NM_001048174.2(MUTYH):c.1131G>C (p.Pro377=) AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (1 submission)
Last evaluated:: Aug 13, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV003367918.2

Allele description [Variation Report for NM_001048174.2(MUTYH):c.1131G>C (p.Pro377=)]

NM_001048174.2(MUTYH):c.1131G>C (p.Pro377=)

Gene:

MUTYH:mutY DNA glycosylase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p34.1

Genomic location:

Preferred name:

NM_001048174.2(MUTYH):c.1131G>C (p.Pro377=)

HGVS:

NC_000001.11:g.45331528C>G
NG_008189.1:g.13943G>C
NM_001048171.2:c.1131G>C
NM_001048172.2:c.1134G>C
NM_001048173.2:c.1131G>C
NM_001048174.2:c.1131G>CMANE SELECT
NM_001128425.2:c.1215G>C
NM_001293190.2:c.1176G>C
NM_001293191.2:c.1164G>C
NM_001293192.2:c.855G>C
NM_001293195.2:c.1131G>C
NM_001293196.2:c.855G>C
NM_001350650.2:c.786G>C
NM_001350651.2:c.786G>C
NM_001407069.1:c.1164G>C
NM_001407070.1:c.1131G>C
NM_001407071.1:c.1134G>C
NM_001407072.1:c.1131G>C
NM_001407073.1:c.1131G>C
NM_001407075.1:c.1047G>C
NM_001407077.1:c.1164G>C
NM_001407078.1:c.1134G>C
NM_001407079.1:c.1092G>C
NM_001407080.1:c.1089G>C
NM_001407081.1:c.1131G>C
NM_001407082.1:c.786G>C
NM_001407083.1:c.1173G>C
NM_001407085.1:c.1173G>C
NM_001407086.1:c.1134G>C
NM_001407087.1:c.1152G>C
NM_001407088.1:c.1131G>C
NM_001407089.1:c.1131G>C
NM_001407091.1:c.855G>C
NM_012222.3:c.1206G>C
NP_001041636.2:p.Pro377=
NP_001041637.1:p.Pro378=
NP_001041638.1:p.Pro377=
NP_001041639.1:p.Pro377=
NP_001121897.1:p.Pro405=
NP_001121897.1:p.Pro405=
NP_001280119.1:p.Pro392=
NP_001280120.1:p.Pro388=
NP_001280121.1:p.Pro285=
NP_001280124.1:p.Pro377=
NP_001280125.1:p.Pro285=
NP_001337579.1:p.Pro262=
NP_001337580.1:p.Pro262=
NP_001393998.1:p.Pro388=
NP_001393999.1:p.Pro377=
NP_001394000.1:p.Pro378=
NP_001394001.1:p.Pro377=
NP_001394002.1:p.Pro377=
NP_001394004.1:p.Pro349=
NP_001394006.1:p.Pro388=
NP_001394007.1:p.Pro378=
NP_001394008.1:p.Pro364=
NP_001394009.1:p.Pro363=
NP_001394010.1:p.Pro377=
NP_001394011.1:p.Pro262=
NP_001394012.1:p.Pro391=
NP_001394014.1:p.Pro391=
NP_001394015.1:p.Pro378=
NP_001394016.1:p.Pro384=
NP_001394017.1:p.Pro377=
NP_001394018.1:p.Pro377=
NP_001394020.1:p.Pro285=
NP_036354.1:p.Pro402=
LRG_220t1:c.1215G>C
LRG_220:g.13943G>C
LRG_220p1:p.Pro405=
NC_000001.10:g.45797200C>G
NM_001128425.1:c.1215G>C
NR_146882.2:n.1359G>C
NR_146883.2:n.1208G>C
NR_176269.1:n.1355G>C
NR_176270.1:n.1295G>C
NR_176271.1:n.1218G>C
NR_176272.1:n.1282G>C
NR_176273.1:n.1240G>C
NR_176274.1:n.1295G>C

Molecular consequence:

NR_146882.2:n.1359G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_146883.2:n.1208G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176269.1:n.1355G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176271.1:n.1218G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176272.1:n.1282G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176273.1:n.1240G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176274.1:n.1295G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_001048171.2:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001048172.2:c.1134G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001048173.2:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001048174.2:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001128425.2:c.1215G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001293190.2:c.1176G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001293191.2:c.1164G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001293192.2:c.855G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001293195.2:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001293196.2:c.855G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001350650.2:c.786G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001350651.2:c.786G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407069.1:c.1164G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407070.1:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407071.1:c.1134G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407072.1:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407073.1:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407075.1:c.1047G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407077.1:c.1164G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407078.1:c.1134G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407079.1:c.1092G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407080.1:c.1089G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407081.1:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407082.1:c.786G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407083.1:c.1173G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407085.1:c.1173G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407086.1:c.1134G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407087.1:c.1152G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407088.1:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407089.1:c.1131G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001407091.1:c.855G>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_012222.3:c.1206G>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

Recent activity

Clear Turn Off Turn On

COX6A subunit VIa of cytochrome c oxidase [Agaricus bisporus var. bisporus H97]
COX6A subunit VIa of cytochrome c oxidase [Agaricus bisporus var. bisporus H97]
gi|426201798|gb|EKV51721.1||gnl|WGS |AGABI2DRAFT_133378

Protein
Cytochrome c oxidase subunit 6a [Picochlorum sp. SENEW3]
Cytochrome c oxidase subunit 6a [Picochlorum sp. SENEW3]
gi|2629885730|gnl|PSENEW3|PSENEW3_0 32-RA:cds|gb|WPT15291.1|

Protein
UNVERIFIED: Meiogyne virgata voucher PSU Leeratiwong 17-952 COX6A gene, partial ...
UNVERIFIED: Meiogyne virgata voucher PSU Leeratiwong 17-952 COX6A gene, partial sequence
gi|2515603443|gb|OP739722.1|

Nucleotide
Agaricus bisporus var. bisporus H97 COX6A subunit VIa of cytochrome c oxidase (A...
Agaricus bisporus var. bisporus H97 COX6A subunit VIa of cytochrome c oxidase (AGABI2DRAFT_133378), mRNA
gi|568436679|ref|XM_006454637.1||gn _WGS:AEOK|mrna.AGABI2DRAFT_133378

Nucleotide
PREDICTED: Bos taurus aldehyde dehydrogenase 6 family member A1 (ALDH6A1), trans...
PREDICTED: Bos taurus aldehyde dehydrogenase 6 family member A1 (ALDH6A1), transcript variant X2, mRNA
gi|2587622020|ref|XM_024997298.2|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004055759	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Aug 13, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004055759

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Aug 13, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004055759.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine