Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79097 |
| ensemblid | ENSG00000150244.12 |
| hgncid | 19021 |
| symbol | TRIM48 |
| name | tripartite motif containing 48 |
| refseq_nuc | NM_024114.5 |
| refseq_prot | NP_077019.2 |
| ensembl_nuc | ENST00000417545.5 |
| ensembl_prot | ENSP00000402414.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 55262155 |
| end | 55271114 |
| strand | + |
| ver | v1.2 |
| region | chr11:55262155-55271114 |
| region5000 | chr11:55257155-55276114 |
| regionname0 | TRIM48_chr11_55262155_55271114 |
| regionname5000 | TRIM48_chr11_55257155_55276114 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 224 | 237 | 65 | 52 | 88 | 6 | 24 | 75 | TRIM48_chr11_55257155_55276114 | TRIM48 | MSRRI others(219): Show |
chr11 | 55257155 | 55276114 |
| a0002 | 0/0 | 224 | 26 | 9 | 4 | 7 | 2 | 4 | 4 | TRIM48_chr11_55257155_55276114 | TRIM48 | MSRRI others(219): Show |
chr11 | 55257155 | 55276114 |
| a0003 | 0/0 | 14 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | TRIM48_chr11_55257155_55276114 | TRIM48 | MSRRI others(9): Show |
chr11 | 55257155 | 55276114 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 672 | 237 | 65 | 52 | 88 | 6 | 24 | TRIM48_chr11_55257155_55276114 | TRIM48 | ATGTC others(667): Show |
chr11 | 55257155 | 55276114 | ||
| a0002c0002 | 0/0 | 672 | 26 | 9 | 4 | 7 | 2 | 4 | TRIM48_chr11_55257155_55276114 | TRIM48 | ATGTC others(667): Show |
chr11 | 55257155 | 55276114 | ||
| a0003c0003 | 0/0 | 44 | 9 | 0 | 0 | 9 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | ATGTC others(39): Show |
chr11 | 55257155 | 55276114 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1467 | 232 | 63 | 51 | 86 | 6 | 24 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0001c0001t0005 | 0/0 | 1467 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0001c0001t0006 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0001c0001t0007 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0001c0001t0008 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0002c0002t0001 | 0/0 | 1467 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0002c0002t0002 | 0/0 | 1467 | 18 | 1 | 4 | 7 | 2 | 4 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(1462): Show |
chr11 | 55257155 | 55276114 |
| a0003c0003t0003 | 0/0 | 207 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(202): Show |
chr11 | 55257155 | 55276114 |
| a0003c0003t0004 | 0/0 | 207 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | AGTTT others(202): Show |
chr11 | 55257155 | 55276114 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 122 | 17 | 36 | 45 | 5 | 19 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0002 | 0/0 | 34 | 6 | 4 | 20 | 0 | 4 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0003 | 0/0 | 19 | 0 | 1 | 18 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0004 | 0/0 | 16 | 14 | 1 | 0 | 1 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0010 | 1/0 | 5 | 3 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0001g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0002c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0002c0002t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0002c0002t0002g0001 | 0/0 | 13 | 0 | 2 | 7 | 0 | 4 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0002c0002t0002g0007 | 0/0 | 5 | 1 | 2 | 0 | 2 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0003c0003t0003g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| a0003c0003t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0007 | EUR | GBR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0007 | EUR | IBS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18941 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18943 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18963 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18966 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18974 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19056 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19062 | hp2 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19082 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | YRI | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | GIH | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0024 | REF | REF | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | TRIM48_chr11_55257155_55276114 | TRIM48 | chr11 | 55257155 | 55276114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:55262311 | G | A | 1 | a0002 | 26 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(23): Show |
missense_variant&splice_region_variant | MODERATE | c.44G>A | p.Arg15Gln | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/6 | 157/1467 | 44/675 | 15/224 | chr11 | 55262311 | |||
| chr11:55264123 | AATTACAC others(6934): Show |
A | 1 | a0003 | 9 | NA18941.hp1 NA18943.hp2 NA18963.hp2 others(6): Show |
exon_loss_variant | HIGH | c.45-772_*633del | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 55264123 | ||||||
| chr11:55265052 | C | A | 1 | a0001 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.197C>A | p.Thr66Asn | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 310/1467 | 197/675 | 66/224 | chr11 | 55265052 | |||
| chr11:55265069 | A | G | 1 | a0001 | 2 | NA19007.hp1 NA19009.hp2 |
missense_variant | MODERATE | c.214A>G | p.Ile72Val | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 327/1467 | 214/675 | 72/224 | chr11 | 55265069 | |||
| chr11:55265106 | T | C | 1 | a0001 | 6 | HG01346.hp2 HG01433.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.251T>C | p.Ile84Thr | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 364/1467 | 251/675 | 84/224 | chr11 | 55265106 | |||
| chr11:55265220 | T | C | 1 | a0002 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.365T>C | p.Val122Ala | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 478/1467 | 365/675 | 122/224 | chr11 | 55265220 | |||
| chr11:55265268 | G | A | 1 | a0001 | 5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.413G>A | p.Arg138Gln | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 526/1467 | 413/675 | 138/224 | chr11 | 55265268 | |||
| chr11:55265634 | A | G | 1 | a0001 | 2 | HG01433.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.494A>G | p.Glu165Gly | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/6 | 607/1467 | 494/675 | 165/224 | chr11 | 55265634 | |||
| chr11:55269286 | C | T | 1 | a0001 | 4 | NA18941.hp2 NA18970.hp2 NA19007.hp2 others(1): Show |
missense_variant | MODERATE | c.623C>T | p.Ala208Val | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/6 | 736/1467 | 623/675 | 208/224 | chr11 | 55269286 | |||
