chr12:112926887:G>C Detail (hg19) (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	chr12:112,926,887-112,926,887
hg38	chr12:112,489,083-112,489,083 View the variant detail on this assembly version.

HGVS

PTPN11

Type	Transcript	Protein
RefSeq	NM_002834.3:c.1507G>C	NP_002825.3:p.Gly503Arg
	NM_001330437.1:c.1519G>C	NP_001317366.1:p.Gly507Arg
Ensemble	ENST00000351677.7:c.1507G>C	ENST00000351677.7:p.Gly503Arg
	ENST00000635625.1:c.1519G>C	ENST00000635625.1:p.Gly507Arg
	ENST00000639857.2:c.1507G>C	ENST00000639857.2:p.Gly503Arg
	ENST00000687906.1:c.1393G>C	ENST00000687906.1:p.Gly465Arg
	ENST00000688597.1:c.1224+6878G>C
	ENST00000690210.1:c.1507G>C	ENST00000690210.1:p.Gly503Arg

Summary

MGeND

Clinical significance	not provided
Variant entry	1
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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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
	COSMIC	COSM4384772	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
not provided		Acute myeloblastic leukaemia	somatic	MGS000005 (TMGS000006)	Keizo Horibe	National Hospital Organization Nagoya Medical Center

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2023-11-28	criteria provided, multiple submitters, no conflicts	RASopathy	germline	Detail
Pathogenic	2023-09-22	criteria provided, multiple submitters, no conflicts	not provided	germline unknown	Detail
Pathogenic	2017-05-18	criteria provided, single submitter	Noonan syndrome 1,LEOPARD syndrome 1,metachondromatosis,juvenile myelomonocytic leukemia	unknown	Detail
Pathogenic	2017-05-18	criteria provided, single submitter	Noonan syndrome 1,LEOPARD syndrome 1,metachondromatosis,juvenile myelomonocytic leukemia	unknown	Detail
Pathogenic	2017-05-18	criteria provided, single submitter	Noonan syndrome 1,LEOPARD syndrome 1,metachondromatosis,juvenile myelomonocytic leukemia	unknown	Detail
Pathogenic	2017-05-18	criteria provided, single submitter	Noonan syndrome 1,LEOPARD syndrome 1,metachondromatosis,juvenile myelomonocytic leukemia	unknown	Detail
Pathogenic	2018-03-23	criteria provided, single submitter	Noonan syndrome,juvenile myelomonocytic leukemia	germline	Detail
Pathogenic	2018-03-23	criteria provided, single submitter	Noonan syndrome,juvenile myelomonocytic leukemia	germline	Detail
Pathogenic	2024-03-26	criteria provided, multiple submitters, no conflicts	Noonan syndrome 1	germline maternal unknown	Detail
Pathogenic	2021-02-24	criteria provided, single submitter	Neurodevelopmental disorder	germline	Detail
Pathogenic	2020-10-28	criteria provided, single submitter		germline	Detail
Pathogenic	2023-02-24	criteria provided, single submitter	PTPN11-related disorder	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	Turner Syndrome, Male	NA	CLINVAR		Detail
0.694	Noonan syndrome	NA	CLINVAR		Detail
0.582	juvenile myelomonocytic leukemia	NA	CLINVAR		Detail
0.694	Noonan syndrome	The baby had no dysmorphic facial features and was diagnosed postmortem with Noo...	BeFree	24754368	Detail

Annotation

Annotations

Descrption	Source	Links
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND RASopathy	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND not provided	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND multiple conditions	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND multiple conditions	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND multiple conditions	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND multiple conditions	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND Noonan Syndrome with Juvenile Myelomonocytic Leukemi...	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND Noonan Syndrome with Juvenile Myelomonocytic Leukemi...	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND Noonan syndrome 1	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND Neurodevelopmental disorder	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND Cardiovascular phenotype	ClinVar	Detail
NM_002834.5(PTPN11):c.1507G>C (p.Gly503Arg) AND PTPN11-related disorder	ClinVar	Detail
NA	DisGeNET	Detail
NA	DisGeNET	Detail
NA	DisGeNET	Detail
The baby had no dysmorphic facial features and was diagnosed postmortem with Noonan syndrome by geno...	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: rs397507545 dbSNP
Genome: hg19
Position: chr12:112,926,887-112,926,887
Variant Type: snv
Reference Allele: G
Alternative Allele: C

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