chr11:108326116:CT> Detail (hg38) (ATM, C11orf65)

Information

Genome

Assembly Position
hg19 chr11:108,196,843-108,196,844 
hg38 chr11:108,326,116-108,326,117

HGVS

Type Transcript Protein
RefSeq NM_000051.3:c.6866_6867delCT NP_000042.3:p.Ser2289Ter
NM_001351834.1:c.6866_6867delCT NP_001338763.1:p.Ser2289Ter
Ensemble ENST00000278616.10:c.6866_6867delCT ENST00000278616.10:p.Ser2289Ter
Type Transcript Protein
RefSeq NM_001330368.1:c.641-17046_641-17045delAG
Ensemble ENST00000525729.5:c.641-17046_641-17045delAG
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 607585 OMIM
HGNC 795 HGNC
Ensembl ENSG00000149311 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM5547795 COSMIC
MONDO
Type Database ID Link
Gene MIM
HGNC 28519 HGNC
Ensembl ENSG00000166323 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM5547795 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
prostate cancer Olaparib C Predictive Supports Sensitivity/Response Somatic 3 26510020 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Treatment with the PARP inhibitor olaparib in patients whose prostate cancers were no longer respond... 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
hg38
Position
chr11:108,326,116-108,326,117
Variant Type
snv
Reference Allele
CT
Alternative Allele
-
Variant (CIViC) (CIViC Variant)
V2288FS*1
Transcript 1 (CIViC Variant)
ENST00000278616.4
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/243
Summary (CIViC Variant)
A frameshift mutation predicted to cause truncation before the C-terminal phosphoinositide 3-kinase (PI3K) catalytic domain.
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