chr12:25362828:G>C Detail (hg19) (KRAS)

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

Genome

Assembly	Position
hg19	chr12:25,362,828-25,362,828
hg38	chr12:25,209,894-25,209,894 View the variant detail on this assembly version.

HGVS

KRAS

Type	Transcript	Protein
RefSeq	NM_004985.4:c.468C>G	NP_004976.2:p.Phe156Leu
	NM_033360.3:c.468C>G	NP_203524.1:p.Phe156Leu
Ensemble	ENST00000311936.8:c.468C>G	ENST00000311936.8:p.Phe156Leu
	ENST00000693229.1:c.393C>G	ENST00000693229.1:p.Phe131Leu
	ENST00000692768.1:c.270C>G	ENST00000692768.1:p.Phe90Leu
	ENST00000685328.1:c.468C>G	ENST00000685328.1:p.Phe156Leu
	ENST00000557334.6:c.129C>G	ENST00000557334.6:p.Phe43Leu
	ENST00000688940.1:c.468C>G	ENST00000688940.1:p.Phe156Leu
	ENST00000256078.10:c.*22C>G

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

KRAS

Type	Database	ID	Link
Gene	MIM	190070	OMIM
	HGNC	6407	HGNC
	Ensembl	ENSG00000133703	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM5347094	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2008-05-01	no assertion criteria provided	cardiofaciocutaneous syndrome 2	germline	Detail
Pathogenic	2017-05-19	criteria provided, single submitter	not provided	germline	Detail
Pathogenic	2021-08-31	criteria provided, single submitter	RASopathy	germline	Detail
Pathogenic	2023-03-29	criteria provided, single submitter	KRAS-related disorder	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.240	cardiofaciocutaneous syndrome 2	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_033360.4(KRAS):c.*22C>G AND Cardiofaciocutaneous syndrome 2	ClinVar	Detail
NM_033360.4(KRAS):c.*22C>G AND not provided	ClinVar	Detail
NM_033360.4(KRAS):c.*22C>G AND RASopathy	ClinVar	Detail
NM_033360.4(KRAS):c.*22C>G AND KRAS-related disorder	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: rs104894362 dbSNP
Genome: hg19
Position: chr12:25,362,828-25,362,828
Variant Type: snv
Reference Allele: G
Alternative Allele: C

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