chr16:2070571:G>A Detail (hg38) (TSC2)

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

Genome

Assembly	Position
hg19	chr16:2,120,572-2,120,572 View the variant detail on this assembly version.
hg38	chr16:2,070,571-2,070,571

HGVS

TSC2

Type	Transcript	Protein
RefSeq	NM_000548.4:c.1832G>A	NP_000539.2:p.Arg611Gln
	NM_001114382.2:c.1832G>A	NP_001107854.1:p.Arg611Gln
	NM_001318829.1:c.1685G>A	NP_001305758.1:p.Arg562Gln
	NM_001077183.2:c.1832G>A	NP_001070651.1:p.Arg611Gln
	NM_001318827.1:c.1721G>A	NP_001305756.1:p.Arg574Gln
	NM_001318831.1:c.1721G>A	NP_001305760.1:p.Arg574Gln
	NM_001318832.1:c.1865G>A	NP_001305761.1:p.Arg622Gln
Ensemble	ENST00000219476.9:c.1832G>A	ENST00000219476.9:p.Arg611Gln
	ENST00000350773.9:c.1832G>A	ENST00000350773.9:p.Arg611Gln
	ENST00000382538.10:c.1685G>A	ENST00000382538.10:p.Arg562Gln
	ENST00000401874.7:c.1832G>A	ENST00000401874.7:p.Arg611Gln
	ENST00000439673.6:c.1721G>A	ENST00000439673.6:p.Arg574Gln
	ENST00000568454.6:c.1865G>A	ENST00000568454.6:p.Arg622Gln
	ENST00000642206.2:c.1877G>A	ENST00000642206.2:p.Arg626Gln
	ENST00000642365.2:c.1832G>A	ENST00000642365.2:p.Arg611Gln
	ENST00000642561.1:c.1832G>A	ENST00000642561.1:p.Arg611Gln
	ENST00000642797.1:c.1832G>A	ENST00000642797.1:p.Arg611Gln
	ENST00000642936.1:c.1832G>A	ENST00000642936.1:p.Arg611Gln
	ENST00000643088.1:c.1832G>A	ENST00000643088.1:p.Arg611Gln
	ENST00000643946.1:c.1832G>A	ENST00000643946.1:p.Arg611Gln
	ENST00000644043.1:c.1832G>A	ENST00000644043.1:p.Arg611Gln
	ENST00000644329.1:c.1832G>A	ENST00000644329.1:p.Arg611Gln
	ENST00000644335.1:c.1832G>A	ENST00000644335.1:p.Arg611Gln
	ENST00000645186.2:c.1832G>A	ENST00000645186.2:p.Arg611Gln
	ENST00000646388.1:c.1832G>A	ENST00000646388.1:p.Arg611Gln

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
Review star
Show details

Links

TSC2

Type	Database	ID	Link
Gene	MIM	191092	OMIM
	HGNC	12363	HGNC
	Ensembl	ENSG00000103197	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM1636646	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic Likely pathogenic	2024-03-25	criteria provided, multiple submitters, no conflicts	tuberous sclerosis 2	germline not provided	Detail
not provided		no assertion provided	Tuberous sclerosis syndrome	germline	Detail
Pathogenic	2000-05-23	no assertion criteria provided	Lymphangiomyomatosis	germline somatic	Detail
Pathogenic	2024-04-01	criteria provided, multiple submitters, no conflicts	not provided	germline unknown	Detail
Pathogenic	2023-06-08	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2022-03-02	criteria provided, multiple submitters, no conflicts	Lymphangiomyomatosis,Isolated focal cortical dysplasia type II,tuberous sclerosis 2	unknown germline	Detail
Pathogenic	2022-03-02	criteria provided, multiple submitters, no conflicts	Lymphangiomyomatosis,Isolated focal cortical dysplasia type II,tuberous sclerosis 2	germline unknown	Detail
Pathogenic	2022-03-02	criteria provided, multiple submitters, no conflicts	Lymphangiomyomatosis,Isolated focal cortical dysplasia type II,tuberous sclerosis 2	germline unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.441	TUBEROUS SCLEROSIS 2 (disorder)	NA	CLINVAR		Detail
0.494	tuberous sclerosis	NA	CLINVAR		Detail
0.577	lymphangioleiomyomatosis	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND Tuberous sclerosis 2	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND Tuberous sclerosis syndrome	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND Lymphangiomyomatosis	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND not provided	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND multiple conditions	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND multiple conditions	ClinVar	Detail
NM_000548.5(TSC2):c.1832G>A (p.Arg611Gln) AND multiple conditions	ClinVar	Detail
NA	DisGeNET	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: rs28934872 dbSNP
Genome: hg38
Position: chr16:2,070,571-2,070,571
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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