Item | Value |
---|---|
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 | 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 | MDSDD others(444): Show |
chr11 | 89961037 | 89979072 |
a0002 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | MDSDD others(444): Show |
chr11 | 89961037 | 89979072 |
a0003 | 0/0 | 449 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | MDSDD others(444): Show |
chr11 | 89961037 | 89979072 |
a0004 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM64_chr11_89961037_89979072 | TRIM64 | MDSDD others(444): Show |
chr11 | 89961037 | 89979072 |
a0005 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM64_chr11_89961037_89979072 | TRIM64 | MDSDD others(444): Show |
chr11 | 89961037 | 89979072 |
a0006 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM64_chr11_89961037_89979072 | TRIM64 | MDSDD others(444): Show |
chr11 | 89961037 | 89979072 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1347 | 20 | 0 | 5 | 14 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | ATGGA others(1342): Show |
chr11 | 89961037 | 89979072 | ||
a0002c0004 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | ATGGA others(1342): Show |
chr11 | 89961037 | 89979072 | ||
a0003c0002 | 0/0 | 1347 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | ATGGA others(1342): Show |
chr11 | 89961037 | 89979072 | ||
a0004c0005 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | ATGGA others(1342): Show |
chr11 | 89961037 | 89979072 | ||
a0005c0003 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | ATGGA others(1342): Show |
chr11 | 89961037 | 89979072 | ||
a0006c0006 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | ATGGA others(1342): Show |
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 | CTCTC others(1648): Show |
chr11 | 89961037 | 89979072 |
a0002c0004t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | CTCTC others(1648): Show |
chr11 | 89961037 | 89979072 |
a0003c0002t0001 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | CTCTC others(1648): Show |
chr11 | 89961037 | 89979072 |
a0004c0005t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | CTCTC others(1648): Show |
chr11 | 89961037 | 89979072 |
a0005c0003t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | CTCTC others(1648): Show |
chr11 | 89961037 | 89979072 |
a0006c0006t0001 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | CTCTC others(1648): Show |
chr11 | 89961037 | 89979072 |
actghapid | grch38/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 |
a0002c0004t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
a0003c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0005c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
a0006c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 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 | a0002 | 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 | a0003 | 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 | a0005 | 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 | a0006 | 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 | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | TRIM64_chr11_89961037_89979072 | TRIM64 | chr11 | 89961037 | 89979072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:89968676 | T | C | 1 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 a0004 a0006 |
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 | a0003 a0004 a0005 |
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 | a0003 a0004 a0005 |
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 | a0002 a0003 a0004 others(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 | a0002 a0003 a0004 others(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 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:89966185 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0003c0002t0001g0013 others(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 | a0003c0002t0001g0013 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | |||||||
chr11:89969118 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(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 | a0003c0002t0001g0013 a0004c0005t0001g0007 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0003c0002t0001g0013 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0003c0002t0001g0013 others(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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 |
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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 |
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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0003c0002t0001g0013 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0003c0002t0001g0013 others(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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 |
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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 |
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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 others(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 | a0003c0002t0001g0013 a0004c0005t0001g0007 a0005c0003t0001g0012 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 |
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 | a0002c0004t0001g0005 a0003c0002t0001g0013 a0004c0005t0001g0007 others(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 | a0002c0004t0001g0005 a0003c0002t0001g0013 a0005c0003t0001g0012 |
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 | a0002c0004t0001g0005 a0003c0002t0001g0013 a0004c0005t0001g0007 others(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 |