| chr11:55269298 | G | A | 1 | a0001 | 2 | NA19058.hp2 NA19087.hp2 |
missense_variant | MODERATE | c.635G>A | p.Gly212Glu | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/6 | 748/1467 | 635/675 | 212/224 | chr11 | 55269298 | |||
| chr11:55269336 | T | C | 1 | a0001 | 11 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
stop_lost | HIGH | c.673T>C | p.Ter225Argext*? | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/6 | 786/1467 | 673/675 | 225/224 | chr11 | 55269336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:55264921 | G | A | 1 | a0001c0001 | 8 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
synonymous_variant | LOW | c.66G>A | p.Ser22Ser | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 179/1467 | 66/675 | 22/224 | chr11 | 55264921 | |||
| chr11:55264939 | A | G | 1 | a0001c0001 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.84A>G | p.Glu28Glu | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 197/1467 | 84/675 | 28/224 | chr11 | 55264939 | |||
| chr11:55265011 | G | A | 1 | a0001c0001 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.156G>A | p.Arg52Arg | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/6 | 269/1467 | 156/675 | 52/224 | chr11 | 55265011 | |||
| chr11:55265608 | T | G | 1 | a0001c0001 | 10 | HG01081.hp2 HG01123.hp2 HG01167.hp1 others(7): Show |
synonymous_variant | LOW | c.468T>G | p.Leu156Leu | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/6 | 581/1467 | 468/675 | 156/224 | chr11 | 55265608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:55262180 | C | T | 1 | a0001c0001t0005 | 2 | NA19007.hp1 NA19009.hp2 |
5_prime_UTR_variant | MODIFIER | c.-88C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/6 | 88 | chr11 | 55262180 | ||||||
| chr11:55262230 | G | A | 1 | a0003c0003t0004 | 2 | NA19056.hp1 NA19062.hp2 |
5_prime_UTR_variant | MODIFIER | c.-38G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/6 | 38 | chr11 | 55262230 | ||||||
| chr11:55262242 | G | A | 1 | a0001c0001t0006 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/6 | 26 | chr11 | 55262242 | ||||||
| chr11:55270591 | T | C | 3 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 |
11 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*156T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1253 | chr11 | 55270591 | ||||||
| chr11:55270742 | T | A | 1 | a0001c0001t0001 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307T>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1404 | chr11 | 55270742 | ||||||
| chr11:55270899 | T | C | 4 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(1): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*464T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1561 | chr11 | 55270899 | ||||||
| chr11:55270909 | A | G | 3 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 |
11 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*474A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1571 | chr11 | 55270909 | ||||||
| chr11:55271079 | A | C | 1 | a0001c0001t0008 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1741 | chr11 | 55271079 | ||||||
| chr11:55271082 | G | A | 1 | a0001c0001t0007 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1744 | chr11 | 55271082 | ||||||
| chr11:55271098 | T | C | 1 | a0002c0002t0002 | 18 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*663T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 6/6 | 1760 | chr11 | 55271098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:55262463 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(23): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.44+152T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262463 | |||||||
| chr11:55262480 | G | A | 1 | a0001c0001t0001g0002 | 34 | HG00558.hp1 HG01081.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.44+169G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262480 | |||||||
| chr11:55262599 | A | T | 2 | a0001c0001t0001g0007 a0002c0002t0002g0007 |
6 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+288A>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262599 | |||||||
| chr11:55262647 | G | A | 1 | a0001c0001t0001g0002 | 34 | HG00558.hp1 HG01081.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.44+336G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262647 | |||||||
| chr11:55262700 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+389A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262700 | |||||||
| chr11:55262739 | G | A | 2 | a0003c0003t0003g0005 a0003c0003t0004g0005 |
9 | NA18941.hp1 NA18943.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+428G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262739 | |||||||
| chr11:55262751 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0023 |
20 | HG00558.hp2 HG02071.hp2 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.44+440A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262751 | |||||||
| chr11:55262794 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
5 | HG01433.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+483A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262794 | |||||||
| chr11:55262817 | T | TAC | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+507_44+508insCA | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 55262817 | ||||||
| chr11:55262821 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+510T>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262821 | |||||||
| chr11:55262821 | T | TAA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(26): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.44+510_44+511insAA | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262821 | |||||||
| chr11:55262836 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.44+525T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262836 | |||||||
| chr11:55262971 | G | A | 1 | a0001c0001t0001g0009 | 5 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+660G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55262971 | |||||||
| chr11:55263002 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.44+691C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263002 | |||||||
| chr11:55263034 | T | C | 1 | a0002c0002t0001g0015 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.44+723T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263034 | |||||||
| chr11:55263094 | A | T | 2 | a0003c0003t0003g0005 a0003c0003t0004g0005 |
9 | NA18941.hp1 NA18943.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+783A>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263094 | |||||||
