chr2:233760236:>TATATATATATATA Detail (hg38) (UGT1A10, UGT1A8, UGT1A7, UGT1A6, UGT1A5, UGT1A9, UGT1A4, UGT1A1, UGT1A3)

Information

Genome

Assembly Position
hg19 chr2:234,668,882-234,668,882 
hg38 chr2:233,760,236-233,760,236

HGVS

Type Transcript Protein
RefSeq
Type Transcript Protein
RefSeq NM_019075.2:c.856-6799_856-6798insTATATATATATATA
Ensemble ENST00000344644.10:c.856-6799_856-6798insTATATATATATATA
ENST00000373445.1:c.856-6799_856-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_019093.2:c.868-6799_868-6798insTATATATATATATA
Ensemble ENST00000482026.6:c.868-6799_868-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_007120.2:c.868-6799_868-6798insTATATATATATATA
Ensemble ENST00000373409.8:c.868-6799_868-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_019078.1:c.868-6799_868-6798insTATATATATATATA
Ensemble ENST00000373414.4:c.868-6799_868-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_001072.3:c.862-6799_862-6798insTATATATATATATA
NM_205862.1:c.61-6799_61-6798insTATATATATATATA
Ensemble ENST00000305139.11:c.862-6799_862-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_019077.2:c.856-6799_856-6798insTATATATATATATA
Ensemble ENST00000373426.4:c.856-6799_856-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_019076.4:c.856-6799_856-6798insTATATATATATATA
Ensemble ENST00000373450.5:c.856-6799_856-6798insTATATATATATATA
Type Transcript Protein
RefSeq NM_021027.2:c.856-6799_856-6798insTATATATATATATA
Ensemble ENST00000354728.5:c.856-6799_856-6798insTATATATATATATA
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 191740 OMIM
HGNC 12530 HGNC
Ensembl ENSG00000241635 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606435 OMIM
HGNC 12531 HGNC
Ensembl ENSG00000242515 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606428 OMIM
HGNC 12535 HGNC
Ensembl ENSG00000288702 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606429 OMIM
HGNC 12536 HGNC
Ensembl ENSG00000244474 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606430 OMIM
HGNC 12537 HGNC
Ensembl ENSG00000288705 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606431 OMIM
HGNC 12538 HGNC
Ensembl ENSG00000167165 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606432 OMIM
HGNC 12539 HGNC
Ensembl ENSG00000244122 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606433 OMIM
HGNC 12540 HGNC
Ensembl ENSG00000242366 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM 606434 OMIM
HGNC 12541 HGNC
Ensembl ENSG00000241119 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
cancer Belinostat A Predictive Supports Adverse Response Common Germline 5 26313268 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
The FDA approved package insert for Belinostat recommends dose adjustment for UGT1A1*28 allele homoz... CIViC Evidence Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr2:233,760,236-233,760,236
Variant Type
snv
Reference Allele
-
Alternative Allele
TATATATATATATA
Variant (CIViC) (CIViC Variant)
UGT1A1*28
Transcript 1 (CIViC Variant)
ENST00000305208.5
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/729
Genome browser