Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 152877 |
| ensemblid | ENSG00000174137.14 |
| hgncid | 31860 |
| symbol | FAM53A |
| name | family with sequence similarity 53 member A |
| refseq_nuc | NM_001174070.3 |
| refseq_prot | NP_001167541.1 |
| ensembl_nuc | ENST00000308132.11 |
| ensembl_prot | ENSP00000310057.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 1639887 |
| end | 1684313 |
| strand | - |
| ver | v1.2 |
| region | chr4:1639887-1684313 |
| region5000 | chr4:1634887-1689313 |
| regionname0 | FAM53A_chr4_1639887_1684313 |
| regionname5000 | FAM53A_chr4_1634887_1689313 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 398 | 286 | 56 | 68 | 109 | 10 | 41 | 72 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0002 | 0/0 | 398 | 48 | 31 | 8 | 9 | 0 | 0 | 7 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0003 | 0/0 | 398 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0004 | 0/0 | 398 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0005 | 0/0 | 398 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0006 | 0/0 | 398 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0007 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0008 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0009 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0010 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0011 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0012 | 0/0 | 398 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| a0013 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | MVTLI others(393): Show |
chr4 | 1634887 | 1689313 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1194 | 229 | 50 | 51 | 97 | 6 | 23 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0001c0002 | 0/0 | 1194 | 53 | 6 | 17 | 9 | 4 | 17 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0001c0010 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0001c0013 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0001c0014 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0001c0017 | 0/0 | 1194 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0002c0003 | 0/0 | 1194 | 48 | 31 | 8 | 9 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0003c0004 | 0/0 | 1194 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0004c0006 | 0/0 | 1194 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0005c0005 | 0/0 | 1194 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0006c0007 | 0/0 | 1194 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0007c0018 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0008c0012 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0009c0016 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0010c0011 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0011c0008 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0012c0009 | 0/0 | 1194 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 | ||
| a0013c0015 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | ATGGT others(1189): Show |
chr4 | 1634887 | 1689313 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2848 | 94 | 9 | 22 | 48 | 2 | 12 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0002 | 0/0 | 2848 | 11 | 10 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0003 | 0/0 | 2848 | 13 | 13 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0004 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0006 | 0/0 | 2848 | 18 | 0 | 3 | 9 | 3 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0007 | 1/0 | 2848 | 18 | 0 | 3 | 12 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0008 | 0/0 | 2848 | 16 | 0 | 13 | 0 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0009 | 0/0 | 2848 | 14 | 0 | 4 | 7 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0010 | 0/0 | 2848 | 10 | 0 | 0 | 10 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0011 | 0/0 | 2848 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0013 | 0/0 | 2848 | 5 | 0 | 0 | 5 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0014 | 0/0 | 2848 | 4 | 0 | 3 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0017 | 0/0 | 2848 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0019 | 0/0 | 2848 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0021 | 0/0 | 2847 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2842): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0022 | 0/0 | 2667 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2662): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0024 | 0/0 | 2848 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0025 | 0/0 | 2848 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0026 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2842): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0030 | 0/0 | 2849 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0031 | 0/0 | 2848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0032 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2842): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0035 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2781): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0037 | 0/0 | 2785 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2780): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0038 | 0/0 | 2785 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2780): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0039 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0043 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0001t0044 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0004 | 0/0 | 2848 | 18 | 0 | 4 | 9 | 0 | 5 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0005 | 0/0 | 2849 | 19 | 3 | 8 | 0 | 2 | 6 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0012 | 0/0 | 2849 | 6 | 0 | 3 | 0 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0015 | 0/0 | 2849 | 5 | 2 | 0 | 0 | 2 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0027 | 0/0 | 2848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0033 | 0/0 | 2848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0040 | 0/0 | 2849 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0041 | 0/0 | 2848 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0002t0045 | 0/0 | 2849 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0001c0010t0001 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0013t0013 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0014t0001 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0001c0017t0005 | 0/0 | 2849 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0002 | 0/0 | 2848 | 23 | 12 | 3 | 8 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0003 | 0/0 | 2848 | 12 | 11 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0011 | 0/0 | 2848 | 4 | 1 | 2 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0016 | 0/0 | 2848 | 3 | 1 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0020 | 0/0 | 2848 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0023 | 0/0 | 2786 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2781): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0029 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0002c0003t0034 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0003c0004t0018 | 0/0 | 2848 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0004c0006t0028 | 0/0 | 2849 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0004c0006t0042 | 0/0 | 2849 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0005c0005t0002 | 0/0 | 2848 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0006c0007t0004 | 0/0 | 2848 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0007c0018t0005 | 0/0 | 2849 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0008c0012t0010 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0009c0016t0004 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0010c0011t0036 | 0/0 | 2849 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2844): Show |
chr4 | 1634887 | 1689313 |
| a0011c0008t0016 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0012c0009t0014 | 0/0 | 2848 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| a0013c0015t0001 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | GGCTG others(2843): Show |
chr4 | 1634887 | 1689313 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0009g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0013g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0013g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0013g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0014g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0014g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0014g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0017g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0017g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0017g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0019g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0019g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0021g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0021g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0022g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0022g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0024g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0024g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0025g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0025g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0026g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0030g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0031g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0032g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0035g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0037g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0038g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0039g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0043g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0001t0044g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0012g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0012g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0012g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0012g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0012g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0015g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0015g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0015g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0027g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0033g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0040g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0041g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0002t0045g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0010t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0013t0013g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0014t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0001c0017t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0011g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0011g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0011g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0016g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0016g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0020g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0020g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0023g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0023g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0029g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0002c0003t0034g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0003c0004t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0003c0004t0018g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0003c0004t0018g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0004c0006t0028g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0004c0006t0042g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0005c0005t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0006c0007t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0006c0007t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0007c0018t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0008c0012t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0009c0016t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0010c0011t0036g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0011c0008t0016g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0012c0009t0014g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| a0013c0015t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00099 | hp2 | a0001 | c0002 | t0015 | g0004 | EUR | GBR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00280 | hp1 | a0001 | c0002 | t0005 | g0304 | EUR | FIN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0048 | EUR | FIN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00423 | hp1 | a0001 | c0001 | t0017 | g0106 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0254 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00438 | hp1 | a0001 | c0010 | t0001 | g0240 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0267 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00558 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00609 | hp1 | a0001 | c0013 | t0013 | g0249 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00609 | hp2 | a0001 | c0001 | t0013 | g0255 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0327 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00621 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00639 | hp1 | a0001 | c0002 | t0005 | g0298 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00642 | hp1 | a0001 | c0002 | t0005 | g0299 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00673 | hp2 | a0001 | c0001 | t0009 | g0232 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00733 | hp1 | a0002 | c0003 | t0011 | g0022 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00735 | hp1 | a0001 | c0002 | t0005 | g0263 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00735 | hp2 | a0001 | c0001 | t0031 | g0055 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00738 | hp1 | a0001 | c0002 | t0004 | g0162 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0020 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0121 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0195 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0120 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01074 | hp2 | a0001 | c0002 | t0012 | g0017 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0073 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01106 | hp2 | a0001 | c0002 | t0005 | g0323 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01109 | hp1 | a0002 | c0003 | t0016 | g0316 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0071 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01168 | hp1 | a0001 | c0001 | t0014 | g0015 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01168 | hp2 | a0001 | c0002 | t0012 | g0058 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01169 | hp2 | a0001 | c0002 | t0012 | g0057 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0143 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01243 | hp2 | a0002 | c0003 | t0003 | g0109 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01255 | hp1 | a0001 | c0001 | t0019 | g0064 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0260 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0009 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01257 | hp2 | a0001 | c0002 | t0005 | g0159 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0009 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01358 | hp2 | a0001 | c0002 | t0005 | g0301 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01361 | hp1 | a0001 | c0002 | t0005 | g0305 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0198 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0205 | EUR | IBS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0049 | EUR | IBS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0322 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01891 | hp1 | a0002 | c0003 | t0003 | g0069 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01891 | hp2 | a0002 | c0003 | t0002 | g0138 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0312 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01943 | hp1 | a0002 | c0003 | t0002 | g0295 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0085 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0262 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01975 | hp1 | a0002 | c0003 | t0016 | g0308 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0072 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01978 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0078 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01981 | hp1 | a0001 | c0002 | t0027 | g0018 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01981 | hp2 | a0001 | c0002 | t0033 | g0066 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0082 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0080 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0206 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02027 | hp2 | a0002 | c0003 | t0002 | g0186 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02040 | hp1 | a0001 | c0001 | t0007 | g0065 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02040 | hp2 | a0007 | c0018 | t0005 | g0319 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0325 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02071 | hp2 | a0008 | c0012 | t0010 | g0038 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0264 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02132 | hp1 | a0009 | c0016 | t0004 | g0191 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0247 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02135 | hp1 | a0001 | c0001 | t0009 | g0200 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02135 | hp2 | a0001 | c0001 | t0017 | g0098 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02145 | hp1 | a0002 | c0003 | t0002 | g0139 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02145 | hp2 | a0001 | c0001 | t0022 | g0132 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0075 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | CDX | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02257 | hp1 | a0004 | c0006 | t0028 | g0012 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02257 | hp2 | a0002 | c0003 | t0002 | g0276 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02258 | hp2 | a0010 | c0011 | t0036 | g0122 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02273 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02280 | hp1 | a0001 | c0001 | t0021 | g0324 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02293 | hp1 | a0002 | c0003 | t0011 | g0024 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0196 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0077 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0335 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02602 | hp1 | a0001 | c0002 | t0005 | g0307 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02602 | hp2 | a0001 | c0002 | t0015 | g0070 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02615 | hp1 | a0002 | c0003 | t0020 | g0123 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0140 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02622 | hp2 | a0002 | c0003 | t0002 | g0311 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02630 | hp1 | a0002 | c0003 | t0003 | g0112 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02630 | hp2 | a0001 | c0001 | t0038 | g0315 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02647 | hp1 | a0001 | c0001 | t0035 | g0118 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02647 | hp2 | a0002 | c0003 | t0011 | g0019 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0074 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02698 | hp2 | a0001 | c0002 | t0012 | g0051 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02717 | hp2 | a0011 | c0008 | t0016 | g0277 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02723 | hp1 | a0002 | c0003 | t0003 | g0113 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02723 | hp2 | a0001 | c0001 | t0043 | g0130 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0330 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02735 | hp2 | a0001 | c0002 | t0005 | g0302 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02809 | hp1 | a0002 | c0003 | t0002 | g0146 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02809 | hp2 | a0002 | c0003 | t0003 | g0111 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02818 | hp1 | a0002 | c0003 | t0003 | g0117 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02886 | hp1 | a0002 | c0003 | t0023 | g0135 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02895 | hp2 | a0002 | c0003 | t0002 | g0156 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02896 | hp1 | a0002 | c0003 | t0020 | g0108 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02896 | hp2 | a0002 | c0003 | t0003 | g0115 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02897 | hp1 | a0002 | c0003 | t0003 | g0114 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0157 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0270 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02965 | hp2 | a0003 | c0004 | t0018 | g0150 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02976 | hp2 | a0001 | c0001 | t0030 | g0056 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03017 | hp2 | a0001 | c0002 | t0005 | g0306 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03041 | hp1 | a0004 | c0006 | t0042 | g0142 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03041 | hp2 | a0002 | c0003 | t0003 | g0124 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0278 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03130 | hp1 | a0002 | c0003 | t0002 | g0320 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03195 | hp1 | a0002 | c0003 | t0023 | g0147 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0318 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03209 | hp2 | a0002 | c0003 | t0002 | g0271 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03239 | hp1 | a0001 | c0002 | t0012 | g0059 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0044 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0144 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03453 | hp2 | a0001 | c0002 | t0015 | g0125 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0261 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03490 | hp2 | a0001 | c0002 | t0004 | g0194 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0154 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0155 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0189 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03516 | hp1 | a0002 | c0003 | t0003 | g0127 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03540 | hp2 | a0002 | c0003 | t0029 | g0060 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03579 | hp1 | a0003 | c0004 | t0018 | g0313 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03579 | hp2 | a0001 | c0001 | t0024 | g0149 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0332 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0052 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0153 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0079 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03704 | hp2 | a0012 | c0009 | t0014 | g0014 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03710 | hp1 | a0001 | c0002 | t0005 | g0300 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03710 | hp2 | a0001 | c0002 | t0041 | g0329 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0081 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03927 | hp2 | a0001 | c0002 | t0005 | g0160 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0093 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04115 | hp2 | a0001 | c0002 | t0005 | g0279 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0076 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04204 | hp2 | a0001 | c0002 | t0012 | g0016 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04228 | hp1 | a0001 | c0017 | t0005 | g0163 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18522 | hp1 | a0002 | c0003 | t0034 | g0107 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18612 | hp1 | a0001 | c0001 | t0025 | g0166 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18939 | hp1 | a0001 | c0001 | t0009 | g0253 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18947 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18951 | hp1 | a0005 | c0005 | t0002 | g0010 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18951 | hp2 | a0001 | c0001 | t0010 | g0032 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0042 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18953 | hp2 | a0001 | c0001 | t0013 | g0252 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18954 | hp2 | a0002 | c0003 | t0002 | g0248 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18956 | hp2 | a0001 | c0001 | t0009 | g0257 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18957 | hp1 | a0001 | c0001 | t0044 | g0290 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18957 | hp2 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0197 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18961 | hp2 | a0001 | c0002 | t0004 | g0161 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0193 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18965 | hp2 | a0013 | c0015 | t0001 | g0210 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0202 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18970 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18977 | hp1 | a0002 | c0003 | t0011 | g0023 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0039 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0203 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18990 | hp1 | a0001 | c0001 | t0017 | g0097 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0184 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18991 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18994 | hp1 | a0002 | c0003 | t0002 | g0204 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0084 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18998 | hp2 | a0001 | c0001 | t0013 | g0250 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18999 | hp1 | a0001 | c0001 | t0025 | g0213 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19009 | hp2 | a0006 | c0007 | t0004 | g0331 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19010 | hp1 | a0001 | c0014 | t0001 | g0223 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19010 | hp2 | a0006 | c0007 | t0004 | g0328 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19030 | hp2 | a0001 | c0001 | t0032 | g0067 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19068 | hp2 | a0001 | c0001 | t0013 | g0251 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19070 | hp2 | a0005 | c0005 | t0002 | g0010 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19077 | hp1 | a0001 | c0001 | t0013 | g0258 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19078 | hp2 | a0001 | c0001 | t0009 | g0256 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0192 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19087 | hp2 | a0002 | c0003 | t0002 | g0185 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19088 | hp1 | a0001 | c0002 | t0004 | g0190 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0105 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20129 | hp1 | a0001 | c0002 | t0040 | g0321 | AFR | ASW | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ASW | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20752 | hp1 | a0001 | c0001 | t0014 | g0054 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20752 | hp2 | a0001 | c0002 | t0015 | g0004 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0045 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20905 | hp2 | a0001 | c0002 | t0045 | g0303 | SAS | GIH | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02109 | hp2 | a0001 | c0001 | t0026 | g0050 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0053 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02559 | hp1 | a0003 | c0004 | t0018 | g0131 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0309 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03471 | hp1 | a0002 | c0003 | t0016 | g0148 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0314 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG06807 | hp1 | a0001 | c0001 | t0037 | g0129 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| HG06807 | hp2 | a0001 | c0001 | t0039 | g0151 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18955 | hp1 | a0001 | c0001 | t0009 | g0209 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0110 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA21309 | hp1 | a0002 | c0003 | t0003 | g0100 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| NA21309 | hp2 | a0001 | c0002 | t0015 | g0094 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0158 | REF | REF | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0061 | REF | REF | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1641397 | G | A | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1093C>T | p.Arg365Cys | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1338/2848 | 1093/1197 | 365/398 | chr4 | 1641397 | |||
