Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 120146 |
|---|---|
| ensemblid | ENSG00000204450.9 |
| hgncid | 14663 |
| symbol | TRIM64 |
| name | tripartite motif containing 64 |
| refseq_nuc | NM_001136486.2 |
| refseq_prot | NP_001129958.1 |
| ensembl_nuc | ENST00000533122.4 |
| ensembl_prot | ENSP00000483764.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 89966037 |
| end | 89974072 |
| strand | + |
| ver | v1.2 |
| region | chr11:89966037-89974072 |
| region5000 | chr11:89961037-89979072 |
| regionname0 | TRIM64_chr11_89966037_89974072 |
| regionname5000 | TRIM64_chr11_89961037_89979072 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 449 | 20 | 0 | 5 | 14 | 0 | 0 | 11 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0002 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0003 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0004 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0005 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0006 | 0/0 | 449 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1350 | 20 | 0 | 5 | 14 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| c0002 | 0/0 | 1350 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| c0003 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| c0004 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| c0005 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| c0006 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 304 | 25 | 0 | 6 | 18 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1350 | 20 | 0 | 5 | 14 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0002c0003 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0003c0004 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0004c0005 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0005c0006 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0006c0002 | 0/0 | 1350 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1653 | 20 | 0 | 5 | 14 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0002c0003t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0003c0004t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0004c0005t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0005c0006t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| a0006c0002t0001 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | copy fasta | chr11 | 89961037 | 89979072 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0002c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0003c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0004c0005t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0005c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| a0006c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | CHS | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG00741 | hp2 | a0006 | c0002 | t0001 | g0013 | AMR | PUR | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA18999 | hp1 | a0004 | c0005 | t0001 | g0007 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19070 | hp1 | a0005 | c0006 | t0001 | g0011 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89968676
|
T | C | 1 | a0006 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.173T>C | p.Ile58Thr | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/7 | 293/1653 | 173/1350 | 58/449 | chr11 | 89968676 | ||
| chr11:89968705
|
G | C | 1 | a0006 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.202G>C | p.Val68Leu | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/7 | 322/1653 | 202/1350 | 68/449 | chr11 | 89968705 | ||
| chr11:89968790
|
A | C | 1 | a0006 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.287A>C | p.Glu96Ala | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/7 | 407/1653 | 287/1350 | 96/449 | chr11 | 89968790 | ||
| chr11:89969527
|
A | C | 3 | a0004a0005a0006 | 3 | HG00741.hp2 NA18999.hp1 NA19070.hp1 |
missense_variant | MODERATE | c.486A>C | p.Arg162Ser | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 3/7 | 606/1653 | 486/1350 | 162/449 | chr11 | 89969527 | ||
| chr11:89970451
|
G | A | 3 | a0002a0004a0006 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
missense_variant | MODERATE | c.712G>A | p.Val238Met | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 4/7 | 832/1653 | 712/1350 | 238/449 | chr11 | 89970451 | ||
| chr11:89970464
|
A | T | 3 | a0002a0004a0006 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
missense_variant | MODERATE | c.725A>T | p.Glu242Val | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 4/7 | 845/1653 | 725/1350 | 242/449 | chr11 | 89970464 | ||
| chr11:89973612
|
A | G | 5 | a0002a0003a0004others(2): Show | 5 | HG00408.hp1 HG00741.hp2 NA18999.hp1 others(2): Show |
missense_variant | MODERATE | c.1073A>G | p.Gln358Arg | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 7/7 | 1193/1653 | 1073/1350 | 358/449 | chr11 | 89973612 | ||
| chr11:89973753
|
A | G | 4 | a0003a0004a0005others(1): Show | 4 | HG00408.hp1 HG00741.hp2 NA18999.hp1 others(1): Show |
missense_variant | MODERATE | c.1214A>G | p.Gln405Arg | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 7/7 | 1334/1653 | 1214/1350 | 405/449 | chr11 | 89973753 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89966185
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0010a0002c0003t0001g0012others(2): Show | 9 | HG00741.hp2 HG02083.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+33C>T | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 1/6 | chr11 | 89966185 | ||||||
| chr11:89969043
|
A | G | 1 | a0006c0002t0001g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.408+132A>G | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/6 | chr11 | 89969043 | ||||||
| chr11:89969088
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(8): Show | 23 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.408+177T>C | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/6 | chr11 | 89969088 | ||||||
| chr11:89969106
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 24 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.408+195G>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/6 | chr11 | 89969106 | ||||||
