chr3:12585761:C>T Detail (hg38) (RAF1, MKRN2)

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

Genome

Assembly	Position
hg19	chr3:12,627,260-12,627,260 View the variant detail on this assembly version.
hg38	chr3:12,585,761-12,585,761

HGVS

MKRN2
RAF1

Type	Transcript	Protein
RefSeq
Ensemble	ENST00000676541.1:c.*3508C>T
	ENST00000677142.1:c.*3508C>T

Type	Transcript	Protein
RefSeq	NM_002880.3:c.1456G>A	NP_002871.1:p.Asp486Asn
Ensemble	ENST00000251849.9:c.1456G>A	ENST00000251849.9:p.Asp486Asn
	ENST00000442415.7:c.1516G>A	ENST00000442415.7:p.Asp506Asn
	ENST00000685437.1:c.1357G>A	ENST00000685437.1:p.Asp453Asn
	ENST00000685653.1:c.1456G>A	ENST00000685653.1:p.Asp486Asn
	ENST00000687923.1:c.1345G>A	ENST00000687923.1:p.Asp449Asn
	ENST00000688543.1:c.1357G>A	ENST00000688543.1:p.Asp453Asn
	ENST00000689389.1:c.1279G>A	ENST00000689389.1:p.Asp427Asn
	ENST00000690397.1:c.1345G>A	ENST00000690397.1:p.Asp449Asn
	ENST00000690460.1:c.1444G>A	ENST00000690460.1:p.Asp482Asn
	ENST00000691899.1:c.1456G>A	ENST00000691899.1:p.Asp486Asn
	ENST00000692093.1:c.1357G>A	ENST00000692093.1:p.Asp453Asn
	ENST00000693312.1:c.1231G>A	ENST00000693312.1:p.Asp411Asn

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	not provided
Review star
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Links

MKRN2
RAF1

Type	Database	ID	Link
Gene	MIM	608426	OMIM
	HGNC	7113	HGNC
	Ensembl	ENSG00000075975	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Type	Database	ID	Link
Gene	MIM	164760	OMIM
	HGNC	9829	HGNC
	Ensembl	ENSG00000132155	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
not provided		no assertion provided	Noonan syndrome with multiple lentigines	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.369	LEOPARD Syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_002880.4(RAF1):c.1456G>A (p.Asp486Asn) AND Noonan syndrome with multiple lentigines	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: rs80338798 dbSNP
Genome: hg38
Position: chr3:12,585,761-12,585,761
Variant Type: snv
Reference Allele: C
Alternative Allele: T

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