chr7:148508726:> Detail (hg19) (EZH2)

Information

Genome

Assembly Position
hg19 chr7:148,508,726-148,508,728
hg38 chr7:148,811,634-148,811,636 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
skin melanoma GSK126 D Predictive Supports Sensitivity/Response Somatic 2 26304929 Detail
diffuse large B-cell lymphoma B Diagnostic Supports Positive Somatic 4 20081860 Detail
follicular lymphoma B Diagnostic Supports Positive Somatic 4 20081860 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Preclinical study in melanoma cell lines. EZH2 expression was higher in EZH2 mutant (N=3) and wild-t... CIViC Evidence Detail
Heterozygous mutations in EZH2 at Y641 were the second most frequent genetic event (after BCL2 t(14;... CIViC Evidence Detail
Heterozygous mutations in EZH2 at Y641 were the second most frequent genetic event (after BCL2 t(14;... CIViC Evidence Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr7:148,508,726-148,508,728
Variant Type
snv
Variant (CIViC) (CIViC Variant)
Y646
Transcript 1 (CIViC Variant)
ENST00000320356.2
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/165
Summary (CIViC Variant)
Mutations of Y646 are associated with a diagnosis of Germinal Center B type DLBCL and Follicular non-Hodgkin Lymphoma. In vitro experimental findings suggest that this may be due to reduced methyltransferase activity of EZH2 on protein H3K27 (Morin et al., 2010).
Variant (CIViC) (CIViC Variant)
Y641S
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/2666
Variant (CIViC) (CIViC Variant)
Y646F
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/2989
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