| chr4:1641477 | C | T | 1 | a0005 | 2 | NA18951.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.1013G>A | p.Cys338Tyr | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1258/2848 | 1013/1197 | 338/398 | chr4 | 1641477 | |||
| chr4:1655033 | C | T | 1 | a0003 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.827G>A | p.Arg276His | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1072/2848 | 827/1197 | 276/398 | chr4 | 1655033 | |||
| chr4:1655049 | G | C | 1 | a0004 | 2 | HG02257.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.811C>G | p.Arg271Gly | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1056/2848 | 811/1197 | 271/398 | chr4 | 1655049 | |||
| chr4:1655109 | C | T | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.751G>A | p.Gly251Arg | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 996/2848 | 751/1197 | 251/398 | chr4 | 1655109 | |||
| chr4:1655129 | G | A | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.731C>T | p.Thr244Met | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 976/2848 | 731/1197 | 244/398 | chr4 | 1655129 | |||
| chr4:1655156 | G | C | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.704C>G | p.Pro235Arg | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 949/2848 | 704/1197 | 235/398 | chr4 | 1655156 | |||
| chr4:1655255 | G | A | 1 | a0008 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.605C>T | p.Ala202Val | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 850/2848 | 605/1197 | 202/398 | chr4 | 1655255 | |||
| chr4:1655400 | C | T | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.460G>A | p.Asp154Asn | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 705/2848 | 460/1197 | 154/398 | chr4 | 1655400 | |||
| chr4:1655423 | G | C | 1 | a0006 | 2 | NA19009.hp2 NA19010.hp2 |
missense_variant | MODERATE | c.437C>G | p.Thr146Ser | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 682/2848 | 437/1197 | 146/398 | chr4 | 1655423 | |||
| chr4:1655459 | C | G | 1 | a0009 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.401G>C | p.Arg134Pro | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 646/2848 | 401/1197 | 134/398 | chr4 | 1655459 | |||
| chr4:1655469 | C | G | 1 | a0011 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.391G>C | p.Val131Leu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 636/2848 | 391/1197 | 131/398 | chr4 | 1655469 | |||
| chr4:1655522 | G | A | 1 | a0013 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.338C>T | p.Thr113Met | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 583/2848 | 338/1197 | 113/398 | chr4 | 1655522 | |||
| chr4:1657435 | C | T | 3 | a0002 a0005 a0011 |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
missense_variant | MODERATE | c.109G>A | p.Gly37Ser | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/5 | 354/2848 | 109/1197 | 37/398 | chr4 | 1657435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1641311 | C | T | 1 | a0001c0010 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1179G>A | p.Glu393Glu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1424/2848 | 1179/1197 | 393/398 | chr4 | 1641311 | |||
| chr4:1655074 | A | C | 6 | a0001c0002 a0001c0017 a0006c0007 others(3): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
synonymous_variant | LOW | c.786T>G | p.Pro262Pro | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1031/2848 | 786/1197 | 262/398 | chr4 | 1655074 | |||
| chr4:1655095 | C | G | 1 | a0004c0006 | 2 | HG02257.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.765G>C | p.Leu255Leu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1010/2848 | 765/1197 | 255/398 | chr4 | 1655095 | |||
| chr4:1655164 | C | T | 1 | a0001c0017 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.696G>A | p.Ala232Ala | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 941/2848 | 696/1197 | 232/398 | chr4 | 1655164 | |||
| chr4:1655230 | G | A | 1 | a0003c0004 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.630C>T | p.Ser210Ser | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 875/2848 | 630/1197 | 210/398 | chr4 | 1655230 | |||
| chr4:1655314 | G | A | 1 | a0001c0013 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.546C>T | p.Pro182Pro | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 791/2848 | 546/1197 | 182/398 | chr4 | 1655314 | |||
| chr4:1655401 | G | A | 1 | a0001c0014 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.459C>T | p.Cys153Cys | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 704/2848 | 459/1197 | 153/398 | chr4 | 1655401 | |||
| chr4:1655476 | C | T | 1 | a0003c0004 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.384G>A | p.Glu128Glu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 629/2848 | 384/1197 | 128/398 | chr4 | 1655476 | |||
| chr4:1655554 | G | A | 5 | a0001c0002 a0001c0017 a0006c0007 others(2): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
synonymous_variant | LOW | c.306C>T | p.Thr102Thr | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 551/2848 | 306/1197 | 102/398 | chr4 | 1655554 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1639895 | T | C | 1 | a0001c0002t0045 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1398A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1398 | chr4 | 1639895 | ||||||
| chr4:1639968 | G | T | 7 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(4): Show |
34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1325C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1325 | chr4 | 1639968 | ||||||
| chr4:1640002 | C | T | 1 | a0003c0004t0018 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1291G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1291 | chr4 | 1640002 | ||||||
| chr4:1640033 | G | A | 1 | a0001c0002t0041 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1260 | chr4 | 1640033 | ||||||
| chr4:1640094 | T | G | 1 | a0001c0001t0025 | 2 | NA18612.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1199A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1199 | chr4 | 1640094 | ||||||
| chr4:1640182 | G | A | 2 | a0001c0001t0021 a0001c0001t0032 |
3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1111 | chr4 | 1640182 | ||||||
| chr4:1640311 | C | T | 4 | a0002c0003t0016 a0002c0003t0029 a0002c0003t0034 others(1): Show |
6 | HG01109.hp1 HG01975.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*982G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 982 | chr4 | 1640311 | ||||||
| chr4:1640334 | C | T | 1 | a0001c0001t0031 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*959G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 959 | chr4 | 1640334 | ||||||
| chr4:1640339 | G | C | 1 | a0001c0001t0024 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*954C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 954 | chr4 | 1640339 | ||||||
| chr4:1640344 | G | GA | 11 | a0001c0001t0030 a0001c0002t0005 a0001c0002t0012 others(8): Show |
38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*948_*949insT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 948 | chr4 | 1640344 | ||||||
| chr4:1640437 | C | T | 5 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0017 others(2): Show |
20 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 856 | chr4 | 1640437 | ||||||
| chr4:1640612 | C | T | 1 | a0001c0001t0026 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 681 | chr4 | 1640612 | ||||||
| chr4:1640619 | T | C | 1 | a0001c0001t0044 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 674 | chr4 | 1640619 | ||||||
| chr4:1640623 | C | T | 2 | a0001c0001t0019 a0001c0001t0043 |
3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 670 | chr4 | 1640623 | ||||||
| chr4:1640639 | G | T | 1 | a0001c0001t0037 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 654 | chr4 | 1640639 | ||||||
| chr4:1640647 | A | G | 50 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(47): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*646T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 646 | chr4 | 1640647 | ||||||
| chr4:1640674 | T | G | 9 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(6): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*619A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 619 | chr4 | 1640674 | ||||||
| chr4:1640683 | G | C | 9 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(6): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 610 | chr4 | 1640683 | ||||||
| chr4:1640694 | A | G | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 599 | chr4 | 1640694 | ||||||
| chr4:1640707 | C | T | 2 | a0004c0006t0028 a0004c0006t0042 |
2 | HG02257.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 586 | chr4 | 1640707 | ||||||
| chr4:1640715 | G | A | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 578 | chr4 | 1640715 | ||||||
| chr4:1640715 | GTGGCCCC others(55): Show |
G | 1 | a0002c0003t0023 | 2 | HG02886.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516_*577delTGGCTG others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 516 | chr4 | 1640715 | ||||||
| chr4:1640728 | A | G | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0022 others(30): Show |
120 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*565T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 565 | chr4 | 1640728 | ||||||
| chr4:1640754 | C | T | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 539 | chr4 | 1640754 | ||||||
| chr4:1640755 | A | G | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*538T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 538 | chr4 | 1640755 | ||||||
| chr4:1640766 | C | A | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 527 | chr4 | 1640766 | ||||||
| chr4:1640769 | T | C | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 524 | chr4 | 1640769 | ||||||
| chr4:1640769 | T | TGGCAGCC others(55): Show |
2 | a0001c0001t0019 a0001c0001t0043 |
3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*462_*523dupGCCTGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 523 | chr4 | 1640769 | ||||||
| chr4:1640769 | TGGCAGCC others(55): Show |
T | 1 | a0001c0001t0001 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462_*523delGCCTGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 462 | chr4 | 1640769 | ||||||
| chr4:1640770 | G | A | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*523C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 523 | chr4 | 1640770 | ||||||
| chr4:1640792 | T | A | 8 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 others(5): Show |
68 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 501 | chr4 | 1640792 | ||||||
| chr4:1640806 | C | G | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*487G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 487 | chr4 | 1640806 | ||||||
| chr4:1640817 | G | A | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 476 | chr4 | 1640817 | ||||||
| chr4:1640820 | G | T | 8 | a0001c0001t0004 a0001c0001t0022 a0001c0002t0004 others(5): Show |
27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*473C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 473 | chr4 | 1640820 | ||||||
| chr4:1640839 | A | G | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 454 | chr4 | 1640839 | ||||||
| chr4:1640868 | CTCTGTGC others(55): Show |
C | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*363_*424delCTAGGT others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 363 | chr4 | 1640868 | ||||||
| chr4:1640878 | T | C | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
83 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*415A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 415 | chr4 | 1640878 | ||||||
| chr4:1640879 | G | A | 2 | a0001c0001t0026 a0001c0002t0040 |
2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 414 | chr4 | 1640879 | ||||||
| chr4:1640890 | A | C | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 403 | chr4 | 1640890 | ||||||
| chr4:1640894 | A | G | 2 | a0001c0001t0026 a0001c0002t0040 |
2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*399T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 399 | chr4 | 1640894 | ||||||
| chr4:1640901 | A | G | 2 | a0001c0001t0026 a0001c0002t0040 |
2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 392 | chr4 | 1640901 | ||||||
| chr4:1640920 | A | T | 1 | a0001c0001t0001 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 373 | chr4 | 1640920 | ||||||
| chr4:1640930 | G | C | 2 | a0001c0001t0026 a0001c0002t0040 |
2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*363C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 363 | chr4 | 1640930 | ||||||
| chr4:1640930 | GTCTGTGC others(54): Show |
G | 1 | a0001c0001t0030 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302_*362delGTAGGT others(55): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 302 | chr4 | 1640930 | ||||||
| chr4:1640951 | A | C | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 342 | chr4 | 1640951 | ||||||
| chr4:1640954 | CGGCAGCC others(55): Show |
C | 1 | a0001c0001t0035 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277_*338delACCGGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 277 | chr4 | 1640954 | ||||||
| chr4:1640959 | G | T | 1 | a0001c0001t0002 | 4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*334C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 334 | chr4 | 1640959 | ||||||
| chr4:1641013 | C | A | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*280G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 280 | chr4 | 1641013 | ||||||
| chr4:1641016 | T | A | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0022 others(17): Show |
79 | HG00544.hp1 HG00621.hp1 HG00733.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*277A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 277 | chr4 | 1641016 | ||||||
| chr4:1641016 | T | C | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0030 others(13): Show |
45 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*277A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 277 | chr4 | 1641016 | ||||||
| chr4:1641016 | T | TGGCAGCC others(55): Show |
2 | a0001c0001t0001 a0001c0001t0006 |
3 | HG02165.hp1 HG02258.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*215_*276dupGCCGGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 276 | chr4 | 1641016 | ||||||
| chr4:1641024 | G | A | 2 | a0001c0001t0021 a0001c0001t0032 |
3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*269C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 269 | chr4 | 1641024 | ||||||
| chr4:1641078 | C | A | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*215G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 215 | chr4 | 1641078 | ||||||
| chr4:1641086 | GTGGCCCC others(174): Show |
G | 1 | a0001c0001t0022 | 2 | HG02145.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*26_*206del | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 26 | chr4 | 1641086 | ||||||
| chr4:1641094 | G | A | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 199 | chr4 | 1641094 | ||||||
| chr4:1641099 | G | A | 8 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0027 others(5): Show |
28 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 194 | chr4 | 1641099 | ||||||
| chr4:1641138 | G | GGGCCGTG others(50): Show |
2 | a0004c0006t0028 a0004c0006t0042 |
2 | HG02257.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*154_*155insTGGCAC others(51): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 154 | chr4 | 1641138 | ||||||
| chr4:1641144 | AGCCGTGG others(50): Show |
A | 22 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0026 others(19): Show |
82 | HG00544.hp1 HG00621.hp1 HG00733.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*92_*148delCCGGCAC others(50): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 92 | chr4 | 1641144 | ||||||
| chr4:1641147 | C | T | 1 | a0001c0002t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 146 | chr4 | 1641147 | ||||||
| chr4:1641148 | G | A | 1 | a0001c0002t0012 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 145 | chr4 | 1641148 | ||||||
| chr4:1641201 | G | GCGGCA | 7 | a0001c0001t0021 a0001c0001t0032 a0001c0001t0037 others(4): Show |
8 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*91_*92insTGCCG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 91 | chr4 | 1641201 | ||||||
| chr4:1641201 | G | GCGGCAGC others(60): Show |
1 | a0001c0002t0005 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91_*92insTGCCGCCG others(59): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 91 | chr4 | 1641201 | ||||||
| chr4:1641201 | G | GCGGCAGC others(122): Show |
6 | a0001c0002t0005 a0001c0002t0012 a0001c0002t0015 others(3): Show |
32 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*91_*92insTGCCGCCG others(121): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 91 | chr4 | 1641201 | ||||||
| chr4:1641204 | C | T | 1 | a0001c0002t0005 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 89 | chr4 | 1641204 | ||||||
| chr4:1641213 | G | A | 11 | a0001c0001t0003 a0002c0003t0002 a0002c0003t0003 others(8): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 80 | chr4 | 1641213 | ||||||
| chr4:1641236 | C | G | 7 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0027 others(4): Show |
25 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*57G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 57 | chr4 | 1641236 | ||||||
| chr4:1668765 | C | T | 1 | a0001c0001t0039 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 24 | chr4 | 1668765 | ||||||
| chr4:1668781 | T | C | 1 | a0010c0011t0036 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 40 | chr4 | 1668781 | ||||||
| chr4:1668790 | G | A | 1 | a0002c0003t0020 | 2 | HG02615.hp1 HG02896.hp1 |
5_prime_UTR_variant | MODIFIER | c.-49C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 49 | chr4 | 1668790 | ||||||
| chr4:1668875 | TC | T | 5 | a0001c0001t0021 a0001c0001t0026 a0001c0001t0032 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-135delG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 135 | chr4 | 1668875 | ||||||
| chr4:1684252 | T | G | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(45): Show |
273 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
5_prime_UTR_variant | MODIFIER | c.-184A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/5 | 15511 | chr4 | 1684252 | ||||||
| chr4:1684272 | G | T | 14 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0011 others(11): Show |
52 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-204C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/5 | 15531 | chr4 | 1684272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1641675 | C | T | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-68G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641675 | |||||||
| chr4:1641731 | G | A | 4 | a0001c0001t0030g0056 a0004c0006t0028g0012 a0004c0006t0042g0142 others(1): Show |
4 | HG02257.hp1 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-124C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641731 | |||||||
| chr4:1641850 | G | A | 3 | a0001c0001t0019g0064 a0001c0001t0019g0105 a0001c0001t0043g0130 |
3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-243C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641850 | |||||||
| chr4:1641863 | C | T | 2 | a0001c0001t0006g0045 a0004c0006t0042g0142 |
2 | HG03041.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.883-256G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641863 | |||||||
| chr4:1641984 | G | A | 36 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 others(33): Show |
37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.883-377C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641984 | |||||||
| chr4:1642135 | C | T | 1 | a0002c0003t0002g0009 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.883-528G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642135 | |||||||
| chr4:1642141 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.883-534G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642141 | |||||||
| chr4:1642170 | C | T | 2 | a0001c0001t0025g0166 a0001c0001t0025g0213 |
2 | NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.883-563G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642170 | |||||||
| chr4:1642241 | C | T | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-634G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642241 | |||||||
| chr4:1642301 | G | A | 67 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0102 others(64): Show |
72 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.883-694C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642301 | |||||||
| chr4:1642403 | G | A | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.883-796C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642403 | |||||||
| chr4:1642404 | G | A | 1 | a0002c0003t0002g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-797C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642404 | |||||||
| chr4:1642422 | C | A | 33 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.883-815G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642422 | |||||||
| chr4:1642435 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.883-828G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642435 | |||||||
| chr4:1642436 | C | A | 27 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(24): Show |
27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.883-829G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642436 | |||||||
| chr4:1642440 | C | T | 1 | a0001c0002t0005g0159 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.883-833G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642440 | |||||||
| chr4:1642441 | G | A | 42 | a0001c0001t0003g0104 a0002c0003t0002g0009 a0002c0003t0002g0138 others(39): Show |
44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.883-834C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642441 | |||||||
| chr4:1642524 | A | G | 119 | a0001c0001t0003g0104 a0001c0001t0004g0335 a0001c0001t0022g0132 others(116): Show |
122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-917T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642524 | |||||||
| chr4:1642675 | C | T | 1 | a0001c0001t0006g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.883-1068G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642675 | |||||||
