||||||
| chr5:175502223 | G | T | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-6809G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502223 | |||||||
| chr5:175502286 | A | T | 1 | a0001c0002t0002g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165-6746A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502286 | |||||||
| chr5:175502373 | A | G | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-6659A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502373 | |||||||
| chr5:175502553 | G | A | 1 | a0001c0002t0002g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.165-6479G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502553 | |||||||
| chr5:175502597 | G | A | 1 | a0001c0002t0015g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.165-6435G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502597 | |||||||
| chr5:175502656 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-6376A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502656 | |||||||
| chr5:175502698 | G | A | 1 | a0001c0001t0003g0171 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.165-6334G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502698 | |||||||
| chr5:175502829 | A | G | 53 | a0001c0001t0001g0137 a0001c0001t0009g0180 a0001c0001t0013g0063 others(50): Show |
53 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.165-6203A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502829 | |||||||
| chr5:175502861 | T | TAATA | 28 | a0001c0001t0001g0137 a0001c0001t0013g0063 a0001c0001t0013g0240 others(25): Show |
28 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.165-6157_165-6154d others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175502861 | ||||||
| chr5:175502988 | G | A | 2 | a0001c0001t0020g0195 a0001c0001t0020g0196 |
2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.165-6044G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175502988 | |||||||
| chr5:175503237 | A | G | 14 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-5795A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503237 | |||||||
| chr5:175503316 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.165-5716C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503316 | |||||||
| chr5:175503396 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.165-5636C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503396 | |||||||
| chr5:175503449 | G | A | 168 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(165): Show |
180 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.165-5583G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503449 | |||||||
| chr5:175503453 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0003g0185 a0001c0001t0045g0198 |
3 | HG02486.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.165-5579A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503453 | |||||||
| chr5:175503661 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.165-5371C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503661 | |||||||
| chr5:175503744 | C | T | 111 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(108): Show |
113 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.165-5288C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503744 | |||||||
| chr5:175503745 | A | G | 191 | a0001c0001t0001g0137 a0001c0001t0002g0169 a0001c0001t0004g0004 others(188): Show |
203 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.165-5287A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503745 | |||||||
| chr5:175503831 | C | T | 21 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(18): Show |
21 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.165-5201C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503831 | |||||||
| chr5:175503870 | G | A | 1 | a0001c0001t0003g0297 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.165-5162G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503870 | |||||||
| chr5:175503875 | G | A | 1 | a0001c0001t0017g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165-5157G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503875 | |||||||
| chr5:175503904 | T | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-5128T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503904 | |||||||
| chr5:175503912 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.165-5120G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503912 | |||||||
| chr5:175503927 | CT | C | 60 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(57): Show |
62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5104delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503927 | |||||||
| chr5:175503928 | T | C | 23 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(20): Show |
23 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.165-5104T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503928 | |||||||
| chr5:175503929 | G | C | 60 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(57): Show |
62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5103G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503929 | |||||||
| chr5:175503931 | G | C | 60 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(57): Show |
62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5101G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503931 | |||||||
| chr5:175503932 | A | T | 60 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(57): Show |
62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.165-5100A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503932 | |||||||
| chr5:175503959 | C | T | 78 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(75): Show |
88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165-5073C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503959 | |||||||
| chr5:175503972 | T | C | 20 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(17): Show |
20 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-5060T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503972 | |||||||
| chr5:175503993 | C | T | 78 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(75): Show |
88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165-5039C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175503993 | |||||||
| chr5:175504003 | C | CAA | 23 | a0001c0001t0005g0033 a0001c0001t0013g0063 a0001c0001t0013g0240 others(20): Show |
23 | HG01169.hp2 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.165-5013_165-5012d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | ||||||
| chr5:175504003 | C | CAAA | 27 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0034 others(24): Show |
28 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.165-5014_165-5012d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | ||||||
| chr5:175504003 | C | CAAAAA | 38 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(35): Show |
39 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.165-5016_165-5012d others(7): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | ||||||
| chr5:175504003 | CA | C | 6 | a0001c0001t0001g0136 a0001c0001t0003g0324 a0001c0001t0003g0335 others(3): Show |
6 | HG01257.hp2 HG01515.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-5012delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504003 | ||||||
| chr5:175504023 | G | A | 99 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(96): Show |
101 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.165-5009G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504023 | |||||||
| chr5:175504054 | G | A | 1 | a0001c0003t0008g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.165-4978G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504054 | |||||||
| chr5:175504416 | AAC | A | 23 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(20): Show |
23 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.165-4612_165-4611d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504416 | ||||||
| chr5:175504429 | A | G | 36 | a0001c0001t0009g0180 a0001c0002t0002g0057 a0001c0002t0002g0058 others(33): Show |
36 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.165-4603A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504429 | |||||||
| chr5:175504431 | C | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-4601C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504431 | |||||||
| chr5:175504443 | C | T | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-4589C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504443 | |||||||
| chr5:175504504 | G | A | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.165-4528G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504504 | |||||||
| chr5:175504573 | C | CA | 9 | a0001c0001t0003g0218 a0001c0001t0014g0186 a0001c0001t0014g0187 others(6): Show |
10 | HG02109.hp2 HG02155.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.165-4445dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504573 | ||||||
| chr5:175504573 | CA | C | 12 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(9): Show |
12 | HG01256.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.165-4445delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175504573 | ||||||
| chr5:175504577 | A | C | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-4455A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504577 | |||||||
| chr5:175504768 | G | T | 1 | a0001c0001t0013g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165-4264G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504768 | |||||||
| chr5:175504821 | C | T | 5 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0014g0186 others(2): Show |
5 | NA18747.hp2 NA18939.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-4211C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504821 | |||||||
| chr5:175504829 | C | T | 5 | a0001c0001t0003g0035 a0001c0001t0003g0129 a0001c0001t0003g0130 others(2): Show |
5 | HG01192.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-4203C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504829 | |||||||
| chr5:175504874 | G | A | 12 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(9): Show |
12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-4158G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504874 | |||||||
| chr5:175504936 | G | T | 58 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(55): Show |
60 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.165-4096G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175504936 | |||||||
| chr5:175505008 | A | G | 113 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(110): Show |
123 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.165-4024A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505008 | |||||||
| chr5:175505020 | A | G | 131 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(128): Show |
141 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.165-4012A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505020 | |||||||
| chr5:175505026 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.165-4006C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505026 | |||||||
| chr5:175505067 | C | T | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165-3965C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505067 | |||||||
| chr5:175505083 | C | T | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-3949C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505083 | |||||||
| chr5:175505125 | A | T | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165-3907A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505125 | |||||||
| chr5:175505206 | A | G | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0101 others(3): Show |
6 | HG01106.hp2 HG01433.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-3826A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505206 | |||||||
| chr5:175505218 | A | G | 1 | a0001c0002t0002g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.165-3814A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505218 | |||||||
| chr5:175505312 | A | C | 1 | a0001c0002t0002g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.165-3720A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505312 | |||||||
| chr5:175505390 | A | G | 6 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-3642A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505390 | |||||||
| chr5:175505536 | A | T | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-3496A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505536 | |||||||
| chr5:175505537 | C | CAAT | 13 | a0001c0001t0001g0152 a0001c0001t0003g0025 a0001c0001t0003g0141 others(10): Show |
13 | HG01952.hp2 HG02165.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-3461_165-3459d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | C | CAATAAT | 9 | a0001c0001t0001g0252 a0001c0001t0003g0035 a0001c0001t0003g0129 others(6): Show |
9 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-3464_165-3459d others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | C | CAATAATA others(2): Show |
20 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0105 others(17): Show |
21 | HG00558.hp2 HG00609.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.165-3467_165-3459d others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | C | CAATAATA others(5): Show |
51 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0029 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.165-3470_165-3459d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | C | CAATAATA others(8): Show |
19 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0055 others(16): Show |
19 | HG00140.hp1 HG00544.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.165-3473_165-3459d others(17): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | C | CAATAATA others(11): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0062 a0001c0001t0001g0121 others(2): Show |
5 | HG00558.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-3476_165-3459d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | C | CAATAATA others(17): Show |
1 | a0001c0001t0014g0189 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.165-3482_165-3459d others(26): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | CAAT | C | 55 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(52): Show |
57 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.165-3461_165-3459d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | CAATAATA others(2): Show |
C | 2 | a0001c0002t0002g0015 a0001c0002t0064g0153 |
3 | HG02109.hp2 NA18969.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.165-3467_165-3459d others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505537 | CAATAATA others(5): Show |
C | 108 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(105): Show |
117 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.165-3470_165-3459d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175505537 | ||||||
| chr5:175505582 | T | G | 102 | a0001c0001t0009g0180 a0001c0002t0002g0001 a0001c0002t0002g0008 others(99): Show |
112 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.165-3450T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505582 | |||||||
| chr5:175505663 | G | C | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-3369G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505663 | |||||||
| chr5:175505671 | T | C | 1 | a0001c0001t0003g0297 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.165-3361T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505671 | |||||||
| chr5:175505711 | A | G | 130 | a0001c0001t0001g0137 a0001c0001t0009g0180 a0001c0001t0013g0063 others(127): Show |
140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.165-3321A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505711 | |||||||
| chr5:175505809 | T | C | 125 | a0001c0001t0001g0137 a0001c0001t0009g0180 a0001c0001t0013g0063 others(122): Show |
135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.165-3223T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505809 | |||||||
| chr5:175505875 | A | G | 4 | a0001c0001t0003g0218 a0001c0001t0003g0244 a0001c0001t0003g0308 others(1): Show |
4 | HG02083.hp1 NA18981.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-3157A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505875 | |||||||
| chr5:175505937 | T | C | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-3095T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505937 | |||||||
| chr5:175505961 | C | T | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-3071C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175505961 | |||||||
| chr5:175506060 | T | C | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2972T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506060 | |||||||
| chr5:175506088 | G | C | 112 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(109): Show |
122 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.165-2944G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506088 | |||||||
| chr5:175506339 | G | A | 2 | a0001c0001t0024g0219 a0001c0002t0064g0153 |
2 | HG02071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.165-2693G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506339 | |||||||
| chr5:175506362 | A | T | 8 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(5): Show |
8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-2670A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506362 | |||||||
| chr5:175506410 | G | A | 1 | a0001c0001t0055g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165-2622G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506410 | |||||||
| chr5:175506459 | T | C | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-2573T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506459 | |||||||
| chr5:175506479 | C | A | 2 | a0001c0002t0006g0322 a0001c0002t0031g0256 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.165-2553C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506479 | |||||||
| chr5:175506576 | T | C | 1 | a0001c0001t0016g0079 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165-2456T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506576 | |||||||
| chr5:175506653 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.165-2379A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506653 | |||||||
| chr5:175506659 | T | A | 189 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(186): Show |
201 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.165-2373T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506659 | |||||||
| chr5:175506728 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2304A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506728 | |||||||
| chr5:175506754 | C | T | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2278C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506754 | |||||||
| chr5:175506817 | A | C | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2215A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506817 | |||||||
| chr5:175506924 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-2108A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506924 | |||||||
| chr5:175506953 | C | T | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-2079C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506953 | |||||||
| chr5:175506961 | G | A | 1 | a0004c0006t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165-2071G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175506961 | |||||||
| chr5:175507043 | A | G | 1 | a0001c0001t0013g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165-1989A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507043 | |||||||
| chr5:175507059 | A | G | 91 | a0001c0001t0009g0180 a0001c0002t0002g0001 a0001c0002t0002g0008 others(88): Show |
101 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.165-1973A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507059 | |||||||
| chr5:175507122 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1910A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507122 | |||||||
| chr5:175507128 | C | T | 2 | a0001c0002t0002g0212 a0001c0002t0002g0278 |
2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.165-1904C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507128 | |||||||
| chr5:175507168 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.165-1864A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507168 | |||||||
| chr5:175507198 | A | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-1834A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507198 | |||||||
| chr5:175507211 | A | G | 7 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(4): Show |
7 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-1821A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507211 | |||||||
| chr5:175507333 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1699A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507333 | |||||||
| chr5:175507434 | A | G | 14 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1598A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507434 | |||||||
| chr5:175507435 | A | T | 14 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1597A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507435 | |||||||
| chr5:175507473 | A | C | 14 | a0001c0001t0001g0137 a0001c0003t0004g0072 a0001c0003t0007g0021 others(11): Show |
14 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1559A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507473 | |||||||
| chr5:175507479 | A | G | 58 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(55): Show |
60 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.165-1553A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507479 | |||||||
| chr5:175507553 | T | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1479T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507553 | |||||||
| chr5:175507554 | A | G | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165-1478A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507554 | |||||||
| chr5:175507586 | A | T | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1446A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507586 | |||||||
| chr5:175507594 | T | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1438T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507594 | |||||||
| chr5:175507620 | C | T | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1412C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507620 | |||||||
| chr5:175507627 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165-1405C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507627 | |||||||
| chr5:175507652 | A | G | 39 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(36): Show |
40 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.165-1380A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507652 | |||||||
| chr5:175507658 | C | T | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-1374C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507658 | |||||||
| chr5:175507663 | A | G | 1 | a0004c0006t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165-1369A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507663 | |||||||
| chr5:175507682 | G | A | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-1350G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507682 | |||||||
| chr5:175507804 | C | T | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-1228C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507804 | |||||||
| chr5:175507850 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-1182A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507850 | |||||||
| chr5:175507970 | C | CT | 38 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(35): Show |
39 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.165-1059dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507970 | ||||||
| chr5:175507973 | T | TAAAAAAA | 10 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.165-1046_165-1040d others(9): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | ||||||
| chr5:175507973 | T | TAAAATAA others(2): Show |
16 | a0001c0002t0002g0057 a0001c0002t0002g0083 a0001c0002t0002g0150 others(13): Show |
16 | HG01884.hp2 HG02080.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.165-1055_165-1054i others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | ||||||
| chr5:175507973 | T | TAAAATAA others(3): Show |
3 | a0001c0002t0002g0058 a0001c0002t0015g0082 a0001c0002t0041g0151 |
3 | HG02257.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.165-1055_165-1054i others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | ||||||
| chr5:175507973 | TA | T | 100 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(97): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.165-1040delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507973 | ||||||
| chr5:175507974 | A | AAAATAAA others(3): Show |
6 | a0001c0002t0015g0081 a0001c0002t0015g0085 a0001c0002t0015g0096 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-1055_165-1054i others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507974 | ||||||
| chr5:175507975 | A | AAATAAAA others(2): Show |
71 | a0001c0001t0009g0180 a0001c0002t0002g0001 a0001c0002t0002g0008 others(68): Show |
81 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.165-1055_165-1054i others(11): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175507975 | ||||||
| chr5:175507992 | A | G | 3 | a0001c0002t0002g0224 a0001c0002t0002g0318 a0001c0002t0029g0319 |
3 | HG00738.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.165-1040A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507992 | |||||||
| chr5:175507994 | T | C | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-1038T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175507994 | |||||||
| chr5:175508080 | A | G | 3 | a0001c0003t0004g0072 a0001c0003t0008g0023 a0003c0011t0004g0074 |
3 | HG00741.hp2 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.165-952A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508080 | |||||||
| chr5:175508110 | A | G | 13 | a0001c0003t0004g0072 a0001c0003t0007g0021 a0001c0003t0007g0070 others(10): Show |
13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-922A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508110 | |||||||
| chr5:175508156 | A | G | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-876A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508156 | |||||||
| chr5:175508217 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-815A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508217 | |||||||
| chr5:175508222 | A | AT | 52 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(49): Show |
54 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.165-784dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | ||||||
| chr5:175508222 | A | ATT | 12 | a0001c0001t0002g0169 a0001c0001t0004g0160 a0001c0001t0004g0162 others(9): Show |
12 | HG00621.hp2 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-785_165-784dup others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | ||||||
| chr5:175508222 | AT | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(206): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.165-784delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | ||||||
| chr5:175508222 | ATT | A | 16 | a0001c0001t0003g0091 a0001c0001t0014g0186 a0001c0001t0014g0187 others(13): Show |
16 | HG02155.hp2 HG02717.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-785_165-784del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | ||||||
| chr5:175508222 | ATTTT | A | 11 | a0001c0003t0007g0070 a0001c0003t0007g0073 a0001c0003t0007g0075 others(8): Show |
11 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.165-787_165-784del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | ||||||
| chr5:175508222 | ATTTTT | A | 10 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(7): Show |
10 | HG01257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.165-788_165-784del others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508222 | ||||||
| chr5:175508281 | A | G | 2 | a0001c0002t0002g0329 a0001c0002t0002g0330 |
2 | HG00597.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.165-751A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508281 | |||||||
| chr5:175508291 | T | C | 1 | a0001c0002t0002g0194 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165-741T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508291 | |||||||
| chr5:175508319 | G | A | 2 | a0001c0002t0002g0209 a0001c0002t0064g0153 |
2 | HG01993.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.165-713G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508319 | |||||||
| chr5:175508325 | A | C | 2 | a0001c0001t0001g0273 a0001c0001t0061g0270 |
2 | NA18946.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.165-707A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508325 | |||||||
| chr5:175508416 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-616A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508416 | |||||||
| chr5:175508443 | A | C | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-589A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508443 | |||||||
| chr5:175508457 | A | G | 13 | a0001c0003t0004g0072 a0001c0003t0007g0021 a0001c0003t0007g0070 others(10): Show |
13 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165-575A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508457 | |||||||
| chr5:175508474 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-558A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508474 | |||||||
| chr5:175508526 | C | T | 4 | a0001c0001t0016g0079 a0001c0001t0016g0080 a0001c0001t0016g0155 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-506C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508526 | |||||||
| chr5:175508568 | A | G | 111 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-464A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508568 | |||||||
| chr5:175508610 | C | G | 1 | a0001c0004t0038g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165-422C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508610 | |||||||
| chr5:175508645 | A | AT | 111 | a0001c0001t0005g0148 a0001c0001t0009g0180 a0001c0001t0013g0063 others(108): Show |
121 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.165-376dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 175508645 | ||||||
| chr5:175508793 | G | A | 102 | a0001c0001t0009g0180 a0001c0002t0002g0001 a0001c0002t0002g0008 others(99): Show |
112 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.165-239G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508793 | |||||||
| chr5:175508826 | C | T | 27 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(24): Show |
27 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.165-206C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508826 | |||||||
| chr5:175508857 | T | G | 102 | a0001c0001t0009g0180 a0001c0002t0002g0001 a0001c0002t0002g0008 others(99): Show |
112 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.165-175T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508857 | |||||||
| chr5:175508913 | A | G | 129 | a0001c0001t0009g0180 a0001c0001t0013g0063 a0001c0001t0013g0240 others(126): Show |
139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.165-119A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508913 | |||||||
| chr5:175508973 | T | A | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165-59T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 2/10 | chr5 | 175508973 | |||||||
| chr5:175509230 | T | C | 23 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0004g0040 others(20): Show |
23 | HG00621.hp2 HG00673.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.335+28T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509230 | |||||||
| chr5:175509309 | T | G | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.335+107T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509309 | |||||||
| chr5:175509315 | GACAA | G | 3 | a0001c0002t0064g0153 a0002c0005t0023g0182 a0002c0005t0023g0184 |
3 | HG02109.hp2 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.335+118_335+121del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 175509315 | ||||||
| chr5:175509364 | A | G | 13 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(10): Show |
13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.335+162A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509364 | |||||||
| chr5:175509455 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.335+253A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509455 | |||||||
| chr5:175509517 | C | CT | 8 | a0001c0001t0001g0031 a0001c0001t0001g0108 a0001c0001t0001g0109 others(5): Show |
8 | HG01981.hp1 HG01981.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.335+326dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 175509517 | ||||||
| chr5:175509559 | T | C | 12 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(9): Show |
12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.335+357T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509559 | |||||||
| chr5:175509699 | A | G | 86 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(83): Show |
96 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.336-410A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509699 | |||||||
| chr5:175509699 | A | T | 12 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(9): Show |
12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.336-410A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175509699 | |||||||
| chr5:175510061 | C | A | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.336-48C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 3/10 | chr5 | 175510061 | |||||||
| chr5:175510417 | T | C | 1 | a0001c0001t0046g0089 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.434+210T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510417 | |||||||
| chr5:175510480 | T | G | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.434+273T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510480 | |||||||
| chr5:175510500 | A | G | 1 | a0001c0002t0041g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.434+293A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510500 | |||||||
| chr5:175510520 | G | A | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.434+313G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510520 | |||||||
| chr5:175510732 | TA | T | 8 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(5): Show |
8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.434+535delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 175510732 | ||||||
| chr5:175510772 | G | A | 98 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(95): Show |
108 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.434+565G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510772 | |||||||
| chr5:175510795 | A | T | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.434+588A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510795 | |||||||
| chr5:175510972 | T | C | 129 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(126): Show |
139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.435-479T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510972 | |||||||
| chr5:175510980 | CTT | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0121 a0001c0001t0001g0134 others(4): Show |
7 | HG00558.hp1 NA18747.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-470_435-469del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175510980 | |||||||
| chr5:175511009 | T | G | 98 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(95): Show |
108 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.435-442T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175511009 | |||||||
| chr5:175511141 | G | T | 1 | a0001c0001t0005g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.435-310G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175511141 | |||||||
| chr5:175511439 | T | C | 1 | a0001c0001t0004g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.435-12T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 4/10 | chr5 | 175511439 | |||||||
| chr5:175511691 | A | T | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+165A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511691 | |||||||
| chr5:175511740 | CTG | C | 85 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.510+218_510+219del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511740 | ||||||
| chr5:175511763 | C | G | 1 | a0001c0002t0012g0214 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510+237C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511763 | |||||||
| chr5:175511817 | A | T | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.510+291A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511817 | |||||||
| chr5:175511821 | C | G | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-290C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511821 | |||||||
| chr5:175511822 | T | C | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-289T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511822 | |||||||
| chr5:175511823 | C | A | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-288C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511823 | |||||||
| chr5:175511824 | T | G | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-287T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511824 | |||||||
| chr5:175511838 | A | C | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-273A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511838 | |||||||
| chr5:175511839 | G | A | 1 | a0001c0001t0024g0246 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.511-272G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511839 | |||||||
| chr5:175511841 | A | ATC | 3 | a0001c0002t0064g0153 a0002c0005t0023g0182 a0002c0005t0023g0184 |
3 | HG02109.hp2 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-249_511-248dup others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | ||||||
| chr5:175511841 | A | ATCTCTC | 84 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(81): Show |
94 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.511-253_511-248dup others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | ||||||
| chr5:175511841 | A | ATCTCTCT others(1): Show |
9 | a0001c0002t0002g0283 a0001c0002t0002g0284 a0001c0002t0002g0285 others(6): Show |
9 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-255_511-248dup others(8): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | ||||||
| chr5:175511841 | A | ATCTCTCT others(3): Show |
1 | a0001c0002t0006g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.511-257_511-248dup others(10): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | ||||||
| chr5:175511841 | A | ATCTCTCT others(5): Show |
2 | a0001c0002t0031g0256 a0001c0004t0038g0038 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.511-259_511-248dup others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511841 | ||||||
| chr5:175511860 | TCTCC | T | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.511-249_511-246del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511860 | ||||||
| chr5:175511862 | TCC | T | 19 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(16): Show |
19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.511-246_511-245del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr5 | 175511862 | ||||||
| chr5:175511864 | C | T | 95 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(92): Show |
105 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.511-247C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175511864 | |||||||
| chr5:175512013 | A | T | 2 | a0001c0001t0003g0295 a0001c0001t0003g0303 |
2 | NA18984.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.511-98A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175512013 | |||||||
| chr5:175512075 | A | G | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.511-36A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 5/10 | chr5 | 175512075 | |||||||
| chr5:175512211 | C | T | 101 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(98): Show |
111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.596+15C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512211 | |||||||
| chr5:175512223 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.596+27G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512223 | |||||||
| chr5:175512334 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.596+138A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512334 | |||||||
| chr5:175512387 | G | A | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+191G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512387 | |||||||
| chr5:175512424 | G | A | 101 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0013 others(98): Show |
111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.596+228G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512424 | |||||||
| chr5:175512461 | C | T | 337 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(334): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.596+265C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512461 | |||||||
| chr5:175512631 | G | T | 27 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(24): Show |
27 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.596+435G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512631 | |||||||
| chr5:175512636 | A | G | 4 | a0001c0001t0018g0238 a0001c0001t0018g0311 a0001c0001t0018g0312 others(1): Show |
4 | HG01433.hp2 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+440A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512636 | |||||||
| chr5:175512692 | G | A | 12 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0083 others(9): Show |
12 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.596+496G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512692 | |||||||
| chr5:175512703 | G | T | 5 | a0001c0001t0013g0240 a0001c0001t0013g0241 a0001c0001t0013g0248 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+507G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512703 | |||||||
| chr5:175512780 | T | C | 1 | a0001c0007t0040g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.596+584T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512780 | |||||||
| chr5:175512855 | A | C | 4 | a0001c0002t0002g0083 a0001c0002t0002g0150 a0001c0002t0002g0191 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-608A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175512855 | |||||||
| chr5:175513000 | A | T | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.597-463A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513000 | |||||||
| chr5:175513027 | G | A | 1 | a0001c0003t0007g0231 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.597-436G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513027 | |||||||
| chr5:175513138 | T | TAAAAATA others(337): Show |
1 | a0001c0001t0004g0046 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.597-308_597-307ins others(344): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513138 | ||||||
| chr5:175513175 | C | T | 19 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(16): Show |
19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.597-288C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513175 | |||||||
| chr5:175513177 | G | A | 19 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(16): Show |
19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.597-286G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513177 | |||||||
| chr5:175513191 | T | C | 2 | a0001c0002t0006g0322 a0001c0002t0031g0256 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.597-272T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513191 | |||||||
| chr5:175513193 | G | T | 1 | a0001c0004t0038g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.597-270G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513193 | |||||||
| chr5:175513233 | A | G | 129 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(126): Show |
139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.597-230A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513233 | |||||||
| chr5:175513294 | TGTAAAAA others(8): Show |
T | 1 | a0001c0003t0004g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.597-168_597-154del others(15): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513294 | |||||||
| chr5:175513296 | TA | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0029 others(66): Show |
75 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.597-139delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513296 | TAA | T | 88 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0017 others(85): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.597-140_597-139del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513296 | TAAA | T | 51 | a0001c0001t0002g0169 a0001c0001t0004g0041 a0001c0001t0004g0043 others(48): Show |
57 | HG00099.hp1 HG00597.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-141_597-139del others(3): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513296 | TAAAA | T | 82 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(79): Show |
84 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.597-142_597-139del others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513296 | TAAAAA | T | 15 | a0001c0001t0004g0004 a0001c0001t0004g0275 a0001c0001t0026g0233 others(12): Show |
15 | HG00140.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-143_597-139del others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513296 | TAAAAAA | T | 8 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(5): Show |
8 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-144_597-139del others(6): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513296 | TAAAAAAA others(6): Show |
T | 18 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(15): Show |
18 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.597-151_597-139del others(13): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 175513296 | ||||||
| chr5:175513310 | A | C | 1 | a0001c0001t0003g0344 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.597-153A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513310 | |||||||
| chr5:175513313 | A | C | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.597-150A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513313 | |||||||
| chr5:175513366 | G | C | 3 | a0001c0002t0002g0284 a0001c0002t0002g0285 a0001c0002t0012g0214 |
3 | NA18957.hp1 NA18965.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.597-97G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513366 | |||||||
| chr5:175513394 | A | G | 1 | a0001c0001t0009g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.597-69A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 6/10 | chr5 | 175513394 | |||||||
| chr5:175513678 | C | T | 5 | a0001c0001t0013g0240 a0001c0001t0013g0241 a0001c0001t0013g0248 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+88C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513678 | |||||||
| chr5:175513691 | A | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+101A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513691 | |||||||
| chr5:175513787 | G | A | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.724+197G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513787 | |||||||
| chr5:175513789 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+199G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513789 | |||||||
| chr5:175513795 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0232 |
3 | NA18948.hp1 NA18969.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.724+205G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513795 | |||||||
| chr5:175513849 | T | A | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.724+259T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513849 | |||||||
| chr5:175513996 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0121 a0001c0001t0001g0134 others(4): Show |
7 | HG00558.hp1 NA18747.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+406C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175513996 | |||||||
| chr5:175514036 | C | T | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.724+446C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514036 | |||||||
| chr5:175514136 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.724+546G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514136 | |||||||
| chr5:175514222 | G | A | 21 | a0001c0001t0003g0093 a0001c0001t0014g0186 a0001c0001t0014g0187 others(18): Show |
21 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.724+632G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514222 | |||||||
| chr5:175514347 | C | G | 90 | a0001c0001t0002g0169 a0001c0002t0002g0001 a0001c0002t0002g0008 others(87): Show |
100 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.724+757C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514347 | |||||||
| chr5:175514421 | C | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+831C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514421 | |||||||
| chr5:175514435 | G | A | 1 | a0004c0006t0003g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.724+845G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514435 | |||||||
| chr5:175514633 | G | A | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.724+1043G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514633 | |||||||
| chr5:175514687 | AG | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+1099delG | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 175514687 | ||||||
| chr5:175514715 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+1125G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514715 | |||||||
| chr5:175514807 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.724+1217C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514807 | |||||||
| chr5:175514862 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0110 |
2 | HG00099.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.724+1272G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514862 | |||||||
| chr5:175514882 | A | G | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.724+1292A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514882 | |||||||
| chr5:175514929 | A | G | 19 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(16): Show |
19 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.724+1339A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514929 | |||||||
| chr5:175514936 | T | A | 2 | a0001c0002t0002g0314 a0001c0002t0002g0317 |
2 | HG02683.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.724+1346T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514936 | |||||||
| chr5:175514974 | C | T | 5 | a0001c0002t0002g0067 a0001c0002t0002g0225 a0001c0002t0002g0229 others(2): Show |
5 | HG02723.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+1384C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175514974 | |||||||
| chr5:175515026 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.724+1436T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515026 | |||||||
| chr5:175515069 | C | T | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.724+1479C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515069 | |||||||
| chr5:175515176 | C | G | 101 | a0001c0001t0002g0169 a0001c0001t0057g0179 a0001c0002t0002g0001 others(98): Show |
111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.725-1438C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515176 | |||||||
| chr5:175515205 | CAG | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.725-1408_725-1407d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515205 | |||||||
| chr5:175515302 | C | T | 1 | a0001c0001t0003g0320 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.725-1312C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515302 | |||||||
| chr5:175515303 | G | A | 1 | a0001c0001t0062g0049 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.725-1311G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515303 | |||||||
| chr5:175515323 | T | C | 1 | a0001c0001t0003g0293 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.725-1291T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515323 | |||||||
| chr5:175515365 | T | A | 38 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(35): Show |
39 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.725-1249T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515365 | |||||||
| chr5:175515381 | G | C | 6 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.725-1233G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515381 | |||||||
| chr5:175515470 | T | C | 12 | a0001c0003t0004g0072 a0001c0003t0007g0021 a0001c0003t0007g0070 others(9): Show |
12 | HG00423.hp2 HG00741.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.725-1144T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515470 | |||||||
| chr5:175515496 | T | C | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.725-1118T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515496 | |||||||
| chr5:175515515 | T | C | 4 | a0001c0001t0013g0063 a0001c0001t0019g0064 a0001c0001t0019g0065 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.725-1099T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515515 | |||||||
| chr5:175515516 | G | A | 1 | a0001c0001t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.725-1098G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515516 | |||||||
| chr5:175515554 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.725-1060G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515554 | |||||||
| chr5:175515858 | C | T | 57 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(54): Show |
59 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.725-756C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515858 | |||||||
| chr5:175515915 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02647.hp1 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.725-699G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175515915 | |||||||
| chr5:175516033 | TAATGCGG others(42): Show |
T | 8 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(5): Show |
8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-576_725-528del others(49): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 175516033 | ||||||
| chr5:175516035 | A | G | 58 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(55): Show |
60 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.725-579A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516035 | |||||||
| chr5:175516150 | A | G | 16 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(13): Show |
16 | HG02155.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.725-464A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516150 | |||||||
| chr5:175516218 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.725-396C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516218 | |||||||
| chr5:175516261 | T | C | 78 | a0001c0001t0002g0169 a0001c0002t0002g0001 a0001c0002t0002g0008 others(75): Show |
88 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.725-353T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | chr5 | 175516261 | |||||||
| chr5:175516548 | GA | G | 69 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(66): Show |
71 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.725-57delA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 175516548 | ||||||
| chr5:175516738 | G | C | 1 | a0001c0001t0005g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.774+75G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175516738 | |||||||
| chr5:175516858 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.774+195A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175516858 | |||||||
| chr5:175517088 | A | T | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.774+425A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517088 | |||||||
| chr5:175517237 | G | A | 1 | a0001c0001t0053g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.774+574G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517237 | |||||||
| chr5:175517324 | C | T | 1 | a0001c0002t0002g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.774+661C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517324 | |||||||
| chr5:175517393 | G | A | 1 | a0001c0003t0004g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.774+730G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517393 | |||||||
| chr5:175517528 | C | G | 1 | a0001c0001t0004g0046 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.774+865C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517528 | |||||||
| chr5:175517611 | A | G | 117 | a0001c0001t0002g0169 a0001c0001t0013g0063 a0001c0001t0013g0240 others(114): Show |
127 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.774+948A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517611 | |||||||
| chr5:175517836 | C | T | 9 | a0001c0003t0007g0021 a0001c0003t0007g0070 a0001c0003t0007g0073 others(6): Show |
9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+1173C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517836 | |||||||
| chr5:175517905 | G | A | 101 | a0001c0001t0002g0169 a0001c0001t0057g0179 a0001c0002t0002g0001 others(98): Show |
111 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.774+1242G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175517905 | |||||||
| chr5:175518033 | C | A | 1 | a0001c0001t0003g0299 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.774+1370C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518033 | |||||||
| chr5:175518050 | C | T | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1387C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518050 | |||||||
| chr5:175518300 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
66 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.774+1637A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518300 | |||||||
| chr5:175518383 | GTT | G | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+1726_774+1727d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175518383 | ||||||
| chr5:175518462 | C | T | 186 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(183): Show |
198 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.774+1799C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518462 | |||||||