| chr11:55263209 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.44+898C>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263209 | |||||||
| chr11:55263231 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44+920A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263231 | |||||||
| chr11:55263246 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44+935A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263246 | |||||||
| chr11:55263250 | G | A | 1 | a0001c0001t0001g0011 | 4 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+939G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263250 | |||||||
| chr11:55263418 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
5 | HG01433.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+1107C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263418 | |||||||
| chr11:55263419 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG02818.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44+1108G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263419 | |||||||
| chr11:55263424 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0021 others(5): Show |
19 | HG01433.hp1 HG02109.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.44+1113A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263424 | |||||||
| chr11:55263492 | G | GA | 2 | a0001c0001t0001g0006 a0002c0002t0001g0006 |
6 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+1193dupA | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 55263492 | ||||||
| chr11:55263518 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.44+1207C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263518 | |||||||
| chr11:55263654 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0021 others(3): Show |
10 | HG01433.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-1246C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263654 | |||||||
| chr11:55263784 | G | T | 1 | a0001c0001t0001g0012 | 4 | HG01496.hp2 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-1116G>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263784 | |||||||
| chr11:55263905 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.45-995C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55263905 | |||||||
| chr11:55264007 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.45-893C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264007 | |||||||
| chr11:55264009 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.45-891C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264009 | |||||||
| chr11:55264121 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.45-779A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264121 | |||||||
| chr11:55264128 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-772C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264128 | |||||||
| chr11:55264278 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-622C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264278 | |||||||
| chr11:55264291 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.45-609G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264291 | |||||||
| chr11:55264292 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.45-608T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264292 | |||||||
| chr11:55264311 | G | T | 1 | a0001c0001t0001g0001 | 3 | HG01891.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45-589G>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264311 | |||||||
| chr11:55264324 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-576C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264324 | |||||||
| chr11:55264325 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG01891.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45-575G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264325 | |||||||
| chr11:55264350 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-550C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264350 | |||||||
| chr11:55264498 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.45-402G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264498 | |||||||
| chr11:55264509 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.45-391G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264509 | |||||||
| chr11:55264511 | C | T | 1 | a0001c0001t0001g0001 | 3 | HG01891.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45-389C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264511 | |||||||
| chr11:55264591 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
5 | HG01433.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-309G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264591 | |||||||
| chr11:55264683 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.45-217A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264683 | |||||||
| chr11:55264701 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(7): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.45-199G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264701 | |||||||
| chr11:55264736 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45-164G>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264736 | |||||||
| chr11:55264738 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.45-162C>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264738 | |||||||
| chr11:55264838 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.45-62C>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264838 | |||||||
| chr11:55264891 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45-9C>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 1/5 | chr11 | 55264891 | |||||||
| chr11:55265371 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
5 | HG01433.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+57C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/5 | chr11 | 55265371 | |||||||
| chr11:55265445 | C | G | 1 | a0001c0001t0001g0017 | 2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.459+131C>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/5 | chr11 | 55265445 | |||||||
| chr11:55265463 | C | T | 1 | a0002c0002t0001g0006 | 4 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-137C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/5 | chr11 | 55265463 | |||||||
| chr11:55265500 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-100G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/5 | chr11 | 55265500 | |||||||
| chr11:55265580 | A | G | 3 | a0001c0001t0001g0007 a0002c0002t0002g0001 a0002c0002t0002g0007 |
19 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-20A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2/5 | chr11 | 55265580 | |||||||