| chr4:1642676 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0007g0083 |
2 | NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.883-1069C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642676 | |||||||
| chr4:1642708 | T | TCTGTGGT others(28): Show |
1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.883-1136_883-1102d others(37): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642708 | |||||||
| chr4:1642849 | C | G | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-1242G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642849 | |||||||
| chr4:1642872 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.883-1265A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642872 | |||||||
| chr4:1642961 | C | T | 1 | a0001c0002t0004g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.883-1354G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642961 | |||||||
| chr4:1643023 | C | G | 1 | a0012c0009t0014g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.883-1416G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643023 | |||||||
| chr4:1643233 | G | A | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.883-1626C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643233 | |||||||
| chr4:1643241 | C | T | 35 | a0001c0001t0014g0015 a0001c0001t0014g0021 a0001c0001t0014g0054 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-1634G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643241 | |||||||
| chr4:1643246 | C | T | 50 | a0001c0001t0006g0026 a0001c0001t0006g0037 a0001c0001t0006g0041 others(47): Show |
55 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-1639G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643246 | |||||||
| chr4:1643263 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0002g0326 a0001c0001t0007g0080 others(3): Show |
6 | HG01168.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1656T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643263 | |||||||
| chr4:1643266 | A | G | 1 | a0001c0002t0004g0327 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.883-1659T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643266 | |||||||
| chr4:1643289 | G | A | 2 | a0001c0001t0001g0170 a0002c0003t0002g0248 |
2 | HG02683.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.883-1682C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643289 | |||||||
| chr4:1643320 | A | G | 6 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0116 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1713T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643320 | |||||||
| chr4:1643323 | A | G | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-1716T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643323 | |||||||
| chr4:1643334 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.883-1727G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643334 | |||||||
| chr4:1643335 | G | A | 1 | a0001c0002t0004g0330 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.883-1728C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643335 | |||||||
| chr4:1643346 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.883-1739C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643346 | |||||||
| chr4:1643464 | T | C | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-1857A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643464 | |||||||
| chr4:1643567 | A | AT | 91 | a0001c0001t0001g0212 a0001c0001t0001g0236 a0001c0001t0001g0242 others(88): Show |
93 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.883-1961dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643567 | |||||||
| chr4:1643585 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-1978C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643585 | |||||||
| chr4:1643587 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-1980C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643587 | |||||||
| chr4:1643704 | C | T | 1 | a0005c0005t0002g0010 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.883-2097G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643704 | |||||||
| chr4:1643727 | G | A | 1 | a0001c0001t0025g0213 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.883-2120C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643727 | |||||||
| chr4:1643738 | T | G | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-2131A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643738 | |||||||
| chr4:1643752 | C | T | 33 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.883-2145G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643752 | |||||||
| chr4:1643859 | G | A | 3 | a0001c0001t0014g0015 a0001c0001t0014g0021 a0001c0001t0014g0054 |
3 | HG01168.hp1 HG01978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.883-2252C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643859 | |||||||
| chr4:1644031 | C | A | 35 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-2424G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644031 | |||||||
| chr4:1644047 | T | C | 37 | a0001c0001t0030g0056 a0001c0002t0005g0140 a0001c0002t0005g0143 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-2440A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644047 | |||||||
| chr4:1644157 | A | G | 37 | a0001c0001t0030g0056 a0001c0002t0005g0140 a0001c0002t0005g0143 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-2550T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644157 | |||||||
| chr4:1644196 | G | A | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-2589C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644196 | |||||||
| chr4:1644290 | C | G | 119 | a0001c0001t0003g0104 a0001c0001t0004g0335 a0001c0001t0022g0132 others(116): Show |
122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-2683G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644290 | |||||||
| chr4:1644311 | C | T | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-2704G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644311 | |||||||
| chr4:1644350 | G | A | 1 | a0001c0001t0044g0290 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.883-2743C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644350 | |||||||
| chr4:1644381 | C | T | 3 | a0001c0001t0019g0064 a0001c0001t0019g0105 a0001c0001t0043g0130 |
3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-2774G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644381 | |||||||
| chr4:1644401 | A | G | 1 | a0001c0001t0010g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.883-2794T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644401 | |||||||
| chr4:1644406 | A | T | 1 | a0001c0001t0003g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.883-2799T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644406 | |||||||
| chr4:1644453 | G | A | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-2846C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644453 | |||||||
| chr4:1644487 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-2880G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644487 | |||||||
| chr4:1644502 | G | A | 35 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-2895C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644502 | |||||||
| chr4:1644516 | C | A | 1 | a0002c0003t0003g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.883-2909G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644516 | |||||||
| chr4:1644556 | G | A | 1 | a0001c0001t0008g0072 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.883-2949C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644556 | |||||||
| chr4:1644560 | C | T | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-2953G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644560 | |||||||
| chr4:1644563 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-2956C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644563 | |||||||
| chr4:1644595 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-2988G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644595 | |||||||
| chr4:1644627 | G | C | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-3020C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644627 | |||||||
| chr4:1644630 | T | C | 40 | a0001c0001t0003g0104 a0002c0003t0002g0009 a0002c0003t0002g0138 others(37): Show |
42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.883-3023A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644630 | |||||||
| chr4:1644637 | T | C | 70 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-3030A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644637 | |||||||
| chr4:1644739 | C | T | 4 | a0002c0003t0002g0309 a0002c0003t0003g0114 a0002c0003t0003g0115 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-3132G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644739 | |||||||
| chr4:1644764 | G | A | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-3157C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644764 | |||||||
| chr4:1644778 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0096 a0001c0001t0003g0103 others(2): Show |
5 | HG02809.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-3171C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644778 | |||||||
| chr4:1645100 | G | A | 27 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(24): Show |
27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.883-3493C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645100 | |||||||
| chr4:1645130 | G | C | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-3523C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645130 | |||||||
| chr4:1645193 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-3586G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645193 | |||||||
| chr4:1645206 | G | GCCAGC | 70 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-3600_883-3599i others(7): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645206 | |||||||
| chr4:1645209 | G | A | 27 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(24): Show |
27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.883-3602C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645209 | |||||||
| chr4:1645285 | C | T | 1 | a0001c0001t0009g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.883-3678G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645285 | |||||||
| chr4:1645376 | A | G | 1 | a0001c0002t0005g0304 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.883-3769T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645376 | |||||||
| chr4:1645432 | G | A | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-3825C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645432 | |||||||
| chr4:1645625 | T | C | 35 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-4018A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645625 | |||||||
| chr4:1645687 | G | A | 1 | a0002c0003t0002g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.883-4080C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645687 | |||||||
| chr4:1645793 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883-4186C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645793 | |||||||
| chr4:1645813 | G | A | 1 | a0001c0001t0006g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.883-4206C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645813 | |||||||
| chr4:1645837 | A | G | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-4230T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645837 | |||||||
| chr4:1645869 | G | A | 73 | a0001c0001t0002g0272 a0001c0001t0003g0062 a0001c0001t0003g0068 others(70): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.883-4262C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645869 | |||||||
| chr4:1645871 | A | G | 70 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-4264T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645871 | |||||||
| chr4:1645873 | A | C | 119 | a0001c0001t0003g0104 a0001c0001t0004g0335 a0001c0001t0022g0132 others(116): Show |
122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-4266T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645873 | |||||||
| chr4:1645891 | T | C | 1 | a0001c0001t0007g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.883-4284A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645891 | |||||||
| chr4:1645917 | C | T | 22 | a0002c0003t0002g0009 a0002c0003t0002g0139 a0002c0003t0002g0184 others(19): Show |
23 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-4310G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645917 | |||||||
| chr4:1646015 | A | G | 17 | a0001c0001t0010g0002 a0001c0001t0010g0027 a0001c0001t0010g0028 others(14): Show |
19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-4408T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646015 | |||||||
| chr4:1646016 | C | T | 66 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0102 others(63): Show |
71 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-4409G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646016 | |||||||
| chr4:1646103 | C | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-4496G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646103 | |||||||
| chr4:1646122 | A | G | 3 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0032g0067 |
3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.883-4515T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646122 | |||||||
| chr4:1646123 | C | T | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-4516G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646123 | |||||||
| chr4:1646162 | G | A | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-4555C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646162 | |||||||
| chr4:1646238 | A | C | 37 | a0001c0001t0030g0056 a0001c0002t0005g0140 a0001c0002t0005g0143 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-4631T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646238 | |||||||
| chr4:1646331 | CCTCATGA others(1): Show |
C | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-4732_883-4725d others(10): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646331 | |||||||
| chr4:1646348 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-4741G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646348 | |||||||
| chr4:1646367 | G | C | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-4760C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646367 | |||||||
| chr4:1646378 | C | T | 1 | a0002c0003t0016g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.883-4771G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646378 | |||||||
| chr4:1646466 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG00642.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.883-4859C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646466 | |||||||
| chr4:1646467 | C | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG00642.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.883-4860G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646467 | |||||||
| chr4:1646611 | C | T | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-5004G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646611 | |||||||
| chr4:1646625 | C | T | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-5018G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646625 | |||||||
| chr4:1646668 | G | A | 1 | a0001c0001t0038g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883-5061C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646668 | |||||||
| chr4:1646744 | C | A | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-5137G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646744 | |||||||
| chr4:1646787 | C | T | 1 | a0001c0001t0006g0052 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.883-5180G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646787 | |||||||
| chr4:1646899 | C | T | 30 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(27): Show |
30 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.883-5292G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646899 | |||||||
| chr4:1647043 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.883-5436G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647043 | |||||||
| chr4:1647085 | A | G | 120 | a0001c0001t0003g0063 a0001c0001t0003g0104 a0001c0001t0004g0335 others(117): Show |
123 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.883-5478T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647085 | |||||||
| chr4:1647153 | A | G | 35 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-5546T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647153 | |||||||
| chr4:1647164 | CT | C | 29 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(26): Show |
29 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.883-5558delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647164 | |||||||
| chr4:1647234 | A | G | 119 | a0001c0001t0003g0104 a0001c0001t0004g0335 a0001c0001t0022g0132 others(116): Show |
122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-5627T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647234 | |||||||
| chr4:1647292 | A | G | 77 | a0001c0001t0002g0272 a0001c0001t0003g0062 a0001c0001t0003g0063 others(74): Show |
82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.883-5685T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647292 | |||||||
| chr4:1647313 | T | C | 67 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.883-5706A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647313 | |||||||
| chr4:1647322 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883-5715C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647322 | |||||||
| chr4:1647337 | G | GA | 20 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0001g0266 others(17): Show |
20 | HG00621.hp2 HG00642.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-5731dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647337 | |||||||
| chr4:1647582 | T | C | 327 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(324): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.883-5975A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647582 | |||||||
| chr4:1647585 | G | A | 1 | a0001c0002t0033g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.883-5978C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647585 | |||||||
| chr4:1647606 | C | T | 1 | a0002c0003t0002g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.883-5999G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647606 | |||||||
| chr4:1647623 | T | C | 78 | a0001c0001t0001g0235 a0001c0001t0003g0063 a0001c0001t0004g0335 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.883-6016A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647623 | |||||||
| chr4:1647655 | G | A | 3 | a0001c0001t0008g0071 a0001c0001t0008g0120 a0001c0001t0008g0121 |
3 | HG01070.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.883-6048C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647655 | |||||||
| chr4:1647690 | C | T | 113 | a0001c0001t0003g0104 a0001c0001t0004g0335 a0001c0001t0022g0132 others(110): Show |
116 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.883-6083G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647690 | |||||||
| chr4:1647710 | T | C | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-6103A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647710 | |||||||
| chr4:1648053 | G | C | 1 | a0001c0001t0011g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883-6446C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648053 | |||||||
| chr4:1648091 | C | T | 1 | a0001c0010t0001g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.883-6484G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648091 | |||||||
| chr4:1648120 | G | C | 3 | a0001c0001t0007g0005 a0001c0001t0007g0087 a0001c0001t0007g0090 |
4 | NA18947.hp1 NA18963.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-6513C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648120 | |||||||
| chr4:1648190 | C | G | 20 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0169 others(17): Show |
20 | HG00544.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-6583G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648190 | |||||||
| chr4:1648433 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.882+6545C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648433 | |||||||
| chr4:1648464 | T | G | 1 | a0001c0001t0031g0055 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.882+6514A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648464 | |||||||
| chr4:1648513 | G | A | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+6465C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648513 | |||||||
| chr4:1648516 | G | A | 1 | a0001c0001t0008g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.882+6462C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648516 | |||||||
| chr4:1648593 | T | C | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+6385A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648593 | |||||||
| chr4:1648603 | C | T | 3 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0032g0067 |
3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.882+6375G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648603 | |||||||
| chr4:1648632 | G | A | 13 | a0002c0003t0002g0009 a0002c0003t0002g0184 a0002c0003t0002g0185 others(10): Show |
14 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+6346C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648632 | |||||||
| chr4:1648728 | G | T | 1 | a0001c0001t0009g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.882+6250C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648728 | |||||||
| chr4:1648771 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0245 |
2 | NA18991.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.882+6207A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648771 | |||||||
| chr4:1648809 | A | C | 35 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.882+6169T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648809 | |||||||
| chr4:1648819 | G | A | 49 | a0001c0001t0003g0104 a0002c0003t0002g0009 a0002c0003t0002g0138 others(46): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.882+6159C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648819 | |||||||
| chr4:1648830 | A | T | 1 | a0001c0002t0005g0323 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.882+6148T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648830 | |||||||
| chr4:1648835 | G | A | 1 | a0001c0002t0005g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.882+6143C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648835 | |||||||
| chr4:1648867 | C | A | 1 | a0001c0002t0005g0159 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.882+6111G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648867 | |||||||
| chr4:1648890 | A | G | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+6088T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648890 | |||||||
| chr4:1648972 | G | C | 1 | a0001c0002t0005g0314 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+6006C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648972 | |||||||
| chr4:1648977 | G | T | 1 | a0001c0001t0008g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.882+6001C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648977 | |||||||
| chr4:1649072 | C | T | 8 | a0002c0003t0002g0139 a0002c0003t0002g0271 a0002c0003t0002g0278 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+5906G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649072 | |||||||
| chr4:1649134 | G | GGGGAAGG others(17): Show |
1 | a0001c0001t0009g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.882+5820_882+5843d others(26): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649134 | |||||||
| chr4:1649134 | GGGGAAGG others(5): Show |
G | 1 | a0008c0012t0010g0038 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.882+5832_882+5843d others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649134 | |||||||
| chr4:1649140 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+5838C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649140 | |||||||
| chr4:1649152 | G | A | 8 | a0001c0002t0012g0016 a0001c0002t0012g0017 a0001c0002t0012g0051 others(5): Show |
8 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+5826C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649152 | |||||||
| chr4:1649152 | G | GGGGAAA | 28 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(25): Show |
29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.882+5820_882+5825d others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649152 | |||||||
| chr4:1649158 | A | G | 8 | a0001c0002t0012g0016 a0001c0002t0012g0017 a0001c0002t0012g0051 others(5): Show |
8 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+5820T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649158 | |||||||
| chr4:1649164 | G | A | 8 | a0001c0002t0012g0016 a0001c0002t0012g0017 a0001c0002t0012g0051 others(5): Show |
8 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+5814C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649164 | |||||||
| chr4:1649170 | A | AGGGAAGG others(41): Show |
2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+5807_882+5808i others(50): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649170 | |||||||
| chr4:1649170 | A | AGGGAAGG others(17): Show |
2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.882+5807_882+5808i others(26): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649170 | |||||||
| chr4:1649176 | A | AGGGAAG | 98 | a0001c0001t0003g0063 a0001c0001t0003g0104 a0001c0001t0004g0335 others(95): Show |
101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.882+5796_882+5801d others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649176 | |||||||
| chr4:1649176 | A | AGGGAAGG others(5): Show |
1 | a0001c0017t0005g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.882+5790_882+5801d others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649176 | |||||||
