chr1:45333436:G>A Detail (hg38) (MUTYH)

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

Information

Genome

Assembly	Position
hg19	chr1:45,799,108-45,799,108 View the variant detail on this assembly version.
hg38	chr1:45,333,436-45,333,436

HGVS

MUTYH

Type	Transcript	Protein
RefSeq	NM_001048172.1:c.241C>T	NP_001041637.1:p.Arg81Trp
	NM_001048173.1:c.241C>T	NP_001041638.1:p.Arg81Trp
	NM_001293196.1:c.241C>T	NP_001280125.1:p.Arg81Trp
	NM_001293195.1:c.241C>T	NP_001280124.1:p.Arg81Trp
	NM_001048171.1:c.283C>T	NP_001041636.1:p.Arg95Trp
	NM_001293190.1:c.283C>T	NP_001280119.1:p.Arg95Trp
	NM_001293192.1:c.283C>T	NP_001280121.1:p.Arg95Trp
	NM_012222.2:c.283C>T	NP_036354.1:p.Arg95Trp
	NM_001048174.1:c.241C>T	NP_001041639.1:p.Arg81Trp
	NM_001293191.1:c.241C>T	NP_001280120.1:p.Arg81Trp
Ensemble	ENST00000354383.10:c.244C>T	ENST00000354383.10:p.Arg82Trp
	ENST00000355498.6:c.241C>T	ENST00000355498.6:p.Arg81Trp
	ENST00000372098.7:c.316C>T	ENST00000372098.7:p.Arg106Trp
	ENST00000372104.5:c.241C>T	ENST00000372104.5:p.Arg81Trp
	ENST00000372110.7:c.286C>T	ENST00000372110.7:p.Arg96Trp
	ENST00000372115.7:c.283C>T	ENST00000372115.7:p.Arg95Trp
	ENST00000412971.6:c.37-602C>T
	ENST00000448481.5:c.274C>T	ENST00000448481.5:p.Arg92Trp
	ENST00000456914.7:c.241C>T	ENST00000456914.7:p.Arg81Trp
	ENST00000483127.2:c.259C>T	ENST00000483127.2:p.Arg87Trp
	ENST00000488731.6:c.116-602C>T
	ENST00000528013.6:c.283C>T	ENST00000528013.6:p.Arg95Trp
	ENST00000529892.6:c.283C>T	ENST00000529892.6:p.Arg95Trp
	ENST00000529984.5:c.116-602C>T
	ENST00000531105.5:c.115+955C>T
	ENST00000672314.2:c.241C>T	ENST00000672314.2:p.Arg81Trp
	ENST00000672818.3:c.316C>T	ENST00000672818.3:p.Arg106Trp
	ENST00000710952.2:c.325C>T	ENST00000710952.2:p.Arg109Trp
	ENST00000713750.1:c.241C>T	ENST00000713750.1:p.Arg81Trp
	ENST00000713751.1:c.262C>T	ENST00000713751.1:p.Arg88Trp

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

JP	HGVD:[No Data.]
	ToMMo:[No Data.]
	NCBN:[No Data.]
	NCBN(Hondo):[No Data.]
	NCBN(Ryukyu):[No Data.]
East asia	ExAC:<0.001

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	tgv298240835	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2023-10-10	criteria provided, multiple submitters, no conflicts	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic Likely pathogenic	2024-01-24	criteria provided, multiple submitters, no conflicts	familial adenomatous polyposis 2	germline unknown	Detail
Pathogenic Likely pathogenic	2021-11-03	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Pathogenic		no assertion criteria provided	Carcinoma of colon	unknown	Detail
Pathogenic	2021-07-01	no assertion criteria provided	Gastric cancer	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.241C>T (p.Arg81Trp) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) AND Familial adenomatous polyposis 2	ClinVar	Detail
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) AND not provided	ClinVar	Detail
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) AND Carcinoma of colon	ClinVar	Detail
NM_001048174.2(MUTYH):c.241C>T (p.Arg81Trp) AND Gastric cancer	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: rs765123255 dbSNP
Genome: hg38
Position: chr1:45,333,436-45,333,436
Variant Type: snv
Reference Allele: G
Alternative Allele: A
East Asian Chromosome Counts (ExAC): 8654
East Asian Allele Counts (ExAC): 0
East Asian Heterozygous Counts (ExAC): 0
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 0.0
Chromosome Counts in All Race (ExAC): 121394
Allele Counts in All Race (ExAC): 6
Heterozygous Counts in All Race (ExAC): 6
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 4.9425836532283306E-5

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