chr12:112454636:A>T Detail (hg38) (PTPN11)

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

Genome

Assembly	Position
hg19	chr12:112,892,440-112,892,440 View the variant detail on this assembly version.
hg38	chr12:112,454,636-112,454,636

HGVS

PTPN11

Type	Transcript	Protein
RefSeq	NM_002834.3:c.598A>T	NP_002825.3:p.Asn200Tyr
	NM_080601.1:c.598A>T	NP_542168.1:p.Asn200Tyr
	NM_001330437.1:c.598A>T	NP_001317366.1:p.Asn200Tyr
Ensemble	ENST00000351677.7:c.598A>T	ENST00000351677.7:p.Asn200Tyr
	ENST00000392597.5:c.598A>T	ENST00000392597.5:p.Asn200Tyr
	ENST00000635625.1:c.598A>T	ENST00000635625.1:p.Asn200Tyr
	ENST00000639857.2:c.598A>T	ENST00000639857.2:p.Asn200Tyr
	ENST00000687906.1:c.598A>T	ENST00000687906.1:p.Asn200Tyr
	ENST00000688597.1:c.598A>T	ENST00000688597.1:p.Asn200Tyr
	ENST00000690210.1:c.598A>T	ENST00000690210.1:p.Asn200Tyr

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

PTPN11

Type	Database	ID	Link
Gene	MIM	176876	OMIM
	HGNC	9644	HGNC
	Ensembl	ENSG00000179295	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv381245203	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2015-01-08	criteria provided, single submitter	Noonan syndrome	germline unknown	Detail
Pathogenic Likely pathogenic	2023-02-10	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Pathogenic	2022-02-05	criteria provided, single submitter	RASopathy	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	Turner Syndrome, Male	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_002834.5(PTPN11):c.598A>T (p.Asn200Tyr) AND Noonan syndrome	ClinVar	Detail
NM_002834.5(PTPN11):c.598A>T (p.Asn200Tyr) AND not provided	ClinVar	Detail
NM_002834.5(PTPN11):c.598A>T (p.Asn200Tyr) AND RASopathy	ClinVar	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: rs727503381 dbSNP
Genome: hg38
Position: chr12:112,454,636-112,454,636
Variant Type: snv
Reference Allele: A
Alternative Allele: T

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