| chr4:1649176 | A | G | 12 | a0001c0001t0030g0056 a0001c0002t0012g0016 a0001c0002t0012g0017 others(9): Show |
12 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+5802T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649176 | |||||||
| chr4:1649182 | G | GGGGAAGG others(17): Show |
1 | a0001c0001t0002g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+5772_882+5795d others(26): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649182 | |||||||
| chr4:1649183 | G | A | 3 | a0001c0001t0019g0064 a0001c0001t0019g0105 a0001c0001t0043g0130 |
3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882+5795C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649183 | |||||||
| chr4:1649188 | GGGGAAGG others(5): Show |
G | 1 | a0002c0003t0003g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.882+5778_882+5789d others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649188 | |||||||
| chr4:1649200 | A | G | 48 | a0001c0001t0003g0104 a0002c0003t0002g0009 a0002c0003t0002g0138 others(45): Show |
50 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.882+5778T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649200 | |||||||
| chr4:1649227 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+5751C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649227 | |||||||
| chr4:1649434 | C | A | 1 | a0001c0001t0017g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.882+5544G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649434 | |||||||
| chr4:1649453 | T | C | 5 | a0002c0003t0002g0009 a0002c0003t0002g0295 a0002c0003t0011g0022 others(2): Show |
6 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+5525A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649453 | |||||||
| chr4:1649473 | C | T | 1 | a0002c0003t0002g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+5505G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649473 | |||||||
| chr4:1649517 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.882+5461C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649517 | |||||||
| chr4:1649672 | T | C | 50 | a0001c0001t0003g0104 a0001c0001t0011g0053 a0002c0003t0002g0009 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.882+5306A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649672 | |||||||
| chr4:1649753 | G | A | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+5225C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649753 | |||||||
| chr4:1649818 | A | G | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+5160T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649818 | |||||||
| chr4:1649842 | T | C | 36 | a0001c0001t0001g0141 a0001c0002t0005g0140 a0001c0002t0005g0143 others(33): Show |
37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+5136A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649842 | |||||||
| chr4:1649855 | A | T | 120 | a0001c0001t0003g0063 a0001c0001t0003g0104 a0001c0001t0004g0335 others(117): Show |
123 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.882+5123T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649855 | |||||||
| chr4:1649870 | G | A | 27 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(24): Show |
27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.882+5108C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649870 | |||||||
| chr4:1649872 | G | A | 42 | a0001c0001t0003g0104 a0002c0003t0002g0009 a0002c0003t0002g0138 others(39): Show |
44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.882+5106C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649872 | |||||||
| chr4:1649876 | TGTTTGTG others(18): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+5077_882+5101d others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649876 | |||||||
| chr4:1649879 | T | TTGTGAGG others(51): Show |
1 | a0001c0001t0014g0015 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.882+5041_882+5098d others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649879 | |||||||
| chr4:1649879 | TTGTGAGG others(22): Show |
T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0222 a0001c0001t0001g0231 others(10): Show |
13 | HG00423.hp2 HG02083.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+5070_882+5098d others(31): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649879 | |||||||
| chr4:1649879 | TTGTGAGG others(51): Show |
T | 3 | a0001c0001t0001g0170 a0001c0001t0030g0056 a0010c0011t0036g0122 |
3 | HG02258.hp2 HG02683.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.882+5041_882+5098d others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649879 | |||||||
| chr4:1649897 | G | A | 1 | a0001c0001t0007g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.882+5081C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649897 | |||||||
| chr4:1649908 | C | CTGTGAGG others(18): Show |
2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.882+5069_882+5070i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649908 | |||||||
| chr4:1649930 | C | G | 24 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(21): Show |
24 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.882+5048G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649930 | |||||||
| chr4:1649937 | C | CTGTGAGG others(18): Show |
1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+5040_882+5041i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649937 | |||||||
| chr4:1649959 | C | T | 26 | a0001c0001t0003g0104 a0002c0003t0002g0138 a0002c0003t0002g0139 others(23): Show |
27 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+5019G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649959 | |||||||
| chr4:1649962 | TTGACTGT others(26): Show |
T | 27 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(24): Show |
27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.882+4983_882+5015d others(35): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649962 | |||||||
| chr4:1649962 | TTGACTGT others(55): Show |
T | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+4954_882+5015d others(64): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649962 | |||||||
| chr4:1649985 | TG | T | 3 | a0002c0003t0002g0202 a0002c0003t0002g0203 a0002c0003t0002g0204 |
3 | NA18969.hp2 NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.882+4992delC | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649985 | |||||||
| chr4:1649995 | C | CTGTGAGG others(18): Show |
1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+4982_882+4983i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649995 | |||||||
| chr4:1650012 | C | CGTGGCGT others(22): Show |
32 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(29): Show |
33 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+4965_882+4966i others(31): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650012 | |||||||
| chr4:1650020 | TTGAC | T | 17 | a0001c0001t0003g0104 a0002c0003t0002g0138 a0002c0003t0002g0156 others(14): Show |
18 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.882+4954_882+4957d others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650020 | |||||||
| chr4:1650037 | C | CAGTCATG others(134): Show |
1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+4940_882+4941i others(143): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650037 | |||||||
| chr4:1650041 | C | T | 1 | a0001c0002t0015g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.882+4937G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650041 | |||||||
| chr4:1650046 | C | T | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4932G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650046 | |||||||
| chr4:1650046 | CGTTTGAC others(76): Show |
C | 2 | a0001c0001t0003g0104 a0002c0003t0002g0311 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.882+4849_882+4931d others(85): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650046 | |||||||
| chr4:1650053 | C | CTGTGAGG others(18): Show |
1 | a0001c0002t0015g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.882+4924_882+4925i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650053 | |||||||
| chr4:1650075 | T | C | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4903A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650075 | |||||||
| chr4:1650094 | G | A | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.882+4884C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650094 | |||||||
| chr4:1650094 | G | T | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4884C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650094 | |||||||
| chr4:1650096 | G | A | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4882C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650096 | |||||||
| chr4:1650100 | C | T | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4878G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650100 | |||||||
| chr4:1650123 | T | G | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4855A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650123 | |||||||
| chr4:1650125 | A | G | 3 | a0001c0001t0007g0128 a0001c0001t0030g0056 a0010c0011t0036g0122 |
3 | HG02258.hp2 HG02976.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.882+4853T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650125 | |||||||
| chr4:1650161 | T | C | 1 | a0002c0003t0002g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.882+4817A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650161 | |||||||
| chr4:1650161 | TTGTGAGG others(51): Show |
T | 1 | a0001c0001t0001g0207 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.882+4759_882+4816d others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650161 | |||||||
| chr4:1650178 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+4800G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650178 | |||||||
| chr4:1650213 | A | G | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+4765T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650213 | |||||||
| chr4:1650241 | C | T | 1 | a0002c0003t0002g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+4737G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650241 | |||||||
| chr4:1650266 | G | A | 1 | a0002c0003t0011g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.882+4712C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650266 | |||||||
| chr4:1650385 | T | TTGAC | 197 | a0001c0001t0002g0272 a0001c0001t0003g0062 a0001c0001t0003g0063 others(194): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.882+4592_882+4593i others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650385 | |||||||
| chr4:1650398 | T | C | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+4580A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650398 | |||||||
| chr4:1650557 | C | T | 13 | a0001c0002t0005g0143 a0001c0002t0005g0160 a0001c0002t0005g0279 others(10): Show |
14 | HG00099.hp2 HG01074.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+4421G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650557 | |||||||
| chr4:1650560 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+4418C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650560 | |||||||
| chr4:1650594 | C | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+4384G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650594 | |||||||
| chr4:1650641 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.882+4337C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650641 | |||||||
| chr4:1650691 | T | C | 33 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.882+4287A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650691 | |||||||
| chr4:1650716 | G | A | 1 | a0001c0001t0032g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.882+4262C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650716 | |||||||
| chr4:1650743 | G | A | 1 | a0001c0001t0006g0040 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.882+4235C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650743 | |||||||
| chr4:1650807 | T | G | 30 | a0001c0001t0004g0335 a0001c0001t0022g0132 a0001c0001t0022g0157 others(27): Show |
30 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+4171A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650807 | |||||||
| chr4:1650918 | T | C | 1 | a0002c0003t0002g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882+4060A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650918 | |||||||
| chr4:1651210 | G | A | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.882+3768C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651210 | |||||||
| chr4:1651223 | G | GA | 41 | a0001c0001t0001g0207 a0001c0001t0001g0237 a0001c0001t0001g0317 others(38): Show |
42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.882+3754dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651223 | |||||||
| chr4:1651223 | GA | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0006g0045 others(5): Show |
8 | HG00544.hp1 HG03490.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+3754delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651223 | |||||||
| chr4:1651224 | A | G | 2 | a0001c0001t0030g0056 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+3754T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651224 | |||||||
| chr4:1651260 | G | A | 36 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(33): Show |
37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+3718C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651260 | |||||||
| chr4:1651271 | T | C | 201 | a0001c0001t0001g0296 a0001c0001t0002g0272 a0001c0001t0003g0062 others(198): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.882+3707A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651271 | |||||||
| chr4:1651283 | G | A | 5 | a0001c0002t0005g0159 a0001c0002t0005g0205 a0001c0002t0005g0300 others(2): Show |
5 | HG01257.hp2 HG01358.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+3695C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651283 | |||||||
| chr4:1651298 | G | A | 1 | a0011c0008t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.882+3680C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651298 | |||||||
| chr4:1651479 | C | T | 1 | a0001c0001t0038g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+3499G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651479 | |||||||
| chr4:1651519 | C | T | 4 | a0001c0001t0019g0064 a0001c0001t0021g0324 a0001c0001t0021g0325 others(1): Show |
4 | HG01255.hp1 HG02055.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+3459G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651519 | |||||||
| chr4:1651532 | T | TA | 12 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0231 others(9): Show |
13 | HG01081.hp2 HG01346.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+3445dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651532 | |||||||
| chr4:1651532 | TA | T | 70 | a0001c0001t0002g0136 a0001c0001t0004g0335 a0001c0001t0019g0064 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.882+3445delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651532 | |||||||
| chr4:1651532 | TAA | T | 120 | a0001c0001t0001g0296 a0001c0001t0002g0272 a0001c0001t0003g0062 others(117): Show |
127 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.882+3444_882+3445d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651532 | |||||||
| chr4:1651608 | C | A | 5 | a0001c0001t0002g0272 a0001c0001t0003g0102 a0001c0001t0003g0116 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+3370G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651608 | |||||||
| chr4:1651625 | T | C | 108 | a0001c0001t0001g0141 a0001c0001t0001g0297 a0001c0001t0002g0133 others(105): Show |
111 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.882+3353A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651625 | |||||||
| chr4:1651630 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.882+3348C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651630 | |||||||
| chr4:1651675 | C | T | 1 | a0001c0001t0021g0325 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+3303G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651675 | |||||||
| chr4:1651681 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.882+3297T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651681 | |||||||
| chr4:1651699 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.882+3279G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651699 | |||||||
| chr4:1651707 | T | TGGACAGG others(73): Show |
1 | a0002c0003t0003g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882+3191_882+3270d others(82): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651707 | |||||||
| chr4:1651707 | T | TGGACAGG others(73): Show |
1 | a0001c0001t0003g0095 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.882+3270_882+3271i others(82): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651707 | |||||||
| chr4:1651707 | TGGACAGG others(33): Show |
T | 13 | a0002c0003t0002g0009 a0002c0003t0002g0184 a0002c0003t0002g0185 others(10): Show |
14 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+3231_882+3270d others(42): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651707 | |||||||
| chr4:1651720 | G | GCAGGCTC others(33): Show |
32 | a0001c0001t0021g0325 a0001c0002t0005g0140 a0001c0002t0005g0143 others(29): Show |
33 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+3218_882+3257d others(42): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651720 | |||||||
| chr4:1651720 | GCAGGCTC others(33): Show |
G | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+3218_882+3257d others(42): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651720 | |||||||
| chr4:1651736 | A | G | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+3242T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651736 | |||||||
| chr4:1651799 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.882+3179G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651799 | |||||||
| chr4:1651858 | G | A | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+3120C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651858 | |||||||
| chr4:1651890 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.882+3088C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651890 | |||||||
| chr4:1651964 | C | T | 37 | a0001c0001t0002g0326 a0001c0001t0011g0013 a0002c0003t0002g0009 others(34): Show |
39 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.882+3014G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651964 | |||||||
| chr4:1651985 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.882+2993C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651985 | |||||||
| chr4:1652011 | G | A | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+2967C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652011 | |||||||
| chr4:1652012 | T | TCACACAC others(13): Show |
4 | a0001c0001t0011g0013 a0001c0001t0026g0050 a0002c0003t0023g0135 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2946_882+2965d others(22): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652012 | |||||||
| chr4:1652012 | TCACACAC others(13): Show |
T | 63 | a0001c0001t0019g0064 a0001c0001t0021g0324 a0001c0001t0021g0325 others(60): Show |
64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.882+2946_882+2965d others(22): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652012 | |||||||
| chr4:1652076 | T | A | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+2902A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652076 | |||||||
| chr4:1652080 | A | G | 4 | a0001c0001t0022g0132 a0001c0001t0022g0157 a0002c0003t0003g0124 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2898T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652080 | |||||||
| chr4:1652099 | T | C | 4 | a0001c0001t0003g0063 a0001c0001t0003g0096 a0001c0001t0003g0103 others(1): Show |
4 | HG02818.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2879A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652099 | |||||||
| chr4:1652131 | T | A | 216 | a0001c0001t0001g0282 a0001c0001t0002g0133 a0001c0001t0002g0134 others(213): Show |
224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.882+2847A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652131 | |||||||
| chr4:1652138 | CCA | C | 50 | a0001c0001t0002g0136 a0001c0001t0002g0268 a0002c0003t0002g0009 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.882+2838_882+2839d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652138 | |||||||
| chr4:1652172 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.882+2806G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652172 | |||||||
| chr4:1652173 | G | GCCACACA others(358): Show |
1 | a0002c0003t0002g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+2804_882+2805i others(367): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652173 | |||||||
| chr4:1652190 | CGCCACAC others(11): Show |
C | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.882+2770_882+2787d others(20): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652190 | |||||||
| chr4:1652229 | T | TAC | 59 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.882+2748_882+2749i others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652229 | |||||||
| chr4:1652243 | C | CCACACAC others(66): Show |
2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.882+2662_882+2734d others(75): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652243 | |||||||
| chr4:1652316 | TCA | T | 48 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(45): Show |
50 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.882+2660_882+2661d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652316 | |||||||
| chr4:1652346 | ACAC | A | 8 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+2629_882+2631d others(5): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652346 | |||||||
| chr4:1652361 | C | G | 1 | a0001c0001t0003g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+2617G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652361 | |||||||
| chr4:1652388 | T | C | 60 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+2590A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652388 | |||||||
| chr4:1652389 | G | GCACACCA | 60 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+2582_882+2588d others(9): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652389 | |||||||
| chr4:1652414 | C | G | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+2564G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652414 | |||||||
| chr4:1652416 | C | T | 3 | a0002c0003t0002g0202 a0002c0003t0002g0203 a0002c0003t0002g0204 |
3 | NA18969.hp2 NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.882+2562G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652416 | |||||||
| chr4:1652472 | C | T | 1 | a0011c0008t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.882+2506G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652472 | |||||||
| chr4:1652522 | T | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+2456A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652522 | |||||||
| chr4:1652620 | C | G | 1 | a0002c0003t0002g0184 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.882+2358G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652620 | |||||||
| chr4:1652667 | A | G | 15 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(12): Show |
15 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.882+2311T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652667 | |||||||
| chr4:1652771 | C | A | 4 | a0001c0002t0005g0263 a0001c0002t0005g0298 a0001c0002t0005g0304 others(1): Show |
4 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2207G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652771 | |||||||
| chr4:1652836 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+2142G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652836 | |||||||
| chr4:1652889 | C | A | 1 | a0001c0002t0005g0279 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.882+2089G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652889 | |||||||
| chr4:1652964 | G | A | 78 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.882+2014C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652964 | |||||||
| chr4:1653017 | C | T | 2 | a0001c0002t0004g0162 a0001c0002t0004g0206 |
2 | HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.882+1961G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653017 | |||||||
| chr4:1653061 | T | C | 70 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(67): Show |
72 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.882+1917A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653061 | |||||||
| chr4:1653094 | CCA | C | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+1882_882+1883d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653094 | |||||||
| chr4:1653132 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0310 |
2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.882+1846T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653132 | |||||||
| chr4:1653136 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+1842G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653136 | |||||||
| chr4:1653201 | A | C | 58 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.882+1777T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653201 | |||||||
| chr4:1653225 | A | G | 2 | a0001c0001t0019g0064 a0001c0001t0019g0105 |
2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.882+1753T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653225 | |||||||
| chr4:1653248 | C | T | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.882+1730G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653248 | |||||||
| chr4:1653284 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.882+1694C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653284 | |||||||
| chr4:1653291 | C | A | 1 | a0005c0005t0002g0010 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.882+1687G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653291 | |||||||
| chr4:1653382 | C | T | 12 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(9): Show |