| chr11:55265706 | T | A | 1 | a0002c0002t0001g0001 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.555+11T>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55265706 | |||||||
| chr11:55265779 | C | G | 1 | a0001c0001t0001g0003 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.555+84C>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55265779 | |||||||
| chr11:55265797 | C | CA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(5): Show |
76 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.555+118dupA | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55265797 | ||||||
| chr11:55265797 | C | CAA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(6): Show |
73 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.555+117_555+118dup others(2): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55265797 | ||||||
| chr11:55265797 | CA | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
8 | HG01109.hp1 HG01433.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.555+118delA | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55265797 | ||||||
| chr11:55265808 | A | G | 1 | a0001c0001t0001g0011 | 4 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+113A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55265808 | |||||||
| chr11:55265843 | C | T | 1 | a0001c0001t0001g0003 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.555+148C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55265843 | |||||||
| chr11:55265893 | C | G | 2 | a0002c0002t0001g0001 a0002c0002t0001g0015 |
3 | HG02809.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.555+198C>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55265893 | |||||||
| chr11:55265910 | G | C | 1 | a0001c0001t0001g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.555+215G>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55265910 | |||||||
| chr11:55266019 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.555+324A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266019 | |||||||
| chr11:55266207 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+512C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266207 | |||||||
| chr11:55266523 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.555+828T>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266523 | |||||||
| chr11:55266541 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.555+846A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266541 | |||||||
| chr11:55266552 | G | A | 1 | a0002c0002t0001g0015 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.555+857G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266552 | |||||||
| chr11:55266865 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG01891.hp1 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.555+1170G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266865 | |||||||
| chr11:55266946 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(4): Show |
11 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+1251T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266946 | |||||||
| chr11:55266970 | C | T | 2 | a0001c0001t0001g0001 a0002c0002t0001g0001 |
2 | HG02735.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.555+1275C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266970 | |||||||
| chr11:55266981 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0008g0013 |
3 | HG02896.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.555+1286T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55266981 | |||||||
| chr11:55267257 | A | C | 3 | a0001c0001t0001g0007 a0002c0002t0002g0001 a0002c0002t0002g0007 |
19 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.556-1093A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267257 | |||||||
| chr11:55267314 | C | T | 1 | a0001c0001t0001g0001 | 3 | HG01109.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.556-1036C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267314 | |||||||
| chr11:55267438 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(22): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.556-912A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267438 | |||||||
| chr11:55267567 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
5 | HG01433.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-783G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267567 | |||||||
| chr11:55267572 | AT | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0021 others(3): Show |
10 | HG01433.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.556-773delT | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55267572 | ||||||
| chr11:55267577 | T | TAAGAGGA others(21): Show |
1 | a0001c0001t0001g0001 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.556-771_556-744dup others(28): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55267577 | ||||||
| chr11:55267650 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-700C>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267650 | |||||||
| chr11:55267881 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | HG01346.hp2 HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.556-469A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267881 | |||||||
| chr11:55267971 | G | A | 6 | a0001c0001t0001g0001 a0002c0002t0001g0001 a0002c0002t0001g0006 others(3): Show |
28 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.556-379G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55267971 | |||||||
| chr11:55268139 | T | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.556-211T>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55268139 | |||||||
| chr11:55268197 | T | C | 1 | a0001c0001t0001g0012 | 4 | HG01496.hp2 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-153T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55268197 | |||||||
| chr11:55268283 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.556-67A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | chr11 | 55268283 | |||||||
| chr11:55268333 | A | AT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
34 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.556-5dupT | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55268333 | ||||||
| chr11:55268333 | AT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(3): Show |
16 | HG01109.hp1 HG01433.hp1 HG02109.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.556-5delT | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 55268333 | ||||||
| chr11:55268376 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG00323.hp1 | splice_region_variant&intron_variant | LOW | c.578+4A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268376 | |||||||