| chr5:175518490 | A | G | 6 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1827A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518490 | |||||||
| chr5:175518496 | T | G | 2 | a0001c0001t0013g0248 a0001c0001t0047g0247 |
2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.774+1833T>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518496 | |||||||
| chr5:175518530 | G | A | 1 | a0001c0001t0013g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.774+1867G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518530 | |||||||
| chr5:175518558 | G | T | 1 | a0001c0001t0016g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.774+1895G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518558 | |||||||
| chr5:175518678 | G | A | 2 | a0001c0002t0041g0151 a0001c0007t0040g0181 |
2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.774+2015G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518678 | |||||||
| chr5:175518813 | A | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+2150A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518813 | |||||||
| chr5:175518827 | C | T | 3 | a0001c0001t0009g0267 a0001c0001t0009g0268 a0001c0001t0010g0144 |
3 | HG01069.hp1 HG01070.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.774+2164C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518827 | |||||||
| chr5:175518833 | A | G | 8 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(5): Show |
8 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+2170A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518833 | |||||||
| chr5:175518836 | C | A | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+2173C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518836 | |||||||
| chr5:175518899 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.774+2236T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175518899 | |||||||
| chr5:175519038 | T | A | 1 | a0001c0001t0055g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.774+2375T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519038 | |||||||
| chr5:175519082 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.774+2419C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519082 | |||||||
| chr5:175519180 | A | G | 1 | a0001c0004t0038g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.774+2517A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519180 | |||||||
| chr5:175519191 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+2528G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519191 | |||||||
| chr5:175519388 | A | T | 1 | a0001c0001t0003g0301 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.775-2531A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519388 | |||||||
| chr5:175519468 | C | T | 60 | a0001c0001t0004g0004 a0001c0001t0004g0006 a0001c0001t0004g0039 others(57): Show |
62 | HG00140.hp2 HG00544.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.775-2451C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519468 | |||||||
| chr5:175519480 | A | G | 1 | a0001c0002t0031g0256 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.775-2439A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519480 | |||||||
| chr5:175519538 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.775-2381G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519538 | |||||||
| chr5:175519688 | CAAG | C | 6 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-2228_775-2226d others(5): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519688 | ||||||
| chr5:175519858 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0045g0198 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.775-2061T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519858 | |||||||
| chr5:175519864 | C | CT | 50 | a0001c0001t0001g0009 a0001c0001t0001g0062 a0001c0001t0001g0107 others(47): Show |
51 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.775-2031dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519864 | ||||||
| chr5:175519864 | C | CTT | 6 | a0001c0001t0001g0325 a0001c0001t0025g0114 a0001c0002t0002g0193 others(3): Show |
6 | HG00609.hp2 HG02109.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-2032_775-2031d others(4): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519864 | ||||||
| chr5:175519864 | CT | C | 20 | a0001c0001t0001g0175 a0001c0001t0003g0130 a0001c0001t0003g0335 others(17): Show |
20 | HG01167.hp1 HG01168.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-2031delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175519864 | ||||||
| chr5:175519932 | T | C | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1987T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175519932 | |||||||
| chr5:175520058 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.775-1861C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520058 | |||||||
| chr5:175520220 | T | C | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1699T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520220 | |||||||
| chr5:175520260 | A | C | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.775-1659A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520260 | |||||||
| chr5:175520426 | G | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0104 a0001c0001t0001g0136 others(1): Show |
4 | HG01081.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1493G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520426 | |||||||
| chr5:175520428 | G | A | 4 | a0001c0002t0002g0083 a0001c0002t0002g0150 a0001c0002t0002g0191 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1491G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520428 | |||||||
| chr5:175520538 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.775-1381C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520538 | |||||||
| chr5:175520573 | G | C | 1 | a0001c0001t0003g0091 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.775-1346G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520573 | |||||||
| chr5:175520712 | C | T | 1 | a0001c0004t0006g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.775-1207C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520712 | |||||||
| chr5:175520745 | A | G | 6 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(3): Show |
6 | HG02055.hp1 HG02155.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-1174A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520745 | |||||||
| chr5:175520870 | A | G | 9 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1049A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520870 | |||||||
| chr5:175520925 | G | A | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.775-994G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520925 | |||||||
| chr5:175520945 | C | T | 99 | a0001c0001t0002g0169 a0001c0002t0002g0001 a0001c0002t0002g0008 others(96): Show |
109 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.775-974C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175520945 | |||||||
| chr5:175521003 | T | A | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.775-916T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521003 | |||||||
| chr5:175521026 | C | T | 1 | a0001c0002t0002g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.775-893C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521026 | |||||||
| chr5:175521253 | T | TA | 345 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(342): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.775-653dupA | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 175521253 | ||||||
| chr5:175521554 | A | G | 145 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(142): Show |
156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.775-365A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521554 | |||||||
| chr5:175521709 | T | C | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-210T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521709 | |||||||
| chr5:175521813 | A | C | 19 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(16): Show |
19 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-106A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521813 | |||||||
| chr5:175521832 | G | A | 15 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(12): Show |
16 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.775-87G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 8/10 | chr5 | 175521832 | |||||||
| chr5:175522093 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0010g0286 |
3 | HG01928.hp2 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.824+125G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522093 | |||||||
| chr5:175522115 | A | G | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.824+147A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522115 | |||||||
| chr5:175522138 | A | G | 9 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(6): Show |
9 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.824+170A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522138 | |||||||
| chr5:175522203 | T | C | 116 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(113): Show |
127 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.825-172T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522203 | |||||||
| chr5:175522275 | G | T | 1 | a0001c0001t0009g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.825-100G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522275 | |||||||
| chr5:175522287 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.825-88G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522287 | |||||||
| chr5:175522290 | G | A | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.825-85G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 9/10 | chr5 | 175522290 | |||||||
| chr5:175522472 | C | A | 18 | a0001c0001t0013g0063 a0001c0001t0013g0240 a0001c0001t0013g0241 others(15): Show |
18 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.872+50C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522472 | |||||||
| chr5:175522476 | T | C | 1 | a0001c0002t0030g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.872+54T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522476 | |||||||
| chr5:175522482 | G | A | 1 | a0001c0001t0003g0259 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.872+60G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522482 | |||||||
| chr5:175522649 | C | CT | 116 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(113): Show |
127 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.872+230dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175522649 | ||||||
| chr5:175522736 | C | G | 1 | a0001c0001t0003g0341 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.872+314C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522736 | |||||||
| chr5:175522809 | G | C | 1 | a0001c0001t0005g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.872+387G>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522809 | |||||||
| chr5:175522870 | A | G | 136 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(133): Show |
147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.872+448A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522870 | |||||||
| chr5:175522882 | G | A | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+460G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522882 | |||||||
| chr5:175522885 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.872+463A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175522885 | |||||||
| chr5:175523117 | G | A | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.872+695G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523117 | |||||||