12 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+1596G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653382 | |||||||
| chr4:1653459 | C | T | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+1519G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653459 | |||||||
| chr4:1653479 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+1499G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653479 | |||||||
| chr4:1653482 | A | G | 78 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(75): Show |
79 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.882+1496T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653482 | |||||||
| chr4:1653485 | C | T | 18 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(15): Show |
18 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.882+1493G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653485 | |||||||
| chr4:1653766 | G | A | 1 | a0001c0001t0006g0033 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.882+1212C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653766 | |||||||
| chr4:1653978 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.882+1000G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653978 | |||||||
| chr4:1654088 | G | A | 2 | a0001c0002t0005g0270 a0001c0002t0040g0321 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.882+890C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654088 | |||||||
| chr4:1654197 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.882+781G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654197 | |||||||
| chr4:1654209 | C | T | 11 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(8): Show |
11 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+769G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654209 | |||||||
| chr4:1654277 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.882+701G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654277 | |||||||
| chr4:1654283 | C | T | 69 | a0001c0001t0002g0272 a0001c0001t0003g0062 a0001c0001t0003g0068 others(66): Show |
74 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.882+695G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654283 | |||||||
| chr4:1654409 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.882+569C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654409 | |||||||
| chr4:1654519 | C | G | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+459G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654519 | |||||||
| chr4:1654590 | C | G | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+388G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654590 | |||||||
| chr4:1654611 | A | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+367T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654611 | |||||||
| chr4:1654650 | C | T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0283 a0001c0001t0001g0289 |
3 | HG01069.hp2 HG01071.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.882+328G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654650 | |||||||
| chr4:1654726 | C | T | 23 | a0002c0003t0002g0009 a0002c0003t0002g0139 a0002c0003t0002g0146 others(20): Show |
24 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.882+252G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654726 | |||||||
| chr4:1654740 | C | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+238G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654740 | |||||||
| chr4:1654746 | T | C | 2 | a0001c0001t0008g0073 a0001c0001t0008g0079 |
2 | HG01081.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.882+232A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654746 | |||||||
| chr4:1654815 | G | A | 2 | a0001c0001t0006g0049 a0001c0001t0009g0261 |
2 | HG01515.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.882+163C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654815 | |||||||
| chr4:1655837 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.137-114G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655837 | |||||||
| chr4:1655849 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.137-126C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655849 | |||||||
| chr4:1655864 | G | A | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.137-141C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655864 | |||||||
| chr4:1655892 | C | T | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.137-169G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655892 | |||||||
| chr4:1655924 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0293 |
2 | NA18953.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.137-201C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655924 | |||||||
| chr4:1655931 | T | C | 2 | a0001c0001t0006g0049 a0001c0001t0009g0261 |
2 | HG01515.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.137-208A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655931 | |||||||
| chr4:1656002 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.137-279G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656002 | |||||||
| chr4:1656043 | G | A | 1 | a0001c0002t0005g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.137-320C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656043 | |||||||
| chr4:1656048 | C | T | 49 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(46): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.137-325G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656048 | |||||||
| chr4:1656137 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137-414C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656137 | |||||||
| chr4:1656138 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137-415G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656138 | |||||||
| chr4:1656155 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.137-432G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656155 | |||||||
| chr4:1656186 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.137-463G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656186 | |||||||
| chr4:1656218 | T | A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0211 a0001c0001t0001g0212 others(2): Show |
5 | HG00673.hp1 NA18965.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-495A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656218 | |||||||
| chr4:1656370 | G | A | 1 | a0001c0001t0009g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.137-647C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656370 | |||||||
| chr4:1656394 | T | TGGCTTGT others(16): Show |
2 | a0001c0002t0004g0189 a0001c0002t0004g0194 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.137-694_137-672dup others(23): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656394 | |||||||
| chr4:1656409 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.137-686G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656409 | |||||||
| chr4:1656484 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137-761C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656484 | |||||||
| chr4:1656609 | A | C | 25 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(22): Show |
25 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+799T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656609 | |||||||
| chr4:1656633 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.136+775C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656633 | |||||||
| chr4:1656654 | G | A | 49 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(46): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.136+754C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656654 | |||||||
| chr4:1656736 | G | A | 1 | a0001c0002t0041g0329 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136+672C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656736 | |||||||
| chr4:1656765 | C | T | 1 | a0001c0002t0004g0267 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.136+643G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656765 | |||||||
| chr4:1656766 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.136+642C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656766 | |||||||
| chr4:1656912 | C | T | 40 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(37): Show |
42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.136+496G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656912 | |||||||
| chr4:1656918 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.136+490G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656918 | |||||||
| chr4:1656976 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.136+432C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656976 | |||||||
| chr4:1657076 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136+332G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657076 | |||||||
| chr4:1657079 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.136+329C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657079 | |||||||
| chr4:1657230 | C | T | 1 | a0001c0002t0005g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136+178G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657230 | |||||||
| chr4:1657270 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136+138G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657270 | |||||||
| chr4:1657401 | T | C | 217 | a0001c0001t0001g0141 a0001c0001t0002g0133 a0001c0001t0002g0134 others(214): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
splice_region_variant&intron_variant | LOW | c.136+7A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657401 | |||||||
| chr4:1657681 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.76-213T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657681 | |||||||
| chr4:1657698 | C | T | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.76-230G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657698 | |||||||
| chr4:1657782 | C | T | 18 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(15): Show |
18 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-314G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657782 | |||||||
| chr4:1657799 | G | A | 15 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(12): Show |
15 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-331C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657799 | |||||||
| chr4:1657944 | C | G | 1 | a0001c0002t0004g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.76-476G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657944 | |||||||
| chr4:1657963 | TA | T | 3 | a0001c0001t0010g0029 a0001c0001t0013g0258 a0002c0003t0002g0202 |
3 | NA18957.hp2 NA18969.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.76-496delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657963 | |||||||
| chr4:1657969 | A | T | 16 | a0002c0003t0002g0138 a0002c0003t0002g0156 a0002c0003t0002g0311 others(13): Show |
17 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-501T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657969 | |||||||
| chr4:1658004 | G | A | 128 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(125): Show |
131 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.76-536C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658004 | |||||||
| chr4:1658071 | T | C | 60 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.76-603A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658071 | |||||||
| chr4:1658242 | G | A | 4 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-774C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658242 | |||||||
| chr4:1658247 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.76-779G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658247 | |||||||
| chr4:1658299 | T | C | 63 | a0001c0001t0003g0063 a0001c0001t0003g0096 a0001c0001t0003g0103 others(60): Show |
64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.76-831A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658299 | |||||||
| chr4:1658349 | T | C | 42 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(39): Show |
44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.76-881A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658349 | |||||||
| chr4:1658358 | T | G | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.76-890A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658358 | |||||||
| chr4:1658393 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0291 |
2 | HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.76-925C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658393 | |||||||
| chr4:1658419 | C | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-951G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658419 | |||||||
| chr4:1658490 | A | G | 59 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.76-1022T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658490 | |||||||
| chr4:1658746 | C | G | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76-1278G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658746 | |||||||
| chr4:1658755 | G | A | 12 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(9): Show |
12 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-1287C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658755 | |||||||
| chr4:1658803 | G | A | 15 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(12): Show |
15 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1335C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658803 | |||||||
| chr4:1658889 | C | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0215 |
2 | NA18965.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.76-1421G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658889 | |||||||
| chr4:1658924 | T | C | 60 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.76-1456A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658924 | |||||||
| chr4:1658976 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0007g0088 |
2 | NA18983.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.76-1508G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658976 | |||||||
| chr4:1659019 | C | T | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-1551G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659019 | |||||||
| chr4:1659092 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.76-1624G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659092 | |||||||
| chr4:1659143 | G | A | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76-1675C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659143 | |||||||
| chr4:1659144 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.76-1676C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659144 | |||||||
| chr4:1659261 | G | A | 4 | a0001c0001t0002g0133 a0001c0001t0002g0273 a0001c0001t0002g0274 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1793C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659261 | |||||||
| chr4:1659332 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-1864G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659332 | |||||||
| chr4:1659339 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-1871G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659339 | |||||||
| chr4:1659343 | G | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-1875C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659343 | |||||||
| chr4:1659401 | C | A | 60 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.76-1933G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659401 | |||||||
| chr4:1659423 | G | A | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-1955C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659423 | |||||||
| chr4:1659551 | C | T | 1 | a0001c0001t0006g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.76-2083G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659551 | |||||||
| chr4:1659555 | G | A | 2 | a0001c0001t0025g0166 a0001c0001t0025g0213 |
2 | NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.76-2087C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659555 | |||||||
| chr4:1659790 | C | T | 1 | a0001c0001t0007g0088 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-2322G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659790 | |||||||
| chr4:1659966 | G | A | 19 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(16): Show |
19 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-2498C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659966 | |||||||
| chr4:1660025 | G | A | 49 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(46): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.76-2557C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660025 | |||||||
| chr4:1660090 | G | A | 4 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0032g0067 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-2622C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660090 | |||||||
| chr4:1660198 | G | A | 1 | a0001c0001t0017g0097 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.76-2730C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660198 | |||||||
| chr4:1660358 | G | GA | 133 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(130): Show |
136 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.76-2891_76-2890ins others(1): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660358 | |||||||
| chr4:1660489 | T | C | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76-3021A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660489 | |||||||
| chr4:1660629 | C | T | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-3161G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660629 | |||||||
| chr4:1660704 | C | T | 1 | a0001c0001t0007g0091 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.76-3236G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660704 | |||||||
| chr4:1660705 | G | A | 5 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0102 others(2): Show |
5 | HG01884.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-3237C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660705 | |||||||
| chr4:1660832 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3364C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660832 | |||||||
| chr4:1661113 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3645C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661113 | |||||||
| chr4:1661116 | C | T | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.76-3648G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661116 | |||||||
| chr4:1661238 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.76-3770G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661238 | |||||||
| chr4:1661354 | T | C | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-3886A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661354 | |||||||
| chr4:1661383 | T | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3915A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661383 | |||||||
| chr4:1661473 | C | T | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-4005G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661473 | |||||||
| chr4:1661484 | G | A | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-4016C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661484 | |||||||
| chr4:1661624 | T | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
217 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.76-4156A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661624 | |||||||
| chr4:1661650 | A | AC | 7 | a0001c0001t0001g0245 a0001c0001t0010g0002 a0001c0001t0010g0029 others(4): Show |
9 | HG00408.hp1 HG00609.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-4183dupG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661650 | |||||||
| chr4:1661661 | C | G | 2 | a0002c0003t0020g0108 a0002c0003t0020g0123 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.76-4193G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661661 | |||||||
| chr4:1661758 | C | T | 5 | a0001c0001t0001g0246 a0001c0001t0007g0005 a0001c0001t0007g0083 others(2): Show |
6 | NA18947.hp1 NA18963.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-4290G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661758 | |||||||
| chr4:1661835 | G | A | 40 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(37): Show |
42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.76-4367C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661835 | |||||||
| chr4:1661861 | G | A | 59 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.76-4393C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661861 | |||||||
| chr4:1661909 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-4441C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661909 | |||||||
| chr4:1662120 | A | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-4652T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662120 | |||||||
| chr4:1662362 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-4894G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662362 | |||||||
| chr4:1662479 | C | CA | 17 | a0001c0001t0003g0068 a0001c0001t0003g0096 a0001c0001t0006g0025 others(14): Show |
17 | HG00609.hp2 HG02080.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-5012dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | |||||||
| chr4:1662479 | CA | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
119 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.76-5012delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | |||||||
| chr4:1662479 | CAA | C | 28 | a0001c0001t0001g0214 a0001c0001t0001g0281 a0001c0001t0001g0282 others(25): Show |
29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.76-5013_76-5012del others(2): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | |||||||
| chr4:1662479 | CAAA | C | 38 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(35): Show |
38 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.76-5014_76-5012del others(3): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | |||||||
| chr4:1662479 | CAAAAAAA others(6): Show |
C | 42 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(39): Show |
44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.76-5024_76-5012del others(13): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | |||||||
| chr4:1662505 | C | T | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.76-5037G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662505 | |||||||
| chr4:1662636 | C | T | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.76-5168G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662636 | |||||||
| chr4:1662649 | C | CA | 8 | a0001c0001t0001g0187 a0002c0003t0002g0144 a0002c0003t0002g0320 others(5): Show |
8 | HG00438.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-5182dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662649 | |||||||
| chr4:1662649 | CA | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.76-5182delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662649 | |||||||
| chr4:1662649 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0245 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.76-5191_76-5182del others(10): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662649 | |||||||
| chr4:1662788 | C | T | 4 | a0001c0001t0002g0133 a0001c0001t0002g0273 a0001c0001t0002g0274 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5320G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662788 | |||||||
| chr4:1662887 | G | A | 49 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(46): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.76-5419C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662887 | |||||||
| chr4:1662946 | C | A | 1 | a0001c0002t0041g0329 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-5478G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662946 | |||||||
| chr4:1662976 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.76-5508G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662976 | |||||||
| chr4:1663011 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.76-5543C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663011 | |||||||
| chr4:1663030 | TA | T | 320 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(317): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.76-5563delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663030 | |||||||
| chr4:1663116 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75+5551C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663116 | |||||||
| chr4:1663171 | G | GA | 40 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(37): Show |
42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.75+5495dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663171 | |||||||
| chr4:1663216 | A | C | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.75+5451T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663216 | |||||||
| chr4:1663217 | G | T | 24 | a0001c0002t0005g0143 a0001c0002t0005g0159 a0001c0002t0005g0160 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.75+5450C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663217 | |||||||
| chr4:1663237 | A | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.75+5430T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663237 | |||||||
| chr4:1663287 | A | C | 1 | a0001c0001t0007g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.75+5380T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663287 | |||||||
| chr4:1663513 | C | T | 42 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(39): Show |
44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.75+5154G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663513 | |||||||
| chr4:1663550 | G | A | 1 | a0001c0001t0003g0104 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.75+5117C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663550 | |||||||
| chr4:1663590 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.75+5077G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663590 | |||||||
| chr4:1663798 | G | C | 39 | a0002c0003t0002g0009 a0002c0003t0002g0138 a0002c0003t0002g0139 others(36): Show |
41 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.75+4869C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663798 | |||||||
| chr4:1663831 | C | A | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.75+4836G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663831 | |||||||
| chr4:1663840 | T | TA | 6 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0003g0068 others(3): Show |
6 | HG00423.hp1 HG02145.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4826dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663840 | |||||||
| chr4:1663840 | TA | T | 60 | a0001c0001t0001g0287 a0001c0001t0006g0049 a0001c0001t0007g0086 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.75+4826delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663840 | |||||||
| chr4:1664127 | G | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+4540C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664127 | |||||||
| chr4:1664349 | G | A | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.75+4318C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664349 | |||||||
| chr4:1664354 | G | A | 1 | a0001c0001t0007g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.75+4313C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664354 | |||||||
| chr4:1664371 | G | A | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.75+4296C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664371 | |||||||
| chr4:1664411 | C | T | 1 | a0001c0002t0015g0004 | 2 | HG00099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.75+4256G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664411 | |||||||
| chr4:1664427 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.75+4240G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664427 | |||||||
| chr4:1664433 | G | T | 58 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.75+4234C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664433 | |||||||
| chr4:1664612 | A | C | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.75+4055T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664612 | |||||||
| chr4:1664654 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.75+4013T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664654 | |||||||
| chr4:1664857 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.75+3810T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664857 | |||||||
| chr4:1665179 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+3488C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665179 | |||||||
| chr4:1665243 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.75+3424C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665243 | |||||||
| chr4:1665421 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.75+3246C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665421 | |||||||
| chr4:1665435 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+3232C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665435 | |||||||
| chr4:1665487 | CA | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0201 others(25): Show |
29 | HG00438.hp1 HG00558.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+3179delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665487 | |||||||
| chr4:1665580 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0310 |
2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.75+3087C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665580 | |||||||
| chr4:1665668 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.75+2999C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665668 | |||||||
| chr4:1665963 | C | CTGTATCT others(27): Show |
3 | a0001c0002t0005g0314 a0001c0002t0005g0323 a0001c0002t0015g0125 |
3 | HG01106.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.75+2703_75+2704ins others(34): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665963 | |||||||
| chr4:1665964 | A | G | 5 | a0001c0002t0005g0140 a0001c0002t0005g0314 a0001c0002t0005g0323 others(2): Show |
5 | HG01106.hp2 HG02615.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+2703T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665964 | |||||||
| chr4:1665997 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2670C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665997 | |||||||
| chr4:1666025 | C | A | 1 | a0001c0002t0005g0300 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.75+2642G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666025 | |||||||
| chr4:1666045 | T | C | 313 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.75+2622A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666045 | |||||||
| chr4:1666057 | C | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2610G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666057 | |||||||
| chr4:1666063 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+2604C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666063 | |||||||
| chr4:1666156 | C | A | 1 | a0001c0001t0010g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2511G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666156 | |||||||
| chr4:1666189 | A | C | 1 | a0001c0001t0010g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2478T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666189 | |||||||
| chr4:1666208 | A | G | 1 | a0001c0001t0010g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2459T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666208 | |||||||
| chr4:1666212 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2455C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666212 | |||||||
| chr4:1666213 | C | CACCTGCA others(20): Show |
1 | a0001c0001t0010g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2453_75+2454ins others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666213 | |||||||
| chr4:1666241 | G | A | 2 | a0001c0001t0010g0042 a0001c0002t0005g0306 |
2 | HG03017.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.75+2426C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666241 | |||||||
| chr4:1666255 | A | C | 2 | a0001c0001t0010g0042 a0012c0009t0014g0014 |
2 | HG03704.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.75+2412T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666255 | |||||||
| chr4:1666273 | A | AACCTGCA others(52): Show |
1 | a0001c0001t0001g0245 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.75+2393_75+2394ins others(59): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | |||||||
| chr4:1666273 | A | AACCTGCA others(59): Show |
1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2328_75+2393dup others(66): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | |||||||
| chr4:1666273 | A | AACGTGCA others(59): Show |
56 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(53): Show |
57 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.75+2393_75+2394ins others(66): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | |||||||
| chr4:1666273 | A | AGCCTGCA others(92): Show |
1 | a0012c0009t0014g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.75+2393_75+2394ins others(99): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | |||||||
| chr4:1666276 | C | G | 1 | a0001c0002t0005g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+2391G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666276 | |||||||
| chr4:1666319 | T | TGTATCTA others(24): Show |
1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+2317_75+2347dup others(31): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666319 | |||||||
| chr4:1666319 | T | TGTATCTA others(57): Show |
254 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
268 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.75+2284_75+2347dup others(64): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666319 | |||||||
| chr4:1666383 | C | CCTGTATC others(93): Show |
1 | a0001c0002t0005g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+2283_75+2284ins others(100): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666383 | |||||||
| chr4:1666417 | C | A | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.75+2250G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666417 | |||||||
| chr4:1666451 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2216C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666451 | |||||||
| chr4:1666480 | T | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(313): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.75+2187A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666480 | |||||||
| chr4:1666553 | G | A | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+2114C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666553 | |||||||
| chr4:1666577 | G | C | 322 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(319): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.75+2090C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666577 | |||||||
| chr4:1666592 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0002g0275 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+2075G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666592 | |||||||
| chr4:1666598 | C | G | 1 | a0001c0001t0017g0106 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75+2069G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666598 | |||||||
| chr4:1666609 | T | C | 1 | a0003c0004t0018g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+2058A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666609 | |||||||
| chr4:1666610 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.75+2057C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666610 | |||||||
| chr4:1666648 | G | A | 1 | a0002c0003t0016g0308 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.75+2019C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666648 | |||||||
| chr4:1666682 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.75+1985A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666682 | |||||||
| chr4:1666740 | G | A | 3 | a0002c0003t0003g0114 a0002c0003t0003g0115 a0002c0003t0003g0124 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.75+1927C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666740 | |||||||
| chr4:1666777 | G | A | 1 | a0002c0003t0016g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+1890C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666777 | |||||||
| chr4:1666795 | G | A | 1 | a0001c0002t0005g0205 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.75+1872C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666795 | |||||||
| chr4:1666855 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.75+1812A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666855 | |||||||
| chr4:1667058 | G | T | 1 | a0001c0001t0009g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+1609C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667058 | |||||||
| chr4:1667104 | G | A | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.75+1563C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667104 | |||||||
| chr4:1667111 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.75+1556C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667111 | |||||||
| chr4:1667127 | C | CAAA | 53 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(50): Show |
54 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.75+1537_75+1539dup others(3): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667127 | |||||||
| chr4:1667169 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.75+1498A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667169 | |||||||
| chr4:1667267 | C | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.75+1400G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667267 | |||||||
| chr4:1667268 | C | T | 7 | a0001c0001t0010g0028 a0001c0001t0010g0039 a0001c0001t0010g0042 others(4): Show |
7 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+1399G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667268 | |||||||
| chr4:1667326 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0231 a0001c0001t0001g0285 others(6): Show |
10 | HG01074.hp1 HG01081.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+1341C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667326 | |||||||
| chr4:1667420 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0265 |
2 | HG00558.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.75+1247C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667420 | |||||||
| chr4:1667451 | A | C | 1 | a0001c0001t0007g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+1216T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667451 | |||||||
| chr4:1667472 | C | T | 1 | a0001c0002t0033g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.75+1195G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667472 | |||||||
| chr4:1667479 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+1188G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667479 | |||||||
| chr4:1667512 | C | T | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1155G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667512 | |||||||
| chr4:1667525 | C | T | 5 | a0001c0002t0012g0016 a0001c0002t0012g0017 a0001c0002t0012g0051 others(2): Show |
5 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1142G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667525 | |||||||
| chr4:1667526 | G | A | 4 | a0001c0001t0037g0129 a0003c0004t0018g0131 a0003c0004t0018g0150 others(1): Show |
4 | HG02559.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1141C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667526 | |||||||
| chr4:1667548 | C | G | 1 | a0001c0002t0005g0307 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.75+1119G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667548 | |||||||
| chr4:1668028 | G | A | 1 | a0001c0002t0004g0330 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.75+639C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668028 | |||||||
| chr4:1668032 | T | C | 322 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(319): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.75+635A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668032 | |||||||
| chr4:1668090 | C | G | 4 | a0001c0001t0002g0133 a0001c0001t0002g0273 a0001c0001t0002g0274 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+577G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668090 | |||||||
| chr4:1668108 | T | C | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.75+559A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668108 | |||||||
| chr4:1668109 | T | C | 1 | a0002c0003t0002g0295 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.75+558A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668109 | |||||||
| chr4:1668148 | C | CT | 314 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(311): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.75+518dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668148 | |||||||
| chr4:1668203 | G | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+464C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668203 | |||||||
| chr4:1668237 | G | T | 1 | a0001c0001t0008g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+430C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668237 | |||||||
| chr4:1668240 | T | C | 1 | a0001c0001t0008g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+427A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668240 | |||||||
| chr4:1668264 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+403G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668264 | |||||||
| chr4:1668285 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75+382C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668285 | |||||||
| chr4:1668391 | T | C | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.75+276A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668391 | |||||||
| chr4:1668470 | A | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+197T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668470 | |||||||
| chr4:1668489 | G | A | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+178C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668489 | |||||||
| chr4:1668549 | A | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+118T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668549 | |||||||
| chr4:1668563 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+104C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668563 | |||||||
| chr4:1668972 | A | C | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-67T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1668972 | |||||||
| chr4:1668975 | T | C | 1 | a0001c0001t0038g0315 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-164-70A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1668975 | |||||||
| chr4:1669092 | TA | T | 6 | a0002c0003t0016g0148 a0002c0003t0016g0308 a0002c0003t0016g0316 others(3): Show |
6 | HG01109.hp1 HG01975.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-188delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669092 | |||||||
| chr4:1669127 | G | A | 32 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(29): Show |
32 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-164-222C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669127 | |||||||
| chr4:1669137 | A | G | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-232T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669137 | |||||||
| chr4:1669228 | G | A | 1 | a0001c0001t0010g0027 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-164-323C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669228 | |||||||
| chr4:1669233 | T | C | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-164-328A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669233 | |||||||
| chr4:1669395 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-164-490C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669395 | |||||||
| chr4:1669404 | G | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-499C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669404 | |||||||
| chr4:1669427 | C | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-522G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669427 | |||||||
| chr4:1669450 | G | C | 5 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-545C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669450 | |||||||
| chr4:1669579 | C | T | 1 | a0001c0002t0005g0323 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-164-674G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669579 | |||||||
| chr4:1669738 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-164-833C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669738 | |||||||
| chr4:1669803 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-164-898C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669803 | |||||||
| chr4:1669896 | C | T | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-164-991G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669896 | |||||||
| chr4:1669984 | C | T | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-1079G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669984 | |||||||
| chr4:1669985 | G | A | 6 | a0001c0002t0004g0153 a0001c0002t0004g0189 a0001c0002t0004g0194 others(3): Show |
6 | HG01070.hp2 HG02300.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-1080C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669985 | |||||||
| chr4:1670001 | C | A | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-1096G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670001 | |||||||
| chr4:1670024 | C | T | 2 | a0001c0001t0024g0149 a0001c0001t0024g0318 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-164-1119G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670024 | |||||||
| chr4:1670045 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
194 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-164-1140C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670045 | |||||||
| chr4:1670117 | GGCCAT | G | 5 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-1217_-164-121 others(9): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670117 | |||||||
| chr4:1670320 | C | T | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-1415G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670320 | |||||||
| chr4:1670369 | G | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
125 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-164-1464C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670369 | |||||||
| chr4:1670491 | C | G | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-1586G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670491 | |||||||
| chr4:1670649 | A | G | 4 | a0001c0001t0030g0056 a0003c0004t0018g0131 a0003c0004t0018g0150 others(1): Show |
4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-1744T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670649 | |||||||
| chr4:1670695 | G | A | 1 | a0001c0001t0009g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-164-1790C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670695 | |||||||
| chr4:1670896 | G | A | 3 | a0001c0001t0007g0089 a0002c0003t0023g0135 a0002c0003t0023g0147 |
3 | HG02886.hp1 HG03195.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-164-1991C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670896 | |||||||
| chr4:1670900 | G | A | 1 | a0002c0003t0003g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-164-1995C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670900 | |||||||
| chr4:1671032 | G | A | 1 | a0001c0001t0006g0033 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-164-2127C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671032 | |||||||
| chr4:1671047 | C | G | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-2142G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671047 | |||||||
| chr4:1671061 | A | ACCAGCTC others(49): Show |
7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-2157_-164-215 others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671061 | |||||||
| chr4:1671073 | C | CCACAGCC others(473): Show |
1 | a0002c0003t0002g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-164-2169_-164-216 others(484): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671073 | |||||||
| chr4:1671073 | C | CCACAGCC others(473): Show |
41 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(38): Show |
43 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-164-2169_-164-216 others(484): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671073 | |||||||
| chr4:1671095 | C | T | 1 | a0001c0002t0004g0327 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-164-2190G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671095 | |||||||
| chr4:1671117 | A | C | 2 | a0001c0002t0012g0059 a0002c0003t0003g0111 |
2 | HG02809.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-164-2212T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671117 | |||||||
| chr4:1671118 | C | A | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-2213G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671118 | |||||||
| chr4:1671129 | C | CCACAGCC others(417): Show |
1 | a0002c0003t0003g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-164-2225_-164-222 others(428): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671129 | |||||||
| chr4:1671129 | C | T | 9 | a0001c0002t0004g0188 a0001c0002t0004g0190 a0001c0002t0004g0192 others(6): Show |
9 | HG00621.hp1 HG01981.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-2224G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671129 | |||||||
| chr4:1671138 | T | C | 44 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(41): Show |
46 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-164-2233A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671138 | |||||||
| chr4:1671173 | A | C | 42 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(39): Show |
44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.-164-2268T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671173 | |||||||
| chr4:1671189 | A | G | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2284T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671189 | |||||||
| chr4:1671212 | C | G | 2 | a0001c0002t0012g0059 a0010c0011t0036g0122 |
2 | HG02258.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-164-2307G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671212 | |||||||
| chr4:1671223 | C | A | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2318G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671223 | |||||||
| chr4:1671245 | A | G | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2340T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671245 | |||||||
| chr4:1671250 | G | A | 58 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-164-2345C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671250 | |||||||
| chr4:1671270 | G | A | 43 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(40): Show |
45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-2365C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671270 | |||||||
| chr4:1671276 | G | A | 12 | a0001c0002t0005g0160 a0001c0002t0005g0279 a0001c0002t0005g0306 others(9): Show |
13 | HG00099.hp2 HG01074.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-164-2371C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671276 | |||||||
| chr4:1671279 | A | C | 1 | a0002c0003t0003g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-164-2374T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671279 | |||||||
| chr4:1671300 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0265 |
2 | HG00558.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-164-2395G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671300 | |||||||
| chr4:1671316 | C | T | 3 | a0001c0001t0026g0050 a0001c0001t0037g0129 a0001c0001t0038g0315 |
3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-2411G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671316 | |||||||
| chr4:1671335 | C | A | 4 | a0001c0001t0001g0174 a0001c0001t0008g0077 a0001c0002t0012g0059 others(1): Show |