| chr11:89969118
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(8): Show | 23 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.408+207T>C | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/6 | chr11 | 89969118 | ||||||
| chr11:89969205
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(7): Show | 22 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.409-245G>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/6 | chr11 | 89969205 | ||||||
| chr11:89969384
|
ATT | A | 2 | a0004c0005t0001g0007a0006c0002t0001g0013 | 2 | HG00741.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.409-65_409-64delTT | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 2/6 | chr11 | 89969384 | ||||||
| chr11:89969632
|
C | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 15 | HG00408.hp1 HG00408.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.504+87C>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 3/6 | chr11 | 89969632 | ||||||
| chr11:89969678
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 15 | HG00408.hp1 HG00408.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.504+133G>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 3/6 | chr11 | 89969678 | ||||||
| chr11:89969828
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 15 | HG00408.hp1 HG00408.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.504+283T>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 3/6 | chr11 | 89969828 | ||||||
| chr11:89969888
|
TA | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 15 | HG00408.hp1 HG00408.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.505-347delA | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89969888 | |||||
| chr11:89971260
|
T | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0008a0002c0003t0001g0012others(2): Show | 5 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.758+5T>G | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971260 | ||||||
| chr11:89971341
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0008 | 2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.758+86G>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971341 | ||||||
| chr11:89971441
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0002c0003t0001g0012others(2): Show | 9 | HG00741.hp2 HG02083.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.758+186T>C | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971441 | ||||||
| chr11:89971524
|
A | G | 3 | a0002c0003t0001g0012a0004c0005t0001g0007a0006c0002t0001g0013 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.758+269A>G | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971524 | ||||||
| chr11:89971607
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.758+352G>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971607 | ||||||
| chr11:89971626
|
A | T | 3 | a0002c0003t0001g0012a0004c0005t0001g0007a0006c0002t0001g0013 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.758+371A>T | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971626 | ||||||
| chr11:89971746
|
A | G | 3 | a0002c0003t0001g0012a0004c0005t0001g0007a0006c0002t0001g0013 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.759-451A>G | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971746 | ||||||
| chr11:89971803
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0004a0002c0003t0001g0012others(1): Show | 8 | HG00741.hp2 HG02083.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.759-394T>C | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971803 | ||||||
| chr11:89971846
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0002c0003t0001g0012others(2): Show | 9 | HG00741.hp2 HG02083.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.759-351T>C | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971846 | ||||||
| chr11:89971864
|
G | C | 3 | a0002c0003t0001g0012a0004c0005t0001g0007a0006c0002t0001g0013 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.759-333G>C | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89971864 | ||||||
| chr11:89972011
|
T | TTGGGTTT others(3): Show |
3 | a0002c0003t0001g0012a0004c0005t0001g0007a0006c0002t0001g0013 | 3 | HG00741.hp2 NA18999.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.759-183_759-182ins others(10): Show |
TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 89972011 | |||||
| chr11:89972101
|
C | G | 4 | a0002c0003t0001g0012a0004c0005t0001g0007a0005c0006t0001g0011others(1): Show | 4 | HG00741.hp2 NA18999.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-96C>G | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | chr11 | 89972101 | ||||||
| chr11:89972183
|
AT | A | 4 | a0002c0003t0001g0012a0004c0005t0001g0007a0005c0006t0001g0011others(1): Show | 4 | HG00741.hp2 NA18999.hp1 NA19003.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.759-5delT | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 89972183 | |||||
| chr11:89972412
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0008 | 2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.856+118C>T | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 6/6 | chr11 | 89972412 | ||||||
| chr11:89973101
|
GA | G | 5 | a0002c0003t0001g0012a0003c0004t0001g0005a0004c0005t0001g0007others(2): Show | 5 | HG00408.hp1 HG00741.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-285delA | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 89973101 | |||||
| chr11:89973134
|
C | A | 3 | a0002c0003t0001g0012a0003c0004t0001g0005a0006c0002t0001g0013 | 3 | HG00408.hp1 HG00741.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.857-262C>A | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 6/6 | chr11 | 89973134 | ||||||
| chr11:89973261
|
A | G | 5 | a0002c0003t0001g0012a0003c0004t0001g0005a0004c0005t0001g0007others(2): Show | 5 | HG00408.hp1 HG00741.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-135A>G | TRIM64 | ENSG00000204450.9 | transcript | ENST00000533122.4 | protein_coding | 6/6 | chr11 | 89973261 |