| chr5:175523173 | A | G | 1 | a0001c0001t0018g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.872+751A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523173 | |||||||
| chr5:175523220 | G | A | 2 | a0001c0001t0026g0233 a0001c0001t0059g0207 |
2 | HG02559.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.872+798G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523220 | |||||||
| chr5:175523236 | A | G | 2 | a0002c0005t0023g0182 a0002c0005t0023g0184 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.872+814A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523236 | |||||||
| chr5:175523671 | C | T | 125 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(122): Show |
136 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+1249C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523671 | |||||||
| chr5:175523767 | G | A | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.872+1345G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523767 | |||||||
| chr5:175523795 | C | A | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.872+1373C>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523795 | |||||||
| chr5:175523875 | C | G | 6 | a0001c0002t0015g0081 a0001c0002t0015g0082 a0001c0002t0015g0085 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+1453C>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175523875 | |||||||
| chr5:175524003 | A | G | 1 | a0001c0002t0012g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.872+1581A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524003 | |||||||
| chr5:175524019 | G | A | 1 | a0001c0001t0016g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.872+1597G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524019 | |||||||
| chr5:175524111 | AAAAAAAA others(27): Show |
A | 1 | a0001c0002t0041g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872+1691_872+1724d others(36): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524111 | ||||||
| chr5:175524114 | AAAAAAAA others(24): Show |
A | 1 | a0001c0002t0012g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.872+1694_872+1724d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524114 | ||||||
| chr5:175524115 | AAAAAAAA others(25): Show |
A | 1 | a0001c0002t0002g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.872+1695_872+1726d others(34): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524115 | ||||||
| chr5:175524116 | AAAAAAAA others(22): Show |
A | 1 | a0001c0002t0034g0338 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.872+1696_872+1724d others(31): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524116 | ||||||
| chr5:175524116 | AAAAAAAA others(24): Show |
A | 32 | a0001c0001t0002g0169 a0001c0002t0002g0001 a0001c0002t0002g0008 others(29): Show |
34 | HG00099.hp1 HG01167.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.872+1696_872+1726d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524116 | ||||||
| chr5:175524116 | AAAAAAAA others(28): Show |
A | 2 | a0001c0002t0002g0083 a0001c0002t0002g0191 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.872+1696_872+1730d others(37): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524116 | ||||||
| chr5:175524117 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0055g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.872+1697_872+1712d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524117 | ||||||
| chr5:175524117 | AAAAAAAA others(23): Show |
A | 2 | a0001c0002t0002g0001 a0001c0002t0002g0013 |
2 | HG00673.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.872+1697_872+1726d others(32): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524117 | ||||||
| chr5:175524117 | AAAAAAAA others(27): Show |
A | 1 | a0001c0002t0030g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.872+1697_872+1730d others(36): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524117 | ||||||
| chr5:175524118 | AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0003g0323 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.872+1698_872+1718d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | ||||||
| chr5:175524118 | AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0003g0141 a0001c0001t0003g0217 |
2 | NA18985.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.872+1698_872+1722d others(27): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | ||||||
| chr5:175524118 | AAAAAAAA others(24): Show |
A | 43 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(40): Show |
48 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.872+1698_872+1728d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | ||||||
| chr5:175524118 | AAAAAAAA others(28): Show |
A | 9 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0150 others(6): Show |
9 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.872+1698_872+1732d others(37): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | ||||||
| chr5:175524118 | AAAAAAAA others(30): Show |
A | 1 | a0001c0002t0002g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.872+1698_872+1734d others(39): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524118 | ||||||
| chr5:175524119 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.872+1699_872+1708d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | ||||||
| chr5:175524119 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0298 |
2 | HG01255.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.872+1699_872+1710d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | ||||||
| chr5:175524119 | AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0005g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.872+1699_872+1724d others(28): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | ||||||
| chr5:175524119 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0005g0333 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.872+1699_872+1726d others(30): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | ||||||
| chr5:175524119 | AAAAAAAA others(23): Show |
A | 2 | a0001c0002t0002g0326 a0001c0007t0040g0181 |
2 | HG03579.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.872+1699_872+1728d others(32): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524119 | ||||||
| chr5:175524120 | AAAAAAAT | A | 6 | a0001c0001t0003g0011 a0001c0001t0003g0255 a0001c0001t0003g0263 others(3): Show |
7 | HG00735.hp2 HG01099.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+1700_872+1706d others(9): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(4): Show |
A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0220 a0001c0001t0003g0305 others(2): Show |
5 | HG00280.hp2 HG01109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1700_872+1710d others(13): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0004g0046 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.872+1700_872+1712d others(15): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(10): Show |
A | 1 | a0001c0001t0001g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.872+1700_872+1716d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(12): Show |
A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0037 |
2 | NA18968.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.872+1700_872+1718d others(21): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0016g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.872+1700_872+1720d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(18): Show |
A | 1 | a0001c0001t0005g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.872+1700_872+1724d others(27): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(20): Show |
A | 4 | a0001c0001t0005g0147 a0001c0001t0020g0195 a0001c0001t0020g0196 others(1): Show |
4 | HG01109.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1700_872+1726d others(29): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524120 | AAAAAAAT others(24): Show |
A | 1 | a0001c0002t0002g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.872+1700_872+1730d others(33): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524120 | ||||||
| chr5:175524121 | A | T | 6 | a0001c0001t0003g0344 a0001c0002t0015g0082 a0001c0002t0015g0085 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+1699A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524121 | |||||||
| chr5:175524121 | AAAAAATA others(5): Show |
A | 9 | a0001c0001t0003g0014 a0001c0001t0003g0025 a0001c0001t0003g0054 others(6): Show |
10 | HG01952.hp2 NA18945.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+1701_872+1712d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | ||||||
| chr5:175524121 | AAAAAATA others(9): Show |
A | 1 | a0001c0001t0004g0164 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.872+1701_872+1716d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | ||||||
| chr5:175524121 | AAAAAATA others(11): Show |
A | 8 | a0001c0001t0001g0116 a0001c0001t0004g0275 a0001c0001t0026g0069 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+1701_872+1718d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | ||||||
| chr5:175524121 | AAAAAATA others(13): Show |
A | 2 | a0001c0001t0003g0129 a0001c0001t0003g0130 |
2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.872+1701_872+1720d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524121 | ||||||
| chr5:175524122 | AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.872+1702_872+1716d others(17): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | ||||||
| chr5:175524122 | AAAAATAT others(10): Show |
A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0252 a0001c0001t0003g0091 |
3 | HG02004.hp2 HG03492.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.872+1702_872+1718d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | ||||||
| chr5:175524122 | AAAAATAT others(12): Show |
A | 10 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0118 others(7): Show |
10 | HG01243.hp1 HG01978.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.872+1702_872+1720d others(21): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | ||||||
| chr5:175524122 | AAAAATAT others(14): Show |
A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0062 a0001c0001t0001g0152 others(9): Show |
12 | HG02630.hp2 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.872+1702_872+1722d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | ||||||
| chr5:175524122 | AAAAATAT others(16): Show |
A | 1 | a0001c0001t0052g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.872+1702_872+1724d others(25): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | ||||||
| chr5:175524122 | AAAAATAT others(20): Show |
A | 9 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(6): Show |
9 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.872+1702_872+1728d others(29): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524122 | ||||||
| chr5:175524123 | A | T | 9 | a0001c0001t0003g0094 a0001c0001t0003g0254 a0001c0001t0003g0344 others(6): Show |
9 | HG02074.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+1701A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524123 | |||||||
| chr5:175524123 | AAAATATA others(3): Show |
A | 1 | a0001c0001t0003g0307 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.872+1703_872+1712d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524123 | AAAATATA others(5): Show |
A | 1 | a0001c0001t0003g0300 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.872+1703_872+1714d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524123 | AAAATATA others(9): Show |
A | 1 | a0001c0001t0008g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.872+1703_872+1718d others(18): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524123 | AAAATATA others(11): Show |
A | 22 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0004g0040 others(19): Show |