4 | HG02015.hp2 HG02258.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-2430G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671335 | |||||||
| chr4:1671350 | C | T | 1 | a0002c0003t0002g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-164-2445G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671350 | |||||||
| chr4:1671356 | G | A | 1 | a0001c0001t0008g0077 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-164-2451C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671356 | |||||||
| chr4:1671385 | A | C | 8 | a0001c0001t0006g0052 a0001c0001t0008g0001 a0001c0001t0008g0071 others(5): Show |
11 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-164-2480T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671385 | |||||||
| chr4:1671391 | T | TCACAGCC others(585): Show |
1 | a0001c0001t0001g0233 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-164-2487_-164-248 others(596): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671391 | |||||||
| chr4:1671401 | G | A | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2496C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671401 | |||||||
| chr4:1671424 | G | C | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-2519C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671424 | |||||||
| chr4:1671435 | A | ACCAGCTC others(1333): Show |
7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-2531_-164-253 others(1344): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671435 | |||||||
| chr4:1671435 | A | ACCAGCTC others(155): Show |
43 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(40): Show |
45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-2531_-164-253 others(166): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671435 | |||||||
| chr4:1671435 | A | C | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-2530T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671435 | |||||||
| chr4:1671447 | C | CCACAGCC others(261): Show |
1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(272): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(529): Show |
1 | a0001c0001t0001g0226 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(540): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(529): Show |
3 | a0001c0001t0009g0253 a0001c0001t0009g0256 a0001c0001t0009g0257 |
3 | NA18939.hp1 NA18956.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(540): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(473): Show |
1 | a0001c0001t0007g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(484): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(579): Show |
177 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
189 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(579): Show |
2 | a0001c0001t0024g0149 a0001c0001t0024g0318 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(841): Show |
1 | a0001c0001t0008g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(852): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(579): Show |
2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(579): Show |
5 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0102 others(2): Show |
5 | HG01884.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(579): Show |
6 | a0001c0001t0006g0025 a0001c0001t0006g0030 a0001c0001t0006g0031 others(3): Show |
6 | HG00423.hp2 HG02080.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(261): Show |
4 | a0001c0002t0005g0270 a0001c0002t0040g0321 a0004c0006t0028g0012 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(272): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(579): Show |
2 | a0001c0001t0001g0230 a0010c0011t0036g0122 |
2 | HG02129.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(417): Show |
1 | a0001c0001t0008g0077 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(428): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(205): Show |
29 | a0001c0002t0005g0140 a0001c0002t0005g0143 a0001c0002t0005g0159 others(26): Show |
29 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(216): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(205): Show |
23 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(20): Show |
23 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(216): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671447 | C | CCACAGCC others(205): Show |
1 | a0001c0002t0015g0004 | 2 | HG00099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(216): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | |||||||
| chr4:1671457 | A | G | 52 | a0001c0001t0001g0141 a0001c0001t0022g0132 a0001c0002t0004g0206 others(49): Show |
54 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-164-2552T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671457 | |||||||
| chr4:1671461 | G | C | 313 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-164-2556C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671461 | |||||||
| chr4:1671480 | G | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(258): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-164-2575C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671480 | |||||||
| chr4:1671491 | C | A | 52 | a0001c0001t0001g0141 a0001c0001t0022g0132 a0001c0002t0004g0206 others(49): Show |
54 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-164-2586G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671491 | |||||||
| chr4:1671491 | C | CCCAGCTC others(99): Show |
3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-2587_-164-258 others(110): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671491 | |||||||
| chr4:1671498 | C | T | 1 | a0001c0002t0004g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2593G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671498 | |||||||
| chr4:1671503 | C | CCACGGCC others(149): Show |
1 | a0001c0002t0004g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2599_-164-259 others(160): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671503 | |||||||
| chr4:1671513 | G | A | 262 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-164-2608C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671513 | |||||||
| chr4:1671513 | G | GGCCCGGA others(261): Show |
6 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0026g0050 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-2609_-164-260 others(272): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671513 | |||||||
| chr4:1671518 | G | A | 2 | a0001c0001t0001g0141 a0001c0002t0041g0329 |
2 | HG02258.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-164-2613C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671518 | |||||||
| chr4:1671536 | G | C | 1 | a0001c0002t0004g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2631C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671536 | |||||||
| chr4:1671547 | A | ACCAGCTC others(523): Show |
1 | a0001c0001t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-164-2643_-164-264 others(534): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671547 | |||||||
| chr4:1671547 | A | C | 1 | a0001c0002t0004g0206 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2642T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671547 | |||||||
| chr4:1671569 | A | G | 320 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(317): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-164-2664T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671569 | |||||||
| chr4:1671573 | G | C | 322 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(319): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.-164-2668C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671573 | |||||||
| chr4:1671665 | G | C | 2 | a0002c0003t0003g0109 a0002c0003t0003g0110 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-164-2760C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671665 | |||||||
| chr4:1671672 | T | C | 1 | a0001c0002t0004g0330 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-164-2767A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671672 | |||||||
| chr4:1671773 | C | T | 63 | a0001c0001t0030g0056 a0001c0002t0004g0153 a0001c0002t0004g0161 others(60): Show |
64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-2868G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671773 | |||||||
| chr4:1671837 | C | T | 266 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-164-2932G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671837 | |||||||
| chr4:1672004 | C | T | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-3099G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672004 | |||||||
| chr4:1672024 | C | CACCCAGG others(17): Show |
63 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(60): Show |
64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-3120_-164-311 others(28): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672024 | |||||||
| chr4:1672035 | C | A | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-3130G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672035 | |||||||
| chr4:1672043 | CT | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-3139delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672043 | |||||||
| chr4:1672048 | A | AT | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-3144_-164-314 others(5): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672048 | |||||||
| chr4:1672086 | G | A | 43 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(40): Show |
45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-3181C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672086 | |||||||
| chr4:1672093 | CGAACCCA others(17): Show |
C | 1 | a0001c0001t0006g0034 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-164-3212_-164-318 others(28): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672093 | |||||||
| chr4:1672124 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-164-3219T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672124 | |||||||
| chr4:1672133 | G | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-164-3228C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672133 | |||||||
| chr4:1672161 | CCCAGGAA others(48): Show |
C | 59 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-3311_-164-325 others(59): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672161 | |||||||
| chr4:1672175 | AACCCACG others(1): Show |
A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-3278_-164-327 others(12): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672175 | |||||||
| chr4:1672262 | GACCCACA others(16): Show |
G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-3380_-164-335 others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672262 | |||||||
| chr4:1672285 | C | T | 59 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-3380G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672285 | |||||||
| chr4:1672309 | AACCCATG others(25): Show |
A | 59 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-3436_-164-340 others(36): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672309 | |||||||
| chr4:1672325 | AACCCAGG others(17): Show |
A | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-3444_-164-342 others(28): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672325 | |||||||
| chr4:1672347 | T | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-3442A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672347 | |||||||
| chr4:1672349 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
214 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.-164-3444C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672349 | |||||||
| chr4:1672363 | G | C | 2 | a0001c0001t0001g0246 a0001c0001t0007g0083 |
2 | NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-164-3458C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672363 | |||||||
| chr4:1672363 | GGAACCCA others(1): Show |
G | 53 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(50): Show |
55 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.-164-3466_-164-345 others(12): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672363 | |||||||
| chr4:1672435 | G | A | 1 | a0002c0003t0020g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-164-3530C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672435 | |||||||
| chr4:1672481 | G | A | 2 | a0001c0001t0010g0027 a0001c0001t0010g0035 |
2 | HG00621.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-164-3576C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672481 | |||||||
| chr4:1672521 | A | G | 1 | a0001c0001t0007g0091 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-164-3616T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672521 | |||||||
| chr4:1672579 | C | T | 1 | a0001c0001t0019g0105 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-164-3674G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672579 | |||||||
| chr4:1672628 | G | GCT | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-3725_-164-372 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672628 | |||||||
| chr4:1672632 | G | A | 1 | a0001c0002t0005g0323 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-164-3727C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672632 | |||||||
| chr4:1672759 | CT | C | 9 | a0001c0002t0004g0161 a0001c0002t0004g0189 a0001c0002t0004g0264 others(6): Show |
9 | HG00642.hp1 HG01243.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-164-3855delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672759 | CTT | C | 48 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0026g0050 others(45): Show |
49 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-164-3856_-164-385 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672759 | CTTT | C | 21 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0280 others(18): Show |
21 | HG00438.hp1 HG01109.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-164-3857_-164-385 others(7): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672759 | CTTTT | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
194 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.-164-3858_-164-385 others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672759 | CTTTTTTT others(3): Show |
C | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-3864_-164-385 others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672759 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0024g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-164-3865_-164-385 others(15): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672759 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0006g0041 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-164-3870_-164-385 others(20): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | |||||||
| chr4:1672914 | C | G | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-4009G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672914 | |||||||
| chr4:1673156 | C | T | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-164-4251G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673156 | |||||||
| chr4:1673217 | T | C | 1 | a0001c0002t0005g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-164-4312A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673217 | |||||||
| chr4:1673224 | C | T | 11 | a0001c0001t0002g0133 a0001c0001t0002g0273 a0001c0001t0002g0274 others(8): Show |
11 | HG02572.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-164-4319G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673224 | |||||||
| chr4:1673254 | G | A | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-4349C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673254 | |||||||
| chr4:1673282 | G | A | 1 | a0001c0002t0005g0205 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-164-4377C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673282 | |||||||
| chr4:1673400 | G | A | 1 | a0001c0001t0006g0036 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-164-4495C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673400 | |||||||
| chr4:1673416 | C | G | 43 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(40): Show |
45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-4511G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673416 | |||||||
| chr4:1673459 | C | T | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-4554G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673459 | |||||||
| chr4:1673514 | A | G | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-4609T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673514 | |||||||
| chr4:1673550 | T | C | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-4645A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673550 | |||||||
| chr4:1673615 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-164-4710G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673615 | |||||||
| chr4:1673624 | T | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-4719A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673624 | |||||||
| chr4:1673649 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-164-4744G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673649 | |||||||
| chr4:1673720 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-164-4815C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673720 | |||||||
| chr4:1673728 | G | A | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-4823C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673728 | |||||||
| chr4:1673949 | G | A | 10 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0116 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-164-5044C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673949 | |||||||
| chr4:1674013 | G | A | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-5108C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674013 | |||||||
| chr4:1674090 | C | T | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-164-5185G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674090 | |||||||
| chr4:1674261 | G | A | 1 | a0001c0001t0010g0027 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-164-5356C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674261 | |||||||
| chr4:1674272 | C | T | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-5367G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674272 | |||||||
| chr4:1674367 | A | G | 4 | a0001c0001t0002g0133 a0001c0001t0002g0273 a0001c0001t0002g0274 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-5462T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674367 | |||||||
| chr4:1674407 | C | T | 2 | a0002c0003t0023g0135 a0002c0003t0023g0147 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-164-5502G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674407 | |||||||
| chr4:1674466 | G | A | 1 | a0001c0001t0008g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-164-5561C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674466 | |||||||
| chr4:1674540 | G | A | 1 | a0001c0001t0007g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-164-5635C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674540 | |||||||
| chr4:1674668 | CA | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.-164-5764delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674668 | |||||||
| chr4:1674767 | T | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-5862A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674767 | |||||||
| chr4:1674832 | G | A | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0235 others(4): Show |
7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-5927C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674832 | |||||||
| chr4:1674871 | C | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0236 others(2): Show |
5 | HG02056.hp2 NA18939.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-5966G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674871 | |||||||
| chr4:1674961 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-164-6056G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674961 | |||||||
| chr4:1674998 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-164-6093C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674998 | |||||||
| chr4:1675028 | A | AC | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-6124dupG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675028 | |||||||
| chr4:1675062 | G | A | 15 | a0001c0001t0006g0052 a0001c0001t0008g0001 a0001c0001t0008g0071 others(12): Show |
18 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-164-6157C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675062 | |||||||
| chr4:1675291 | T | C | 322 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(319): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.-164-6386A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675291 | |||||||
| chr4:1675305 | C | T | 1 | a0001c0002t0005g0298 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-164-6400G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675305 | |||||||
| chr4:1675382 | T | G | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-6477A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675382 | |||||||
| chr4:1675593 | G | C | 312 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-164-6688C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675593 | |||||||
| chr4:1675703 | G | A | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-6798C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675703 | |||||||
| chr4:1675712 | G | A | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-164-6807C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675712 | |||||||
| chr4:1675757 | G | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-164-6852C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675757 | |||||||
| chr4:1675764 | G | A | 4 | a0001c0001t0030g0056 a0003c0004t0018g0131 a0003c0004t0018g0150 others(1): Show |
4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-6859C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675764 | |||||||
| chr4:1675764 | G | T | 3 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0032g0067 |
3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-164-6859C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675764 | |||||||
| chr4:1675802 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-164-6897G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675802 | |||||||
| chr4:1675818 | C | T | 1 | a0002c0003t0002g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-164-6913G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675818 | |||||||
| chr4:1675906 | G | A | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-164-7001C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675906 | |||||||
| chr4:1675936 | A | T | 1 | a0001c0002t0004g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-164-7031T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675936 | |||||||
| chr4:1675950 | C | T | 1 | a0001c0001t0009g0260 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-164-7045G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675950 | |||||||
| chr4:1676066 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-164-7161C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676066 | |||||||
| chr4:1676126 | A | C | 7 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0116 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-164-7221T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676126 | |||||||
| chr4:1676155 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-164-7250G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676155 | |||||||
| chr4:1676239 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0291 |
2 | HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-164-7334C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676239 | |||||||
| chr4:1676259 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-164-7354G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676259 | |||||||
| chr4:1676269 | A | G | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-7364T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676269 | |||||||
| chr4:1676358 | G | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0238 |
2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-164-7453C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676358 | |||||||
| chr4:1676701 | G | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
269 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-165+7532C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676701 | |||||||
| chr4:1676706 | G | A | 1 | a0001c0002t0004g0195 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-165+7527C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676706 | |||||||
| chr4:1676747 | C | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(329): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.-165+7486G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676747 | |||||||
| chr4:1676835 | C | T | 6 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0026g0050 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+7398G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676835 | |||||||
| chr4:1676871 | G | C | 2 | a0001c0001t0037g0129 a0001c0001t0038g0315 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-165+7362C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676871 | |||||||
| chr4:1677044 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(210): Show |
225 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-165+7189C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677044 | |||||||
| chr4:1677050 | C | T | 2 | a0004c0006t0028g0012 a0004c0006t0042g0142 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-165+7183G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677050 | |||||||
| chr4:1677051 | A | G | 114 | a0001c0001t0022g0132 a0001c0001t0030g0056 a0001c0002t0004g0153 others(111): Show |
117 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-165+7182T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677051 | |||||||
| chr4:1677098 | T | C | 10 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0116 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+7135A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677098 | |||||||