| chr11:55268386 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.578+14T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268386 | |||||||
| chr11:55268433 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.578+61C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268433 | |||||||
| chr11:55268509 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(2): Show |
69 | HG00323.hp1 HG00438.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.578+137G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268509 | |||||||
| chr11:55268709 | A | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(4): Show |
11 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.578+337A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268709 | |||||||
| chr11:55268757 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(16): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.578+385C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268757 | |||||||
| chr11:55268797 | A | G | 1 | a0002c0002t0001g0006 | 4 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+425A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268797 | |||||||
| chr11:55268835 | T | C | 1 | a0001c0001t0001g0002 | 4 | NA18946.hp2 NA18953.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-407T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268835 | |||||||
| chr11:55268915 | T | C | 1 | a0001c0001t0001g0009 | 5 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-327T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268915 | |||||||
| chr11:55268966 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0008 |
2 | HG02004.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.579-276G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268966 | |||||||
| chr11:55268987 | C | A | 1 | a0001c0001t0001g0008 | 3 | HG02109.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.579-255C>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55268987 | |||||||
| chr11:55269032 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | HG01346.hp2 HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.579-210C>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55269032 | |||||||
| chr11:55269094 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.579-148G>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55269094 | |||||||
| chr11:55269230 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.579-12T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 4/5 | chr11 | 55269230 | |||||||
| chr11:55269444 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(4): Show |
11 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.*1+105A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269444 | |||||||
| chr11:55269617 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*1+278G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269617 | |||||||
| chr11:55269698 | T | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(22): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.*1+359T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269698 | |||||||
| chr11:55269745 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.*1+406G>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269745 | |||||||
| chr11:55269749 | T | C | 1 | a0001c0001t0001g0002 | 4 | HG01081.hp1 HG02273.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1+410T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269749 | |||||||
| chr11:55269757 | T | TTAAATGG others(72): Show |
1 | a0001c0001t0001g0006 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.*1+419_*1+420insAA others(77): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 55269757 | ||||||
| chr11:55269848 | A | C | 1 | a0001c0001t0001g0001 | 7 | HG01123.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.*1+509A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269848 | |||||||
| chr11:55269907 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*2-530A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269907 | |||||||
| chr11:55269935 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.*2-502C>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269935 | |||||||
| chr11:55269949 | G | A | 1 | a0001c0001t0001g0012 | 4 | HG01496.hp2 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-488G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269949 | |||||||
| chr11:55269966 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 |
3 | HG01346.hp2 HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*2-471A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269966 | |||||||
| chr11:55269995 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*2-442G>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269995 | |||||||
| chr11:55269997 | A | G | 1 | a0001c0001t0001g0012 | 4 | HG01496.hp2 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-440A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55269997 | |||||||
| chr11:55270048 | T | C | 1 | a0001c0001t0001g0001 | 3 | HG01109.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.*2-389T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270048 | |||||||
| chr11:55270058 | C | A | 1 | a0001c0001t0001g0011 | 4 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-379C>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270058 | |||||||
| chr11:55270088 | A | T | 1 | a0002c0002t0001g0006 | 4 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2-349A>T | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270088 | |||||||
| chr11:55270091 | A | C | 1 | a0001c0001t0001g0001 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.*2-346A>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270091 | |||||||
| chr11:55270192 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.*2-245C>A | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270192 | |||||||
| chr11:55270234 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.*2-203T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270234 | |||||||
| chr11:55270299 | A | G | 1 | a0002c0002t0002g0007 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*2-138A>G | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270299 | |||||||
| chr11:55270340 | T | C | 1 | a0001c0001t0001g0001 | 3 | NA18948.hp1 NA18953.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.*2-97T>C | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | chr11 | 55270340 | |||||||
| chr11:55270390 | TTTTC | T | 2 | a0001c0001t0001g0008 a0001c0001t0007g0008 |
5 | HG02109.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-29_*2-26delTTCT | TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 55270390 |