chr1:45798838:C>T Detail (hg19) (MUTYH)

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

Information

Genome

Assembly	Position
hg19	chr1:45,798,838-45,798,838
hg38	chr1:45,333,166-45,333,166 View the variant detail on this assembly version.

HGVS

MUTYH

Type	Transcript	Protein
RefSeq	NM_001048171.1:c.351G>A	NP_001041636.1:p.Trp117Ter
	NM_001293190.1:c.351G>A	NP_001280119.1:p.Trp117Ter
	NM_001293192.1:c.351G>A	NP_001280121.1:p.Trp117Ter
	NM_012222.2:c.351G>A	NP_036354.1:p.Trp117Ter
	NM_001048174.1:c.309G>A	NP_001041639.1:p.Trp103Ter
	NM_001293191.1:c.309G>A	NP_001280120.1:p.Trp103Ter
	NM_001293195.1:c.309G>A	NP_001280124.1:p.Trp103Ter
	NM_001048172.1:c.309G>A	NP_001041637.1:p.Trp103Ter
	NM_001048173.1:c.309G>A	NP_001041638.1:p.Trp103Ter
	NM_001293196.1:c.309G>A	NP_001280125.1:p.Trp103Ter
Ensemble	ENST00000710952.2:c.393G>A	ENST00000710952.2:p.Trp131Ter
	ENST00000713750.1:c.309G>A	ENST00000713750.1:p.Trp103Ter
	ENST00000372110.7:c.354G>A	ENST00000372110.7:p.Trp118Ter
	ENST00000531105.5:c.115+1225G>A
	ENST00000672818.3:c.384G>A	ENST00000672818.3:p.Trp128Ter
	ENST00000372098.7:c.384G>A	ENST00000372098.7:p.Trp128Ter
	ENST00000448481.5:c.342G>A	ENST00000448481.5:p.Trp114Ter
	ENST00000529892.6:c.351G>A	ENST00000529892.6:p.Trp117Ter
	ENST00000713751.1:c.330G>A	ENST00000713751.1:p.Trp110Ter
	ENST00000488731.6:c.116-332G>A
	ENST00000372115.7:c.351G>A	ENST00000372115.7:p.Trp117Ter
	ENST00000529984.5:c.116-332G>A
	ENST00000354383.10:c.312G>A	ENST00000354383.10:p.Trp104Ter
	ENST00000456914.7:c.309G>A	ENST00000456914.7:p.Trp103Ter
	ENST00000483127.2:c.327G>A	ENST00000483127.2:p.Trp109Ter
	ENST00000672314.2:c.309G>A	ENST00000672314.2:p.Trp103Ter
	ENST00000412971.6:c.37-332G>A
	ENST00000528013.6:c.351G>A	ENST00000528013.6:p.Trp117Ter
	ENST00000372104.5:c.309G>A	ENST00000372104.5:p.Trp103Ter
	ENST00000355498.6:c.309G>A	ENST00000355498.6:p.Trp103Ter

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

MUTYH

Type	Database	ID	Link
Gene	MIM	604933	OMIM
	HGNC	7527	HGNC
	Ensembl	ENSG00000132781	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
Pathogenic Likely pathogenic	2021-03-04	criteria provided, multiple submitters, no conflicts	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2017-06-26	criteria provided, single submitter	not provided	germline	Detail
Pathogenic Likely pathogenic	2023-11-09	criteria provided, multiple submitters, no conflicts	familial adenomatous polyposis 2	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_001048174.2(MUTYH):c.309G>A (p.Trp103Ter) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_001048174.2(MUTYH):c.309G>A (p.Trp103Ter) AND not provided	ClinVar	Detail
NM_001048174.2(MUTYH):c.309G>A (p.Trp103Ter) AND Familial adenomatous polyposis 2	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: rs587781295 dbSNP
Genome: hg19
Position: chr1:45,798,838-45,798,838
Variant Type: snv
Reference Allele: C
Alternative Allele: T

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