| chr4:1677351 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0025g0166 |
2 | NA18612.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-165+6882G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677351 | |||||||
| chr4:1677390 | G | A | 1 | a0002c0003t0002g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-165+6843C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677390 | |||||||
| chr4:1677402 | C | A | 1 | a0001c0002t0012g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-165+6831G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677402 | |||||||
| chr4:1677417 | G | A | 4 | a0002c0003t0002g0138 a0002c0003t0002g0156 a0002c0003t0003g0112 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-165+6816C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677417 | |||||||
| chr4:1677524 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+6709C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677524 | |||||||
| chr4:1677561 | T | G | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+6672A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677561 | |||||||
| chr4:1677699 | A | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-165+6534T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677699 | |||||||
| chr4:1677730 | G | A | 1 | a0001c0001t0021g0325 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-165+6503C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677730 | |||||||
| chr4:1677876 | C | T | 10 | a0002c0003t0003g0109 a0002c0003t0003g0110 a0002c0003t0016g0148 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-165+6357G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677876 | |||||||
| chr4:1677932 | G | C | 57 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-165+6301C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677932 | |||||||
| chr4:1677955 | T | G | 3 | a0003c0004t0018g0131 a0003c0004t0018g0150 a0003c0004t0018g0313 |
3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-165+6278A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677955 | |||||||
| chr4:1678083 | C | T | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+6150G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678083 | |||||||
| chr4:1678134 | G | A | 9 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(6): Show |
9 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-165+6099C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678134 | |||||||
| chr4:1678157 | C | A | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+6076G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678157 | |||||||
| chr4:1678360 | T | G | 1 | a0002c0003t0002g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-165+5873A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678360 | |||||||
| chr4:1678377 | C | T | 312 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-165+5856G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678377 | |||||||
| chr4:1678407 | C | T | 322 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(319): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.-165+5826G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678407 | |||||||
| chr4:1678550 | G | A | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+5683C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678550 | |||||||
| chr4:1678582 | G | A | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+5651C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678582 | |||||||
| chr4:1678696 | T | C | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+5537A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678696 | |||||||
| chr4:1678725 | G | C | 3 | a0001c0001t0001g0182 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG00642.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-165+5508C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678725 | |||||||
| chr4:1678746 | C | T | 58 | a0001c0001t0001g0218 a0001c0002t0004g0153 a0001c0002t0004g0161 others(55): Show |
59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-165+5487G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678746 | |||||||
| chr4:1678835 | G | A | 10 | a0001c0001t0002g0272 a0001c0001t0003g0101 a0001c0001t0003g0116 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+5398C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678835 | |||||||
| chr4:1679206 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+5027C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679206 | |||||||
| chr4:1679270 | C | T | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+4963G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679270 | |||||||
| chr4:1679309 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-165+4924G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679309 | |||||||
| chr4:1679316 | G | A | 1 | a0001c0001t0024g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-165+4917C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679316 | |||||||
| chr4:1679379 | A | C | 14 | a0001c0001t0006g0026 a0001c0001t0006g0037 a0001c0001t0006g0044 others(11): Show |
14 | HG00280.hp2 HG00733.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-165+4854T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679379 | |||||||
| chr4:1679386 | C | CA | 106 | a0001c0001t0001g0201 a0001c0001t0001g0208 a0001c0001t0001g0239 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-165+4846dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679386 | |||||||
| chr4:1679386 | C | CAA | 8 | a0001c0001t0001g0212 a0001c0001t0006g0037 a0001c0001t0009g0155 others(5): Show |
8 | HG02027.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+4845_-165+484 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679386 | |||||||
| chr4:1679484 | GAGACCAG others(627): Show |
G | 1 | a0001c0001t0037g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-165+4115_-165+474 others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679484 | |||||||
| chr4:1679542 | C | T | 3 | a0001c0001t0009g0253 a0001c0001t0009g0256 a0001c0001t0009g0257 |
3 | NA18939.hp1 NA18956.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-165+4691G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679542 | |||||||
| chr4:1679547 | G | A | 50 | a0001c0001t0022g0132 a0002c0003t0002g0009 a0002c0003t0002g0138 others(47): Show |
52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+4686C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679547 | |||||||
| chr4:1679680 | C | A | 1 | a0001c0001t0001g0003 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-165+4553G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679680 | |||||||
| chr4:1679684 | T | TA | 18 | a0001c0001t0001g0266 a0001c0001t0002g0133 a0001c0001t0002g0273 others(15): Show |
18 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.-165+4548dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679684 | |||||||
| chr4:1679684 | T | TAA | 49 | a0001c0001t0022g0132 a0001c0002t0005g0143 a0002c0003t0002g0009 others(46): Show |
51 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-165+4547_-165+454 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679684 | |||||||
| chr4:1679684 | TA | T | 56 | a0001c0001t0001g0221 a0001c0001t0008g0001 a0001c0001t0025g0166 others(53): Show |
57 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-165+4548delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679684 | |||||||
| chr4:1679815 | G | A | 4 | a0001c0001t0030g0056 a0003c0004t0018g0131 a0003c0004t0018g0150 others(1): Show |
4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-165+4418C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679815 | |||||||
| chr4:1679847 | G | A | 2 | a0001c0001t0024g0149 a0001c0001t0024g0318 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-165+4386C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679847 | |||||||
| chr4:1679875 | C | T | 1 | a0001c0001t0006g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-165+4358G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679875 | |||||||
| chr4:1679987 | C | T | 1 | a0001c0001t0014g0054 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-165+4246G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679987 | |||||||
| chr4:1680012 | G | C | 51 | a0001c0001t0022g0132 a0001c0002t0005g0143 a0002c0003t0002g0009 others(48): Show |
53 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+4221C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680012 | |||||||
| chr4:1680024 | G | GA | 300 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(297): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-165+4208dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680024 | |||||||
| chr4:1680024 | G | GAA | 11 | a0001c0001t0001g0246 a0001c0001t0006g0026 a0001c0001t0007g0093 others(8): Show |
11 | HG01099.hp2 HG02027.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-165+4207_-165+420 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680024 | |||||||
| chr4:1680135 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-165+4098G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680135 | |||||||
| chr4:1680166 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-165+4067T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680166 | |||||||
| chr4:1680235 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.-165+3998A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680235 | |||||||
| chr4:1680260 | G | A | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+3973C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680260 | |||||||
| chr4:1680274 | G | A | 1 | a0001c0002t0027g0018 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-165+3959C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680274 | |||||||
| chr4:1680283 | C | A | 4 | a0001c0001t0021g0324 a0001c0001t0021g0325 a0001c0001t0026g0050 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+3950G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680283 | |||||||
| chr4:1680296 | G | A | 1 | a0001c0002t0004g0197 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-165+3937C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680296 | |||||||
| chr4:1680305 | G | C | 1 | a0001c0001t0010g0027 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-165+3928C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680305 | |||||||
| chr4:1680319 | C | CA | 9 | a0001c0001t0002g0136 a0001c0001t0002g0268 a0001c0001t0002g0269 others(6): Show |
9 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+3913dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | |||||||
| chr4:1680319 | C | CAA | 59 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0137 others(56): Show |
64 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-165+3912_-165+391 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | |||||||
| chr4:1680319 | C | CAAA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
113 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-165+3911_-165+391 others(7): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | |||||||
| chr4:1680319 | C | CAAAA | 38 | a0001c0001t0001g0152 a0001c0001t0001g0177 a0001c0001t0001g0178 others(35): Show |
38 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-165+3910_-165+391 others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | |||||||
| chr4:1680319 | CA | C | 93 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(90): Show |
95 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-165+3913delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | |||||||
| chr4:1680330 | A | C | 1 | a0001c0002t0004g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-165+3903T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680330 | |||||||
| chr4:1680331 | A | C | 54 | a0001c0002t0004g0153 a0001c0002t0004g0161 a0001c0002t0004g0162 others(51): Show |
55 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-165+3902T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680331 | |||||||
| chr4:1680337 | A | C | 30 | a0001c0002t0005g0140 a0001c0002t0005g0159 a0001c0002t0005g0160 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-165+3896T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680337 | |||||||
| chr4:1680468 | T | C | 1 | a0010c0011t0036g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+3765A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680468 | |||||||
| chr4:1680614 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-165+3619C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680614 | |||||||
| chr4:1680632 | A | G | 51 | a0001c0001t0022g0132 a0001c0002t0005g0143 a0002c0003t0002g0009 others(48): Show |
53 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+3601T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680632 | |||||||
| chr4:1680714 | T | C | 1 | a0001c0002t0005g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-165+3519A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680714 | |||||||
| chr4:1680721 | C | T | 5 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0214 others(2): Show |
5 | HG00673.hp1 NA18965.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+3512G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680721 | |||||||
| chr4:1680750 | T | C | 7 | a0002c0003t0002g0144 a0002c0003t0002g0320 a0002c0003t0002g0322 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+3483A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680750 | |||||||
| chr4:1680797 | C | CA | 51 | a0001c0001t0014g0021 a0001c0001t0022g0132 a0002c0003t0002g0009 others(48): Show |
53 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.-165+3435dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680797 | |||||||
| chr4:1680847 | A | AGGGCACA others(7): Show |
1 | a0001c0001t0007g0083 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-165+3372_-165+338 others(18): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680847 | |||||||
| chr4:1680864 | G | C | 1 | a0001c0002t0004g0197 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-165+3369C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680864 | |||||||
| chr4:1680890 | T | C | 10 | a0001c0001t0022g0132 a0002c0003t0002g0139 a0002c0003t0002g0146 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+3343A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680890 | |||||||
| chr4:1680955 | A | C | 114 | a0001c0001t0001g0259 a0001c0001t0022g0132 a0001c0001t0030g0056 others(111): Show |
117 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-165+3278T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680955 | |||||||
| chr4:1681223 | A | G | 1 | a0013c0015t0001g0210 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-165+3010T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681223 | |||||||
| chr4:1681234 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-165+2999A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681234 | |||||||
| chr4:1681299 | T | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
125 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-165+2934A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681299 | |||||||
| chr4:1681342 | C | T | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+2891G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681342 | |||||||
| chr4:1681386 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-165+2847G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681386 | |||||||
| chr4:1681439 | G | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-165+2794C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681439 | |||||||
| chr4:1681448 | C | T | 1 | a0011c0008t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-165+2785G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681448 | |||||||
| chr4:1681489 | T | C | 51 | a0001c0001t0022g0132 a0001c0002t0005g0143 a0002c0003t0002g0009 others(48): Show |
53 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+2744A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681489 | |||||||
| chr4:1681523 | C | CT | 52 | a0001c0001t0010g0027 a0001c0002t0004g0153 a0001c0002t0004g0161 others(49): Show |
53 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+2709dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681523 | |||||||
| chr4:1681523 | CT | C | 54 | a0001c0001t0001g0294 a0001c0001t0006g0043 a0001c0001t0008g0121 others(51): Show |
56 | HG00733.hp1 HG01070.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.-165+2709delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681523 | |||||||
| chr4:1681531 | T | C | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+2702A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681531 | |||||||
| chr4:1681575 | C | A | 1 | a0001c0001t0006g0049 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-165+2658G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681575 | |||||||
| chr4:1681658 | A | G | 113 | a0001c0001t0022g0132 a0001c0001t0030g0056 a0001c0002t0004g0153 others(110): Show |
116 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-165+2575T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681658 | |||||||
| chr4:1681729 | C | T | 14 | a0002c0003t0002g0009 a0002c0003t0002g0184 a0002c0003t0002g0185 others(11): Show |
15 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-165+2504G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681729 | |||||||
| chr4:1681761 | C | T | 1 | a0002c0003t0020g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-165+2472G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681761 | |||||||
| chr4:1681816 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0317 |
3 | HG00408.hp2 HG02015.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-165+2417G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681816 | |||||||
| chr4:1681881 | T | C | 13 | a0001c0001t0006g0026 a0001c0001t0006g0044 a0001c0001t0006g0045 others(10): Show |
13 | HG00280.hp2 HG00733.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+2352A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681881 | |||||||
| chr4:1681911 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-165+2322G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681911 | |||||||
| chr4:1681963 | G | A | 1 | a0001c0002t0005g0307 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-165+2270C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681963 | |||||||
| chr4:1682239 | A | G | 64 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(61): Show |
65 | HG00609.hp1 HG00733.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.-165+1994T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682239 | |||||||
| chr4:1682264 | C | CT | 82 | a0001c0001t0001g0141 a0001c0001t0001g0152 a0001c0001t0001g0207 others(79): Show |
87 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-165+1968dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682264 | |||||||
| chr4:1682264 | CT | C | 46 | a0001c0001t0003g0116 a0001c0001t0013g0250 a0001c0001t0013g0251 others(43): Show |
47 | HG00609.hp1 HG00733.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-165+1968delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682264 | |||||||
| chr4:1682313 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-165+1920G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682313 | |||||||
| chr4:1682408 | A | G | 1 | a0001c0001t0030g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-165+1825T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682408 | |||||||
| chr4:1682506 | C | T | 1 | a0001c0001t0013g0252 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-165+1727G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682506 | |||||||
| chr4:1682574 | T | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-165+1659A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682574 | |||||||
| chr4:1682643 | C | G | 2 | a0003c0004t0018g0150 a0003c0004t0018g0313 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-165+1590G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682643 | |||||||
| chr4:1682682 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.-165+1551G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682682 | |||||||
| chr4:1682702 | A | G | 1 | a0001c0001t0026g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+1531T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682702 | |||||||
| chr4:1682715 | TGAGCAAC others(30): Show |
T | 1 | a0002c0003t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-165+1481_-165+151 others(41): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682715 | |||||||
| chr4:1682730 | A | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-165+1503T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682730 | |||||||
| chr4:1682772 | T | C | 6 | a0001c0001t0003g0119 a0001c0001t0035g0118 a0002c0003t0002g0146 others(3): Show |
6 | HG01891.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+1461A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682772 | |||||||
| chr4:1682869 | G | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0207 others(185): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.-165+1364C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682869 | |||||||
| chr4:1682883 | A | G | 1 | a0001c0002t0005g0263 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-165+1350T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682883 | |||||||
| chr4:1682900 | G | C | 118 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0145 others(115): Show |
120 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-165+1333C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682900 | |||||||
| chr4:1682907 | G | A | 324 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(321): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-165+1326C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682907 | |||||||
| chr4:1682916 | C | G | 1 | a0002c0003t0002g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-165+1317G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682916 | |||||||
| chr4:1682959 | A | G | 5 | a0001c0001t0022g0132 a0001c0001t0038g0315 a0001c0002t0005g0314 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+1274T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682959 | |||||||
| chr4:1682960 | C | T | 2 | a0001c0001t0009g0154 a0001c0001t0009g0155 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-165+1273G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682960 | |||||||
| chr4:1683116 | T | C | 1 | a0002c0003t0002g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-165+1117A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683116 | |||||||
| chr4:1683118 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-165+1115G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683118 | |||||||
| chr4:1683355 | T | A | 9 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0004g0335 others(6): Show |
9 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+878A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683355 | |||||||
| chr4:1683399 | C | A | 1 | a0001c0001t0009g0312 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-165+834G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683399 | |||||||
| chr4:1683410 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
251 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.-165+823G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683410 | |||||||
| chr4:1683416 | C | T | 1 | a0001c0002t0004g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-165+817G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683416 | |||||||
| chr4:1683484 | T | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-165+749A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683484 | |||||||
| chr4:1683512 | A | C | 9 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0136 others(6): Show |
9 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-165+721T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683512 | |||||||
| chr4:1683586 | A | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0004g0335 others(5): Show |
8 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+647T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683586 | |||||||
| chr4:1683604 | T | C | 4 | a0001c0001t0002g0326 a0001c0001t0021g0324 a0001c0001t0021g0325 others(1): Show |
4 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+629A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683604 | |||||||
| chr4:1683614 | G | A | 6 | a0001c0002t0004g0327 a0001c0002t0004g0330 a0001c0002t0004g0332 others(3): Show |
6 | HG00621.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+619C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683614 | |||||||
| chr4:1683730 | C | T | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0136 others(5): Show |
8 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+503G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683730 | |||||||
| chr4:1683779 | G | A | 1 | a0001c0001t0007g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-165+454C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683779 | |||||||
| chr4:1683910 | G | C | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG00642.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-165+323C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683910 | |||||||
| chr4:1683976 | C | G | 8 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0136 others(5): Show |
8 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+257G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683976 | |||||||
| chr4:1683980 | C | T | 2 | a0001c0001t0043g0130 a0003c0004t0018g0131 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-165+253G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683980 | |||||||
| chr4:1684031 | A | G | 1 | a0001c0001t0037g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-165+202T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1684031 | |||||||
| chr4:1684092 | G | A | 1 | a0001c0001t0004g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+141C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1684092 |