chr11:108098600:G>A Detail (hg19) (ATM)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
Genome browser

Information

Genome

Assembly	Position
hg19	chr11:108,098,600-108,098,600
hg38	chr11:108,227,873-108,227,873 View the variant detail on this assembly version.

HGVS

ATM

Type	Transcript	Protein
RefSeq	NM_000051.3:c.170G>A	NP_000042.3:p.Trp57Ter
	NM_001351834.1:c.170G>A	NP_001338763.1:p.Trp57Ter
Ensemble	ENST00000531525.3:c.170G>A	ENST00000531525.3:p.Trp57Ter
	ENST00000530958.5:c.170G>A	ENST00000530958.5:p.Trp57Ter
	ENST00000532931.6:c.170G>A	ENST00000532931.6:p.Trp57Ter
	ENST00000683150.1:c.170G>A	ENST00000683150.1:p.Trp57Ter
	ENST00000713846.1:c.170G>A	ENST00000713846.1:p.Trp57Ter
	ENST00000713844.1:c.170G>A	ENST00000713844.1:p.Trp57Ter
	ENST00000713845.1:c.170G>A	ENST00000713845.1:p.Trp57Ter
	ENST00000526567.5:c.170G>A	ENST00000526567.5:p.Trp57Ter
	ENST00000713847.1:c.170G>A	ENST00000713847.1:p.Trp57Ter
	ENST00000601453.3:c.170G>A	ENST00000601453.3:p.Trp57Ter
	ENST00000639240.1:c.170G>A	ENST00000639240.1:p.Trp57Ter
	ENST00000683468.1:c.170G>A	ENST00000683468.1:p.Trp57Ter
	ENST00000683914.2:c.170G>A	ENST00000683914.2:p.Trp57Ter
	ENST00000675843.1:c.170G>A	ENST00000675843.1:p.Trp57Ter
	ENST00000278616.10:c.170G>A	ENST00000278616.10:p.Trp57Ter
	ENST00000452508.7:c.170G>A	ENST00000452508.7:p.Trp57Ter
	ENST00000640388.1:c.170G>A	ENST00000640388.1:p.Trp57Ter
	ENST00000684029.1:c.170G>A	ENST00000684029.1:p.Trp57Ter
	ENST00000682465.1:c.170G>A	ENST00000682465.1:p.Trp57Ter
	ENST00000639953.1:c.170G>A	ENST00000639953.1:p.Trp57Ter

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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Links

ATM

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
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2023-02-17	criteria provided, multiple submitters, no conflicts	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2024-01-31	criteria provided, multiple submitters, no conflicts	Ataxia-telangiectasia syndrome	germline unknown	Detail
Pathogenic	2022-04-15	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Pathogenic	2024-01-09	criteria provided, multiple submitters, no conflicts	Familial cancer of breast	germline unknown	Detail
Pathogenic	2018-10-12	criteria provided, single submitter	Ataxia-telangiectasia syndrome,Breast cancer, susceptibility to	germline	Detail
Pathogenic	2018-10-12	criteria provided, single submitter	Ataxia-telangiectasia syndrome,Breast cancer, susceptibility to	germline	Detail
not provided		no assertion provided	Ataxia-telangiectasia syndrome	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.709	ataxia telangiectasia	NA	CLINVAR		Detail
0.120	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND Ataxia-telangiectasia syndrome	ClinVar	Detail
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND not provided	ClinVar	Detail
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND Familial cancer of breast	ClinVar	Detail
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND multiple conditions	ClinVar	Detail
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND multiple conditions	ClinVar	Detail
NM_000051.4(ATM):c.170G>A (p.Trp57Ter) AND multiple conditions	ClinVar	Detail
NA	DisGeNET	Detail
NA	DisGeNET	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: -
dbSNP: rs587779818 dbSNP
Genome: hg19
Position: chr11:108,098,600-108,098,600
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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