22 | HG00673.hp2 HG01175.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.872+1703_872+1720d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524123 | AAAATATA others(13): Show |
A | 6 | a0001c0001t0001g0197 a0001c0001t0001g0201 a0001c0001t0003g0035 others(3): Show |
6 | HG00280.hp1 HG01192.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.872+1703_872+1722d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524123 | AAAATATA others(15): Show |
A | 3 | a0001c0001t0001g0010 a0001c0001t0010g0144 a0001c0001t0016g0139 |
3 | HG01069.hp2 NA19068.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.872+1703_872+1724d others(24): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524123 | AAAATATA others(21): Show |
A | 2 | a0001c0001t0018g0238 a0001c0001t0018g0311 |
2 | HG01433.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.872+1703_872+1730d others(30): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524123 | ||||||
| chr5:175524124 | A | T | 1 | a0001c0001t0001g0325 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.872+1702A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524124 | |||||||
| chr5:175524124 | AAATATAT others(4): Show |
A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0299 |
2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.872+1704_872+1714d others(13): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | ||||||
| chr5:175524124 | AAATATAT others(6): Show |
A | 1 | a0001c0001t0001g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.872+1704_872+1716d others(15): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | ||||||
| chr5:175524124 | AAATATAT others(10): Show |
A | 5 | a0001c0001t0004g0004 a0001c0001t0008g0053 a0001c0001t0009g0180 others(2): Show |
5 | HG03579.hp1 NA18967.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1704_872+1720d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | ||||||
| chr5:175524124 | AAATATAT others(12): Show |
A | 7 | a0001c0001t0001g0111 a0001c0001t0001g0228 a0001c0001t0001g0289 others(4): Show |
7 | HG00544.hp1 HG00558.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.872+1704_872+1722d others(21): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | ||||||
| chr5:175524124 | AAATATAT others(14): Show |
A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(41): Show |
46 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.872+1704_872+1724d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | ||||||
| chr5:175524124 | AAATATAT others(20): Show |
A | 2 | a0001c0001t0005g0005 a0001c0001t0018g0313 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.872+1704_872+1730d others(29): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524124 | ||||||
| chr5:175524125 | A | T | 19 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0171 others(16): Show |
19 | HG02074.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.872+1703A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524125 | |||||||
| chr5:175524125 | AATATATA others(3): Show |
A | 3 | a0001c0001t0003g0309 a0001c0001t0013g0240 a0001c0001t0013g0241 |
3 | HG00597.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.872+1740_872+1749d others(12): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | ||||||
| chr5:175524125 | AATATATA others(5): Show |
A | 9 | a0001c0003t0007g0021 a0001c0003t0007g0070 a0001c0003t0007g0073 others(6): Show |
9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+1738_872+1749d others(14): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | ||||||
| chr5:175524125 | AATATATA others(11): Show |
A | 5 | a0001c0001t0001g0325 a0001c0001t0004g0043 a0001c0001t0004g0052 others(2): Show |
5 | HG00609.hp2 HG00621.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+1732_872+1749d others(20): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | ||||||
| chr5:175524125 | AATATATA others(13): Show |
A | 4 | a0001c0001t0001g0101 a0001c0001t0025g0114 a0001c0001t0025g0133 others(1): Show |
4 | HG00544.hp2 HG01433.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1730_872+1749d others(22): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | ||||||
| chr5:175524125 | AATATATA others(17): Show |
A | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+1726_872+1749d others(26): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175524125 | ||||||
| chr5:175524126 | ATATATAT others(10): Show |
A | 1 | a0002c0005t0023g0184 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.872+1705_872+1721d others(19): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524126 | |||||||
| chr5:175524126 | ATATATAT others(14): Show |
A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0122 a0001c0001t0001g0143 others(2): Show |
5 | HG00140.hp1 HG01106.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+1705_872+1725d others(23): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524126 | |||||||
| chr5:175524127 | T | A | 2 | a0001c0001t0009g0269 a0001c0002t0003g0222 |
2 | HG02280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.872+1705T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524127 | |||||||
| chr5:175524129 | T | A | 1 | a0001c0001t0009g0269 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.872+1707T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524129 | |||||||
| chr5:175524131 | T | A | 2 | a0001c0001t0047g0247 a0001c0001t0057g0179 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.872+1709T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524131 | |||||||
| chr5:175524133 | T | A | 4 | a0001c0001t0013g0248 a0001c0001t0013g0249 a0001c0001t0047g0247 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1711T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524133 | |||||||
| chr5:175524135 | T | A | 4 | a0001c0001t0003g0295 a0001c0001t0003g0303 a0001c0001t0013g0248 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1713T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524135 | |||||||
| chr5:175524137 | T | A | 4 | a0001c0001t0003g0309 a0001c0001t0013g0240 a0001c0001t0013g0241 others(1): Show |
4 | HG00597.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+1715T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524137 | |||||||
| chr5:175524139 | T | A | 9 | a0001c0003t0007g0021 a0001c0003t0007g0070 a0001c0003t0007g0073 others(6): Show |
9 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+1717T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524139 | |||||||
| chr5:175524141 | T | A | 4 | a0001c0003t0007g0073 a0001c0003t0007g0078 a0001c0003t0007g0231 others(1): Show |
4 | HG00423.hp2 HG01099.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+1719T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524141 | |||||||
| chr5:175524147 | T | A | 1 | a0001c0001t0050g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.872+1725T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524147 | |||||||
| chr5:175524149 | T | A | 2 | a0001c0001t0001g0122 a0001c0001t0010g0123 |
2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.872+1727T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524149 | |||||||
| chr5:175524151 | T | A | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+1729T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524151 | |||||||
| chr5:175524153 | T | A | 1 | a0001c0002t0064g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+1731T>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524153 | |||||||
| chr5:175524168 | A | C | 16 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(13): Show |
17 | HG00140.hp1 HG00544.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.872+1746A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524168 | |||||||
| chr5:175524170 | A | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
18 | HG00140.hp1 HG00544.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.872+1748A>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524170 | |||||||
| chr5:175524177 | A | G | 1 | a0001c0004t0006g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.872+1755A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524177 | |||||||
| chr5:175524428 | T | C | 125 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(122): Show |
136 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+2006T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524428 | |||||||
| chr5:175524446 | T | C | 1 | a0001c0001t0057g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.872+2024T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524446 | |||||||
| chr5:175524673 | G | T | 145 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(142): Show |
156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.873-1965G>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524673 | |||||||
| chr5:175524945 | A | T | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-1693A>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175524945 | |||||||
| chr5:175525431 | A | G | 37 | a0001c0001t0002g0169 a0001c0002t0002g0001 a0001c0002t0002g0008 others(34): Show |
44 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.873-1207A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175525431 | |||||||
| chr5:175525881 | C | T | 186 | a0001c0001t0002g0169 a0001c0001t0004g0004 a0001c0001t0004g0006 others(183): Show |
198 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.873-757C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175525881 | |||||||
| chr5:175526114 | A | G | 1 | a0001c0002t0006g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.873-524A>G | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526114 | |||||||
| chr5:175526124 | G | GT | 28 | a0001c0001t0001g0055 a0001c0001t0001g0197 a0001c0001t0003g0035 others(25): Show |
28 | HG00741.hp1 HG01070.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.873-498dupT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175526124 | ||||||
| chr5:175526124 | GT | G | 117 | a0001c0001t0002g0169 a0001c0001t0005g0005 a0001c0001t0005g0032 others(114): Show |
128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.873-498delT | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175526124 | ||||||
| chr5:175526184 | TAC | T | 5 | a0001c0001t0014g0186 a0001c0001t0014g0187 a0001c0001t0014g0188 others(2): Show |
5 | HG02155.hp2 NA18939.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-452_873-451del others(2): Show |
SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 175526184 | ||||||
| chr5:175526295 | G | A | 1 | a0001c0001t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.873-343G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526295 | |||||||
| chr5:175526379 | G | A | 2 | a0001c0001t0003g0300 a0001c0001t0003g0307 |
2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.873-259G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526379 | |||||||
| chr5:175526502 | G | A | 7 | a0001c0001t0003g0025 a0001c0002t0015g0081 a0001c0002t0015g0082 others(4): Show |
7 | HG01952.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-136G>A | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526502 | |||||||
| chr5:175526527 | C | T | 1 | a0001c0002t0006g0127 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.873-111C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526527 | |||||||
| chr5:175526570 | T | C | 19 | a0001c0001t0005g0005 a0001c0001t0005g0032 a0001c0001t0005g0033 others(16): Show |
20 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.873-68T>C | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526570 | |||||||
| chr5:175526626 | C | T | 1 | a0001c0002t0006g0280 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.873-12C>T | SFXN1 | ENSG00000164466.13 | transcript | ENST00000321442.10 | protein_coding | 10/10 | chr5 | 175526626 |